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Journal of Pediatric Genetics|August 14, 2019
Investigation of L - Carnitine Concentrations in Treated Patients with Maple Syrup Urine DiseaseBurcu Kumru, Burcu Oztürk Hismi
Cellular and Molecular Neurobiology|December 30, 2017
Effect of Blood Phenylalanine Levels on Oxidative Stress in Classical Phenylketonuric PatientsBurcu Kumru, Davut Sinan Kaplan, Burcu Oztürk Hismi, et al.
International Journal of Pediatric Otorhinolaryngology|May 23, 2006
Effects of GJB2 genotypes on the audiological phenotype: variability is present for all genotypesBurcu Oztürk Hişmi, Suna Tokgöz Yilmaz, Armağan Incesulu, et al.
Cutaneous and Ocular Toxicology|September 7, 2012
Contact sensitivity in Behçet's diseaseEvren Odyakmaz Demirsoy, Rebiay Kiran, Burcu Oztürk, et al.
The Turkish Journal of Pediatrics|February 13, 2007
Mechanical ventilation in childrenTanil Kendirli, Asli Kavaz, Zahide Yalaki, et al.
The Turkish Journal of Pediatrics|May 23, 2013
Detection of other inborn errors of metabolism in hyperphenylalaninemic babies picked up on narrow-spectrum screening programsOzlem Unal, Burcu Oztürk-Hişmi, Turgay Coşkun, et al.
International Journal of Antimicrobial Agents|September 27, 2006
Antibiotic resistance of urinary tract pathogens and evaluation of empirical treatment in Turkish children with urinary tract infectionsSelçuk Yüksel, Burcu Oztürk, Asli Kavaz, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|May 30, 2007
Renal replacement therapies in pediatric intensive care patients: experiences of one center in TurkeyTanil Kendirli, Mesiiha Ekim, Zeynep Birsin Ozçakar, et al.
American Journal of Human Genetics|January 20, 2007
Homozygous mutations in fibroblast growth factor 3 are associated with a new form of syndromic deafness characterized by inner ear agenesis, microtia, and microdontiaMustafa Tekin, Burcu Oztürk Hişmi, Suat Fitoz, et al.
International Journal of Pediatric Otorhinolaryngology|February 4, 2009
Mutations in TMC1 contribute significantly to nonsyndromic autosomal recessive sensorineural hearing loss: a report of five novel mutationsAsli Sirmaci, Duygu Duman, Hatice Oztürkmen-Akay, et al.
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