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Your search keyword '"Momen, Tooba"' showing total 143 results

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1. Clinical, Immunological, and Genetic Findings in Iranian Patients with MHC-II Deficiency: Confirmation of c.162delG RFXANK Founder Mutation in the Iranian Population

2. Clinical heterogeneity in families with multiple cases of inborn errors of immunity

3. Genomic Testing Identifies Monogenic Causes in Patients with Very Early-Onset Inflammatory Bowel Disease: A Multi-center Survey in an Iranian Cohort

5. Expanding the Clinical and Immunological Phenotypes and Natural History of MALT1 Deficiency

6. Clinical, immunological, molecular and therapeutic findings in monogenic immune dysregulation diseases: Middle East and North Africa registry

7. Genomic testing identifies monogenic causes in patients with very early-onset inflammatory bowel disease: a multicenter survey in an Iranian cohort.

9. Extended clinical and immunological phenotype and transplant outcome in CD27 and CD70 deficiency

10. Impact of SARS-CoV-2 Pandemic on Patients with Primary Immunodeficiency

11. Contributors

12. Comparison of Common Monogenic Defects in a Large Predominantly Antibody Deficiency Cohort

13. Fourth Update on the Iranian National Registry of Primary Immunodeficiencies: Integration of Molecular Diagnosis

14. Autoimmune versus Non-autoimmune Cutaneous Features in Monogenic Patients with Inborn Errors of Immunity

15. Clinical, immunological, and genetic findings in Iranian patients with MHC-II deficiency: confirmation of c.121delG RFXANK founder mutation in the Iranian population

18. Clinical, immunological, molecular and therapeutic findings in monogenic immune dysregulation diseases: Middle East and North Africa registry

19. Epidemiology, Sociodemographic Factors and Comorbidity for Allergic Rhinitis, Asthma, and Rhinosinusitis Among 15 to 65-year-Old Iranian Patients

22. Clinical and Epidemiological Features of Patients with Drug-Induced Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis in Iran: Different Points of Children from Adults

24. Congenital disorders of glycosylation with defective fucosylation

25. Global systematic review of primary immunodeficiency registries

26. Extended clinical and immunological phenotype and transplant outcome in CD27 and CD70 deficiency

27. Seroprevalence of ToxocaraCanis in Asthmatic Children and its Relation to the Severity of Diseases - a Case-Control Study

28. Impact of SARS-CoV-2 Pandemic on Patients with Primary Immunodeficiency

29. Global systematic review of primary immunodeficiency registries

30. Exome-first Approach Identified Novel Homozygous Dedicator of Cytokinesis 8 (DOCK8) Mutations in Three Unrelated Iranian Pedigrees Suspected with Hyper-IgE Syndrome

31. Monogenic Primary Immunodeficiency Disorder Associated with Common Variable Immunodeficiency and Autoimmunity

32. Genetic mutations and immunological features of severe combined immunodeficiency patients in Iran

33. Autoimmune manifestations among 461 patients with monogenic inborn errors of immunity.

35. Clinical, immunologic, and genetic spectrum of 696 patients with combined immunodeficiency

40. Effect of Fish Oil on the Level of Interferon Gamma on the Breast Milk of Atopic Mothers: A Randomized Clinical Trial.

41. Demographic, Clinical, and Allergic Characteristics of Children with Eosinophilic Esophagitis in Isfahan, Iran.

45. Comparison of Interleukin-33 Serum Levels in Asthmatic Patients with a Control Group and Relation with the Severity of the Disease.

48. Prevalence of nephrocalcinosis in children with congenital adrenal hyperplasia.

49. Upper Respiratory System Involvement as the Only Manifestation of Granulomatosis with Polyangiitis in a Child with Marfan Phenotype.

50. Para-aortic Lymphadenopathy Associated with Kawasaki Disease.

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