M.D. Gamze Şarbat is a pediatrician trained at Istanbul University Faculty of Medicine, graduating in 1994. She practiced general pediatrics at Maslak Acıbadem Hospital from 2010 to 2018, providing comprehensive care for infants, children, and adolescents. Dr. Şarbat is a member of the Istanbul Medical Chamber and remains dedicated to promoting child health through clinical excellence, preventive care, and family-centered practice.
Education
- 1994 Istanbul University Istanbul Faculty of Medicine Pediatrics
- 1989 Istanbul University Istanbul Faculty of Medicine
Experience
- 2010 – 2018 Maslak Acibadem Hospital General Pediatrics
- 2010 Acibadem Health Group
- 2006 – 2009 Etiler Acibadem Medical Center Healthy Child and General Pediatrics
- 2000 – 2006 Kadikoy Acibadem Hospital General Pediatrics
- 1994 – 2001 Istanbul University Istanbul Faculty of Medicine, Department of Pediatrics, Division of Nutrition and Metabolism Chief Assistant
- 1999 – 2000 The University of Illinois at Chicago Department of Genetics and Metabolism Department of Pediatrics
- 1998 – 1999 Pediatric Metabolic Diseases at the University of Illinois at Chicago
- 1989 – 1994 Istanbul University Istanbul Faculty of Medicine Pediatrics Residency
- 1983 – 1989 Istanbul University Istanbul Faculty of Medicine Medical Doctorate
Memberships
- Istanbul Medical Chamber
Publications
- The molecular basis of glycogen storage disease type Ia.
J Biol Chem 277 (7): 5047-5053 (2002) Shieh JJ, Terzioglu M, Hiraiwa H, et al. - Glycogen storage disease type I: diagnosis and phenotype/genotype correlation.
Eur J Pediatr 161: S10-S19 Suppl. 1 OCT (2002) Matern D, Seydewitz HH, Bali D, et al. - The catalytic center of glucose-6-phosphatase-HIS176 is the nucleophile forming the phosphohistidine-enzyme intermediate during catalysis.
J Biol Chem 277 (36): 32837-32842 (2002) Ghosh A, Shieh JJ, Pan CJ, et al. - Clinical and neuropsychological outcome in 33 patients with biotinidase deficiency ascertained by nationwide newborn screening and family studies in Austria.
Eur J Pediatr 160 (5): 277-282 (2001) Moslinger D, Stockler-Ipsiroglu S, Scheibenreiter S, et al. - Glucose-6-phosphatase gene mutation in Turkish patients with glycogen storage disease type Ia.
Journal of Inherited Metabolic Disease 24 (8): 881-882 (2001) Terzioglu M, Emre S, Ozen H, et al. - Molecular genetics of type I glycogen storage disease.
Mol Genet Metab 73 (2): 117-125 (2001) Janecke AR, Mayatepek E, Utermann G. - . Novel mutations cause biotinidase deficiency in Turkish children.
Journal of Inherited Metabolic Disease 23 (2): 120-128 (2000) Pomponio RJ, Coskun T, Demirkol M, et al. - Glycogen storage disease type Ia: recent experience with mutation analysis a summary of mutations reported in the literature and a newly developed diagnostic flowchart.
Eur J Pediatr 159 (5): 322-330 (2000) Rake JP, ten Berge AM, Visser G, et al. - Heterogeneous mutation in the glucose-6-phosphatase gene in Japanese patients with glycogen storage disease type Ia.
Am J Med Genet 92 (2): 90-94 (2000) Takahashi K, Akanuma J, Matsubara Y, et al. - Molecular aspects of glycogen storage disease type Ia in Turkish patients: a novel mutation in the glucose-6- phosphatase gene.
J Inherit Metab Dis 21: 445-446 (1998) Hüner G, Podskarbi T, Schütz M, Baykal T, Şarbat G, Shin YS, Demirkol M. - Incidence of biotinidase deficiency in Turkish newborns.
T, Huner G, Sarbat G, et al. Acta Paediatrica 87 (10): 1102-1103 (1998) - Five years experience in newborn screening for biotinidase deficiency in Istanbul.
Enzyme Protein 49: 186-187 (1996) Demirkol M, Baykal T, Hüner G, Şarbat G, İnce Z, Cantez T.
