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M Topcu

Showing results (11-20 of 19) with videos related to

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The Journal of Pediatrics|February 1, 1992
Paraneoplastic syndrome manifesting as chronic cerebellar ataxia in a child with Hodgkin diseaseM Topcu, K Gucuyener, H Topaloglu, et al.
International Archives of Occupational and Environmental Health|December 11, 1999
A cross-sectional study of workers in the chemical industry with occupational exposure to hexamethylenetetramineR Merget, M Topcu, K Friese, et al.
Acta Radiologica (Stockholm, Sweden : 1987)|March 1, 1997
Cranial MR findings in Wilson's diseaseI Saatci, M Topcu, F F Baltaoglu, et al.
Clinical Genetics|July 6, 2005
Two novel CLN6 mutations in variant late-infantile neuronal ceroid lipofuscinosis patients of Turkish originE Siintola, M Topcu, A Kohlschütter, et al.
Journal of Inherited Metabolic Disease|January 27, 2009
Peripheral neuropathy in a patient with D-2-hydroxyglutaric aciduriaG Haliloglu, C M Temucin, K K Oguz, et al.
Neuropediatrics|August 2, 2008
L-2-hydroxyglutaric aciduria and brain tumors in children with mutations in the L2HGDH gene: neuroimaging findingsG Haliloglu, F Jobard, K K Oguz, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 18, 2005
Giant axonal neuropathy: clinical and genetic study in six casesE Demir, P Bomont, S Erdem, et al.
Neurology|May 26, 2004
Bilateral generalized polymicrogyria (BGP): a distinct syndrome of cortical malformationB S Chang, X Piao, C Giannini, et al.
Human Molecular Genetics|February 5, 1999
A novel protein tyrosine phosphatase gene is mutated in progressive myoclonus epilepsy of the Lafora type (EPM2)J M Serratosa, P Gómez-Garre, M E Gallardo, et al.
Pageof 2

Showing results (11-20 of 19) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 19 results.
The Journal of Pediatrics|February 1, 1992
Paraneoplastic syndrome manifesting as chronic cerebellar ataxia in a child with Hodgkin diseaseM Topcu, K Gucuyener, H Topaloglu, et al.
International Archives of Occupational and Environmental Health|December 11, 1999
A cross-sectional study of workers in the chemical industry with occupational exposure to hexamethylenetetramineR Merget, M Topcu, K Friese, et al.
Acta Radiologica (Stockholm, Sweden : 1987)|March 1, 1997
Cranial MR findings in Wilson's diseaseI Saatci, M Topcu, F F Baltaoglu, et al.
Clinical Genetics|July 6, 2005
Two novel CLN6 mutations in variant late-infantile neuronal ceroid lipofuscinosis patients of Turkish originE Siintola, M Topcu, A Kohlschütter, et al.
Journal of Inherited Metabolic Disease|January 27, 2009
Peripheral neuropathy in a patient with D-2-hydroxyglutaric aciduriaG Haliloglu, C M Temucin, K K Oguz, et al.
Neuropediatrics|August 2, 2008
L-2-hydroxyglutaric aciduria and brain tumors in children with mutations in the L2HGDH gene: neuroimaging findingsG Haliloglu, F Jobard, K K Oguz, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 18, 2005
Giant axonal neuropathy: clinical and genetic study in six casesE Demir, P Bomont, S Erdem, et al.
Neurology|May 26, 2004
Bilateral generalized polymicrogyria (BGP): a distinct syndrome of cortical malformationB S Chang, X Piao, C Giannini, et al.
Human Molecular Genetics|February 5, 1999
A novel protein tyrosine phosphatase gene is mutated in progressive myoclonus epilepsy of the Lafora type (EPM2)J M Serratosa, P Gómez-Garre, M E Gallardo, et al.
Pageof 2