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Scientific Reports|February 13, 2016
Heme Oxygenase-1 and 2 Common Genetic Variants and Risk for Multiple SclerosisJosé A G Agúndez, Elena García-Martín, Carmen Martínez, et al.
Journal of Alzheimer'S Disease : JAD|May 11, 2016
Neuroimaging Correlates of Frontotemporal Dementia Associated with SQSTM1 MutationsElkin Luis, Alexandra Ortiz, Luis Eudave, et al.
Medicine|December 4, 2015
Association Between Vitamin D Receptor rs731236 (Taq1) Polymorphism and Risk for Restless Legs Syndrome in the Spanish Caucasian PopulationFélix Javier Jiménez-Jiménez, Elena García-Martín, Hortensia Alonso-Navarro, et al.
Medicine|August 28, 2015
Heme Oxygenase-1 and 2 Common Genetic Variants and Risk for Restless Legs SyndromeElena García-Martín, Félix Javier Jiménez-Jiménez, Hortensia Alonso-Navarro, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|November 13, 2016
Thr105Ile (rs11558538) polymorphism in the histamine-1-methyl-transferase (HNMT) gene and risk for restless legs syndromeFélix Javier Jiménez-Jiménez, Elena García-Martín, Hortensia Alonso-Navarro, et al.
Human Molecular Genetics|July 19, 2015
Missense mutations in TENM4, a regulator of axon guidance and central myelination, cause essential tremorHyun Hor, Ludmila Francescatto, Luca Bartesaghi, et al.
Parkinsonism & Related Disorders|January 15, 2015
TREM2 R47H variant and risk of essential tremor: a cross-sectional international multicenter studySara Ortega-Cubero, Oswaldo Lorenzo-Betancor, Elena Lorenzo, et al.
Human Molecular Genetics|September 24, 2013
Characterization of the repeat expansion size in C9orf72 in amyotrophic lateral sclerosis and frontotemporal dementiaOriol Dols-Icardo, Alberto García-Redondo, Ricard Rojas-García, et al.
Neurobiology of Aging|December 18, 2015
Assessing the role of TUBA4A gene in frontotemporal degenerationOriol Dols-Icardo, Oriol Iborra, Jessica Valdivia, et al.
Acta Neuropathologica|March 31, 2016
A comprehensive study of the genetic impact of rare variants in SORL1 in European early-onset Alzheimer's diseaseJan Verheijen, Tobi Van den Bossche, Julie van der Zee, et al.
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