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Schweizerische Medizinische Wochenschrift|October 14, 1989
[Neurofibromatosis 2 (bilateral acoustic neurofibromatosis)]C Yalcinkaya, A Sarioglu, E Boltshauser
Neuroradiology|September 11, 2002
Progressive white-matter disease with primary cerebellar involvement: a separate entity?C Yalcinkaya, I Arslanoglu, C Islak, et al.
Clinical and Experimental Obstetrics & Gynecology|June 10, 2015
A different technique for the closure of trocar sitesC Yalcinkaya, G Coban, A Parlakgumus, et al.
Neuroradiology|January 1, 1989
MRI in Cockayne syndrome type IE Boltshauser, C Yalcinkaya, W Wichmann, et al.
Clinical and Experimental Obstetrics & Gynecology|March 7, 2014
Operative hysteroscopy preserving virginity: a new techniqueC Yalcinkaya, H Kalayci, E Simsek, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|May 12, 2004
Photosensitive absence epilepsy with myoclonias and heterozygosity for succinic semialdehyde dehydrogenase (SSADH) deficiencyA Dervent, K M Gibson, P L Pearl, et al.
Seizure|December 8, 2006
Seizures during treatment of Vitamin B12 deficiencyG Benbir, S Uysal, S Saltik, et al.
Neuropediatrics|October 12, 2005
Atypical MRI findings in Canavan disease: a patient with a mild courseC Yalcinkaya, G Benbir, G S Salomons, et al.
Neuropediatrics|July 30, 2009
Two cases with progressive cystic leukoencephalopathyZ Yapici, G Benbir, S Saltik, et al.
Clinical Genetics|January 31, 2012
High frequency of GJA12/GJC2 mutations in Turkish patients with Pelizaeus-Merzbacher diseaseB Bilir, Z Yapici, C Yalcinkaya, et al.
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