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The global, regional, and national burden of inflammatory bowel disease in 195 countries and territories, 1990-2017: a systematic analysis for the Global Burden of Disease Study 2017 Gbd 2017 Inflammatory Bowel Dis Co, Alatab S, Sepanlou Sg, Ikuta K, Vahedi H, Bisignano C, et al LANCET GASTROENTEROLOGY & HEPATOLOGY 2020;5(1):17-30
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The global, regional, and national burden of inflammatory bowel disease in 195 countries and territories, 1990-2017: a systematic analysis for the Global Burden of Disease Study 2017 Gbd 2017 Inflammatory Bowel Disease Collaborators The lancet. Gastroenterology & hepatology 2020;5(1):17-30
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The global, regional, and national burden of stomach cancer in 195 countries, 1990-2017: a systematic analysis for the Global Burden of Disease study 2017 Gbd 2017 Stomach Canc Collaborator, Etemadi A, Safiri S, Sepanlou Sg, Ikuta K, Bisignano C, et al LANCET GASTROENTEROLOGY & HEPATOLOGY 2020;5(1):42-54
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The global, regional, and national burden of stomach cancer in 195 countries, 1990-2017: a systematic analysis for the Global Burden of Disease study 2017 Gbd 2017 Stomach Cancer Collaborators The lancet. Gastroenterology & hepatology 2020;5(1):42-54
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Abnormality in the T cell repertoire contributes to immunodeficiency in patients with DNA repair/methylation defects Fang M, Su Z, Abolhassani H, Jiang C, Cheng B, Li T, et al EUROPEAN JOURNAL OF IMMUNOLOGY 2019;:28-28
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Ataxia-telangiectasia: A review of clinical features and molecular pathology Amirifar P, Ranjouri Mr, Yazdani R, Abolhassani H, Aghamohammadi A Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology 2019;30(3):277-288
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Bronchiectasis in common variable immunodeficiency: A systematic review and meta-analysis Ramzi N, Jamee M, Bakhtiyari M, Rafiemanesh H, Zainaldain H, Tavakol M, et al Pediatric pulmonology 2019;():-
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Candidiasis associated with very early onset inflammatory bowel disease: First IL10RB deficient case from the National Iranian Registry and review of the literature Yazdani R, Moazzami B, Madani Sp, Behniafard N, Azizi G, Aflatoonian M, et al Clinical immunology (Orlando, Fla.) 2019;205():35-42
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Challenges in investigating patients with isolated decreased serum IgM: The SIMcal study Simcal Consortium, Janssen Lma, Van Hout Rwnm, De Vries E Scandinavian journal of immunology 2019;89(6):e12763-
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Clinical, Immunological, and Genetic Features in Patients with Activated PI3Kδ Syndrome (APDS): a Systematic Review Jamee M, Moniri S, Zaki-dizaji M, Olbrich P, Yazdani R, Jadidi-niaragh F, et al Clinical reviews in allergy & immunology 2019;():-
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Clinical, Immunologic, and Molecular Spectrum of Patients with LPS-Responsive Beige-Like Anchor Protein Deficiency: A Systematic Review Habibi S, Zaki-dizaji M, Rafiemanesh H, Lo B, Jamee M, Gámez-díaz L, et al The journal of allergy and clinical immunology. In practice 2019;7(7):2379-2386.e5
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Clinical implications of systematic phenotyping and exome sequencing in patients with primary antibody deficiency Abolhassani H, Aghamohammadi A, Fang M, Rezaei N, Jiang C, Liu X, et al Genetics in medicine : official journal of the American College of Medical Genetics 2019;21(1):243-251
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Clinical Manifestations, Immunological Characteristics and Genetic Analysis of Patients with Hyper-Immunoglobulin M Syndrome in Iran Tafakori Delbari M, Cheraghi T, Yazdani R, Fekrvand S, Delavari S, Azizi G, et al International archives of allergy and immunology 2019;180(1):52-63
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Common Variable Immunodeficiency: Epidemiology, Pathogenesis, Clinical manifestations, Diagnosis, Classification and Management Yazdani R, Habibi S, Sharifi L, Azizi G, Abolhassani H, Olbrich P, et al Journal of investigational allergology & clinical immunology 2019;():0-
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Comparison of clinical and immunological features and mortality in common variable immunodeficiency and agammaglobulinemia patients Bagheri Y, Vosughi A, Azizi G, Yazdani R, Kiaee F, Hafezi N, et al Immunology letters 2019;210():55-62
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Comparison of Common Monogenic Defects in a Large Predominantly Antibody Deficiency Cohort Yazdani R, Abolhassani H, Kiaee F, Habibi S, Azizi G, Tavakol M, et al The journal of allergy and clinical immunology. In practice 2019;7(3):864-878.e9
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Compound Heterozygous Mutations of IL2-Inducible T cell Kinase in a Swedish Patient: the Importance of Early Genetic Diagnosis Fang M, Abolhassani H, Pan-hammarström Q, Sandholm E, Liu X, Hammarström L Journal of clinical immunology 2019;39(2):131-134
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Cutaneous Granulomatosis and Class Switching Defect as a Presenting Sign in Ataxia-Telangiectasia: First Case from the National Iranian Registry and Review of the Literature Amirifar P, Yazdani R, Moeini Shad T, Ghanadan A, Abolhassani H, Lavin M, et al Immunological investigations 2019;():1-14
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Diagnostic Approach to The Patients with Suspected Primary Immunodeficiency Tavakol M, Jamee M, Azizi G, Sadri H, Bagheri Y, Zaki-dizaji M, et al Endocrine, metabolic & immune disorders drug targets 2019;():-
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Different Clinical Manifestations in a Large Cohort of Predominantly Antibody Deficiency Patients with Monogenic Defects Yazdani R, Abolhassani H, Aghamohammadi A JOURNAL OF CLINICAL IMMUNOLOGY 2019;:S7-S8
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Fifteen Years of the J Project J Project Study Group, Maródi L Journal of clinical immunology 2019;39(4):363-369
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G2-lymphocyte chromosomal radiosensitivity in patients with LPS responsive beige-like anchor protein (LRBA) deficiency Mozdarani H, Kiaee F, Fekrvand S, Azizi G, Yazdani R, Zaki-dizaji M, et al International journal of radiation biology 2019;95(6):680-690
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Generation of a human induced pluripotent stem cell line (PHAi003) from a primary immunodeficient patient with CD70 mutation Arias-fuenzalida J, Yu J, Abolhassani H, Du L, Custodio J, Pan-hammarström Q Stem cell research 2019;41():101612-
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Genetic mutations and immunological features of severe combined immunodeficiency patients in Iran Shahbazi Z, Yazdani R, Shahkarami S, Shahbazi S, Hamid M, Sadeghi-shabestari M, et al Immunology letters 2019;216():70-78
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Graft versus host disease and microchimerism in a JAK3 deficient patient Shahbazi Z, Parvaneh N, Shahbazi S, Rahimi H, Hamid M, Shahbazi D, et al Allergy, asthma, and clinical immunology : official journal of the Canadian Society of Allergy and Clinical Immunology 2019;15():47-
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IL2RG hypomorphic mutation: identification of a novel pathogenic mutation in exon 8 and a review of the literature Lim Ck, Abolhassani H, Appelberg Sk, Sundin M, Hammarström L Allergy, asthma, and clinical immunology : official journal of the Canadian Society of Allergy and Clinical Immunology 2019;15():2-
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Infectious etiology of chronic diarrhea in patients with primary immunodeficiency diseases Parvaneh L, Sharifi N, Azizi G, Abolhassani H, Sharifi L, Mohebbi A, et al European annals of allergy and clinical immunology 2019;51(1):32-37
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Leishmaniasis and autoimmunity in patient with LPS-responsive beige-like anchor protein (LRBA) deficiency Salami F, Shirkani A, Shahrooei M, Azizi G, Yazdani R, Abolhassani H, et al Endocrine, metabolic & immune disorders drug targets 2019;():-
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Malignancy in common variable immunodeficiency: a systematic review and meta-analysis Kiaee F, Azizi G, Rafiemanesh H, Zainaldain H, Sadaat Rizvi F, Alizadeh M, et al Expert review of clinical immunology 2019;15(10):1105-1113
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Mendelian susceptibility to mycobacterial disease: Clinical and immunological findings of patients suspected for IL12Rβ1 deficiency Moradi L, Cheraghi T, Yazdani R, Azizi G, Rasouli S, Zavareh Ft, et al Allergologia et immunopathologia 2019;47(5):491-498
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Outcomes and Treatment Strategies for Autoimmunity and Hyperinflammation in Patients with RAG Deficiency Farmer Jr, Foldvari Z, Ujhazi B, De Ravin Ss, Chen K, Bleesing Jjh, et al The journal of allergy and clinical immunology. In practice 2019;7(6):1970-1985.e4
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PIK3R1 Mutation Associated with Hyper IgM (APDS2 Syndrome): A Case Report and Review of the Literature Yazdani R, Hamidi Z, Babaha F, Azizi G, Fekrvand S, Abolhassani H, et al Endocrine, metabolic & immune disorders drug targets 2019;19(7):941-958
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Respiratory Complications in Patients with Hyper IgM Syndrome Moazzami B, Yazdani R, Azizi G, Kiaei F, Tafakori M, Modaresi M, et al Journal of clinical immunology 2019;39(6):557-568
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The evaluation of neutropenia in common variable immune deficiency patients Ghorbani M, Fekrvand S, Shahkarami S, Yazdani R, Sohani M, Shaghaghi M, et al Expert review of clinical immunology 2019;15(11):1225-1233
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The first cohort of Iranian patients with hyper immunoglobulin E syndrome: A long-term follow-up and genetic analysis Tavassoli M, Abolhassani H, Yazdani R, Ghadami M, Azizi G, Abdolrahim Poor Heravi S, et al Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology 2019;30(4):469-478
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The First Purine Nucleoside Phosphorylase Deficiency Patient Resembling IgA Deficiency and a Review of the Literature Fekrvand S, Yazdani R, Abolhassani H, Ghaffari J, Aghamohammadi A Immunological investigations 2019;48(4):410-430
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The Heterogeneous Pathogenesis of Selective Immunoglobulin A Deficiency Bagheri Y, Sanaei R, Yazdani R, Shekarabi M, Falak R, Mohammadi J, et al International archives of allergy and immunology 2019;179(3):231-246
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The hyper IgM syndromes: Epidemiology, pathogenesis, clinical manifestations, diagnosis and management Yazdani R, Fekrvand S, Shahkarami S, Azizi G, Moazzami B, Abolhassani H, et al Clinical immunology (Orlando, Fla.) 2019;198():19-30
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The profile of IL-4, IL-5, IL-10 and GATA3 in patients with LRBA deficiency and CVID with no known monogenic disease: Association with disease severity Azizi G, Bagheri Y, Yazdani R, Zaki-dizaji M, Jamee M, Jadidi-niaragh F, et al Allergologia et immunopathologia 2019;47(2):172-178
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Treatment forms and clinical course of LPS-Responsive beige-like anchor protein deficiency and introduction of the immune deficiency and -dysregulation activity (=IDDA) score Tesch Vk, Abolhassani H, Grimbacher B, Lankaster A, Gennery A, Shadur B, et al BONE MARROW TRANSPLANTATION 2019;:98-99
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UNC13D Deficiency Associated With Epileptic Seizures and Antibody Deficiency: The First Case from the Iranian National Registry Yazdani R, Amirifar P, Abolhassani H, Azizi G, Parvaneh N, Rezaei N, et al Journal of investigational allergology & clinical immunology 2019;29(2):160-162
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Vaccine-Derived Poliovirus Infection among Patients with Primary Immunodeficiency and Effect of Patient Screening on Disease Outcomes, Iran Shaghaghi M, Shahmahmoodi S, Nili A, Abolhassani H, Madani Sp, Nejati A, et al Emerging infectious diseases 2019;25(11):2005-2012
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Application of next generation sequencing in the conundrum of primary antibody deficiency Abolhassani H, Aghamohammadi A, Rezaei N, Pan-hammarstrom Q, Hammarstrom L EUROPEAN JOURNAL OF HUMAN GENETICS 2018;:313-313
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Autoimmunity and its association with regulatory T cells and B cell subsets in patients with common variable immunodeficiency Azizi G, Abolhassani H, Kiaee F, Tavakolinia N, Rafiemanesh H, Yazdani R, et al Allergologia et immunopathologia 2018;46(2):127-135
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Circulating Helper T-Cell Subsets and Regulatory T Cells in Patients With Common Variable Immunodeficiency Without Known Monogenic Disease Azizi G, Mirshafiey A, Abolhassani H, Yazdani R, Jafarnezhad-ansariha F, Shaghaghi M, et al Journal of investigational allergology & clinical immunology 2018;28(3):172-181
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Clearing Vaccine-Derived Poliovirus Infection Following Hematopoietic Stem Cell Transplantation: a Case Report and Review of Literature Shaghaghi M, Irannejad M, Abolhassani H, Shahmahmoodi S, Hamidieh Aa, Soleyman-jahi S, et al Journal of clinical immunology 2018;38(5):610-616
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Clinical, immunologic, and genetic spectrum of 696 patients with combined immunodeficiency Abolhassani H, Chou J, Bainter W, Platt Cd, Tavassoli M, Momen T, et al The Journal of allergy and clinical immunology 2018;141(4):1450-1458
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CTLA-4 Expression in CD4+ T Cells From Patients With LRBA Deficiency and Common Variable Immunodeficiency With No Known Monogenic Disease Azizi G, Jamee M, Yazdani R, Bagheri Y, Fayyaz F, Jadidi-niaragh F, et al Journal of investigational allergology & clinical immunology 2018;28(6):422-424
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Defects in plasma cell differentiation are associated with primary immunodeficiency in human subjects Pan-hammarström Q, Abolhassani H, Hammarström L The Journal of allergy and clinical immunology 2018;141(4):1217-1219
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Disease Evolution and Response to Rapamycin in Activated Phosphoinositide 3-Kinase δ Syndrome: The European Society for Immunodeficiencies-Activated Phosphoinositide 3-Kinase δ Syndrome Registry Maccari Me, Abolhassani H, Aghamohammadi A, Aiuti A, Aleinikova O, Bangs C, et al Frontiers in immunology 2018;9():543-
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Fourth Update on the Iranian National Registry of Primary Immunodeficiencies: Integration of Molecular Diagnosis Abolhassani H, Kiaee F, Tavakol M, Chavoshzadeh Z, Mahdaviani Sa, Momen T, et al Journal of clinical immunology 2018;38(7):816-832
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Heterozygous Mutations in NFKB2 Exhibit a Broad Clinical Phenotype Newman En, Feusier J, Jacob Sp, Jorde Lb, Hill Hr, Hanson C, et al JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY 2018;141(2):AB21-AB21
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Inflammation, a significant player of Ataxia-Telangiectasia pathogenesis? Zaki-dizaji M, Akrami Sm, Azizi G, Abolhassani H, Aghamohammadi A Inflammation research : official journal of the European Histamine Research Society ... [et al.] 2018;67(7):559-570
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In vitro chromosomal radiosensitivity in patients with common variable immunodeficiency Mahmoodi M, Abolhassani H, Mozdarani H, Rezaei N, Azizi G, Yazdani R, et al CENTRAL EUROPEAN JOURNAL OF IMMUNOLOGY 2018;43(2):155-161
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Mannose-Binding Lectin Protein Deficiency Among Patients with Primary Immunodeficiency Disease Receiving IVIG Therapy Azizi G, Kiaee F, Yaslianifard S, Rafiemanesh H, Mohammadikhajehdehi S, Mohammadi H, et al Endocrine, metabolic & immune disorders drug targets 2018;18(2):175-183
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Monogenic polyautoimmunity in primary immunodeficiency diseases Azizi G, Yazdani R, Rae W, Abolhassani H, Rojas M, Aghamohammadi A, et al Autoimmunity reviews 2018;17(10):1028-1039
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New insights into physiopathology of immunodeficiency-associated vaccine-derived poliovirus infection; systematic review of over 5 decades of data Shaghaghi M, Soleyman-jahi S, Abolhassani H, Yazdani R, Azizi G, Rezaei N, et al Vaccine 2018;36(13):1711-1719
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Polyautoimmunity in Patients with LPS-Responsive Beige-Like Anchor (LRBA) Deficiency Azizi G, Abolhassani H, Zaki-dizaji M, Habibi S, Mohammadi H, Shaghaghi M, et al Immunological investigations 2018;47(5):457-467
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Predictive markers for humoral influenza vaccine response in patients with common variable immunodeficiency Gardulf A, Abolhassani H, Gustafson R, Eriksson Le, Hammarström L The Journal of allergy and clinical immunology 2018;142(6):1922-1931.e2
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Rheumatologic complications in a cohort of 227 patients with common variable immunodeficiency Azizi G, Kiaee F, Hedayat E, Yazdani R, Dolatshahi E, Alinia T, et al Scandinavian journal of immunology 2018;87(5):e12663-
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Systematic investigation for underlying causes of recurrent infections in children: surveillance of primary immunodeficiency Yousefzadegan S, Tavakol M, Abolhassani H, Nadjafi A, Mansouri S, Yazdani R, et al European annals of allergy and clinical immunology 2018;50(2):72-80
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Targeted next-generation sequencing for genetic diagnosis of 160 patients with primary immunodeficiency in south China Xia Y, He T, Luo Y, Li C, Lim Ck, Abolhassani H, et al Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology 2018;29(8):863-872
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The Clinical and Immunological Features of Patients with Primary Antibody Deficiencies Azizi G, Bagheri Y, Tavakol M, Askarimoghaddam F, Porrostami K, Rafiemanesh H, et al Endocrine, metabolic & immune disorders drug targets 2018;18(5):537-545
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The imbalance of circulating T helper subsets and regulatory T cells in patients with LRBA deficiency: Correlation with disease severity Azizi G, Mirshafiey A, Abolhassani H, Yazdani R, Ghanavatinejad A, Noorbakhsh F, et al Journal of cellular physiology 2018;233(11):8767-8777
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Tuberculosis and impaired IL-23-dependent IFN-γ immunity in humans homozygous for a common TYK2 missense variant Boisson-dupuis S, Ramirez-alejo N, Li Z, Patin E, Rao G, Kerner G, et al Science immunology 2018;3(30):-
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Two Faces of LRBA Deficiency in Siblings: Hypogammaglobulinemia and Normal Immunoglobulin Levels Azizi G, Abolhassani H, Habibi S, Rahamooz T, Mohammadi H, Jafarnezhad-ansariha F, et al Journal of investigational allergology & clinical immunology 2018;28(1):48-50
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A Comparison of Clinical and Immunologic Phenotypes in Familial and Sporadic Forms of Common Variable Immunodeficiency Valizadeh A, Yazdani R, Azizi G, Abolhassani H, Aghamohammadi A Scandinavian journal of immunology 2017;86(4):239-247
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Approach to the Management of Autoimmunity in Primary Immunodeficiency Azizi G, Ziaee V, Tavakol M, Alinia T, Yazdai R, Mohammadi H, et al Scandinavian journal of immunology 2017;85(1):13-29
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Ataxia telangiectasia syndrome: moonlighting ATM Zaki-dizaji M, Akrami Sm, Abolhassani H, Rezaei N, Aghamohammadi A Expert review of clinical immunology 2017;13(12):1155-1172
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Autoimmunity in a cohort of 471 patients with primary antibody deficiencies Azizi G, Tavakol M, Rafiemanesh H, Kiaee F, Yazdani R, Heydari A, et al Expert review of clinical immunology 2017;13(11):1099-1106
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Autoimmunity in common variable immunodeficiency: epidemiology, pathophysiology and management Azizi G, Abolhassani H, Asgardoon Mh, Alinia T, Yazdani R, Mohammadi J, et al Expert review of clinical immunology 2017;13(2):101-115
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Cernunnos deficiency associated with BCG adenitis and autoimmunity: First case from the national Iranian registry and review of the literature Yazdani R, Abolhassani H, Tafaroji J, Azizi G, Hamidieh Aa, Chou J, et al Clinical immunology (Orlando, Fla.) 2017;183():201-206
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Clinical, immunologic, molecular analyses and outcomes of iranian patients with LRBA deficiency: A longitudinal study Azizi G, Abolhassani H, Mahdaviani Sa, Chavoshzadeh Z, Eshghi P, Yazdani R, et al Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology 2017;28(5):478-484
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Combined immunodeficiency and Epstein-Barr virus-induced B cell malignancy in humans with inherited CD70 deficiency Abolhassani H, Edwards Esj, Ikinciogullari A, Jing He, Borte S, Buggert M, et al JOURNAL OF EXPERIMENTAL MEDICINE 2017;214(1):91-106
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COMBINED IMMUNODEFICIENCY AND EPSTEIN-BARR VIRUS-INDUCED B CELL MALIGNANCY IN HUMANS WITH INHERITED CD70 DEFICIENCY Jing He, Abolhassani H, Edwards Esj, Ikinciogullari Ka, Borte S, Buggert M, et al JOURNAL OF CLINICAL IMMUNOLOGY 2017;37(2):230-230
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Comparison of Bone Mineral Density in Common Variable Immunodeficiency and X-Linked Agammaglobulinaemia Patients Mohebbi A, Azizi G, Tavakolinia N, Abbasi F, Sayarifard F, Karimipour M, et al Endocrine, metabolic & immune disorders drug targets 2017;17(2):134-140
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Comparison of various classifications for patients with common variable immunodeficiency (CVID) using measurement of B-cell subsets Yazdani R, Seify R, Ganjalikhani-hakemi M, Abolhassani H, Eskandari N, Golsaz-shirazi F, et al Allergologia et immunopathologia 2017;45(2):183-192
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Costs of Hospital Admission on Primary Immunodeficiency Diseases Gholami K, Laali E, Abolhassani H, Ahmadvand A, Mohebbi N, Javadi Mr, et al IRANIAN JOURNAL OF PUBLIC HEALTH 2017;46(3):342-350
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Epidemiology and pathophysiology of malignancy in common variable immunodeficiency? Tak Manesh A, Azizi G, Heydari A, Kiaee F, Shaghaghi M, Hossein-khannazer N, et al Allergologia et immunopathologia 2017;45(6):602-615
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Evaluation of infectious and non-infectious complications in patients with primary immunodeficiency Bazregari S, Azizi G, Tavakol M, Asgardoon Mh, Kiaee F, Tavakolinia N, et al CENTRAL EUROPEAN JOURNAL OF IMMUNOLOGY 2017;42(4):336-341
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Impaired Akt phosphorylation in B-cells of patients with common variable immunodeficiency Yazdani R, Ganjalikhani-hakemi M, Esmaeili M, Abolhassani H, Vaeli S, Rezaei A, et al Clinical immunology (Orlando, Fla.) 2017;175():124-132
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Infectious and Noninfectious Pulmonary Complications in Patients With Primary Immunodeficiency Disorders Yazdani R, Abolhassani H, Asgardoon Mh, Shaghaghi M, Modaresi M, Azizi G, et al Journal of investigational allergology & clinical immunology 2017;27(4):213-224
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Long-term outcomes of 176 patients with X-linked hyper-IgM syndrome treated with or without hematopoietic cell transplantation De La Morena Mt, Leonard D, Torgerson Tr, Cabral-marques O, Slatter M, Aghamohammadi A, et al The Journal of allergy and clinical immunology 2017;139(4):1282-1292
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Measurement of Health-Related Quality of Life in Primary Antibody-Deficient Patients Ataeinia B, Montazeri A, Tavakol M, Azizi G, Kiaee F, Tavakolinia N, et al Immunological investigations 2017;46(4):329-340
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New therapeutic approach by sirolimus for enteropathy treatment in patients with LRBA deficiency Azizi G, Abolhassani H, Yazdani R, Mohammadikhajehdehi S, Parvaneh N, Negahdari B, et al European annals of allergy and clinical immunology 2017;49(5):235-239
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Novel Mutation of ZAP-70-related Combined Immunodeficiency: First Case from the National Iranian Registry and Review of the Literature Shirkani A, Shahrooei M, Azizi G, Rokni-zadeh H, Abolhassani H, Farrokhi S, et al Immunological investigations 2017;46(1):70-79
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Patients with Primary Immunodeficiencies Are a Reservoir of Poliovirus and a Risk to Polio Eradication Jmf Centers Network Investigators, Aghamohammadi A, Abolhassani H, Kutukculer N, Wassilak Sg, Pallansch Ma, et al FRONTIERS IN IMMUNOLOGY 2017;:685-
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Preference of Genetic Diagnosis of CXCR4 Mutation Compared with Clinical Diagnosis of WHIM Syndrome Aghamohammadi A, Abolhassani H, Puchalka J, Greif-kohistani N, Zoghi S, Klein C, et al Journal of clinical immunology 2017;37(3):282-286
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Role of Apoptosis in the Pathogenesis of Common Variable Immunodeficiency (CVID) Ganjalikhani-hakemi M, Yazdani R, Esmaeili M, Abolhassani H, Rae W, Azizi G, et al Endocrine, metabolic & immune disorders drug targets 2017;17(4):332-340
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Selective IgA Deficiency: Epidemiology, Pathogenesis, Clinical Phenotype, Diagnosis, Prognosis and Management Yazdani R, Azizi G, Abolhassani H, Aghamohammadi A Scandinavian journal of immunology 2017;85(1):3-12
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The clinical significance of complete class switching defect in Ataxia telangiectasia patients Ghiasy S, Parvaneh L, Azizi G, Sadri G, Zaki Dizaji M, Abolhassani H, et al Expert review of clinical immunology 2017;13(5):499-505
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Asthma and Allergic Diseases in a Selected Group of Patients With Common Variable Immunodeficiency Yazdani R, Heydari A, Azizi G, Abolhassani H, Aghamohammadi A Journal of investigational allergology & clinical immunology 2016;26(3):209-11
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Autoimmunity in Primary Antibody Deficiencies Azizi G, Ahmadi M, Abolhassani H, Yazdani R, Mohammadi H, Mirshafiey A, et al International archives of allergy and immunology 2016;171(3-4):180-193
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Autoimmunity in primary T-cell immunodeficiencies Azizi G, Ghanavatinejad A, Abolhassani H, Yazdani R, Rezaei N, Mirshafiey A, et al Expert review of clinical immunology 2016;12(9):989-1006
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Cellular and molecular mechanisms of immune dysregulation and autoimmunity Azizi G, Pouyani Mr, Abolhassani H, Sharifi L, Dizaji Mz, Mohammadi J, et al Cellular immunology 2016;310():14-26
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CLINICAL AND IMMUNOLOGIC PROFILES OF SELECTIVE IgA DEFICIENCY ASSOCIATED WITH AUTOIMMUNE MANIFESTATIONS Asgardoon Mh, Gharib B, Abolhassani H, Rezaei N, Aghamohammadi A JOURNAL OF CLINICAL IMMUNOLOGY 2016;36(3):252-252
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CLINICAL SPECTRUM AND OUTCOME OF TREATMENT FOR AUTOIMMUNE CYTOPENIAS IN RAG DEFICIENCY Foldvari Z, Ujhazi B, Abolhassani H, Abraham R, Adeli M, Aghamohammadi A, et al JOURNAL OF CLINICAL IMMUNOLOGY 2016;36(3):301-303
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Cohort of Iranian Patients with Congenital Agammaglobulinemia: Mutation Analysis and Novel Gene Defects Abolhassani H, Vitali M, Lougaris V, Giliani S, Parvaneh N, Parvaneh L, et al Expert review of clinical immunology 2016;12(4):479-86
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Early onset steroid induced posterior subcapsular cataract in a patient with common variable immunodeficiency: case reports and review of literature Marefat H, Abolhassani H, Ghareje Daghi M, Azizi G, Aghamohammadi A European annals of allergy and clinical immunology 2016;48(5):197-201
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Evaluation of Known Defective Signaling-Associated Molecules in Patients Who Primarily Diagnosed as Common Variable Immunodeficiency Yazdani R, Abolhassani H, Rezaei N, Azizi G, Hammarström L, Aghamohammadi A International reviews of immunology 2016;35(1):7-24
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GENTOYPE-PHENOTYPE CORRELATOIN IN IRANIAN CONGENITAL AGAMMAGLOBULINEMIA COHORT Aghamohammadi A, Abolhassani H, Vitali M, Lougaris V, Giliani S, Parvaneh N, et al JOURNAL OF CLINICAL IMMUNOLOGY 2016;36(3):251-251
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Important Factors Influencing Severity of Common Variable Immunodeficiency Mokhtari M, Shakeri A, Mirminachi B, Abolhassani H, Yazdani R, Grimbacher B, et al Archives of Iranian medicine 2016;19(8):544-50
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Lymphocytic Interstitial Pneumonitis: An Unusual Presentation of X-Linked Hyper Ig M Syndrome Reisi M, Azizi G, Momen T, Abolhassani H, Aghamohammadi A Iranian journal of pediatrics 2016;26(2):e3656-
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Managing patients with side effects and adverse events to immunoglobulin therapy Azizi G, Abolhassani H, Asgardoon Mh, Shaghaghi S, Negahdari B, Mohammadi J, et al Expert review of clinical pharmacology 2016;9(1):91-102
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Monogenic mutations associated with IgA deficiency Abolhassani H, Aghamohammadi A, Hammarström L Expert review of clinical immunology 2016;12(12):1321-1335
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Next Generation Sequencing Data Analysis in Primary Immunodeficiency Disorders - Future Directions Fang M, Abolhassani H, Lim Ck, Zhang J, Hammarström L Journal of clinical immunology 2016;36 Suppl 1():68-75
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Review of local herbal compounds found in the Iranian traditional medicine known to optimise male fertility Nejatbakhsh F, Shirbeigi L, Rahimi R, Abolhassani H Andrologia 2016;48(8):850-9
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Role of apoptosis in common variable immunodeficiency and selective immunoglobulin A deficiency Yazdani R, Fatholahi M, Ganjalikhani-hakemi M, Abolhassani H, Azizi G, Hamid Km, et al Molecular immunology 2016;71():1-9
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Spectrum of Phenotypes Associated with Mutations in LRBA Alkhairy Ok, Abolhassani H, Rezaei N, Fang M, Andersen Kk, Chavoshzadeh Z, et al Journal of clinical immunology 2016;36(1):33-45
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The use of Immunoglobulin Therapy in Primary Immunodeficiency Diseases Azizi G, Abolhassani H, Asgardoon Mh, Rahnavard J, Dizaji Mz, Yazdani R, et al ENDOCRINE METABOLIC & IMMUNE DISORDERS-DRUG TARGETS 2016;16(2):80-88
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Vaccine-Derived Polioviruses and Children with Primary Immunodeficiency, Iran, 1995-2014 Shaghaghi M, Shahmahmoodi S, Abolhassani H, Soleyman-jahi S, Parvaneh L, Mahmoudi S, et al EMERGING INFECTIOUS DISEASES 2016;22(10):1712-9
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Vitamin D Deficiency among Female Nurses of Children's Medical Center Hospital and Its Related Factors Rajebi H, Khodadad A, Fahimi G, Abolhassani H Acta medica Iranica 2016;54(2):146-50
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Autoimmunity in patients with selective IgA deficiency Abolhassani H, Gharib B, Shahinpour S, Masoom Sn, Havaei A, Mirminachi B, et al Journal of investigational allergology & clinical immunology 2015;25(2):112-9
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Class switch recombination process in ataxia telangiectasia patients with elevated serum levels of IgM Mohammadinejad P, Abolhassani H, Aghamohammadi A, Pourhamdi S, Ghosh S, Sadeghi B, et al Journal of immunoassay & immunochemistry 2015;36(1):16-26
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Clinical phenotype classification for selective immunoglobulin A deficiency Yazdani R, Latif A, Tabassomi F, Abolhassani H, Azizi G, Rezaei N, et al Expert review of clinical immunology 2015;11(11):1245-54
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Common Variable Immunodeficiency or Late-Onset Combined Immunodeficiency: A New Hypomorphic JAK3 Patient and Review of the Literature Abolhassani H, Cheraghi T, Rezaei N, Aghamohammadi A, Hammarström L Journal of investigational allergology & clinical immunology 2015;25(3):218-20
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Different brands of intravenous immunoglobulin for primary immunodeficiencies: how to choose the best option for the patient? Abolhassani H, Asgardoon Mh, Rezaei N, Hammarstrom L, Aghamohammadi A Expert review of clinical immunology 2015;11(11):1229-43
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Economic burden of common variable immunodeficiency: annual cost of disease Sadeghi B, Abolhassani H, Naseri A, Rezaei N, Aghamohammadi A Expert review of clinical immunology 2015;11(5):681-8
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IgG anti-IgA antibodies in paediatric antibody-deficient patients receiving intravenous immunoglobulin Torabi Sagvand B, Mirminachi B, Abolhassani H, Shokouhfar T, Keihanian T, Amirzargar A, et al Allergologia et immunopathologia 2015;43(4):403-8
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Important differences in the diagnostic spectrum of primary immunodeficiency in adults versus children Abolhassani H, Rezaei N, Mohammadinejad P, Mirminachi B, Hammarstrom L, Aghamohammadi A EXPERT REVIEW OF CLINICAL IMMUNOLOGY 2015;11(2):289-302
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Mortality and morbidity in patients with X-linked agammaglobulinaemia Abolhassani H, Hirbod-mobarakeh A, Shahinpour S, Panahi M, Mohammadinejad P, Mirminachi B, et al Allergologia et immunopathologia 2015;43(1):62-6
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Novel mutations in TNFRSF7/CD27: Clinical, immunologic, and genetic characterization of human CD27 deficiency Alkhairy Ok, Perez-becker R, Driessen Gj, Abolhassani H, Van Montfrans J, Borte S, et al The Journal of allergy and clinical immunology 2015;136(3):703-712.e10
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Primary Antibody Deficiency in a Tertiary Referral Hospital: A 30-Year Experiment Mohammadinejad P, Pourhamdi S, Abolhassani H, Mirminachi B, Havaei A, Masoom Sn, et al Journal of investigational allergology & clinical immunology 2015;25(6):416-25
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RAC2 loss-of-function mutation in 2 siblings with characteristics of common variable immunodeficiency Alkhairy Ok, Rezaei N, Graham Rr, Abolhassani H, Borte S, Hultenby K, et al The Journal of allergy and clinical immunology 2015;135(5):1380-4.e1
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Report on the First Survey of Iranian Patients with Hereditary Angioedema Shahinpour S, Tavakol M, Abolhassani H, Mohammadinejad P, Movahedi M, Arshi S, et al Iranian journal of immunology : IJI 2015;12(3):209-18
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A hypomorphic recombination-activating gene 1 (RAG1) mutation resulting in a phenotype resembling common variable immunodeficiency Abolhassani H, Wang N, Aghamohammadi A, Rezaei N, Lee Yn, Frugoni F, et al JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY 2014;134(6):1375-1380
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Alteration in Frequency and Function of CD4(+)CD25(+)FOXP3(+) Regulatory T cells in Patients with Immune Thrombocytopenic Purpura Arandi N, Mirshafiey A, Jeddi-tehrani M, Shaghaghi M, Sadeghi B, Abolhassani H, et al IRANIAN JOURNAL OF ALLERGY ASTHMA AND IMMUNOLOGY 2014;13(2):85-92
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Autosomal recessive agammaglobulinemia: a novel non-sense mutation in CD79a Khalili A, Plebani A, Vitali M, Abolhassani H, Lougaris V, Mirminachi B, et al Journal of clinical immunology 2014;34(2):138-41
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Clinical Features and Mutation Analysis of 51 Iranian Patients with Hyper Immunoglobulin E Syndrome Tavassoli M, Ghadami M, Abolhassani H, Kokabee M, Parvaneh N, Yeganeh M, et al JOURNAL OF CLINICAL IMMUNOLOGY 2014;:S314-S314
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Clinical Features and Mutation Analysis of Iranian Patients with Congenital Agammaglobulinemia Abolhassani H, Mirminachi B, Vitali M, Lougaris V, Cheraghi T, Khazaei H, et al JOURNAL OF CLINICAL IMMUNOLOGY 2014;:S385-S386
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Clinical Features and Outcomes of 86 Severe Combined Immunodeficiency Patients Afarideh M, Ghajar A, Mirminachi B, Abolhassani H, Havaei A, Sagvand Bt, et al JOURNAL OF CLINICAL IMMUNOLOGY 2014;:S433-S434
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Combined immunodeficiency presenting with vaccine-associated paralytic poliomyelitis: a case report and narrative review of literature Shaghaghi M, Parvaneh N, Ostad-rahimi P, Fathi Sm, Shahmahmoodi S, Abolhassani H, et al Immunological investigations 2014;43(3):292-8
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Distribution of Primary Immunodeficiency Disorders Diagnosed in a Tertiary Referral Center, Tehran, Iran (2006-2013) Mohammadinejad P, Mirminachi B, Sadeghi B, Movahedi M, Gharagozlou M, Mohammadi J, et al IRANIAN JOURNAL OF IMMUNOLOGY 2014;11(4):282-91
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Ectopic decidual reaction mimicking irritable bowel syndrome: a case report Salehgargari S, Sahebdel B, Zare A, Abolhassani H Acta medica Iranica 2014;52(1):88-90
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Evaluation of Antibody Response to Polysaccharide Vaccine and Switched Memory B Cells in Pediatric Patients with Inflammatory Bowel Disease Fallahi G, Aghamohammadi A, Khodadad A, Hashemi M, Mohammadinejad P, Asgarian-omran H, et al GUT AND LIVER 2014;8(1):24-8
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Evaluation of Physicians' Awareness of Pediatric Diseases in Iran Abolhassani H, Mirminachi B, Daryabeigi M, Agharahimi Z, Aghamohammadi A, Rabbani A, et al IRANIAN JOURNAL OF PEDIATRICS 2014;24(1):87-92
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Genetic defects in B-cell development and their clinical consequences Abolhassani H, Parvaneh N, Rezaei N, Hammarström L, Aghamohammadi A Journal of investigational allergology & clinical immunology 2014;24(1):6-22
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IGG Anti-IGA Antibodies in Patients with Primary Antibody Deficiency Receiving Intravenous Immunoglobulin Mirminachi B, Sagvand Bt, Abolhassani H, Shokouhfar T, Keihanian T, Hedayat E, et al JOURNAL OF CLINICAL IMMUNOLOGY 2014;:S386-S387
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Immunologic Evaluation of Patients with Recurrent Infections Yousefzadegan S, Nadjafi A, Abolhassani H, Mansouri S, Mirminachi B, Tavakol M, et al JOURNAL OF CLINICAL IMMUNOLOGY 2014;:S314-S315
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IMPORTANCE OF DEFINITE DIAGNOSIS OF PRIMARY IMMUNODEFICIENCY DISEASES Abolhassani H, Latif Ah, Tabassomi F, Aghamohammadi A, Rezaei N, Hammarstrom L JOURNAL OF CLINICAL IMMUNOLOGY 2014;34(6):711-712
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Investigation of underlying primary immunodeficiencies in patients with severe atopic dermatitis Aghamohammadi A, Moghaddam Zg, Abolhassani H, Hallaji Z, Mortazavi H, Pourhamdi S, et al Allergologia et immunopathologia 2014;42(4):336-41
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Long-term evaluation of a historical cohort of Iranian common variable immunodeficiency patients Aghamohammadi A, Abolhassani H, Latif A, Tabassomi F, Shokuhfar T, Torabi Sagvand B, et al Expert review of clinical immunology 2014;10(10):1405-17
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Molecular diagnosis of primary immunodeficiency diseases in a developing country: Iran as an example Latif Ah, Tabassomi F, Abolhassani H, Hammarström L Expert review of clinical immunology 2014;10(3):385-96
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Morbidity and mortality of Iranian patients with hyper IgM syndrome: a clinical analysis Abolhassani H, Akbari F, Mirminachi B, Bazregari S, Hedayat E, Rezaei N, et al Iranian journal of immunology : IJI 2014;11(2):123-33
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Otological Findings in Pediatric Patients with Hypogammaglobulinemia Tavakol M, Kouhi A, Abolhassani H, Ghajar A, Afarideh M, Shahinpour S, et al IRANIAN JOURNAL OF ALLERGY ASTHMA AND IMMUNOLOGY 2014;13(3):166-73
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Prediction of the evolution of common variable immunodeficiency: HLA typing for patients with selective IgA deficiency Cheraghi T, Aghamohammadi A, Mirminachi B, Keihanian T, Hedayat E, Abolhassani H, et al Journal of investigational allergology & clinical immunology 2014;24(3):198-200
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Primary Immunodeficiency Disorders in Iran: Update and New Insights from the Third Report of the National Registry Aghamohammadi A, Mohammadinejad P, Abolhassani H, Mirminachi B, Movahedi M, Gharagozlou M, et al JOURNAL OF CLINICAL IMMUNOLOGY 2014;34(4):478-90
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Selective IGA Deficiency: New Insights in Pathogenesis and Classification Aghamohammadi A, Abolhassani H, Hammarstrom L JOURNAL OF CLINICAL IMMUNOLOGY 2014;:S386-S386
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A review on guidelines for management and treatment of common variable immunodeficiency Abolhassani H, Sagvand Bt, Shokuhfar T, Mirminachi B, Rezaei N, Aghamohammadi A EXPERT REVIEW OF CLINICAL IMMUNOLOGY 2013;9(6):561-74
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Autism in a Child with Common Variable Immunodeficiency Sadaghiani Ms, Aghamohammadi A, Ashrafi Mr, Hosseini F, Abolhassani H, Rezaei N IRANIAN JOURNAL OF ALLERGY ASTHMA AND IMMUNOLOGY 2013;12(3):287-9
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Autoimmune Phenotype in Patients With Common Variable Immunodeficiency Abolhassani H, Amirkashani D, Parvaneh N, Mohammadinejad P, Gharib B, Shahinpour S, et al JOURNAL OF INVESTIGATIONAL ALLERGOLOGY AND CLINICAL IMMUNOLOGY 2013;23(5):323-9
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Evaluation of CD4+CD25+FOXP3+ regulatory T cells function in patients with common variable immunodeficiency Arandi N, Mirshafiey A, Jeddi-tehrani M, Abolhassani H, Sadeghi B, Mirminachi B, et al Cellular immunology 2013;281(2):129-33
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Evaluation of class switch recombination in B lymphocytes of patients with common variable immunodeficiency Farrokhi As, Aghamohammadi A, Pourhamdi S, Mohammadinejad P, Abolhassani H, Moazzeni Sm JOURNAL OF IMMUNOLOGICAL METHODS 2013;394(1-2):94-9
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Evaluation of Humoral Immune Function in Patients with Chronic Idiopathic Thrombocytopenic Purpura Rahiminejad Ms, Sadeghi Mm, Mohammadinejad P, Sadeghi B, Abolhassani H, Firoozabadi Mmd, et al IRANIAN JOURNAL OF ALLERGY ASTHMA AND IMMUNOLOGY 2013;12(1):50-6
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Evaluation of Natural Regulatory T Cells in Subjects with Selective IgA Deficiency: From Senior Idea to Novel Opportunities Soheili H, Abolhassani H, Arandi N, Khazaei Ha, Shahinpour S, Hirbod-mobarakeh A, et al INTERNATIONAL ARCHIVES OF ALLERGY AND IMMUNOLOGY 2013;160(2):208-14
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Expression of Activation-Induced Cytidine Deaminase Gene in B Lymphocytes of Patients with Common Variable Immunodeficiency Abolhassani H, Farrokhi As, Pourhamdi S, Mohammadinejad P, Sadeghi B, Moazzeni Sm, et al IRANIAN JOURNAL OF PEDIATRICS 2013;23(4):451-7
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Family Study of Pediatric Patients with Primary Antibody Deficiencies Rezaei N, Abolhassani H, Kasraian A, Mohammadinejad P, Sadeghi B, Aghamohammadi A IRANIAN JOURNAL OF ALLERGY ASTHMA AND IMMUNOLOGY 2013;12(4):377-82
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Frequency and expression of inhibitory markers of CD4(+) CD25(+) FOXP3(+) regulatory T cells in patients with common variable immunodeficiency Arandi N, Mirshafiey A, Abolhassani H, Jeddi-tehrani M, Edalat R, Sadeghi B, et al Scandinavian journal of immunology 2013;77(5):405-12
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Psychiatric Aspects of Primary Immunodeficiency Diseases: The Parental Study Abolhassani H, Aghamohammadi A, Pourjabbar S, Sadaghiani Ms, Nikayin S, Rabiee A, et al IRANIAN JOURNAL OF ALLERGY ASTHMA AND IMMUNOLOGY 2013;12(2):176-81
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A Survey of Complementary and Alternative Medicine in Iran Abolhassani H, Naseri M, Mahmoudzadeh S CHINESE JOURNAL OF INTEGRATIVE MEDICINE 2012;18(6):409-16
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AUTOIMMUNE MANIFESTATIONS IN PATIENTS WITH COMMON VARIABLE IMMUNE DEFICIENCY Afarideh M, Aghamohammadi A, Amirkashani D, Hirbod-mobarake A, Shahinpour S, Abolhassani H, et al JOURNAL OF CLINICAL IMMUNOLOGY 2012;:298-298
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Autoimmunity in X-linked agammaglobulinemia: Kawasaki disease and review of the literature Behniafard N, Aghamohammadi A, Abolhassani H, Pourjabbar S, Sabouni F, Rezaei N Expert review of clinical immunology 2012;8(2):155-9
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CD4(+)CD25(+)FOXP3(+) REGULATORY T CELLS (TREG) ABNORMALITY IN PATIENTS WITH COMMON VARIABLE IMMUNODEFICIENCY (CVID) Arandi N, Mirshafiei A, Abolhassani H, Aghamohammadi A JOURNAL OF CLINICAL IMMUNOLOGY 2012;:329-329
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Circulating retinol-binding protein 4 concentrations in patients with coronary artery disease and patients with type 2 diabetes mellitus Mahmoudi Mj, Mahmoudi M, Siassi F, Hedayat M, Pasalar P, Chamari M, et al INTERNATIONAL JOURNAL OF DIABETES IN DEVELOPING COUNTRIES 2012;32(2):105-110
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EVALUATION OF HUMORAL IMMUNE FUNCTION IN PATIENTS WITH CHRONIC IDIOPATHIC THROMBOCYTOPENIC PURPURA Abolhassani H, Rahiminejad Ms, Sadeghi Mm, Mohammadinejad P, Firoozabadi Mmd, Fathi Sm JOURNAL OF CLINICAL IMMUNOLOGY 2012;:288-288
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EVALUATION OF NATURAL REGULATORY T CELLS IN SUBJECTS WITH SELECTIVE IGA DEFICIENCY: FROM SENIOR IDEA TO NOVEL OPPORTUNITIES Abolhassani H, Aghamohammadi A, Soheili H, Shahinpour S, Hirbod-mobarake A, Arandi N, et al JOURNAL OF CLINICAL IMMUNOLOGY 2012;:287-287
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EVALUATION OF REGULATORY T-CELLS AND AUTOIMMUNITY IN IGA DEFICIENCY Aghamohammadi A, Soheili H, Shahinpour S, Abolhassani H, Hirbod A, Arandi N, et al RHEUMATOLOGY 2012;:I22-I23
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Home-based subcutaneous immunoglobulin versus hospital-based intravenous immunoglobulin in treatment of primary antibody deficiencies: systematic review and meta analysis Abolhassani H, Sadaghiani Ms, Aghamohammadi A, Ochs Hd, Rezaei N Journal of clinical immunology 2012;32(6):1180-92
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LONG TERM OBSERVATION OF CHILDREN SUFFERED FROM COMMON VARIABLE IMMUNODEFICIENCY Aghamohammadi A, Abolhassani H, Mohammadinejad P, Sagvand Bt, Abdollahzade S, Salehi-sadaghiani M, et al JOURNAL OF CLINICAL IMMUNOLOGY 2012;:281-281
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Malignancy phenotype in common variable immunodeficiency Abolhassani H, Aghamohammadi A, Imanzadeh A, Mohammadinejad P, Sadeghi B, Rezaei N Journal of investigational allergology & clinical immunology 2012;22(2):133-4
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MORTALITY AND MORBIDITY IN PATIENTS WITH X-LINKED AGAMMAGLOBULINEMIA Shaghaghi Mr, Aghamohammadi A, Abolhassani H, Hirbod-mobarake A, Rezaei N JOURNAL OF CLINICAL IMMUNOLOGY 2012;:297-297
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Naive CD4+ T cells and recent thymic emigrants in common variable immunodeficiency Oraei M, Aghamohammadi A, Rezaei N, Bidad K, Gheflati Z, Amirkhani A, et al Journal of investigational allergology & clinical immunology 2012;22(3):160-7
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OTOLOGIC INVESTIGATION IN PRIMARY IMMUNODEFICIENCY PATIENTS Ghajar A, Aghamohammadi A, Kouhi A, Afarideh M, Abolhassani H, Hirbod-mobarake A, et al JOURNAL OF CLINICAL IMMUNOLOGY 2012;:232-232
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Pediatric patients with common variable immunodeficiency: long-term follow-up Mohammadinejad P, Aghamohammadi A, Abolhassani H, Sadaghiani Ms, Abdollahzade S, Sadeghi B, et al Journal of investigational allergology & clinical immunology 2012;22(3):208-14
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Physicians awareness on primary immunodeficiency disorders in Iran Nourijelyani K, Aghamohammadi A, Salehi Sadaghiani M, Behniafard N, Abolhassani H, Pourjabar S, et al Iranian journal of allergy, asthma, and immunology 2012;11(1):57-64
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Severe primary antibody deficiency due to a novel mutation of mu heavy chain Mohammadzadeh I, Yeganeh M, Aghamohammadi A, Parvaneh N, Behniafard N, Abolhassani H, et al Journal of investigational allergology & clinical immunology 2012;22(1):78-9
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The approach to children with recurrent infections Aghamohammadi A, Abolhassani H, Mohammadinejad P, Rezaei N Iranian journal of allergy, asthma, and immunology 2012;11(2):89-109
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The uncommon combination of common variable immunodeficiency, macrophage activation syndrome, and cytomegalovirus retinitis Aghamohammadi A, Abolhassani H, Hirbod-mobarakeh A, Ghassemi F, Shahinpour S, Behniafard N, et al Viral immunology 2012;25(2):161-5
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Analysis of switched memory B cells in patients with IgA deficiency Aghamohammadi A, Abolhassani H, Biglari M, Abolmaali S, Moazzami K, Tabatabaeiyan M, et al International archives of allergy and immunology 2011;156(4):462-8
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Health policy for common variable immunodeficiency: burden of the disease Abolhassani H, Aghamohammadi A, Abolhassani F, Eftekhar H, Heidarnia M, Rezaei N Journal of investigational allergology & clinical immunology 2011;21(6):454-8
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Health-related quality of life in primary antibody deficiency Aghamohammadi A, Montazeri A, Abolhassani H, Saroukhani S, Pourjabbar S, Tavassoli M, et al Iranian journal of allergy, asthma, and immunology 2011;10(1):47-51
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Impact of delayed diagnosis in children with primary antibody deficiencies Aghamohammadi A, Bahrami A, Mamishi S, Mohammadi B, Abolhassani H, Parvaneh N, et al Journal of microbiology, immunology, and infection = Wei mian yu gan ran za zhi 2011;44(3):229-34
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Indications and safety of intravenous and subcutaneous immunoglobulin therapy Rezaei N, Abolhassani H, Aghamohammadi A, Ochs Hd Expert review of clinical immunology 2011;7(3):301-16
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Oral and dental health status in patients with primary antibody deficiencies Meighani G, Aghamohammadi A, Javanbakht H, Abolhassani H, Nikayin S, Jafari Sm, et al Iranian journal of allergy, asthma, and immunology 2011;10(4):289-93
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A single center 14 years study of infectious complications leading to hospitalization of patients with primary antibody deficiencies Mamishi S, Eghbali An, Rezaei N, Abolhassani H, Parvaneh N, Aghamohammadi A The Brazilian journal of infectious diseases : an official publication of the Brazilian Society of Infectious Diseases 2010;14(4):351-5
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Ataxia-telangiectasia in a patient presenting with hyper-immunoglobulin M syndrome Aghamohammadi A, Imai K, Moazzami K, Abolhassani H, Tabatabaeiyan M, Parvaneh N, et al Journal of investigational allergology & clinical immunology 2010;20(5):442-5
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Behavior abnormality following intravenous immunoglobulin treatment in patients with primary antibody deficiencies Saroukhani S, Aghamohammadi A, Mahmoudi-gharaei J, Abolhassani H, Cheraghi T, Imanzaeh A, et al Human psychopharmacology 2010;25(5):419-22
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Behaviour abnormality following intravenous immunoglobulin treatment in patients with primary antibody deficiencies Saroukhani S, Aghamohammadi A, Abolhassani H, Imanzaeh A, Moazzami K, Pourjabar S, et al ALLERGY 2010;:478-478
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Bilateral deep peroneal nerve paralysis following kerosene self-injection into external hemorrhoids Rostami K, Farzaneh E, Abolhassani H Case reports in medicine 2010;2010():-
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Comparison of pulmonary diseases in common variable immunodeficiency and X-linked agammaglobulinaemia Aghamohammadi A, Allahverdi A, Abolhassani H, Moazzami K, Alizadeh H, Gharagozlou M, et al Respirology (Carlton, Vic.) 2010;15(2):289-95
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Correlation between common variable immunodeficiency clinical phenotypes and parental consanguinity in children and adults Aghamohammadi A, Abolhassani H, Moazzami K, Parvaneh N, Rezaei N Journal of investigational allergology & clinical immunology 2010;20(5):372-9
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Cutaneous granulomas in common variable immunodeficiency Aghamohammadi A, Abolhassani H, Rezaei N, Kalantari N, Tamizifar B, Cheraghi T, et al ALLERGY 2010;:491-492
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Cutaneous granulomas in common variable immunodeficiency: case report and review of literature Aghamohammadi A, Abolhassani H, Rezaei N, Kalantari N, Tamizifar B, Cheraghi T, et al Acta dermatovenerologica Croatica : ADC 2010;18(2):107-13
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Physicians awareness on primary immunodeficiency diseases in Iran Aghamohammadi A, Sadaghiani Ms, Abolhassani H, Moazzami K, Pourjabar S, Khademy J, et al ALLERGY 2010;:488-489
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Renal amyloidosis in common variable immunodeficiency Aghamohammadi A, Shafiei A, Abolhassani H, Sherkat R, Mahjoub F, Rezaei N Nefrologia : publicacion oficial de la Sociedad Espanola Nefrologia 2010;30(4):474-6
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Renal amyloidosis in common variable immunodeficiency Aghamohammadi A, Shafiei A, Abolhassani H, Sherkat R, Mahjoub F, Rezaei N ALLERGY 2010;:492-493
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Clinical and Laboratory Findings in Hyper-IgM Syndrome with Novel CD40L and AICDA Mutations Aghamohammadi A, Parvaneh N, Rezaei N, Moazzami K, Kashef S, Abolhassani H, et al JOURNAL OF CLINICAL IMMUNOLOGY 2009;29(6):769-76
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COMPARISON OF PULMONARY DISEASES IN COMMON VARIABLE IMMUNODEFICIENCY AND X-LINKED AGAMMAGLOBULINEMIA Aghamohammadi A, Allahverdi A, Abolhassani H, Moazzami K, Gharagozlou M, Kalantari N, et al ANNALS OF ALLERGY ASTHMA & IMMUNOLOGY 2009;103(5):A111-A111
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DIFFERENT CLINICAL PHENOTYPES OF 93 PATIENTS WITH COMMON VARIABLE IMMUNODEFICIENCY Aghamohammadi A, Abolhassani H, Moazzami K, Parvaneh N, Rezaei N ANNALS OF ALLERGY ASTHMA & IMMUNOLOGY 2009;103(5):A111-A112
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IgA deficiency: correlation between clinical and immunological phenotypes Aghamohammadi A, Cheraghi T, Gharagozlou M, Movahedi M, Rezaei N, Yeganeh M, et al Journal of clinical immunology 2009;29(1):130-6
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Infectious and Non-Infectious Complications among Undiagnosed Patients with Common Variable Immunodeficiency Aghamohammadi A, Tavassoli M, Abolhassani H, Parvaneh N, Moazzami K, Allahverdi A, et al IRANIAN JOURNAL OF PEDIATRICS 2009;19(4):367-375
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INFECTIOUS AND NON-INFECTIOUS COMPLICATIONS AMONG UNDIAGNOSED PATIENTS WITH COMMON VARIABLE IMMUNODEFICIENCY COMPARED WITH EARLY DIAGNOSED AND WELL-TREATED PATIENTS Aghamohammadi A, Tavassoli M, Abolhassani H, Parvaneh N, Moazzami K, Mahdaviani A, et al ANNALS OF ALLERGY ASTHMA & IMMUNOLOGY 2009;103(5):A111-A111
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Evaluation of humoral immune function in patients with bronchiectasis Tabatabaie P, Aghamohammadi A, Mamishi S, Isaeian A, Heidari G, Abdollahzade S, et al Iranian journal of allergy, asthma, and immunology 2008;7(2):69-77
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Evaluation of humoral immune function in the patients with bronchiectasis Aghamohammadi A, Tabatabaie P, Mamishi S, Isaeian A, Heidari G, Abdollahzade S, et al CLINICAL AND EXPERIMENTAL IMMUNOLOGY 2008;:107-107
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IgA Deficiency: correlation between clinical and immunological manifestations Aghamohammadi A, Cheraghi T, Gharagozlou M, Movahedi M, Pourpak Z, Rezaei N, et al CLINICAL AND EXPERIMENTAL IMMUNOLOGY 2008;:111-112
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Presence of Idiopathic Thrombocytopenic Purpura and autoimmune hemolytic anemia in the patients with common variable immunodeficiency Ramyar A, Aghamohammadi A, Moazzami K, Rezaei N, Yeganeh M, Cheraghi T, et al Iranian journal of allergy, asthma, and immunology 2008;7(3):169-75
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