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Journal of Diabetes and Metabolic Disorders|June 8, 2022
Familial hypercholesterolemia in an Iranian family due to a mutation in the APOE gene (first case report)Shahab Noorian, Rezvan Razmandeh, Roshanak Jazayeri
Journal of Pediatric Endocrinology & Metabolism : JPEM|March 5, 2016
A novel nonsense mutation in the WFS1 gene causes the Wolfram syndromeShahab Noorian, Shahram Savad, Davood Shah Mohammadi
Journal of Medical Case Reports|May 12, 2026
Spondylo-ocular syndrome: xylosyltransferase 2 gene mutation and clinical observations-a case reportMohammad Javad Amini, Hamed Hajishah, Shahab Noorian, et al.
Endocrinology, Diabetes & Metabolism Case Reports|January 12, 2021
Late infantile form of multiple sulfatase deficiencyNami Mohammadian Khonsari, Benyamin Hakak-Zargar, Tessa Voth, et al.
Iranian Journal of Pediatrics|June 1, 2013
GCK Mutation in a Child with Maturity Onset Diabetes of the Young, Type 2Shahab Noorian, Fatemeh Sayarifard, Elham Farhadi, et al.
Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies|May 2, 2022
Compound Heterozygous Mutations Presented with Quadriparesis and Menopause. A Case ReportShahab Noorian, Sahar Mohammadpoor Nami, Zahra Nouri Ghonbalani, et al.
The International Journal of Neuroscience|April 30, 2020
A novel pathogenic variant of BRAT1 gene causes rigidity and multifocal seizure syndrome, lethal neonatalAzam Pourahmadiyan, Morteza Heidari, Hossein Shojaaldini Ardakani, et al.
Clinical Case Reports|December 8, 2025
A Novel EIF2AK3 Variant Causing Wolcott-Rallison Syndrome With Early Neonatal Diabetic Ketoacidosis as Initial Presentation: A Case ReportShahab Noorian, Fatemeh Aghamahdi, Mahnaz Seifi Alan, et al.
Journal of Diabetes and Metabolic Disorders|September 6, 2022
Associated factors to insulin adherence in type 1 diabetes in Tehran and Karaj, IranFarimah Fayyaz, Fatemeh Aghamahdi, Shahab Noorian, et al.
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