Tehran University of Medical Sciences

Science Communicator Platform

Faculty Members have conducted research related to the A Novel Mutation in the Oxct1 Gene Causing Succinyl-Coa:3-Ketoacid Coa Transferase (Scot) Deficiency Starting With Neurologic Manifestations
Fatemeh Mahjoub

Associate Professor of Pathology

Department Pathology

School of Medicine

Bahrami Hospital

Maternal, Fetal and Neonatal Research Center

Tehran University of Medical Sciences

All Documents
1. Detection of Eosinophilic Cell-Free Granules Based on Expression of Ccr3 and Mbp Markers in Esophageal Biopsy Specimens of Patients With Suspected and Confirmed Eosinophilic Esophagitis, Pediatric Gastroenterology, Hepatology and Nutrition (2025)
2. Bile Acid Synthesis Disorder, the First Reported Case From Iran, (Proven by Genetic Study), How the Unavailability of Drug Affected the Course of Treatment, Iranian Journal of Pediatrics (2023)
3. Previously Unreported Esophageal Lymphoid Polyp in a Child: A Case Report With Histopathology, Fetal and Pediatric Pathology (2023)
4. Assessment of Ige-And Cell-Mediated Immunity in Pediatric Patients With Eosinophilic Esophagitis, European Annals of Allergy and Clinical Immunology (2021)
5. Vascular Changes in Eosinophilic Esophagitis (Eoe), Report of an Unusual Case, Fetal and Pediatric Pathology (2020)
6. Application of Human Acellular Breast Dermal Matrix (Abdm) in Implant-Based Breast Reconstruction: An Experimental Study, Aesthetic Plastic Surgery (2017)
7. The Role of Outer Inflammatory Protein a (Oipa) in Vaccination of the C57bl/6 Mouse Model Infected by Helicobacter Pylori, Turkish Journal of Medical Sciences (2017)
8. Validity of Selected Wbc Differentiation Flags in Sysmex Xt-1800I, Iranian Journal of Pathology (2016)
9. Analysis of Vaca/Caga Genotypes/Status in Helicobacter Pylori Isolates From Iranian Children and Their Association With Clinical Outcome, Turkish Journal of Medical Sciences (2015)
10. Introducing a New Histologic Scoring System for Iron Deposition in Liver of Thalassemic Patients, Compared With Atomic Absorption Spectrometry, Experimental and Toxicologic Pathology (2015)
11. Rosai-Dorfman Disease With Nodal and Extranodal Involvements: A Case Report, Journal of Research in Medical Sciences (2011)
12. Renal Amyloidosis in Common Variable Immunodeficiency, Nefrologia (2010)
13. The Clinical, Immunohematological, and Molecular Study of Iranian Patients With Severe Congenital Neutropenia, Journal of Clinical Immunology (2007)