Showing results (21-30 of 33) with videos related to

Sort By:
Pageof 4
Archives of Iranian Medicine|June 12, 2014
Hyperglycemia in VLBW infants; incidence, risk factors and outcomeMohammad Kazem Sabzehei, Seyyed Abolfazl Afjeh, Marjan Shakiba, et al.
Pediatric Nephrology (Berlin, Germany)|April 18, 2007
Hyperostosis with hyperphosphatemia and tumoral calcinosis: a case reportHasan Otukesh, Rozita Hoseini, Hamid Chalian, et al.
Molecular Genetics and Metabolism Reports|August 26, 2024
Clinical presentation and molecular genetics of Iranian patients with Niemann-pick type C disease and report of 6 NPC1 gene novel variants: A case seriesHedyeh Saneifard, Marjan Shakiba, Mohammadreza Alaei, et al.
Iranian Journal of Child Neurology|July 20, 2021
Clinical and Paraclinical Characteristics of Non-Classic PhenylketonuriaMarjan Shakiba, Hedyeh Saneifard, Mohammad Reza Alaei, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|March 6, 2022
Benefits of metformin add-on insulin therapy (MAIT) for HbA1c and lipid profile in adolescents with type 1 diabetes mellitus: preliminary report from a double-blinded, placebo-controlled, randomized clinical trialAli Sheikhy, Zahra Eydian, Aida Fallahzadeh, et al.
Molecular Genetics and Metabolism Reports|July 15, 2024
Expanded inherited metabolic diseases screening by tandem mass spectrophotometry: The first report from IranMarjan Shakiba, Mehrdad Yasaei, Hedyeh Saneifard, et al.
Advances in Rare Diseases|August 9, 2016
Adenosine kinase deficiency with neurodevelopemental delay and recurrent hepatic dysfunction: A case reportMarjan Shakiba, Fatemeh Mahjoub, Hassan Fazilaty, et al.
Iranian Journal of Child Neurology|February 6, 2020
Utility of Seizure Pattern and Related Clinical Features in the Diagnosis of Neurometabolic DisordersNarjes Jafari, Asieh Mosallanejad, Asieh Ghobadifar, et al.
European Journal of Medical Genetics|January 26, 2021
NGLY1 deficiency: Novel variants and literature reviewAriana Kariminejad, Marjan Shakiba, Mehrvash Shams, et al.
Journal of Clinical Laboratory Analysis|November 11, 2023
Expanding phenotype heterogeneity of NARS2 by presenting subdural hematoma and parenchymal hemorrhageMehrnoosh Khodaeian, Fatemeh Bitarafan, Fatemeh Garrousi, et al.
Pageof 4