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Molecular Syndromology|March 30, 2018
Novel Nonsense Mutation in <i>SLC39A13</i> Initially Presenting as Myopathy: Case Report and Review of the LiteratureMaja Dusanic, Gabriele Dekomien, Thomas Lücke, et al.Electrophoresis|April 7, 2005
Long- and short-haired Weimaraner dogs represent two populations of one breedTanja Schrameyer, Gabriele Dekomien, Sandra M Pasternack, et al.Journal of the Neurological Sciences|October 10, 2017
Monozygotic twins with a new compound heterozygous SPG11 mutation and different disease expressionChristiane Schneider-Gold, Gabriele Dekomien, Martin Regensburger, et al.Neuromuscular Disorders : NMD|November 11, 2008
Sarcoglycanopathies: can muscle immunoanalysis predict the genotype?Lars Klinge, Gabriele Dekomien, Ahmed Aboumousa, et al.Journal of Negative Results in Biomedicine|December 16, 2005
Exclusion of PINK1 as candidate gene for the late-onset form of Parkinson's disease in two European populationsAnna Melissa Schlitter, Martin Kurz, Jan P Larsen, et al.Journal of Geriatric Psychiatry and Neurology|June 6, 2007
FMR1 alleles in Parkinson's disease: relation to cognitive decline and hallucinations, a longitudinal studyMartin Wilhelm Kurz, Anna Melissa Schlitter, Yvonne Klenk, et al.Canine Genetics and Epidemiology|July 12, 2016
A large deletion in RPGR causes XLPRA in Weimaraner dogsRegina Kropatsch, Denis A Akkad, Matthias Frank, et al.Neurogenetics|September 25, 2009
Progressive retinal atrophy in Schapendoes dogs: mutation of the newly identified CCDC66 geneGabriele Dekomien, Conni Vollrath, Elisabeth Petrasch-Parwez, et al.Molecular and Cellular Probes|August 10, 2010
Generalized progressive retinal atrophy in the Irish Glen of Imaal Terrier is associated with a deletion in the ADAM9 geneRegina Kropatsch, Elisabeth Petrasch-Parwez, Dominik Seelow, et al.Neuromuscular Disorders : NMD|March 6, 2015
Two novel nebulin variants in an adult patient with congenital nemaline myopathyAnne K Güttsches, Gabriele Dekomien, Kristl G Claeys, et al.Pageof 5