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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 regulation
B Quintáns, M Fernández Prieto, A Carracedo, et al.
Journal of Biomedical Informatics
|
February 14, 2013
SNOMED CT module-driven clinical archetype management
J L Allones, M Taboada, D Martinez, et al.
Cancer
|
December 26, 2001
Rare HRAS1 alleles are a risk factor for the development of brain tumors
A 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 interpretation
B Quintáns, A Ordóñez-Ugalde, P Cacheiro, et al.
Archives of Neurology
|
November 16, 2001
The SCA12 mutation as a rare cause of spinocerebellar ataxia
J A Cholfin, M J Sobrido, S Perlman, et al.
Neurology
|
October 10, 2001
SCA8 repeat expansions in ataxia: a controversial association
M 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 tumours
M 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.
Page
of 4
Search research articles
Search
Showing results (1-10 of 34) with videos related to
Sort By:
Page
of 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 regulation
B Quintáns, M Fernández Prieto, A Carracedo, et al.
Journal of Biomedical Informatics
|
February 14, 2013
SNOMED CT module-driven clinical archetype management
J L Allones, M Taboada, D Martinez, et al.
Cancer
|
December 26, 2001
Rare HRAS1 alleles are a risk factor for the development of brain tumors
A 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 interpretation
B Quintáns, A Ordóñez-Ugalde, P Cacheiro, et al.
Archives of Neurology
|
November 16, 2001
The SCA12 mutation as a rare cause of spinocerebellar ataxia
J A Cholfin, M J Sobrido, S Perlman, et al.
Neurology
|
October 10, 2001
SCA8 repeat expansions in ataxia: a controversial association
M 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 tumours
M 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.
Page
of 4