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M J Sobrido

Showing results (21-30 of 34) with videos related to

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Journal of Molecular Neuroscience : MN|October 6, 2007
Analysis of candidate genes at the IBGC1 locus associated with idiopathic basal ganglia calcification ("Fahr's disease")J R M Oliveira, M J Sobrido, E Spiteri, et al.
Neurology|March 12, 2003
Possible association of the tau H1/H1 genotype with primary progressive aphasiaM-J Sobrido, A Abu-Khalil, S Weintraub, et al.
Journal of the Neurological Sciences|March 16, 2011
Prevalence of parkinsonism and Parkinson's disease in the Arosa Island (Spain): a community-based door-to-door surveyM Seijo-Martinez, M Castro del Rio, J Rodríguez Alvarez, et al.
Neurologia (Barcelona, Spain)|February 25, 2011
[Usefulness of cholestanol levels in the diagnosis and follow-up of patients with cerebrotendinous xanthomatosis]B Pilo de la Fuente, M J Sobrido, M Girós, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 21, 2009
Association study of the serotoninergic system in migraine in the Spanish populationR Corominas, M J Sobrido, M Ribasés, et al.
European Journal of Neurology|June 8, 2011
Cerebrotendinous xanthomatosis in Spain: clinical, prognostic, and genetic surveyB Pilo-de-la-Fuente, A Jimenez-Escrig, J R Lorenzo, et al.
Cerebellum (London, England)|April 10, 2020
Cerebellar Cognitive Affective Syndrome in Costa da Morte Ataxia (SCA36)R Martínez-Regueiro, M Arias, R Cruz, et al.
Molecular Diagnosis & Therapy|March 15, 2017
Evaluating the Calling Performance of a Rare Disease NGS Panel for Single Nucleotide and Copy Number VariantsP Cacheiro, A Ordóñez-Ugalde, B Quintáns, et al.
Brain : a Journal of Neurology|April 29, 2005
Autosomal dominant congenital fibre type disproportion: a clinicopathological and imaging study of a large familyM J Sobrido, J M Fernández, E Fontoira, et al.
Clinical Genetics|February 27, 2013
Exome sequencing is a useful diagnostic tool for complicated forms of hereditary spastic paraplegiaC Bettencourt, J L López-Sendón, J García-Caldentey, et al.
Pageof 4

Showing results (21-30 of 34) with videos related to

Sort By:
Pageof 4
Journal of Molecular Neuroscience : MN|October 6, 2007
Analysis of candidate genes at the IBGC1 locus associated with idiopathic basal ganglia calcification ("Fahr's disease")J R M Oliveira, M J Sobrido, E Spiteri, et al.
Neurology|March 12, 2003
Possible association of the tau H1/H1 genotype with primary progressive aphasiaM-J Sobrido, A Abu-Khalil, S Weintraub, et al.
Journal of the Neurological Sciences|March 16, 2011
Prevalence of parkinsonism and Parkinson's disease in the Arosa Island (Spain): a community-based door-to-door surveyM Seijo-Martinez, M Castro del Rio, J Rodríguez Alvarez, et al.
Neurologia (Barcelona, Spain)|February 25, 2011
[Usefulness of cholestanol levels in the diagnosis and follow-up of patients with cerebrotendinous xanthomatosis]B Pilo de la Fuente, M J Sobrido, M Girós, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 21, 2009
Association study of the serotoninergic system in migraine in the Spanish populationR Corominas, M J Sobrido, M Ribasés, et al.
European Journal of Neurology|June 8, 2011
Cerebrotendinous xanthomatosis in Spain: clinical, prognostic, and genetic surveyB Pilo-de-la-Fuente, A Jimenez-Escrig, J R Lorenzo, et al.
Cerebellum (London, England)|April 10, 2020
Cerebellar Cognitive Affective Syndrome in Costa da Morte Ataxia (SCA36)R Martínez-Regueiro, M Arias, R Cruz, et al.
Molecular Diagnosis & Therapy|March 15, 2017
Evaluating the Calling Performance of a Rare Disease NGS Panel for Single Nucleotide and Copy Number VariantsP Cacheiro, A Ordóñez-Ugalde, B Quintáns, et al.
Brain : a Journal of Neurology|April 29, 2005
Autosomal dominant congenital fibre type disproportion: a clinicopathological and imaging study of a large familyM J Sobrido, J M Fernández, E Fontoira, et al.
Clinical Genetics|February 27, 2013
Exome sequencing is a useful diagnostic tool for complicated forms of hereditary spastic paraplegiaC Bettencourt, J L López-Sendón, J García-Caldentey, et al.
Pageof 4