Isfahan University of Medical Sciences

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Faculty Members have conducted research related to the Screening of Dfnb3 in Iranian Families With Autosomal Recessive Non-Syndromic Hearing Loss Reveals a Novel Pathogenic Mutation in the Myth4 Domain of the Myo15a Gene in a Linked Family
Noushin Rostampour
Noushin Rostampour

Assistant Professor of Pediatric Endocrinology &

Metabolism

Department of Pediatrics, School of Medicine

Imam Hossein Children's Hospital

Isfahan University of Medical Sciences

Related Documents
1. Molecular Genetic Analysis of the Insulin Gene Variants in Iranian Patients With Permanent Neonatal Diabetes, International Journal of Diabetes in Developing Countries (2023)
All Documents
1. Comprehensive Iranian Guidelines for the Diagnosis and Management of Maple Syrup Urine Disease: An Evidence- and Consensus- Based Approach, Orphanet Journal of Rare Diseases (2025)
2. Comprehensive Iranian Guidelines for the Diagnosis and Management of Maple Syrup Urine Disease: An Evidence- and Consensus- Based Approach, Orphanet Journal of Rare Diseases (2025)
3. Childhood Obesity Is Associated With Subclinical Left Ventricular Dysfunction Detected by Speckle Tracking Echocardiography, Clinical Pediatrics (2024)
4. Evaluation of Cardiac Findings in Mucopolysaccharidosis, International Journal of Cardiovascular Imaging (2024)
5. Quality of Life in Patients With Phenylketonuria: A Systematic Review, Advanced Biomedical Research (2024)
6. Growth and Related Treatment Factors in Mucopolysaccharidoses Type I and Ii: A Systematic Review, Journal of Pediatrics Review (2023)
7. Molecular Genetic Analysis of the Insulin Gene Variants in Iranian Patients With Permanent Neonatal Diabetes, International Journal of Diabetes in Developing Countries (2023)
8. New Molecular Insights Into the A218v Variant Impact on the Steroidogenic Acute Regulatory Protein (Star) Associated With 46, Xy Disorders of Sexual Development, Molecular Genetics and Genomics (2023)
9. Perioperative Management of Endocrine Problems in Pediatric Cardiac Surgery Patients, Congenital Heart Disease in Pediatric and Adult Patients: Anesthetic and Perioperative Management, Second Edition (2023)
10. Cognitive Function in Untreated Subjects With Mild Hyperphenylalaninemia: A Systematic Review, Neurological Sciences (2022)
11. Molecular Characterization of a Large Cohort of Mucopolysaccharidosis Patients: Iran Mucopolysaccharidosis Re-Diagnosis Study (Impression), Human Mutation (2022)
12. Molecular Characterization of a Large Cohort of Mucopolysaccharidosis Patients: Iran Mucopolysaccharidosis Re-Diagnosis Study (Impression), Human Mutation (2022)
13. Prevalence of Nephrocalcinosis in Children With Congenital Adrenal Hyperplasia, Journal of Research in Medical Sciences (2022)
14. Prevalence of Nonalcoholic Fatty Liver Disease in Children With Renal Failure Underwent Treatment With Dialysis, International Journal of Preventive Medicine (2022)
15. The Relationship Between Body Mass Index and Depression, Anxiety, Body Image, and Eating Attitudes in Adolescents in Iran, Advanced Biomedical Research (2022)
16. Acer3-Related Leukoencephalopathy: Expanding the Clinical and Imaging Findings Spectrum Due to Novel Variants, Human Genomics (2021)
17. Acer3-Related Leukoencephalopathy: Expanding the Clinical and Imaging Findings Spectrum Due to Novel Variants, Human Genomics (2021)
18. Effect of Vitamin D on Insulin Resistance in Overweight and Obese Children and Adolescents With Vitamin D Deficiency, Acta Medica Iranica (2020)
19. Instructional Design, Development and Evaluation of Congenital Hypothyroidism Registry System, Webology (2019)
20. Instructional Design, Development and Evaluation of Congenital Hypothyroidism Registry System, Webology (2019)
21. Association Between Vascular Endothelial Markers and Carotid Intima-Media Thickness in Children and Adolescents With Type 1 Diabetes Mellitus, Journal of Clinical and Diagnostic Research (2017)
22. Perioperative Management Endocrine Problems in Pediatric Cardiac Surgical Patients, Congenital Heart Disease in Pediatric and Adult Patients: Anesthetic and Perioperative Management (2017)
23. The Effect of Silymarin on Non-Alcoholic Fatty Liver Disease of Children, Journal of HerbMed Pharmacology (2017)
24. Mutations of Dual Oxidase 2 (Duox2) Gene Among Patients With Permanent and Transient Congenital Hypothyroidism, Pakistan Journal of Medical Sciences (2012)
25. A Case of Atypical Mccune-Albright Syndrome With Vaginal Bleeding, Iranian Journal of Pediatrics (2011)
26. The Mutation of Dual Oxidase 2 (Duox2) Gene Among Patients With Permanent and Transient Congenital Hypothyroidism, Journal of Isfahan Medical School (2011)
27. The Role of Ultrasonography in Primary Congenital Hypothyroidism, Journal of Research in Medical Sciences (2011)
28. Age of Puberty in a Representative Sample of Iranian Girls, World Journal of Pediatrics (2009)
29. Age of Puberty in School-Age Girls Living in Isfahan, Journal of Isfahan Medical School (2007)