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O Combarros

Showing results (81-90 of 102) with videos related to

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Acta Neurologica Scandinavica|December 28, 2000
The butyrylcholinesterase K variant is a protective factor for sporadic Alzheimer's disease in womenA Alvarez-Arcaya, O Combarros, J Llorca, et al.
Acta Neurologica Scandinavica|June 26, 2007
Low serum VEGF levels are associated with Alzheimer's diseaseI Mateo, J Llorca, J Infante, et al.
Acta Neurologica Scandinavica|November 8, 2007
Serum levels and genetic variation of TGF-beta1 are not associated with Alzheimer's diseaseE Rodríguez-Rodríguez, P Sánchez-Juan, I Mateo, et al.
Human Genetics|August 24, 1999
Spinocerebellar ataxias in Spanish patients: genetic analysis of familial and sporadic cases. The Ataxia Study GroupM A Pujana, J Corral, M Gratacòs, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 19, 2007
Autosomal-dominant distal myopathy with a myotilin S55F mutation: sorting out the phenotypeJ Berciano, E Gallardo, R Domínguez-Perles, et al.
Muscle & Nerve|August 9, 2001
Diagnostic strategy for familial and sporadic cases of neuropathy associated with 17p11.2 deletionJ Infante, A García, O Combarros, et al.
Journal of Medical Genetics|February 27, 2004
Autosomal dominant axonal Charcot-Marie-Tooth disease type 2 (CMT2G) maps to chromosome 12q12-q13.3E Nelis, J Berciano, N Verpoorten, et al.
Acta Neurologica Scandinavica|January 22, 2009
Epistasis between tau phosphorylation regulating genes (CDK5R1 and GSK-3beta) and Alzheimer's disease riskI Mateo, J L Vázquez-Higuera, P Sánchez-Juan, et al.
Acta Neurologica Scandinavica|March 3, 1998
Gender effect on apolipoprotein E epsilon4 allele-associated risk for sporadic Alzheimer's diseaseO Combarros, C Leno, A Oterino, et al.
Acta Neurologica Scandinavica|September 30, 2009
Serum heme oxygenase-1 levels are increased in Parkinson's disease but not in Alzheimer's diseaseI Mateo, J Infante, P Sánchez-Juan, et al.
Pageof 11

Showing results (81-90 of 102) with videos related to

Sort By:
Pageof 11
Acta Neurologica Scandinavica|December 28, 2000
The butyrylcholinesterase K variant is a protective factor for sporadic Alzheimer's disease in womenA Alvarez-Arcaya, O Combarros, J Llorca, et al.
Acta Neurologica Scandinavica|June 26, 2007
Low serum VEGF levels are associated with Alzheimer's diseaseI Mateo, J Llorca, J Infante, et al.
Acta Neurologica Scandinavica|November 8, 2007
Serum levels and genetic variation of TGF-beta1 are not associated with Alzheimer's diseaseE Rodríguez-Rodríguez, P Sánchez-Juan, I Mateo, et al.
Human Genetics|August 24, 1999
Spinocerebellar ataxias in Spanish patients: genetic analysis of familial and sporadic cases. The Ataxia Study GroupM A Pujana, J Corral, M Gratacòs, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 19, 2007
Autosomal-dominant distal myopathy with a myotilin S55F mutation: sorting out the phenotypeJ Berciano, E Gallardo, R Domínguez-Perles, et al.
Muscle & Nerve|August 9, 2001
Diagnostic strategy for familial and sporadic cases of neuropathy associated with 17p11.2 deletionJ Infante, A García, O Combarros, et al.
Journal of Medical Genetics|February 27, 2004
Autosomal dominant axonal Charcot-Marie-Tooth disease type 2 (CMT2G) maps to chromosome 12q12-q13.3E Nelis, J Berciano, N Verpoorten, et al.
Acta Neurologica Scandinavica|January 22, 2009
Epistasis between tau phosphorylation regulating genes (CDK5R1 and GSK-3beta) and Alzheimer's disease riskI Mateo, J L Vázquez-Higuera, P Sánchez-Juan, et al.
Acta Neurologica Scandinavica|March 3, 1998
Gender effect on apolipoprotein E epsilon4 allele-associated risk for sporadic Alzheimer's diseaseO Combarros, C Leno, A Oterino, et al.
Acta Neurologica Scandinavica|September 30, 2009
Serum heme oxygenase-1 levels are increased in Parkinson's disease but not in Alzheimer's diseaseI Mateo, J Infante, P Sánchez-Juan, et al.
Pageof 11