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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.
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.
The Turkish Journal of Pediatrics|April 1, 1997
Autoimmune polyglandular syndrome type I. A case reportP Cinaz, A Bideci, A Haznedaroğlu, et al.
Acta Paediatrica (Oslo, Norway : 1992)|August 14, 1999
Plasma leptin levels of large for gestational age and small for gestational age infantsP Cinaz, E Sen, A Bideci, 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.
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