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The Turkish Journal of Pediatrics|January 5, 2002
The role of heterotopic gastric mucosa with or without colonization of Helicobacter pylori upon the diverse symptomatology of Meckel's diverticulum in childrenP Oğuzkurt, B Talim, F C Tanyel, et al.Pediatric Dermatology|May 1, 1997
Pyogenic granuloma with multiple dissemination in a burn lesionM Ceyhan, G Erdem, E Kotiloğlu, et al.Journal of Pediatric Surgery|September 22, 2000
Renal oncocytoma: diagnostic and therapeutic aspectsA O Ciftci, B Talim, M E Senocak, et al.Journal of Pediatric Surgery|April 19, 2000
A comparative histopathologic evaluation of the effects of three different solutions used for whole bowel irrigation: an experimental studyM Bingöl-Koloğlu, M E Senocak, B Talim, et al.Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|June 9, 2005
Clinical spectrum of muscle-eye-brain disease: from the typical presentation to severe autistic featuresG Haliloglu, C Gross, N Senbil, et al.Neurology|March 26, 2003
FKRP gene mutations cause congenital muscular dystrophy, mental retardation, and cerebellar cystsH Topaloglu, M Brockington, Y Yuva, et al.American Journal of Human Genetics|January 23, 1999
Assignment of the muscle-eye-brain disease gene to 1p32-p34 by linkage analysis and homozygosity mappingB Cormand, K Avela, H Pihko, et al.Neuropediatrics|February 7, 2003
Spinal muscular atrophy with progressive myoclonic epilepsy: report of new cases and review of the literatureG Haliloglu, A Chattopadhyay, L Skorodis, et al.Neurology|January 24, 2002
Genetic identity of Marinesco-Sjögren/myoglobinuria and CCFDN syndromesL Merlini, R Gooding, H Lochmüller, et al.Neuromuscular Disorders : NMD|June 19, 1998
Merosin-deficient congenital muscular dystrophy with severe mental retardation and normal cranial MRI: a report of two siblingsH Topaloğlu, B Talim, N Vignier, et al.Pageof 3