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Neuropediatrics|August 1, 1997
Calpain-3 deficiency causes a mild muscular dystrophy in childhoodH Topaloğlu, P Dinçer, I Richard, et al.European Journal of Haematology|January 1, 1997
High-dose methylprednisolone for children with acute lymphoblastic leukemia and unfavorable presenting featuresG Hiçsönmez, F Gümrük, P V Zamani, et al.European Journal of Haematology|April 1, 1992
High remission rate in acute myeloblastic leukemia in children treated with high-dose methylprednisoloneG Hicsönmez, N Karadeniz, V P Zamani, 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.Journal of Inherited Metabolic Disease|July 18, 2002
Maple syrup urine disease: mutation analysis in Turkish patientsA Dursun, M Henneke, K Ozgül, et al.The Turkish Journal of Pediatrics|April 19, 2000
Autoimmune hemolytic anemia with warm antibodies in children: retrospective analysis of 51 casesA Gürgey, I Yenicesu, T Kanra, et al.Human Genetics|January 12, 2001
Molecular analysis of 16 Turkish families with DHPR deficiency using denaturing gradient gel electrophoresis (DGGE)A Romstad, H S Kalkanoğlu, T Coşkun, et al.JIMD Reports|February 23, 2013
Identification of mutations and evaluation of cardiomyopathy in Turkish patients with primary carnitine deficiencyM Kilic, R K Ozgül, T Coşkun, et al.International Journal of Pediatric Otorhinolaryngology|December 13, 2006
Audiologic findings in children with biotinidase deficiency in TurkeyG A Genc, H S Sivri-Kalkanoğlu, A Dursun, et al.Pageof 13