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Journal of Pediatric Endocrinology & Metabolism : JPEM|September 1, 2000
Evaluation of bone mineral metabolism in children receiving carbamazepine and valproic acidE Erbayat Altay, A Serdaroğlu, L Tümer, et al.Balkan Journal of Medical Genetics : BJMG|August 27, 2021
A Case of Glycogen Storage Disease Type 1a Mimicking Familial Chylomicronemia SyndromeA Olgac, I Okur, G Biberoğlu, et al.The European Journal of Surgery = Acta Chirurgica|June 12, 1999
Effects of 5-fluorouracil and zinc on healing of colonic anastomoses in rabbitsA R Tümer, N A Kama, L Tümer, et al.Acta Paediatrica (Oslo, Norway : 1992)|March 1, 1996
Extracorporeal shock wave lithotripsy in childrenE Hasanoğlu, N Buyan, L Tümer, et al.Balkan Journal of Medical Genetics : BJMG|January 17, 2020
A 7-year-old Boy with Hand Tremors and a Novel Mutation for L-2-hydroxyglutaric AciduriaA Olgac, Orgun L Tekin, F S Ezgü, et al.Genetic Counseling (Geneva, Switzerland)|April 25, 2013
An extremely rare case: osteosclerotic metaphyseal dysplasiaC S Kasapkara, A Küçükçongar, O Boyunağa, et al.European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|January 14, 2012
SRD5A3-CDG: a patient with a novel mutationC S Kasapkara, L Tümer, F S Ezgü, et al.Nutritional Neuroscience|February 3, 2005
Serum carnitine levels in newborns with perinatal asphyxia and relation to neurologic prognosisF S Ezgü, Y Atalay, A Hasanoğlu, et al.Genetic Counseling (Geneva, Switzerland)|September 12, 2018
COBALAMIN C DEFICIENCY WITH INFANTILE SPASM AND CUTANEOUS FINDINGS: A UNIQUE CASEZ Öztürk, E Arhan, K Aydin, et al.Pageof 2