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Neurogenetics

Showing results (791-800 of 949) with videos related to

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Neurogenetics|May 14, 2005
Subcellular localization of spastin: implications for the pathogenesis of hereditary spastic paraplegiaIngrid K Svenson, Mark T Kloos, Amy Jacon, et al.
Neurogenetics|October 2, 2004
Mosaic mutations of the FLN1 gene cause a mild phenotype in patients with periventricular heterotopiaElena Parrini, Davide Mei, Micheal Wright, et al.
Neurogenetics|February 16, 2005
A novel NIPA1 mutation associated with a pure form of autosomal dominant hereditary spastic paraplegiaJohanna A Reed, Phillip A Wilkinson, Heema Patel, et al.
Neurogenetics|March 7, 2008
Is the early-onset torsion dystonia (EOTD) linked to TOR1A gene as frequent as expected in France?M Y Frédéric, F Clot, L Cif, et al.
Neurogenetics|March 20, 2008
Detection of low-level somatic and germline mosaicism by denaturing high-performance liquid chromatography in a EURO-MRX family with SLC6A8 deficiencyOfir T Betsalel, Jiddeke M van de Kamp, Cristina Martínez-Muñoz, et al.
Neurogenetics|January 18, 2006
Death of neuronal clusters contributes to variance of age at onset in Huntington's diseaseBranka Cajavec, Hanspeter Herzel, Samuel Bernard
Neurogenetics|January 18, 2006
PLP1 and GPM6B intragenic copy number analysis by MAPH in 262 patients with hypomyelinating leukodystrophies: Identification of one partial triplication and two partial deletions of PLP1Patricia Combes, Marie-Noelle Bonnet-Dupeyron, Fernande Gauthier-Barichard, et al.
Neurogenetics|May 16, 2008
A family with combined mutations of the hemophilia A and X-linked adrenoleukodystrophy genesBrent L Fogel, Pari Young, Arthur R Thompson, et al.
Neurogenetics|February 22, 2008
Structural genomic variation in ischemic strokeMar Matarin, Javier Simon-Sanchez, Hon-Chung Fung, et al.
Neurogenetics|April 17, 2008
Dysregulation of large-conductance Ca2+-activated K+ channel expression in nonsyndromal mental retardation due to a cereblon p.R419X mutationJoseph J Higgins, Jin Hao, Barry E Kosofsky, et al.
Pageof 95

Showing results (791-800 of 949) with videos related to

Sort By:
Pageof 95
Neurogenetics|May 14, 2005
Subcellular localization of spastin: implications for the pathogenesis of hereditary spastic paraplegiaIngrid K Svenson, Mark T Kloos, Amy Jacon, et al.
Neurogenetics|October 2, 2004
Mosaic mutations of the FLN1 gene cause a mild phenotype in patients with periventricular heterotopiaElena Parrini, Davide Mei, Micheal Wright, et al.
Neurogenetics|February 16, 2005
A novel NIPA1 mutation associated with a pure form of autosomal dominant hereditary spastic paraplegiaJohanna A Reed, Phillip A Wilkinson, Heema Patel, et al.
Neurogenetics|March 7, 2008
Is the early-onset torsion dystonia (EOTD) linked to TOR1A gene as frequent as expected in France?M Y Frédéric, F Clot, L Cif, et al.
Neurogenetics|March 20, 2008
Detection of low-level somatic and germline mosaicism by denaturing high-performance liquid chromatography in a EURO-MRX family with SLC6A8 deficiencyOfir T Betsalel, Jiddeke M van de Kamp, Cristina Martínez-Muñoz, et al.
Neurogenetics|January 18, 2006
Death of neuronal clusters contributes to variance of age at onset in Huntington's diseaseBranka Cajavec, Hanspeter Herzel, Samuel Bernard
Neurogenetics|January 18, 2006
PLP1 and GPM6B intragenic copy number analysis by MAPH in 262 patients with hypomyelinating leukodystrophies: Identification of one partial triplication and two partial deletions of PLP1Patricia Combes, Marie-Noelle Bonnet-Dupeyron, Fernande Gauthier-Barichard, et al.
Neurogenetics|May 16, 2008
A family with combined mutations of the hemophilia A and X-linked adrenoleukodystrophy genesBrent L Fogel, Pari Young, Arthur R Thompson, et al.
Neurogenetics|February 22, 2008
Structural genomic variation in ischemic strokeMar Matarin, Javier Simon-Sanchez, Hon-Chung Fung, et al.
Neurogenetics|April 17, 2008
Dysregulation of large-conductance Ca2+-activated K+ channel expression in nonsyndromal mental retardation due to a cereblon p.R419X mutationJoseph J Higgins, Jin Hao, Barry E Kosofsky, et al.
Pageof 95