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Journal of the Neurological Sciences|November 21, 2007
Parkin polymorphisms in progressive supranuclear palsyRaquel Ros, Israel Ampuero, Justo García de Yébenes
Human Mutation|July 4, 2012
Revisiting genotype-phenotype overlap in neurogenetics: triplet-repeat expansions mimicking spastic paraplegiasConceição Bettencourt, Beatriz Quintáns, Raquel Ros, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 5, 2002
Steele-Richardson-Olszewski syndrome in a patient with a single C212Y mutation in the parkin proteinBlas Morales, Armando Martínez, Isabel Gonzalo, et al.
Archives of Neurology|June 12, 2002
Molecular findings in familial Parkinson disease in SpainJanet Hoenicka, Lídice Vidal, Blas Morales, et al.
European Archives of Psychiatry and Clinical Neuroscience|June 22, 2006
(AAT)n repeat in the cannabinoid receptor gene, CNR1: association with schizophrenia in a Spanish populationIsabel Martínez-Gras, Janet Hoenicka, Guillermo Ponce, et al.
Human Molecular Genetics|July 22, 2008
Parkin deletion causes cerebral and systemic amyloidosis in human mutated tau over-expressing miceJose A Rodríguez-Navarro, Ana Gómez, Izaskun Rodal, et al.
Experimental Neurology|October 10, 2009
The effects of parkin suppression on the behaviour, amyloid processing, and cell survival in APP mutant transgenic miceJuan Perucho, Maria J Casarejos, Isabel Rubio, et al.
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