A5014595413- Neonatal Health and Biochemistry
- Childhood Cancer Survivors' Quality of Life
- Liver Disease Diagnosis and Treatment
- Cellular Mechanics and Interactions
- Migraine and Headache Studies
- DNA Repair Mechanisms
- Cell Adhesion Molecules Research
- Metabolism and Genetic Disorders
- Pharmacological Effects and Toxicity Studies
- Thyroid Disorders and Treatments
- Folate and B Vitamins Research
- Genetics and Neurodevelopmental Disorders
- Gestational Diabetes Research and Management
- Cardiovascular Issues in Pregnancy
- Acute Lymphoblastic Leukemia research
- Neonatal and fetal brain pathology
- Epilepsy research and treatment
- Skin and Cellular Biology Research
- Congenital Heart Disease Studies
- Hemoglobinopathies and Related Disorders
Ahvaz Jundishapur University of Medical Sciences
2010-2021
To investigate an association between seasonal changes in temperature and the prevalence of congenital hypothyroidism (CH) Southwest Iran.A prospective two-year study conducted from March 2007 to 2009 during nationwide screening programme for CH Ahvaz, biggest city southwest Iran. Blood samples were taken almost all newborns by heel-stick used a thyroid-stimulating hormone (TSH)-enzyme-linked immunosorbent assay (ELISA). Serum thyroxine (T4) TSH measured if ELISA-TSH was >5 mIU/L (suspicious...
Abstract Cockayne syndrome (CS) is one the rare DNA‐repair deficiency disorders with autosomal recessive inheritance. Failure to thrive and microcephaly are major criteria of diagnosis. Owing genetic heterogeneity CS, whole exome sequencing promising way determine basis disease. Here, we present c.1053delT in ERCC8 gene an Iranian family symptom CS using sequencing. The deletion was novel not previously reported elsewhere.
ENWEndNote BIBJabRef, Mendeley RISPapers, Reference Manager, RefWorks, Zotero AMA Momen A, Riahi K, Jelodar G, et al. Vitamin D status in children with migraine: a case-control study. Pediatria Polska - Polish Journal of Paediatrics. 2020;95(4):228-233. doi:10.5114/polp.2020.103505. APA Momen, A., Riahi, K., Jelodar, G., Nasiri, S., Majidinezjad, & Nilsaz-Dezfouli, H. (2020). Paediatrics, 95(4), 228-233. https://doi.org/10.5114/polp.2020.103505 Chicago Aliakbar, Kourosh Gholamreza Shahram...
Crigler-Najjar syndrome (CNS) type I and II are inherited as autosomal recessive conditions that caused by mutations in the UGT1A1 gene. We present analysis of gene 12 individuals from three different families. This allowed us to identify one novel mutation, which was not previously described. In this study, families with clinically diagnosed CNS referred Khuzestan province, southwest Iran, were screened. After signing informed consent, peripheral blood samples patients their parents...