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Journal of the Neurological Sciences
|
September 29, 2007
Interaction between CD14 and LXRbeta genes modulates Alzheimer's disease risk
Eloy Rodríguez-Rodríguez, Pascual Sánchez-Juan, Ignacio Mateo, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
September 29, 2011
High frequency and reduced penetrance of LRRK2 G2019S mutation among Parkinson's disease patients in Cantabria (Spain)
María Sierra, Isabel González-Aramburu, Pascual Sánchez-Juan, et al.
Journal of Neurology
|
June 19, 2008
Magnetic resonance imaging findings of leg musculature in Charcot-Marie-Tooth disease type 2 due to dynamin 2 mutation
Elena Gallardo, Kristl G Claeys, Eva Nelis, et al.
Neurobiology of Aging
|
December 18, 2015
Comparative blood transcriptome analysis in idiopathic and LRRK2 G2019S-associated Parkinson's disease
Jon Infante, Carlos Prieto, María Sierra, et al.
BMC Neurology
|
June 28, 2011
Detection of early Alzheimer's disease in MCI patients by the combination of MMSE and an episodic memory test
Ana Pozueta, Eloy Rodríguez-Rodríguez, José Luis Vazquez-Higuera, 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 family
Elena Gallardo, Antonio García, César Ramón, et al.
Dementia and Geriatric Cognitive Disorders
|
October 9, 2008
Synergistic effect of heme oxygenase-1 and tau genetic variants on Alzheimer's disease risk
Ignacio Mateo, Pascual Sánchez-Juan, Eloy Rodríguez-Rodríguez, 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 controls
Jon 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 disease
Jon 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 ataxia
Chiara Criscuolo, Francesco Saccà, Giuseppe De Michele, et al.
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of 10
Search research articles
Search
Showing results (41-50 of 92) with videos related to
Sort By:
Page
of 10
Journal of the Neurological Sciences
|
September 29, 2007
Interaction between CD14 and LXRbeta genes modulates Alzheimer's disease risk
Eloy Rodríguez-Rodríguez, Pascual Sánchez-Juan, Ignacio Mateo, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
September 29, 2011
High frequency and reduced penetrance of LRRK2 G2019S mutation among Parkinson's disease patients in Cantabria (Spain)
María Sierra, Isabel González-Aramburu, Pascual Sánchez-Juan, et al.
Journal of Neurology
|
June 19, 2008
Magnetic resonance imaging findings of leg musculature in Charcot-Marie-Tooth disease type 2 due to dynamin 2 mutation
Elena Gallardo, Kristl G Claeys, Eva Nelis, et al.
Neurobiology of Aging
|
December 18, 2015
Comparative blood transcriptome analysis in idiopathic and LRRK2 G2019S-associated Parkinson's disease
Jon Infante, Carlos Prieto, María Sierra, et al.
BMC Neurology
|
June 28, 2011
Detection of early Alzheimer's disease in MCI patients by the combination of MMSE and an episodic memory test
Ana Pozueta, Eloy Rodríguez-Rodríguez, José Luis Vazquez-Higuera, 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 family
Elena Gallardo, Antonio García, César Ramón, et al.
Dementia and Geriatric Cognitive Disorders
|
October 9, 2008
Synergistic effect of heme oxygenase-1 and tau genetic variants on Alzheimer's disease risk
Ignacio Mateo, Pascual Sánchez-Juan, Eloy Rodríguez-Rodríguez, 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 controls
Jon 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 disease
Jon 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 ataxia
Chiara Criscuolo, Francesco Saccà, Giuseppe De Michele, et al.
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of 10