Tehran University of Medical Sciences

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Faculty Members have conducted research related to the Evaluation of Patients Referred to Children's Medical Center Laboratory for Diagnosis of Mucopolysaccharidoses: Eight Years' Experience From Iran
Vahid Ziaee
Vahid Ziaee

Professor of Pediatrics Rheumatology

Department Pediatrics

School of Medicine

Childrens Medical Center

Rheumatology Research Center

Tehran University of Medical Sciences

All Documents
1. Association of Nlrp3 Single Nucleotide Polymorphisms With Juvenile Idiopathic Arthritis: A Case–Control Study, Clinical Rheumatology (2025)
2. Clinicogenetic Characterisation of Slc29a3-Related Syndromes: A Case Series, Tracing Ancestral Variants and Molecular Dynamics Simulation, Journal of Medical Genetics (2025)
3. Hematopoietic Stem Cell Transplantation for C1q Deficiency: A Study on Behalf of the Ebmt Inborn Errors Working Party, Journal of Clinical Immunology (2025)
4. High Occurrence of a Missense Variant (C.471C>A) in the Fgf23 Gene Related to Hyperostosis–Hyperphosphatemia Syndrome With a Possible Founder Effect, Human Mutation (2025)
5. Biallelic Human Sharpin Loss of Function Induces Autoinflammation and Immunodeficiency, Nature Immunology (2024)
6. Comparison of the Efficacy of Three Natural Surfactants (Curosurf, Survanta, and Alveofact) in the Treatment of Respiratory Distress Syndrome Among Neonates: A Randomized Controlled Trial [Iran J Pediatr. 2016;26(5): E5743], Iranian Journal of Pediatrics (2024)
7. Exploring the Association Between Serum Vitamin D Levels and the Development of Coronary Artery Lesions in Kawasaki Disease - a Systematic Review, Pediatric Rheumatology (2024)
8. Fecal Calprotectin and the Complications of Iga-Mediated Vasculitis: A Cohort Study, Journal of Comprehensive Pediatrics (2024)
9. Methylprednisolone Pulses As an Effective Treatment in Multisystem Inflammatory Syndrome in Children Associated With Sars-Cov-2 (Mis-C), and the Best Alternative for Ivig, Iranian Journal of Pediatrics (2024)
10. Rheumatic Disorders and Athletic Achievement: Can Chronic Illness Stop Olympic Dreams?, Asian Journal of Sports Medicine (2024)
11. Three Cases of Autoinflammatory Disease With Novel Nlrc4 Mutations, and the First Mutation Reported in the Card Domain of Nlrc4 Associated With Autoinflammatory Infantile Enterocolitis (Aifec), Pediatric Rheumatology (2024)
12. A Case Series of Ten Plus One Deficiency of Adenosine Deaminase 2 (Dada2) Patients in Iran, Pediatric Rheumatology (2023)
13. A Case Series of Ten Plus One Deficiency of Adenosine Deaminase 2 (Dada2) Patients in Iran, Pediatric Rheumatology (2023)
14. Against War, Peace for Every Child, Everywhere, Iranian Journal of Pediatrics (2023)
15. Editorial: Case Reports in Pediatric Rheumatology 2022, Frontiers in Pediatrics (2023)
16. Evaluation of Bone Mineral Density in Juvenile Systemic Lupus Erythematosus, Archives of Bone and Joint Surgery (2023)
17. Giant Coronary Aneurysms With Multiple Large Resistant Thromboses in an 8-Month-Old Boy With Ivig-Resistant Kawasaki Disease: A Case Report, Journal of Tehran University Heart Center (2023)
18. Multisystem Inflammatory Syndrome in Children and Kawasaki Disease; Comparison of Their Clinical Findings and One-Year Follow-Up—A Cross-Sectional Study, Italian Journal of Pediatrics (2023)
19. Neonatal Multisystem Inflammatory Syndrome Associated With Covid-19 Exposure in Two Cases From Iran, Journal of Comprehensive Pediatrics (2023)
20. Study of Nlrp3 Single Nucleotide Polymorphisms in Juvenile Systemic Lupus Erythematosus (Jsle), Immunological Investigations (2023)
21. The Role of Nailfold Capillaroscopy in Pediatric Patients With Kawasaki Disease; [El Papel De La Capilaroscopia Periungueal Pacientes Pediatricos Con La Enfermedad De Kawasaki], Reumatologia Clinica (2023)
22. Wolman Disease Presenting With Hemophagocytic Lymphohistiocytosis Syndrome and a Novel Lipa Gene Variant: A Case Report and Review of The Literature, Journal of Medical Case Reports (2023)
23. An Unusual Ten-Like Presentation of Juvenile Bullous Pemphigoid: A Diagnostic Challenge, Case Reports in Dermatological Medicine (2022)
24. An Unusual Ten-Like Presentation of Juvenile Bullous Pemphigoid: A Diagnostic Challenge, Case Reports in Dermatological Medicine (2022)
25. Colchicine Versus Cimetidine: The Better Choice for Periodic Fever, Aphthous Stomatitis, Pharyngitis, Adenitis (Pfapa) Syndrome Prophylaxis, and the Role of Mefv Gene Mutations, Pediatric Rheumatology (2022)
26. Diagnostic Value of Nailfold Capillaroscopy Changes in Henoch–Schonlein Purpura Children With Gastrointestinal or Renal Involvement, Egyptian Rheumatologist (2022)
27. Dna Methylation of Cd70 Promoter in Juvenile Systemic Lupus Erythematosus, Fetal and Pediatric Pathology (2022)
28. Editorial: Covid-19 and Hyper Inflammation Syndrome: Different Presentation and Management, Frontiers in Pediatrics (2022)
29. Iran's Higher Education and Covid-19: The New Normal for Tehran University of Medical Sciences, Journal of Clinical and Translational Science (2022)
30. Joint Stiffness Leads to the Diagnosis of a Rare Disease, Iranian Journal of Pediatrics (2022)
31. Methylprednisolone Pulses As an Initial Treatment in Hyperinflammatory Syndrome After Covid-19 in Children: Evaluation of Laboratory Data, Serial Echocardiography and Outcome: A Case Series, Intensive Care Medicine Experimental (2022)
32. The Post-Covid-19 Complications in Children: Hemolytic Uremic Syndrome, New-Onset Vasculitis, and Acute Hepatitis, Iranian Journal of Pediatrics (2022)
33. Tnfaip3 Mutation Causing Haploinsufficiency of A20 With a Hemophagocytic Lymphohistiocytosis Phenotype: A Report of Two Cases, Pediatric Rheumatology (2022)
34. Tnfaip3 Mutation Causing Haploinsufficiency of A20 With a Hemophagocytic Lymphohistiocytosis Phenotype: A Report of Two Cases, Pediatric Rheumatology (2022)
35. Aberrant Dna Methylation of the Promoters of Jak2 and Socs3 in Juvenile Systemic Lupus Erythematosus, European Cytokine Network (2021)
36. An Algorithmic Approach to Management of Covid-19 Associated Multisystem Inflammatory Syndrome in Children, Archives of Pediatric Infectious Diseases (2021)
37. An Algorithmic Approach to Management of Covid-19 Associated Multisystem Inflammatory Syndrome in Children, Archives of Pediatric Infectious Diseases (2021)
38. Covid-19 and Myositis; True Dermatomyositis or Prolonged Post Viral Myositis?, Pediatric Rheumatology (2021)
39. Evaluation of Patients Referred to Children's Medical Center Laboratory for Diagnosis of Mucopolysaccharidoses: Eight Years' Experience From Iran, Journal of Child Science (2021)
40. Homozygous Mefv Gene Variant and Pyrin-Associated Autoinflammation With Neutrophilic Dermatosis: A Family With a Novel Autosomal Recessive Mode of Inheritance, JAMA Dermatology (2021)
41. 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)
42. Management of Childhood Rheumatic Diseases During the Covid-19 Pandemic: A Survey on Parental Approaches and Involvements in the Treatment Procedure, Iranian Journal of Pediatrics (2021)
43. Multimodality Imaging of Constrictive Pericarditis in H Syndrome, Echocardiography (2021)
44. Phenotypic Analysis of Pyrin-Associated Autoinflammation With Neutrophilic Dermatosis Patients During Treatment, Rheumatology (United Kingdom) (2021)
45. Serological Screening of Celiac Disease in Patients With Juvenile Idiopathic Arthritis, Archives of Iranian Medicine (2021)
46. The First Presentation of Localized Scleroderma at Birth: Scleroderma As a Differential Diagnosis of Congenital Skin Lesion, Journal of Child Science (2021)
47. An Algorithmic Approach to Multisystem Inflammatory Syndrome in Children With Covid-19: Tehran Children’S Medical Center Protocol, Iranian Journal of Pediatrics (2020)
48. Childhood-Onset Systemic Lupus Erythematosus: How Is It Associated With Breastfeeding and Mode of Delivery?, Journal of Child Science (2020)
49. Covid-19 Pandemic and Biological Therapy in Rheumatologic Disorders: How to Deal With?, Reumatismo (2020)
50. Griscelli Syndrome Type 2 Sine Albinism: Unraveling Differential Rab27a Effector Engagement, Frontiers in Immunology (2020)
51. Homozygous Il1rn Mutation in Siblings With Deficiency of Interleukin-1 Receptor Antagonist (Dira), Journal of Clinical Immunology (2020)
52. Increased Qt Interval Dispersion Is Associated With Coronary Artery Involvement in Children With Kawasaki Disease, Oman Medical Journal (2020)
53. Interleukin-23 Receptor Gene Polymorphisms in Iranian Patients With Juvenile Systemic Lupus Erythematosus, Allergologia et Immunopathologia (2020)
54. Multisystem Inflammatory Syndrome Associated With Sars-Cov-2 Infection in 45 Children: A First Report From Iran, Epidemiology and Infection (2020)
55. Nckap1l Defects Lead to a Novel Syndrome Combining Immunodeficiency, Lymphoproliferation, and Hyperinflammation, Journal of Experimental Medicine (2020)
56. Ptpn22 Gene Polymorphisms in Pediatric Systemic Lupus Erythematosus, Fetal and Pediatric Pathology (2020)
57. The Comparison of Nailfold Capillaroscopy Between Juvenile Systemic Lupus Erythematosus and Healthy Controls: Correlation With Laboratory and Clinical Parameters, International Journal of Vascular Medicine (2020)
58. The Cytoskeletal Regulator Hem1 Governs B Cell Development and Prevents Autoimmunity, Science Immunology (2020)
59. The Status of Foxp3 Gene Methylation in Pediatric Systemic Lupus Erythematosus, Allergologia et Immunopathologia (2020)
60. A Novel Stk4 Mutation Presenting With Juvenile Idiopathic Arthritis and Epidermodysplasia Verruciformis, Journal of Clinical Immunology (2019)
61. A Rare Disease With a Rare Presentation: Hemi-Atrophy Caused by Fibromuscular Dysplasia in a 27 Month Old Girl, Reumatismo (2019)
62. Adrenal Insufficiency in Children With Juvenile Idiopathic Arthritis (Jia) Treated With Prednisolone, Journal of Comprehensive Pediatrics (2019)
63. Direct Immunofluorescence Results of the Skin Biopsy and Frequency of Systemic Involvement in Children With Henoch-Schonlein Purpura, Fetal and Pediatric Pathology (2019)
64. Farber Disease: Report of Three Cases With Joint Involvement Mimicking Juvenile Idiopathic Arthritis, Journal of Musculoskeletal Neuronal Interactions (2019)
65. Gastrointestinal Calcinosis As a Rare Cause of Death in Juvenile Polymyositis, Iranian Journal of Pediatrics (2019)
66. Interleukin 10 and Transforming Growth Factor Beta Polymorphisms As Risk Factors for Kawasaki Disease: A Case-Control Study and Meta-Analysis, Avicenna Journal of Medical Biotechnology (2019)
67. Macrophage Activation Syndrome As a Complication of Rheumatologic Disorders, a Report From Iran, Reumatismo (2019)
68. Mucopolysaccharidosis Type I in Children, a Forgotten Diagnosis Responsible for Undiagnosed Musculoskeletal Complaints: Report of Two Cases, Acta Medica (2019)
69. Post-Mortem Diagnosis of Heme Oxygenase-1 Deficiency by Whole Exome Sequencing in an Iranian Child, International Journal of Molecular and Cellular Medicine (2019)
70. Prolonged Fever and Intravenous Immunoglobulin Resistance in Kawasaki Disease: Should Macrophage Activation Syndrome Be Considered?, Iranian Journal of Pediatrics (2019)
71. Retraction: Correlation Between Anthropometric, Physical Fitness Traits, Lung Capacity, and Success of Iranian Elite Greco-Roman Wrestlers (Asian J Sports Med., 2018), Asian Journal of Sports Medicine (2019)
72. Yogurt Drink Effectively Rehydrates Athletes After a Strenuous Exercise Session, Acta Medica Bulgarica (2019)
73. Association of Interferon Regulatory Factor 5 (Irf5) Gene Polymorphisms With Juvenile Idiopathic Arthritis, Clinical Rheumatology (2018)
74. Autoimmunity and Its Association With Regulatory T Cells and B Cell Subsets in Patients With Common Variable Immunodeficiency, Allergologia et Immunopathologia (2018)
75. Exome Sequencing Revealed C1q Homozygous Mutation in Pediatric Systemic Lupus Erythematosus, Allergologia et Immunopathologia (2018)
76. Familial Mediterranean Gene (Mefv) Mutation in Parents of Children With Familial Mediterranean Fever: What Are the Exceptions?, International Journal of Inflammation (2018)
77. Growth Failure in a Series of Iranian Patients With Juvenile Idiopathic Arthritis, Iranian Journal of Pediatrics (2018)
78. Interleukin-4 Cytokine Single Nucleotide Polymorphisms in Kawasaki Disease: A Case-Control Study and a Review of Knowledge, International Journal of Rheumatic Diseases (2018)
79. Neuropsychiatric Involvement in Juvenile-Onset Systemic Lupus Erythematosus, Neurology Research International (2018)
80. Pro-Inflammatory Cytokine Single Nucleotide Polymorphisms in Kawasaki Disease, International Journal of Rheumatic Diseases (2018)
81. Rheumatologic Complications in a Cohort of 227 Patients With Common Variable Immunodeficiency, Scandinavian Journal of Immunology (2018)
82. Role of Kobayashi Risk Scoring for Determining Refractory Kawasaki Disease, Journal of Comprehensive Pediatrics (2018)
83. Single Nucleotide Polymorphism of Methyl-Cpg-Binding Protein 2 Gene Associates With Juvenile Idiopathic Arthritis, Clinical Rheumatology (2018)
84. The Farsi Version of the Juvenile Arthritis Multidimensional Assessment Report (Jamar), Rheumatology International (2018)
85. The Genetic Basis of Hyaline Fibromatosis Syndrome in Patients From a Consanguineous Background: A Case Series, BMC Medical Genetics (2018)
86. Approach to the Management of Autoimmunity in Primary Immunodeficiency, Scandinavian Journal of Immunology (2017)
87. Approach to the Management of Autoimmunity in Primary Immunodeficiency, Scandinavian Journal of Immunology (2017)
88. April Gene Polymorphism and Serum Sapril Levels in Children With Systemic Lupus Erythematosus, Clinical Rheumatology (2017)
89. Assessment of Sexual Maturation Among Boys in Special Schools of Tehran, Iran, International Journal of Pediatrics (2017)
90. Association of Interleukin-6 Single Nucleotide Polymorphisms With Juvenile Idiopathic Arthritis, Clinical Rheumatology (2017)
91. Association of Ptpn22 Gene Polymorphisms With Susceptibility to Juvenile Idiopathic Arthritis in Iranian Population, Fetal and Pediatric Pathology (2017)
92. Association of Stat4 Gene Single Nucleotide Polymorphisms With Iranian Juvenile-Onset Systemic Lupus Erythematosus Patients, Turkish Journal of Pediatrics (2017)
93. Association Study of Mecp2 Gene Single Nucleotide Polymorphisms in Juvenile-Onset Systemic Lupus Erythematosus Patients From Iran, Fetal and Pediatric Pathology (2017)
94. Chronic Recurrent Multifocal Osteomyelitis: A Case Report, Iranian Journal of Pediatrics (2017)
95. Comparison of Adenosine Deaminase Level in Serum and Synovial Fluid in Patients With Juvenile Idiopathic Arthritis and Its Relation to Inflammatory Acute Phase Reactants, Iranian Journal of Pediatrics (2017)
96. Comparison of Bone Mineral Density in Common Variable Immunodeficiency and X-Linked Agammaglobulinaemia Patients, Endocrine# Metabolic and Immune Disorders - Drug Targets (2017)
97. Comparison of Bone Mineral Density in Common Variable Immunodeficiency and X-Linked Agammaglobulinaemia Patients, Endocrine, Metabolic and Immune Disorders - Drug Targets (2017)
98. Frequency and Type of Hepatic and Gastrointestinal Involvement in Juvenile Systemic Lupus Erythematosus, Autoimmune Diseases (2017)
99. Hyaline Fibromatosis Syndrome: A Novel Mutation and Recurrent Founder Mutation in the Cmg2/Antxr2 Gene, Acta Dermato-Venereologica (2017)
100. Lack of Association Between Stat4 Single Nucleotide Polymorphisms and Iranian Juvenile Rheumatoid Arthritis Patients, Fetal and Pediatric Pathology (2017)
101. Methylprednisolone Pulse Therapy Can Be Life-Saving in Neonatal Lupus Erythematous: A Case Report, Iranian Journal of Pediatrics (2017)
102. Pdcd1 Single Nucleotide Polymorphisms in Iranian Patients With Juvenile Idiopathic Arthritis, Acta Medica Iranica (2017)
103. Phace(S) Syndrome: Report of a Case With New Ocular and Systemic Manifestations, Journal of Current Ophthalmology (2017)
104. Status of Bone Mineral Density in Children With Type 1 Diabetes Mellitus and Its Related Factors, Iranian Journal of Pediatrics (2017)
105. The Relationship Between Sonographic Findings, and Clinical and Paraclinical Symptoms in Henoch Schonlein Purpura, Iranian Journal of Pediatrics (2017)
106. Association of Interleukin-1 Family Gene Polymorphisms With Juvenile Idiopathic Arthritis in Iranian Population, Allergologia et Immunopathologia (2016)
107. Association of Interleukin-2 and Interferon-Γ Single Nucleotide Polymorphisms With Juvenile Systemic Lupus Erythematosus, Allergologia et Immunopathologia (2016)
108. Association of Interleukin-2, But Not Interferon-Gamma, Single Nucleotide Polymorphisms With Juvenile Idiopathic Arthritis, Allergologia et Immunopathologia (2016)
109. Association of Tumour Necrosis Factor-Alpha G/A -238 and G/A -308 Single Nucleotide Polymorphisms With Juvenile Idiopathic Arthritis, International Journal of Immunogenetics (2016)
110. Changes of Platelet Indices in Juvenile Idiopathic Arthritis in Acute Phase and After Two Months Treatment, Iranian Journal of Pediatrics (2016)
111. Il23r Gene Polymorphism With Juvenile Idiopathic Arthritis and Its Association With Serum Il-17A, International Journal of Rheumatic Diseases (2016)
112. Interleukin 10 and Transforming Growth Factor Beta 1 Gene Polymorphisms in Juvenile Idiopathic Arthritis, Bratislava Medical Journal (2016)
113. Novel Echocardiographic Indices for Assessing the Left Main Coronary Artery in Children With Kawasaki Disease, Iranian Journal of Pediatrics (2016)
114. Polymorphisms of Genes Encoding Interleukin-4 and Its Receptor in Iranian Patients With Juvenile Idiopathic Arthritis, Clinical Rheumatology (2016)
115. Prevalence of Positive Autoimmune Biomarkers in the Brucellosis Patients, Clinical Rheumatology (2016)
116. Biological Motion Perception Is Affected by Age and Cognitive Style in Children Aged 8-15, Neurology Research International (2015)
117. Children With Autism Spectrum Disorder and Patterns of Participation in Daily Physical and Play Activities, Neurology Research International (2015)
118. Dynamic Changes, Cut-Off Points, Sensitivity, and Specificity of Laboratory Data to Differentiate Macrophage Activation Syndrome From Active Disease, Disease Markers (2015)
119. Infantile Systemic Hyalinosis in an Iranian Family With a Mutation in the Cmg2/Antxr2 Gene, Clinical and Experimental Dermatology (2015)
120. Kawasaki Disease and Peripheral Gangrene in Infancy, Iranian Journal of Pediatrics (2015)
121. Lack of Association Between Interleukin-10, Transforming Growth Factor-Beta Gene Polymorphisms and Juvenile-Onset Systemic Lupus Erythematosus, Clinical Rheumatology (2015)
122. Noninvasive Evaluation of Myocardial Systolic Dysfunction in the Early Stage of Kawasaki Disease: A Speckle-Tracking Echocardiography Study, Iranian Journal of Pediatrics (2015)
123. Pdcd1 Single Nucleotide Genes Polymorphisms Confer Susceptibility to Juvenile-Onset Systemic Lupus Erythematosus, Autoimmunity (2015)
124. Penile Skin Involvement As the First Presentation of Henoch-Schonlein Purpura Report of Nine Cases and Review of Literature, Iranian Journal of Pediatrics (2015)
125. Presence of a Juvenile Idiopathic Arthritis and Chronic Granulomatous Disease in a Child, Iranian Journal of Pediatrics (2015)
126. Sport Injuries of Karate During Training: An Epidemiologic Study in Iran, Asian Journal of Sports Medicine (2015)
127. The Role of Cytokines in Systemic Lupus Erythematosis: Review Article, Tehran University Medical Journal (2015)
128. Tumor Necrosis Factor-Alpha Single Nucleotide Polymorphisms in Juvenile Systemic Lupus Erythematosus, Human Immunology (2015)
129. Primary Immunodeficiency Disorders in Iran: Update and New Insights From the Third Report of the National Registry, Journal of Clinical Immunology (2014)
130. The Impact of an After-School Physical Activity Program on Health-Related Fitness of Mother/Daughter Pairs: Caspian Study, Preventive Medicine (2012)
131. A National Experience on Physical Activity Initiatives for Adolescent Girls and Their Mothers: Caspian Study, Iranian Journal of Pediatrics (2010)
132. Association of Physical Activity and the Metabolic Syndrome in Children and Adolescents: Caspian Study, Hormone Research (2007)