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Current Molecular Medicine|March 20, 2002
Molecular mechanisms of neuronal migration disorders, quo vadis?S Couillard-Despres, J Winkler, G Uyanik, et al.Fetal Diagnosis and Therapy|December 9, 2000
Increased nuchal translucency in a case of long-chain 3-hydroxyacyl- coenzyme A dehydrogenase deficiencyS Tercanli, G Uyanik, I Hösli, et al.Neuroimmunomodulation|April 14, 2006
Relation between laterality and immune response after acute cerebral ischemiaH J Koch, G Uyanik, U Bogdahn, et al.Journal of Medical Genetics|November 22, 2005
A filamin A splice mutation resulting in a syndrome of facial dysmorphism, periventricular nodular heterotopia, and severe constipation reminiscent of cerebro-fronto-facial syndromeU Hehr, A Hehr, G Uyanik, et al.Klinische Padiatrie|March 17, 2005
[Congenital muscular dystrophies: muscle-eye-brain disease]S Meyer, T Struffert, G Uyanik, et al.Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|May 10, 2011
Selective bilateral hippocampal lesions after theophylline-induced status epilepticus causes a permanent amnesic syndromeZ Kohl, G Uyanik, R Lürding, et al.Neuropediatrics|July 13, 2004
X-linked lissencephaly with abnormal genitalia associated with renal phosphate wastingA Hahn, C Gross, G Uyanik, 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|July 23, 2003
ARX mutations in X-linked lissencephaly with abnormal genitaliaG Uyanik, L Aigner, P Martin, et al.American Journal of Medical Genetics|May 31, 1997
Analysis of the CAG repeats in the SCA1 and B37 genes in schizophrenic and bipolar I disorder patients: tentative association between B37 and schizophreniaD J Morris-Rosendahl, E Burgert, G Uyanik, et al.Pageof 2