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Journal of Inherited Metabolic Disease|August 7, 2001
Factor V Leiden mutation in Turkish patients with homozygous cystathionine beta-synthase deficiencyH S Kalkanoğlu, T Coşkun, S D Aydoğdu, et al.Mikrobiyoloji Bulteni|October 1, 1984
[A cerebellar abscess caused by anaerobic and aerobic (mixed) microorganisms]A Tokatli, G Kanra, Z Ayhan, et al.The Turkish Journal of Pediatrics|April 19, 2000
Guanosine triphosphate cyclohydrolase I deficiency: a rare cause of hyperphenylalaninemiaT Coşkun, T Karagöz, S Kalkanoğlu, et al.Journal of Pediatric Gastroenterology and Nutrition|March 3, 1998
The effect of zinc-supplemented bread consumption on school children with asymptomatic zinc deficiencyI Kiliç, I Ozalp, T Coŝkun, et al.The Journal of Pediatrics|January 1, 1994
Infantile spasms as the initial symptom of biotinidase deficiencyO Kalayci, T Coskun, A Tokatli, et al.Journal of Inherited Metabolic Disease|May 9, 2000
Novel mutations cause biotinidase deficiency in Turkish childrenR J Pomponio, T Coskun, M Demirkol, et al.Journal of Inherited Metabolic Disease|June 27, 2008
Does maternal knowledge impact blood phenylalanine concentration in Turkish children with phenylketonuria?H Gokmen Ozel, T Kucukkasap, G Koksal, et al.JIMD Reports|February 23, 2013
A Zinc Sulphate-Resistant Acrodermatitis Enteropathica Patient with a Novel Mutation in SLC39A4 GeneM Kilic, M Taskesen, T Coskun, et al.The Turkish Journal of Pediatrics|July 4, 2001
Newborn PKU screening in Turkey: at present and organization for futureI Ozalp, T Coşkun, A Tokatli, et al.Journal of Inherited Metabolic Disease|January 5, 2002
Mutation analysis in Turkish patients with hereditary fructose intoleranceA Dursun, H S Kalkanoğlu, T Coşkun, et al.Pageof 3