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Jon Infante

Showing results (51-60 of 145) with videos related to

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Cerebellum (London, England)|February 13, 2020
Social Cognition in Chiari Malformation Type I: a Preliminary CharacterizationMaitane García, Imanol Amayra, Juan Francisco López-Paz, et al.
Journal of Neurology|July 25, 2009
Charcot–Marie–Tooth disease type 2J with MPZ Thr124Met mutation: clinico-electrophysiological and MRI study of a familyElena Gallardo, Antonio García, César Ramón, et al.
Journal of Neurology|September 3, 2010
Striatal dopamine function in a family with multiple SCA-3 phenotypesEsther Cubo, Mateo Diez López, Jon Infante Ceberio, et al.
Neurobiology of Aging|December 6, 2014
Identification of candidate genes for Parkinson's disease through blood transcriptome analysis in LRRK2-G2019S carriers, idiopathic cases, and controlsJon Infante, Carlos Prieto, María Sierra, et al.
Neuroscience Letters|November 22, 2005
LRRK2 G2019S is a common mutation in Spanish patients with late-onset Parkinson's diseaseJon Infante, Eloy Rodríguez, Onofre Combarros, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 12, 2005
Novel mutation of SACS gene in a Spanish family with autosomal recessive spastic ataxiaChiara Criscuolo, Francesco Saccà, Giuseppe De Michele, et al.
Cerebellum (London, England)|July 10, 2019
Analysis of Visuospatial Abilities in Chiari Malformation Type IMaitane García, Esther Lázaro, Imanol Amayra, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 19, 2007
Association of genetic variants of ABCA1 with Alzheimer's disease riskEloy Rodríguez-Rodríguez, Ignacio Mateo, Javier Llorca, et al.
Neurobiology of Aging|August 21, 2007
Age-dependent association of KIBRA genetic variation and Alzheimer's disease riskEloy Rodríguez-Rodríguez, Jon Infante, Javier Llorca, et al.
Clinical Neurology and Neurosurgery|May 15, 2019
Persistent isolated mydriasis as an early sign of internal carotid artery dissection: Pourfour du petit syndromeJosé Ramón Sánchez-de la Torre, Marta Drake-Pérez, Alfonso Casado, et al.
Pageof 15

Showing results (51-60 of 145) with videos related to

Sort By:
Pageof 15
Cerebellum (London, England)|February 13, 2020
Social Cognition in Chiari Malformation Type I: a Preliminary CharacterizationMaitane García, Imanol Amayra, Juan Francisco López-Paz, et al.
Journal of Neurology|July 25, 2009
Charcot–Marie–Tooth disease type 2J with MPZ Thr124Met mutation: clinico-electrophysiological and MRI study of a familyElena Gallardo, Antonio García, César Ramón, et al.
Journal of Neurology|September 3, 2010
Striatal dopamine function in a family with multiple SCA-3 phenotypesEsther Cubo, Mateo Diez López, Jon Infante Ceberio, et al.
Neurobiology of Aging|December 6, 2014
Identification of candidate genes for Parkinson's disease through blood transcriptome analysis in LRRK2-G2019S carriers, idiopathic cases, and controlsJon Infante, Carlos Prieto, María Sierra, et al.
Neuroscience Letters|November 22, 2005
LRRK2 G2019S is a common mutation in Spanish patients with late-onset Parkinson's diseaseJon Infante, Eloy Rodríguez, Onofre Combarros, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 12, 2005
Novel mutation of SACS gene in a Spanish family with autosomal recessive spastic ataxiaChiara Criscuolo, Francesco Saccà, Giuseppe De Michele, et al.
Cerebellum (London, England)|July 10, 2019
Analysis of Visuospatial Abilities in Chiari Malformation Type IMaitane García, Esther Lázaro, Imanol Amayra, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 19, 2007
Association of genetic variants of ABCA1 with Alzheimer's disease riskEloy Rodríguez-Rodríguez, Ignacio Mateo, Javier Llorca, et al.
Neurobiology of Aging|August 21, 2007
Age-dependent association of KIBRA genetic variation and Alzheimer's disease riskEloy Rodríguez-Rodríguez, Jon Infante, Javier Llorca, et al.
Clinical Neurology and Neurosurgery|May 15, 2019
Persistent isolated mydriasis as an early sign of internal carotid artery dissection: Pourfour du petit syndromeJosé Ramón Sánchez-de la Torre, Marta Drake-Pérez, Alfonso Casado, et al.
Pageof 15