Found: 25
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A fludarabine and melphalan reduced-intensity conditioning regimen for HSCT in fifteen chronic granulomatous disease patients and a literature review.
- Published in:
- 2022
- By:
- Publication type:
- journal article
Purine Nucleoside Phosphorylase Deficiency in Two Unrelated Patients with Autoimmune Hemolytic Anemia and Eosinophilia: Two Novel Mutations.
- Published in:
- Archives of Iranian Medicine (AIM), 2023, v. 26, n. 12, p. 712, doi. 10.34172/aim.2023.105
- By:
- Publication type:
- Article
Three novel mutations in CYBA among 22 Iranians with chronic granulomatous disease.
- Published in:
- Turkish Journal of Immunology, 2016, v. 4, p. 40
- By:
- Publication type:
- Article
Clinical and immunological characteristics of 69 leukocyte adhesion deficiency‐I patients.
- Published in:
- Pediatric Allergy & Immunology, 2023, v. 34, n. 7, p. 1, doi. 10.1111/pai.13990
- By:
- Publication type:
- Article
Investigation of ITGB2 Gene in 12 New Cases of Leukocyte Adhesion Deficiency-Type I Revealed Four Novel Mutations from Iran.
- Published in:
- Archives of Iranian Medicine (AIM), 2015, v. 18, n. 11, p. 760, doi. 0151811/AIM.006
- By:
- Publication type:
- Article
A New Patient with Inherited TYK2 Deficiency.
- Published in:
- 2020
- By:
- Publication type:
- Letter
Molecular, Immunological, and Clinical Features of 16 Iranian Patients with Mendelian Susceptibility to Mycobacterial Disease.
- Published in:
- Journal of Clinical Immunology, 2019, v. 39, n. 3, p. 287, doi. 10.1007/s10875-019-0593-4
- By:
- Publication type:
- Article
Inheritance Pattern and Clinical Aspects of 93 Iranian Patients with Chronic Granulomatous Disease.
- Published in:
- Journal of Clinical Immunology, 2011, v. 31, n. 5, p. 792, doi. 10.1007/s10875-011-9567-x
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- Publication type:
- Article
Molecular findings and clinical manifestations of 18 Iranian children with Griscelli syndrome type 2: Two novel homozygote mutations in RAB27A gene in a patient.
- Published in:
- Scandinavian Journal of Immunology, 2023, v. 97, n. 5, p. 1, doi. 10.1111/sji.13264
- By:
- Publication type:
- Article
Genetic and molecular findings of 38 Iranian patients with chronic granulomatous disease caused by p47‐phox defect.
- Published in:
- Scandinavian Journal of Immunology, 2019, v. 90, n. 1, p. N.PAG, doi. 10.1111/sji.12767
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- Publication type:
- Article
Newborn screening using TREC/KREC assay for severe T and B cell lymphopenia in Iran.
- Published in:
- Scandinavian Journal of Immunology, 2018, v. 88, n. 2, p. 1, doi. 10.1111/sji.12699
- By:
- Publication type:
- Article
Characterization of six novel mutations in CYBA: the gene causing autosomal recessive chronic granulomatous disease.
- Published in:
- British Journal of Haematology, 2008, v. 141, n. 6, p. 848, doi. 10.1111/j.1365-2141.2008.07148.x
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- Publication type:
- Article
The Risk of the Next Child Getting Affected by Chronic Granulomatous Disease in Families with at Least One Autosomal Recessive CGD Child.
- Published in:
- Iranian Journal of Allergy, Asthma & Immunology, 2023, v. 22, n. 1, p. 119, doi. 10.18502/ijaai.v22i1.12014
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- Publication type:
- Article
Investigating the Variation of TREC/KREC in Combined Immunodeficiencies.
- Published in:
- Iranian Journal of Allergy, Asthma & Immunology, 2021, v. 20, n. 4, p. 402, doi. 10.18502/ijaai.v20i4.6950
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- Publication type:
- Article
The Critical Role of Prenatal Genetic Study in Prevention of Primary Immunodeficiency in High-risk Families: The Largest Report of 107 Cases.
- Published in:
- Iranian Journal of Allergy, Asthma & Immunology, 2020, v. 19, n. 5, p. 478
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- Publication type:
- Article
Clinical and Genetic Analysis of Nine Suspected Familial Haemophagocytic Lymphohistiocytosis Patients for MUNC13-4 Deficiency and Introducing Four Novel Mutations in UNC13D.
- Published in:
- Iranian Journal of Allergy, Asthma & Immunology, 2019, v. 18, n. 5, p. 487
- By:
- Publication type:
- Article
In vitro Analysis of Nine MicroRNAs in CD8+ T Cells of Asthmatic Patients and the Effects of Two FDA-approved Drugs.
- Published in:
- Iranian Journal of Allergy, Asthma & Immunology, 2019, v. 18, n. 4, p. 358
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- Publication type:
- Article
Lupus Erythematosus and Chronic Granulomatous Disease: Report of Four Iranian Patients with AR-CGD and One XL-CGD.
- Published in:
- Iranian Journal of Allergy, Asthma & Immunology, 2019, v. 18, n. 4, p. 452
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- Publication type:
- Article
Identifying Two Novel Mutations in UNC13D Gene in Two Iranian Patient with Hemophagocytic Lymphohistiocytosis (HLH).
- Published in:
- 2018
- By:
- Publication type:
- Abstract
Biological and Genetic Biobanks Registry for Primary Immunodeficient, Asthmatic, and Allergic Patients.
- Published in:
- 2018
- By:
- Publication type:
- Abstract
Iranian Genetic Testing Registry for Primary Immunodeficiencies.
- Published in:
- 2018
- By:
- Publication type:
- Abstract
Five Mutations in Six Families Possessing at Least one Member with Leukocyte Adhesion Deficiency I.
- Published in:
- 2018
- By:
- Publication type:
- Abstract
Newborn Screening and early diagnosis of Severe T-cell and B-cell Lymphopenia using TREC/KREC Assay.
- Published in:
- 2018
- By:
- Publication type:
- Abstract
A Novel CYBB Mutation in Chronic Granulomatous Disease in Iran.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Molecular Analysis of Four Cases of Chronic Granulomatous Disease Caused by Defects in NCF-2: The Gene Encoding the p67-phox.
- Published in:
- Iranian Journal of Allergy, Asthma & Immunology, 2012, v. 11, n. 4, p. 340
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- Publication type:
- Article