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M J Sobrido

Showing results (1-10 of 34) with videos related to

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Neurologia (Barcelona, Spain)|January 17, 2015
Spinocerebellar ataxia 36 (SCA36): «Costa da Morte ataxia»M Arias, M García-Murias, M J Sobrido
Revista De Neurologia|February 18, 2009
[Behavioral disorders in Parkinson's disease. Genetic, pharmacological and medico-legal aspects]M J Sobrido, J J Dias-Silva, B Quintáns
Neurologia (Barcelona, Spain)|December 18, 2010
Genetic counselling in neurology: a complex problem that requires regulationB Quintáns, M Fernández Prieto, A Carracedo, et al.
Journal of Biomedical Informatics|February 14, 2013
SNOMED CT module-driven clinical archetype managementJ L Allones, M Taboada, D Martinez, et al.
Cancer|December 26, 2001
Rare HRAS1 alleles are a risk factor for the development of brain tumorsA Vega, M J Sobrido, C Ruiz-Ponte, et al.
Applied & Translational Genomics|June 11, 2016
Medical genomics: The intricate path from genetic variant identification to clinical interpretationB Quintáns, A Ordóñez-Ugalde, P Cacheiro, et al.
Archives of Neurology|November 16, 2001
The SCA12 mutation as a rare cause of spinocerebellar ataxiaJ A Cholfin, M J Sobrido, S Perlman, et al.
Neurology|October 10, 2001
SCA8 repeat expansions in ataxia: a controversial associationM J Sobrido, J A Cholfin, S Perlman, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 17, 2000
Low frequency of replication errors in primary nervous system tumoursM J Sobrido, C R Pereira, F Barros, et al.
Revista De Neurologia|February 1, 1996
[Cerebral hemorrhage and migraine]J M Aldrey, J Castillo, R Leira, et al.
Pageof 4

Showing results (1-10 of 34) with videos related to

Sort By:
Pageof 4
Neurologia (Barcelona, Spain)|January 17, 2015
Spinocerebellar ataxia 36 (SCA36): «Costa da Morte ataxia»M Arias, M García-Murias, M J Sobrido
Revista De Neurologia|February 18, 2009
[Behavioral disorders in Parkinson's disease. Genetic, pharmacological and medico-legal aspects]M J Sobrido, J J Dias-Silva, B Quintáns
Neurologia (Barcelona, Spain)|December 18, 2010
Genetic counselling in neurology: a complex problem that requires regulationB Quintáns, M Fernández Prieto, A Carracedo, et al.
Journal of Biomedical Informatics|February 14, 2013
SNOMED CT module-driven clinical archetype managementJ L Allones, M Taboada, D Martinez, et al.
Cancer|December 26, 2001
Rare HRAS1 alleles are a risk factor for the development of brain tumorsA Vega, M J Sobrido, C Ruiz-Ponte, et al.
Applied & Translational Genomics|June 11, 2016
Medical genomics: The intricate path from genetic variant identification to clinical interpretationB Quintáns, A Ordóñez-Ugalde, P Cacheiro, et al.
Archives of Neurology|November 16, 2001
The SCA12 mutation as a rare cause of spinocerebellar ataxiaJ A Cholfin, M J Sobrido, S Perlman, et al.
Neurology|October 10, 2001
SCA8 repeat expansions in ataxia: a controversial associationM J Sobrido, J A Cholfin, S Perlman, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 17, 2000
Low frequency of replication errors in primary nervous system tumoursM J Sobrido, C R Pereira, F Barros, et al.
Revista De Neurologia|February 1, 1996
[Cerebral hemorrhage and migraine]J M Aldrey, J Castillo, R Leira, et al.
Pageof 4