Tehran University of Medical Sciences

Science Communicator Platform

Stay connected! Follow us on X network (Twitter):
Faculty Members have conducted research related to the Mendelian Susceptibility to Mycobacterial Disease (Msmd): Clinical and Genetic Features of 32 Iranian Patients
Nima Parvaneh
Nima Parvaneh

Associate Professor of Allergy and Clinical Immunology

Department Pediatrics

School of Medicine

Childrens Medical Center

Research Center for Immunodeficiencies

Tehran University of Medical Sciences

Related Documents
1. Inherited and Acquired Immunodeficiencies Underlying Tuberculosis in Childhood, Immunological Reviews (2015)
2. Human Il-23 Is Essential for Ifn-Γ–Dependent Immunity to Mycobacteria, Science Immunology (2023)
3. Impaired Il-23–Dependent Induction of Ifn-Γ Underlies Mycobacterial Disease in Patients With Inherited Tyk2 Deficiency, Journal of Experimental Medicine (2022)
4. Avarietyofalu-Mediated Copy Number Variations Can Underlie Il-12Rβ1 Deficiency, Journal of Clinical Immunology (2018)
5. Human Mcts1-Dependent Translation of Jak2 Is Essential for Ifn-Γ Immunity to Mycobacteria, Cell (2023)
6. Mendelian Susceptibility to Mycobacterial Disease: Clinical and Immunological Findings of Patients Suspected for Il12rβ1 Deficiency, Allergologia et Immunopathologia (2019)
7. Effective Anti-Mycobacterial Treatment for Bcg Disease in Patients With Mendelian Susceptibility to Mycobacterial Disease (Msmd): A Case Series, Annals of Clinical Microbiology and Antimicrobials (2022)
8. Fourth Update on the Iranian National Registry of Primary Immunodeficiencies: Integration of Molecular Diagnosis, Journal of Clinical Immunology (2018)
9. Inherited Human Itk Deficiency Impairs Ifn-Γ Immunity and Underlies Tuberculosis, Journal of Experimental Medicine (2023)
10. Visceral Leishmaniasis in Two Patients With Il-12P40 and Il-12Rβ1 Deficiencies, Pediatric Blood and Cancer (2017)
11. Human Inherited Ccr2 Deficiency Underlies Progressive Polycystic Lung Disease, Cell (2024)
12. Evaluation of Interleukin-12 Receptor Β1 and Interferon Gamma Receptor 1 Deficiency in Patients With Disseminated Bcg Infection, Allergologia et Immunopathologia (2019)
All Documents
1. Antibody Response Before and After the Booster Dose of Inactivated Corona Vaccine in Antibody Deficient Patients, Iranian Journal of Allergy# Asthma and Immunology (2024)
2. Biallelic Human Sharpin Loss of Function Induces Autoinflammation and Immunodeficiency, Nature Immunology (2024)
3. Exploring the Phenotypic Profile of Acute Flaccid Paralysis: Insights From a Third-Level Pediatric Emergency Room, Iranian Journal of Child Neurology (2024)
4. Flt3l Governs the Development of Partially Overlapping Hematopoietic Lineages in Humans and Mice, Cell (2024)
5. Human Inherited Ccr2 Deficiency Underlies Progressive Polycystic Lung Disease, Cell (2024)
6. Patients and Mice With Deficiency in the Snare Protein Syntaxin-11 Have a Secondary B Cell Defect, The Journal of experimental medicine (2024)
7. The Immunopathological Landscape of Human Pre-Tcra Deficiency: From Rare to Common Variants, Science (2024)
8. The Immunopathological Landscape of Human Pre-Tcra Deficiency: From Rare to Common Variants, Science (2024)
9. A Case Series of Ten Plus One Deficiency of Adenosine Deaminase 2 (Dada2) Patients in Iran, Pediatric Rheumatology (2023)
10. A Case Series of Ten Plus One Deficiency of Adenosine Deaminase 2 (Dada2) Patients in Iran, Pediatric Rheumatology (2023)
11. Analysis of Lymphocyte and Clinical Profile in Nonmonogenic Common Variable Immunodeficiency Patients With and Without Class Switch Recombination Defect, Journal of Investigational Allergology and Clinical Immunology (2023)
12. Autoantibodies Against Type I Ifns in Humans With Alternative Nf-Κb Pathway Deficiency, Nature (2023)
13. Chediak Higashi Syndrome With Hemophagocytic Lymphohistiocytosis, Fetal and Pediatric Pathology (2023)
14. Clinical and Immunological Characteristics of 69 Leukocyte Adhesion Deficiency-I Patients, Pediatric Allergy and Immunology (2023)
15. Clinical and Immunological Characteristics of 69 Leukocyte Adhesion Deficiency-I Patients, Pediatric Allergy and Immunology (2023)
16. Clinical, Immunological, and Genetic Findings in Iranian Patients With Mhc-Ii Deficiency: Confirmation of C.162Delg Rfxank Founder Mutation in the Iranian Population, Journal of Clinical Immunology (2023)
17. Clinical, Immunological, and Genetic Findings in Iranian Patients With Mhc-Ii Deficiency: Confirmation of C.162Delg Rfxank Founder Mutation in the Iranian Population, Journal of Clinical Immunology (2023)
18. Demographic, Clinical, Immunological, and Molecular Features of Iranian National Cohort of Patients With Defect in Dclre1c Gene, Allergy# Asthma and Clinical Immunology (2023)
19. Hematologically Important Mutations: Leukocyte Adhesion Deficiency (Second Update), Blood Cells# Molecules# and Diseases (2023)
20. Hematologically Important Mutations: Leukocyte Adhesion Deficiency (Second Update), Blood Cells, Molecules, and Diseases (2023)
21. Human Germline Heterozygous Gain-Of-Function Stat6 Variants Cause Severe Allergic Disease, Journal of Experimental Medicine (2023)
22. Human Il-23 Is Essential for Ifn-Γ–Dependent Immunity to Mycobacteria, Science Immunology (2023)
23. Human Mcts1-Dependent Translation of Jak2 Is Essential for Ifn-Γ Immunity to Mycobacteria, Cell (2023)
24. Immunodeficiency With Susceptibility to Lymphoma With Complex Genotype Affecting Energy Metabolism (Fbp1, Acad9) and Vesicle Trafficking (Rab27a), Frontiers in Immunology (2023)
25. Inherited Arpc5 Mutations Cause an Actinopathy Impairing Cell Motility and Disrupting Cytokine Signaling, Nature Communications (2023)
26. Inherited Human Itk Deficiency Impairs Ifn-Γ Immunity and Underlies Tuberculosis, Journal of Experimental Medicine (2023)
27. Tumor Necrosis Factor-Α (-308G>A) Gene Polymorphism and Its Association With Asthma and Atopy Status, Iranian Journal of Allergy# Asthma and Immunology (2023)
28. Adenosine Deaminase (Ada) Deficiency: Report of Six New Cases and Reappraisal of Cutaneous Hypermelanosis As an Early Feature, Journal of Clinical Immunology (2022)
29. Effective Anti-Mycobacterial Treatment for Bcg Disease in Patients With Mendelian Susceptibility to Mycobacterial Disease (Msmd): A Case Series, Annals of Clinical Microbiology and Antimicrobials (2022)
30. Fatal Invasive Aspergillosis in a Child With Chronic Granulomatous Disease, Journal of wound care (2022)
31. Impaired Il-23–Dependent Induction of Ifn-Γ Underlies Mycobacterial Disease in Patients With Inherited Tyk2 Deficiency, Journal of Experimental Medicine (2022)
32. Impaired Il-23–Dependent Induction of Ifn-Γ Underlies Mycobacterial Disease in Patients With Inherited Tyk2 Deficiency, Journal of Experimental Medicine (2022)
33. Molecular and Clinical Characterization of Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy Syndrome (Apeced) in Iranian Non-Jewish Patients: Report of Two Novel Aire Gene Pathogenic Variants, Orphanet Journal of Rare Diseases (2022)
34. The Efficacy of a New Protocol of Oral Immunotherapy to Wheat for Desensitization and Induction of Tolerance, Iranian Journal of Allergy# Asthma and Immunology (2022)
35. Tnfaip3 Mutation Causing Haploinsufficiency of A20 With a Hemophagocytic Lymphohistiocytosis Phenotype: A Report of Two Cases, Pediatric Rheumatology (2022)
36. Tnfaip3 Mutation Causing Haploinsufficiency of A20 With a Hemophagocytic Lymphohistiocytosis Phenotype: A Report of Two Cases, Pediatric Rheumatology (2022)
37. Consensus Middle East and North Africa Registry on Inborn Errors of Immunity, Journal of Clinical Immunology (2021)
38. Effects of Coronavirus Disease 2019 (Covid-19) on Peripheral Blood Lymphocytes and Their Subsets in Children: Imbalanced Cd4+/Cd8+ T Cell Ratio and Disease Severity, Frontiers in Pediatrics (2021)
39. Homozygous Mefv Gene Variant and Pyrin-Associated Autoinflammation With Neutrophilic Dermatosis: A Family With a Novel Autosomal Recessive Mode of Inheritance, JAMA Dermatology (2021)
40. Identification of a New Variant in Nlrp3 Gene by Whole Exome Sequencing in a Patient With Cryopyrin-Associated Periodic Syndrome, Case Reports in Immunology (2021)
41. Impaired Respiratory Burst Contributes to Infections in Pkcδ-Deficient Patients, Journal of Experimental Medicine (2021)
42. Invasive Rasamsonia Argillacea Infection in Chronic Granulomatous Disease: Report of a New Case and Literature Review, Journal of Medical Mycology (2021)
43. Phenotypic Analysis of Pyrin-Associated Autoinflammation With Neutrophilic Dermatosis Patients During Treatment, Rheumatology (United Kingdom) (2021)
44. A Novel Non-Frameshift Ada Deletion Detected by Whole Exome Sequencing in an Iranian Family With Severe Combined Immunodeficiency, Iranian Journal of Allergy# Asthma and Immunology (2020)
45. Delay in Diagnosis of Two Siblings With Severe Ocular Problems and Autoimmune Polyglandular Syndrome, Iranian Journal of Allergy# Asthma and Immunology (2020)
46. Disparity in Access to Care and Its Impact on Diagnosis and Outcomes of Allergic Diseases, Health Disparities in Allergic Diseases: An Evidence-Based Look at Causes# Conditions# and Outcomes (2020)
47. Griscelli Syndrome Type 2 Sine Albinism: Unraveling Differential Rab27a Effector Engagement, Frontiers in Immunology (2020)
48. Nckap1l Defects Lead to a Novel Syndrome Combining Immunodeficiency, Lymphoproliferation, and Hyperinflammation, Journal of Experimental Medicine (2020)
49. Novel Cyba Mutation in a Family With Bcgitis, Acta Microbiologica et Immunologica Hungarica (2020)
50. Ocular Manifestations of Chronic Granulomatous Disease: First Report of Coats’ Disease and Literature Review, Journal of Clinical Immunology (2020)
51. Serum Sickness-Like Reactions in Iranian Children: A Registry-Based Study in a Referral Center, Allergologia et Immunopathologia (2020)
52. A Novel Stk4 Mutation Presenting With Juvenile Idiopathic Arthritis and Epidermodysplasia Verruciformis, Journal of Clinical Immunology (2019)
53. A Rare Case of Hyper Ige Syndrome With Vocal Cords Involvement, Iranian Journal of Allergy# Asthma and Immunology (2019)
54. Associations of Behavioral Disorders With Asthma in Iranian Children, Iranian Journal of Allergy# Asthma and Immunology (2019)
55. Candidate Predisposition Variants in Kaposi Sarcoma As Detected by Whole-Genome Sequencing, Open Forum Infectious Diseases (2019)
56. Clinical Manifestations, Immunological Characteristics and Genetic Analysis of Patients With Hyper-Immunoglobulin M Syndrome in Iran, International Archives of Allergy and Immunology (2019)
57. Comparison of Common Monogenic Defects in a Large Predominantly Antibody Deficiency Cohort, Journal of Allergy and Clinical Immunology: In Practice (2019)
58. Comparison of Common Monogenic Defects in a Large Predominantly Antibody Deficiency Cohort, Journal of Allergy and Clinical Immunology: In Practice (2019)
59. Different Phenotypes of the Same Xiap Mutation in a Family: A Case of Xiap Deficiency With Juvenile Idiopathic Arthritis, Pediatric Blood and Cancer (2019)
60. Evaluation of Interleukin-12 Receptor Β1 and Interferon Gamma Receptor 1 Deficiency in Patients With Disseminated Bcg Infection, Allergologia et Immunopathologia (2019)
61. Genetic Mutations and Immunological Features of Severe Combined Immunodeficiency Patients in Iran, Immunology Letters (2019)
62. Genetic Mutations and Immunological Features of Severe Combined Immunodeficiency Patients in Iran, Immunology Letters (2019)
63. Graft Versus Host Disease and Microchimerism in a Jak3 Deficient Patient, Allergy# Asthma and Clinical Immunology (2019)
64. Mendelian Susceptibility to Mycobacterial Disease: Clinical and Immunological Findings of Patients Suspected for Il12rβ1 Deficiency, Allergologia et Immunopathologia (2019)
65. Post-Mortem Diagnosis of Heme Oxygenase-1 Deficiency by Whole Exome Sequencing in an Iranian Child, International Journal of Molecular and Cellular Medicine (2019)
66. Recurrent Infections and Easy Bruising, Pediatric Immunology: A Case-Based Collection with MCQs (2019)
67. Unc13d Deficiency Associated With Epileptic Seizures and Antibody Deficiency: The First Case From the Iranian National Registry, Journal of Investigational Allergology and Clinical Immunology (2019)
68. Vaccine-Derived Poliovirus Infection Among Patients With Primary Immunodeficiency and Effect of Patient Screening on Disease Outcomes, Iran, Emerging Infectious Diseases (2019)
69. A Novel Ttc7a Deficiency Presenting With Combined Immunodeficiency and Chronic Gastrointestinal Problems, Journal of Investigational Allergology and Clinical Immunology (2018)
70. Avarietyofalu-Mediated Copy Number Variations Can Underlie Il-12Rβ1 Deficiency, Journal of Clinical Immunology (2018)
71. Clinical Presentation and Outcome in Infantile Sandhoff Disease: A Case Series of 25 Patients From Iranian Neurometabolic Bioregistry With Five Novel Mutations Dr. Segolene Ayme, Orphanet Journal of Rare Diseases (2018)
72. Clinical, Immunologic, and Genetic Spectrum of 696 Patients With Combined Immunodeficiency, Journal of Allergy and Clinical Immunology (2018)
73. Clinical, Immunologic, and Genetic Spectrum of 696 Patients With Combined Immunodeficiency, Journal of Allergy and Clinical Immunology (2018)
74. Fourth Update on the Iranian National Registry of Primary Immunodeficiencies: Integration of Molecular Diagnosis, Journal of Clinical Immunology (2018)
75. Fourth Update on the Iranian National Registry of Primary Immunodeficiencies: Integration of Molecular Diagnosis, Journal of Clinical Immunology (2018)
76. Corrigendum: Natural Killer Cells From Patients With Recombinase-Activating Gene and Non-Homologous End Joining Gene Defects Comprise a Higher Frequency of Cd56bright Nkg2a+++ Cells, and yet Display Increased Degranulation and Higher Perforin Content [Front Immunol, 8, (2017), (798)] Doi: 10.3389/Fimmu.2017.00798, Frontiers in Immunology (2017)
77. New Therapeutic Approach by Sirolimus for Enteropathy Treatment in Patients With Lrba Deficiency, European Annals of Allergy and Clinical Immunology (2017)
78. New Therapeutic Approach by Sirolimus for Enteropathy Treatment in Patients With Lrba Deficiency, European Annals of Allergy and Clinical Immunology (2017)
79. Tumefactive Multiple Sclerosis Variants: Report of Two Cases of Schilder and Balo Diseases, Iranian Journal of Child Neurology (2017)
80. Visceral Leishmaniasis in Two Patients With Il-12P40 and Il-12Rβ1 Deficiencies, Pediatric Blood and Cancer (2017)
81. Cohort of Iranian Patients With Congenital Agammaglobulinemia: Mutation Analysis and Novel Gene Defects, Expert Review of Clinical Immunology (2016)
82. Lps-Responsive Beige-Like Anchor Gene Mutation Associated With Possible Bronchiolitis Obliterans Organizing Pneumonia Associated With Hypogammaglobulinemia and Normal Igm Phenotype and Low Number of B, Acta Medica Iranica (2016)
83. Mutation Spectra of the Itgb2 Gene in Iranian Families With Leukocyte Adhesion Deficiency Type 1, Human Immunology (2016)
84. Impaired In-Vitro Responses to Il-12 and Ifn-Γ in Iranian Patients With Mendelian Susceptibility to Mycobacterial Disease, Allergologia et immunopathologia (2015)
85. Inherited and Acquired Immunodeficiencies Underlying Tuberculosis in Childhood, Immunological Reviews (2015)
86. Primary Antibody Deficiency in a Tertiary Referral Hospital: A 30-Year Experiment, Journal of Investigational Allergology and Clinical Immunology (2015)
87. Primary Antibody Deficiency in a Tertiary Referral Hospital: A 30-Year Experiment, Journal of Investigational Allergology and Clinical Immunology (2015)
88. Long-Term Evaluation of a Historical Cohort of Iranian Common Variable Immunodeficiency Patients, Expert Review of Clinical Immunology (2014)
89. Primary Immunodeficiency Disorders in Iran: Update and New Insights From the Third Report of the National Registry, Journal of Clinical Immunology (2014)
90. Selective Antibody Deficiency and Its Relation to the Igg2 and Igg3 Subclass Titers in Recurrent Respiratory Infections, Iranian Journal of Immunology (2013)
91. Timing of Puberty in Iranian Girls According to Their Living Area: A National Study, Journal of Research in Medical Sciences (2011)
92. Characterization of 11 New Cases of Leukocyte Adhesion Deficiency Type 1 With Seven Novel Mutations in the Itgb2 Gene, Journal of Clinical Immunology (2010)