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Stephan Niemann

Showing results (1-10 of 13) with videos related to

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Familial Cancer|May 11, 2005
SDHC mutations in hereditary paraganglioma/pheochromocytomaUlrich Müller, Christian Troidl, Stephan Niemann
Proceedings of the National Academy of Sciences of the United States of America|August 21, 2003
Specific sequence changes in multiple transcript system DYT3 are associated with X-linked dystonia parkinsonismDagmar Nolte, Stephan Niemann, Ulrich Müller
Human Genetics|March 27, 2003
Autosomal dominant malignant and catecholamine-producing paraganglioma caused by a splice donor site mutation in SDHCStephan Niemann, Ulrich Müller, Dieter Engelhardt, et al.
Muscle & Nerve|July 20, 2007
Analysis of a genetic defect in the TATA box of the SOD1 gene in a patient with familial amyotrophic lateral sclerosisStephan Niemann, Wendy J Broom, Robert H Brown
American Journal of Human Genetics|February 12, 2004
Homozygous WNT3 mutation causes tetra-amelia in a large consanguineous familyStephan Niemann, Chengfeng Zhao, Filon Pascu, et al.
Archives of Neurology|December 15, 2004
Phenotypic and molecular analyses of X-linked dystonia-parkinsonism ("lubag") in womenVirgilio Gerald H Evidente, Dagmar Nolte, Stephan Niemann, et al.
Annals of the New York Academy of Sciences|November 1, 2017
The "CMT Rat": Peripheral Neuropathy and Dysmyelination Caused by Transgenic Overexpression of PMP22Stephan Niemann, Michael W Sereda, Moritz Rossner, et al.
Annals of Neurology|January 6, 2004
Chromosomal translocation t(18;21)(q23;q22.1) indicates novel susceptibility loci for frontotemporal dementia with ALSJohannes Prudlo, Burkhard Alber, Vera M Kalscheuer, et al.
American Journal of Human Genetics|January 20, 2005
PHOX2B genotype allows for prediction of tumor risk in congenital central hypoventilation syndromeDelphine Trochet, Louise M O'Brien, David Gozal, et al.
The European Journal of Neuroscience|September 21, 2007
Genetic ablation of NMDA receptor subunit NR3B in mouse reveals motoneuronal and nonmotoneuronal phenotypesStephan Niemann, Hiroaki Kanki, Yasuyuki Fukui, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
Familial Cancer|May 11, 2005
SDHC mutations in hereditary paraganglioma/pheochromocytomaUlrich Müller, Christian Troidl, Stephan Niemann
Proceedings of the National Academy of Sciences of the United States of America|August 21, 2003
Specific sequence changes in multiple transcript system DYT3 are associated with X-linked dystonia parkinsonismDagmar Nolte, Stephan Niemann, Ulrich Müller
Human Genetics|March 27, 2003
Autosomal dominant malignant and catecholamine-producing paraganglioma caused by a splice donor site mutation in SDHCStephan Niemann, Ulrich Müller, Dieter Engelhardt, et al.
Muscle & Nerve|July 20, 2007
Analysis of a genetic defect in the TATA box of the SOD1 gene in a patient with familial amyotrophic lateral sclerosisStephan Niemann, Wendy J Broom, Robert H Brown
American Journal of Human Genetics|February 12, 2004
Homozygous WNT3 mutation causes tetra-amelia in a large consanguineous familyStephan Niemann, Chengfeng Zhao, Filon Pascu, et al.
Archives of Neurology|December 15, 2004
Phenotypic and molecular analyses of X-linked dystonia-parkinsonism ("lubag") in womenVirgilio Gerald H Evidente, Dagmar Nolte, Stephan Niemann, et al.
Annals of the New York Academy of Sciences|November 1, 2017
The "CMT Rat": Peripheral Neuropathy and Dysmyelination Caused by Transgenic Overexpression of PMP22Stephan Niemann, Michael W Sereda, Moritz Rossner, et al.
Annals of Neurology|January 6, 2004
Chromosomal translocation t(18;21)(q23;q22.1) indicates novel susceptibility loci for frontotemporal dementia with ALSJohannes Prudlo, Burkhard Alber, Vera M Kalscheuer, et al.
American Journal of Human Genetics|January 20, 2005
PHOX2B genotype allows for prediction of tumor risk in congenital central hypoventilation syndromeDelphine Trochet, Louise M O'Brien, David Gozal, et al.
The European Journal of Neuroscience|September 21, 2007
Genetic ablation of NMDA receptor subunit NR3B in mouse reveals motoneuronal and nonmotoneuronal phenotypesStephan Niemann, Hiroaki Kanki, Yasuyuki Fukui, et al.
Pageof 2