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Iranian Journal of Pediatrics|December 24, 2014
A Randomized Clinical Trial of Insulin Glargine and Aspart, Compared to NPH and Regular Insulin in Children with Type 1 Diabetes MellitusParastoo Rostami, Aria Setoodeh, Ali Rabbani, et al.
Orphanet Journal of Rare Diseases|August 5, 2018
Clinical presentation and outcome in infantile Sandhoff disease: a case series of 25 patients from Iranian neurometabolic bioregistry with five novel mutationsAli Reza Tavasoli, Nima Parvaneh, Mahmoud Reza Ashrafi, et al.
Journal of Human Immunity|May 22, 2026
TLR7 F507S gain-of-function mutation presenting with early-onset SLE and hypertriglyceridemia: Response to JAK inhibitionNima Parvaneh, Hossein Karami, Leila Shahbaznejad, et al.
Annales D'Endocrinologie|January 23, 2013
AGPAT2 gene mutation in a child with Berardinelli-Seip congenital lipodystrophy syndromeParastoo Rostami, Maryam Nakhaeimoghadam, Faezeh-Moghimpour Bijani, et al.
Mediterranean Journal of Rheumatology|May 24, 2023
Determination of Bone Density by DEXA Method Based on Bone Age and its Comparison with Chronological Age in Chronic PatientsLeyla Katebi, Ali Rabbani, Fatemeh Sayarifard, et al.
International Journal of Preventive Medicine|June 16, 2022
Hepato-Protection Effect of Curcumin Against Methylphenidate-Induced Hepatotoxicity: Histological and Biochemical EvidencesHaleh Ahmadinasab, Majid Motaghinejad, Bahareh Arabzadeh Nosratabad, et al.
Hormone Research in Paediatrics|June 16, 2026
Genotype-Treatment Correlations in Iranian Children with Congenital Hyperinsulinism: A Single-Center Cohort StudyFarzaneh Sharifi, Saeideh Abdolahpour, Arya Setoudeh, et al.
Minerva Endocrinology|August 4, 2020
Early and delayed puberty among Iranian children with obesityReihaneh Mohsenipour, Farzaneh Abbasi, Aria Setoodeh, et al.
Pharmacological Reports : PR|March 4, 2019
Role of vitamin D and vitamin D receptor gene polymorphisms on residual beta cell function in children with type 1 diabetes mellitusNarges Habibian, Mahsa M Amoli, Farzaneh Abbasi, et al.
Orphanet Journal of Rare Diseases|February 2, 2020
Genotype-phenotype correlation and description of two novel mutations in Iranian patients with glycogen storage disease 1b (GSD1b)Maryam Eghbali, Maryam Abiri, Saeed Talebi, et al.
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