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A Vilaseca

Showing results (91-100 of 133) with videos related to

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Pediatric Research|May 7, 2004
Peripheral neuropathy with ataxia in childhood as a result of the G8363A mutation in mitochondrial DNAMercedes Pineda, Abelardo Solano, Rafael Artuch, et al.
Journal of Molecular Medicine (Berlin, Germany)|July 4, 2001
Large de novo deletion in chromosome 12 affecting the PAH, IGF1, ASCL1, and TRA1 genesJ Mallolas, M A Vilaseca, C Pavia, et al.
Anales Espanoles De Pediatria|December 1, 1988
[The neonatal form of propionic acidemia]J Figueras Aloy, A Ribes Rubio, M A Vilaseca Busca, et al.
Human Genetics|May 26, 1998
Variability of biochemical and clinical phenotype in X-linked liver glycogenosis with mutations in the phosphorylase kinase PHKA2 geneB Burwinkel, L Amat, R G Gray, et al.
Clinical Genetics|June 30, 2010
Ancient origin of the CTH alelle carrying the c.200C>T (p.T67I) variant in patients with cystathioninuriaC Espinós, A García-Cazorla, D Martínez-Rubio, et al.
Molecular Genetics and Metabolism|April 23, 2003
Late-onset form of beta-electron transfer flavoprotein deficiencyA Curcoy, R K J Olsen, A Ribes, et al.
European Journal of Clinical Investigation|February 13, 2001
Homocysteine and the MTHFR 677C-->T allele in premature coronary artery disease. Case control and family studiesX Pintó, M A Vilaseca, N Garcia-Giralt, et al.
Biofactors (Oxford, England)|July 29, 2006
Muscle coenzyme Q10 concentrations in patients with probable and definite diagnosis of respiratory chain disordersR Montero, R Artuch, P Briones, et al.
Annals of Neurology|December 21, 2005
Cerebral folate deficiency and leukoencephalopathy caused by a mitochondrial DNA deletionMerce Pineda, Aida Ormazabal, Esther López-Gallardo, et al.
Actas Urologicas Espanolas|December 22, 2015
Changing patterns in the surgical management of renal massesA Vilaseca, M Musquera, D P Nguyen, et al.
Pageof 14

Showing results (91-100 of 133) with videos related to

Sort By:
Pageof 14
Pediatric Research|May 7, 2004
Peripheral neuropathy with ataxia in childhood as a result of the G8363A mutation in mitochondrial DNAMercedes Pineda, Abelardo Solano, Rafael Artuch, et al.
Journal of Molecular Medicine (Berlin, Germany)|July 4, 2001
Large de novo deletion in chromosome 12 affecting the PAH, IGF1, ASCL1, and TRA1 genesJ Mallolas, M A Vilaseca, C Pavia, et al.
Anales Espanoles De Pediatria|December 1, 1988
[The neonatal form of propionic acidemia]J Figueras Aloy, A Ribes Rubio, M A Vilaseca Busca, et al.
Human Genetics|May 26, 1998
Variability of biochemical and clinical phenotype in X-linked liver glycogenosis with mutations in the phosphorylase kinase PHKA2 geneB Burwinkel, L Amat, R G Gray, et al.
Clinical Genetics|June 30, 2010
Ancient origin of the CTH alelle carrying the c.200C>T (p.T67I) variant in patients with cystathioninuriaC Espinós, A García-Cazorla, D Martínez-Rubio, et al.
Molecular Genetics and Metabolism|April 23, 2003
Late-onset form of beta-electron transfer flavoprotein deficiencyA Curcoy, R K J Olsen, A Ribes, et al.
European Journal of Clinical Investigation|February 13, 2001
Homocysteine and the MTHFR 677C-->T allele in premature coronary artery disease. Case control and family studiesX Pintó, M A Vilaseca, N Garcia-Giralt, et al.
Biofactors (Oxford, England)|July 29, 2006
Muscle coenzyme Q10 concentrations in patients with probable and definite diagnosis of respiratory chain disordersR Montero, R Artuch, P Briones, et al.
Annals of Neurology|December 21, 2005
Cerebral folate deficiency and leukoencephalopathy caused by a mitochondrial DNA deletionMerce Pineda, Aida Ormazabal, Esther López-Gallardo, et al.
Actas Urologicas Espanolas|December 22, 2015
Changing patterns in the surgical management of renal massesA Vilaseca, M Musquera, D P Nguyen, et al.
Pageof 14