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Human Mutation|February 1, 2011
Novel genomic techniques open new avenues in the analysis of monogenic disordersGregor Kuhlenbäumer, Julia Hullmann, Silke AppenzellerMedical Microbiology and Immunology|May 7, 2010
Chlamydia pneumoniae infection and Alzheimer's disease: a connection to remember?Kensuke Shima, Gregor Kuhlenbäumer, Jan RuppNeurology|February 18, 2014
Genetics of essential tremor: meta-analysis and reviewGregor Kuhlenbäumer, Franziska Hopfner, Günther DeuschlMovement Disorders : Official Journal of the Movement Disorder Society|June 5, 2003
Painless legs and moving toes in a mother and her daughterRainer Dziewas, Gregor Kuhlenbäumer, Angelika Okegwo, et al.European Journal of Neurology|October 21, 2025
Inflammatory Episode in a Patient With Probable Iatrogenic Cerebral Amyloid Angiopathy: An ARIA Before the Storm?Ulf Jensen-Kondering, Gregor Kuhlenbäumer, Nils G MargrafNeurogenetics|August 17, 2023
Family and literature analysis demonstrates phenotypic effect of two variants in the calpain-3 geneMaike Tomforde, Meike Steinbach, Tobias B Haack, et al.Journal of Neurology|January 17, 2003
Clinical features and molecular genetics of hereditary peripheral neuropathiesGregor Kuhlenbäumer, Peter Young, Gert Hünermund, et al.Journal of Neural Transmission (Vienna, Austria : 1996)|May 13, 2009
Functional gene variants of the serotonin-synthesizing enzyme tryptophan hydroxylase 2 in migraineMartin Marziniak, Claudia Kienzler, Gregor Kuhlenbäumer, et al.Journal of the Neurological Sciences|September 21, 2010
Hereditary and non-hereditary microangiopathies in the young. An up-dateE Bernd Ringelstein, Ilka Kleffner, Ralf Dittrich, et al.Cerebrovascular Diseases (Basel, Switzerland)|February 28, 2015
Determinants of platelet-leukocyte aggregation and platelet activation in strokeBarbara Schmalbach, Olga Stepanow, Arne Jochens, et al.Pageof 10