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G Morís

Showing results (11-20 of 15) with videos related to

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Revista De Neurologia|January 27, 2023
[Adult-onset sensory neuropathy and ataxia as a clinical manifestation of POLG gene mutations]C García-Cabo, P Carvajal-García, I Fernández-Vega, et al.
Medicina Clinica|November 26, 1999
[Frequency of the APOE-4 allele in Alzheimer's disease and its variation with age in Asturias (Spain)]V Alvarez, R Alvarez, J Peña, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 24, 1999
Angiotensin converting enzyme and endothelial nitric oxide synthase DNA polymorphisms and late onset Alzheimer's diseaseR Alvarez, V Alvarez, C H Lahoz, et al.
Biochemical and Biophysical Research Communications|October 21, 1999
Association between an alpha(2) macroglobulin DNA polymorphism and late-onset Alzheimer's diseaseV Alvarez, R Alvarez, C H Lahoz, et al.
Neurologia|April 21, 2019
Clinical guide for the diagnosis and follow-up of myotonic dystrophy type 1, MD1 or Steinert's diseaseG Gutiérrez Gutiérrez, J Díaz-Manera, M Almendrote, et al.
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Showing results (11-20 of 15) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 15 results.
Revista De Neurologia|January 27, 2023
[Adult-onset sensory neuropathy and ataxia as a clinical manifestation of POLG gene mutations]C García-Cabo, P Carvajal-García, I Fernández-Vega, et al.
Medicina Clinica|November 26, 1999
[Frequency of the APOE-4 allele in Alzheimer's disease and its variation with age in Asturias (Spain)]V Alvarez, R Alvarez, J Peña, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 24, 1999
Angiotensin converting enzyme and endothelial nitric oxide synthase DNA polymorphisms and late onset Alzheimer's diseaseR Alvarez, V Alvarez, C H Lahoz, et al.
Biochemical and Biophysical Research Communications|October 21, 1999
Association between an alpha(2) macroglobulin DNA polymorphism and late-onset Alzheimer's diseaseV Alvarez, R Alvarez, C H Lahoz, et al.
Neurologia|April 21, 2019
Clinical guide for the diagnosis and follow-up of myotonic dystrophy type 1, MD1 or Steinert's diseaseG Gutiérrez Gutiérrez, J Díaz-Manera, M Almendrote, et al.
Pageof 2