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Wanda M Gerding

Showing results (1-10 of 29) with videos related to

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Journal of Neurology|December 18, 2010
Late onset Alexander's disease presenting as cerebellar ataxia associated with a novel mutation in the GFAP geneStephan Schmidt, Mike P Wattjes, Wanda M Gerding, et al.
Canine Genetics and Epidemiology|September 25, 2015
Homozygosity mapping and sequencing identify two genes that might contribute to pointing behavior in hunting dogsDenis A Akkad, Wanda M Gerding, Robin B Gasser, et al.
Journal of the Neurological Sciences|April 7, 2009
Severe demyelinating hypertrophic polyneuropathy caused by a de novo frameshift mutation within the intracellular domain of myelin protein zero (MPZ/P0)Jana Zschüntzsch, Payam Dibaj, Sara Pilgram, et al.
Muscle & Nerve|November 3, 2009
Unusual Charcot-Marie-Tooth phenotype due to a mutation within the intracellular domain of myelin protein zeroChristiane Schneider-Gold, Judith Kötting, Jörg T Epplen, et al.
Cancers|March 29, 2023
Optical Genome Mapping for Cytogenetic Diagnostics in AMLVerena Nilius-Eliliwi, Wanda M Gerding, Roland Schroers, et al.
Plos One|January 24, 2013
Cholecystokinin A receptor (CCKAR) gene variation is associated with language lateralizationSebastian Ocklenburg, Larissa Arning, Wanda M Gerding, et al.
Brain and Language|August 6, 2013
FOXP2 variation modulates functional hemispheric asymmetries for speech perceptionSebastian Ocklenburg, Larissa Arning, Wanda M Gerding, et al.
Leukemia|November 26, 2022
Optical Genome Mapping in MDS and AML as tool for structural variant profiling-comment and data update on Yang et al.: "High-resolution structural variant profiling of myelodysplastic syndromes by optical genome mapping uncovers cryptic aberrations of prognostic and therapeutic significance"Deepak B Vangala, Verena Nilius-Eliliwi, Wanda M Gerding, et al.
Journal of Neurology|December 7, 2010
MS-like presentation of Alexander disease with multifocal lesions and oligoclonal bandsHenriette J Tschampa, Susanne Greschus, Michael Vinahl, et al.
Behavioural Brain Research|August 11, 2011
Variation in the NMDA receptor 2B subunit gene GRIN2B is associated with differential language lateralizationSebastian Ocklenburg, Larissa Arning, Constanze Hahn, et al.
Pageof 3

Showing results (1-10 of 29) with videos related to

Sort By:
Pageof 3
Journal of Neurology|December 18, 2010
Late onset Alexander's disease presenting as cerebellar ataxia associated with a novel mutation in the GFAP geneStephan Schmidt, Mike P Wattjes, Wanda M Gerding, et al.
Canine Genetics and Epidemiology|September 25, 2015
Homozygosity mapping and sequencing identify two genes that might contribute to pointing behavior in hunting dogsDenis A Akkad, Wanda M Gerding, Robin B Gasser, et al.
Journal of the Neurological Sciences|April 7, 2009
Severe demyelinating hypertrophic polyneuropathy caused by a de novo frameshift mutation within the intracellular domain of myelin protein zero (MPZ/P0)Jana Zschüntzsch, Payam Dibaj, Sara Pilgram, et al.
Muscle & Nerve|November 3, 2009
Unusual Charcot-Marie-Tooth phenotype due to a mutation within the intracellular domain of myelin protein zeroChristiane Schneider-Gold, Judith Kötting, Jörg T Epplen, et al.
Cancers|March 29, 2023
Optical Genome Mapping for Cytogenetic Diagnostics in AMLVerena Nilius-Eliliwi, Wanda M Gerding, Roland Schroers, et al.
Plos One|January 24, 2013
Cholecystokinin A receptor (CCKAR) gene variation is associated with language lateralizationSebastian Ocklenburg, Larissa Arning, Wanda M Gerding, et al.
Brain and Language|August 6, 2013
FOXP2 variation modulates functional hemispheric asymmetries for speech perceptionSebastian Ocklenburg, Larissa Arning, Wanda M Gerding, et al.
Leukemia|November 26, 2022
Optical Genome Mapping in MDS and AML as tool for structural variant profiling-comment and data update on Yang et al.: "High-resolution structural variant profiling of myelodysplastic syndromes by optical genome mapping uncovers cryptic aberrations of prognostic and therapeutic significance"Deepak B Vangala, Verena Nilius-Eliliwi, Wanda M Gerding, et al.
Journal of Neurology|December 7, 2010
MS-like presentation of Alexander disease with multifocal lesions and oligoclonal bandsHenriette J Tschampa, Susanne Greschus, Michael Vinahl, et al.
Behavioural Brain Research|August 11, 2011
Variation in the NMDA receptor 2B subunit gene GRIN2B is associated with differential language lateralizationSebastian Ocklenburg, Larissa Arning, Constanze Hahn, et al.
Pageof 3