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Neurogenetics

Showing results (871-880 of 949) with videos related to

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Neurogenetics|September 7, 2007
Evidence of shared risk for Alzheimer's disease and Parkinson's disease using family historyAmi R Rosen, N Kyle Steenland, John Hanfelt, et al.
Neurogenetics|December 18, 2008
Humoral immunodeficiency in congenital insensitivity to pain with anhidrosisSara Sebnem Kilic, Rifatcan Ozturk, Bartu Sarisozen, et al.
Neurogenetics|October 10, 2008
Risk for multiple sclerosis in relatives and spouses of patients diagnosed with autoimmune and related conditionsKari Hemminki, Xinjun Li, Jan Sundquist, et al.
Neurogenetics|October 16, 2008
Analysis of CYP7B1 in non-consanguineous cases of hereditary spastic paraplegiaRebecca Schüle, Elisabeth Brandt, Kathrin N Karle, et al.
Neurogenetics|July 8, 2008
Behavioral effects of a deletion in Kcnn2, the gene encoding the SK2 subunit of small-conductance Ca2+-activated K+ channelsMarek Szatanik, Nicolas Vibert, Isabelle Vassias, et al.
Neurogenetics|July 31, 2007
Refinement of the SPG15 candidate interval and phenotypic heterogeneity in three large Arab familiesNizar Elleuch, Naima Bouslam, Sylvain Hanein, et al.
Neurogenetics|September 24, 2008
Association of dopamine transporter and monoamine oxidase molecular polymorphisms with sudden infant death syndrome and stillbirth: new insights into the serotonin hypothesisLaura Filonzi, Cinzia Magnani, Anna Maria Lavezzi, et al.
Neurogenetics|November 27, 2008
The first missense mutation causing Rett syndrome specifically affecting the MeCP2_e1 isoformYann Fichou, Juliette Nectoux, Nadia Bahi-Buisson, et al.
Neurogenetics|November 21, 2008
LRRK2 G2019S and R1441G mutations associated with Parkinson's disease are common in the Basque Country, but relative prevalence is determined by ethnicityA Gorostidi, J Ruiz-Martínez, A Lopez de Munain, et al.
Neurogenetics|January 28, 2009
A LRRK2 G2019S mutation carrier from Turkey shares the Japanese haplotypeC Pirkevi, S Lesage, C Condroyer, et al.
Pageof 95

Showing results (871-880 of 949) with videos related to

Sort By:
Pageof 95
Neurogenetics|September 7, 2007
Evidence of shared risk for Alzheimer's disease and Parkinson's disease using family historyAmi R Rosen, N Kyle Steenland, John Hanfelt, et al.
Neurogenetics|December 18, 2008
Humoral immunodeficiency in congenital insensitivity to pain with anhidrosisSara Sebnem Kilic, Rifatcan Ozturk, Bartu Sarisozen, et al.
Neurogenetics|October 10, 2008
Risk for multiple sclerosis in relatives and spouses of patients diagnosed with autoimmune and related conditionsKari Hemminki, Xinjun Li, Jan Sundquist, et al.
Neurogenetics|October 16, 2008
Analysis of CYP7B1 in non-consanguineous cases of hereditary spastic paraplegiaRebecca Schüle, Elisabeth Brandt, Kathrin N Karle, et al.
Neurogenetics|July 8, 2008
Behavioral effects of a deletion in Kcnn2, the gene encoding the SK2 subunit of small-conductance Ca2+-activated K+ channelsMarek Szatanik, Nicolas Vibert, Isabelle Vassias, et al.
Neurogenetics|July 31, 2007
Refinement of the SPG15 candidate interval and phenotypic heterogeneity in three large Arab familiesNizar Elleuch, Naima Bouslam, Sylvain Hanein, et al.
Neurogenetics|September 24, 2008
Association of dopamine transporter and monoamine oxidase molecular polymorphisms with sudden infant death syndrome and stillbirth: new insights into the serotonin hypothesisLaura Filonzi, Cinzia Magnani, Anna Maria Lavezzi, et al.
Neurogenetics|November 27, 2008
The first missense mutation causing Rett syndrome specifically affecting the MeCP2_e1 isoformYann Fichou, Juliette Nectoux, Nadia Bahi-Buisson, et al.
Neurogenetics|November 21, 2008
LRRK2 G2019S and R1441G mutations associated with Parkinson's disease are common in the Basque Country, but relative prevalence is determined by ethnicityA Gorostidi, J Ruiz-Martínez, A Lopez de Munain, et al.
Neurogenetics|January 28, 2009
A LRRK2 G2019S mutation carrier from Turkey shares the Japanese haplotypeC Pirkevi, S Lesage, C Condroyer, et al.
Pageof 95