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Y Campos

Showing results (31-40 of 121) with videos related to

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Neuromuscular Disorders : NMD|November 5, 1997
Association of genetically proven deficiencies of myophosphorylase and AMP deaminase: a second case of 'double trouble'J C Rubio, M A Martín, J Bautista, et al.
Biochimica Et Biophysica Acta|April 18, 1998
Mitochondrial gene expression and respiratory enzyme activities in cardiac diseasesB Bornstein, R Huertas, P Ochoa, et al.
Human Mutation|November 26, 1999
A novel missense mutation 15747 T>C in the mitochondrial cytochrome b geneI Aguilera, J R García-Lozano, J Bautista, et al.
Neuromuscular Disorders : NMD|July 19, 2000
A homozygous missense mutation (A659D) in the myophosphorylase gene in a Spanish patient with McArdle's diseaseM A Martín, J C Rubio, Y Campos, et al.
Muscle & Nerve|September 1, 1992
Oculopharyngeal muscular dystrophy and mitochondrial abnormalitiesJ Arenas, R A Huertas, Y Campos, et al.
Acta Neurologica Scandinavica|January 1, 1995
Clinical heterogeneity in two pedigrees with the 3243 bp tRNA(Leu(UUR)) mutation of mitochondrial DNAY Campos, J Bautista, E Gutiérrez-Rivas, et al.
American Journal of Human Genetics|October 16, 1999
About the "Pathological" role of the mtDNA T3308C mutationellipsisH Rocha, C Flores, Y Campos, et al.
Electromyography and Clinical Neurophysiology|March 11, 2004
Single fiber electromyography (SFEMG) in mitochondrial diseases (MD)A Cruz-Martínez, J Arpa, S Santiago, et al.
Revista De Neurologia|December 29, 2000
[Benign congenital myopathy associated with a partial deficiency of complexes I and III of the mitochondrial respiratory chain]]M Castro-Gago, J Eirís, E Pintos, et al.
Medicina Clinica|March 29, 2000
[The use of cardiopulmonary exercise test in patients with mitochondrial myopathies]J Fernández, T Montemayor, J Bautista, et al.
Pageof 13

Showing results (31-40 of 121) with videos related to

Sort By:
Pageof 13
Neuromuscular Disorders : NMD|November 5, 1997
Association of genetically proven deficiencies of myophosphorylase and AMP deaminase: a second case of 'double trouble'J C Rubio, M A Martín, J Bautista, et al.
Biochimica Et Biophysica Acta|April 18, 1998
Mitochondrial gene expression and respiratory enzyme activities in cardiac diseasesB Bornstein, R Huertas, P Ochoa, et al.
Human Mutation|November 26, 1999
A novel missense mutation 15747 T>C in the mitochondrial cytochrome b geneI Aguilera, J R García-Lozano, J Bautista, et al.
Neuromuscular Disorders : NMD|July 19, 2000
A homozygous missense mutation (A659D) in the myophosphorylase gene in a Spanish patient with McArdle's diseaseM A Martín, J C Rubio, Y Campos, et al.
Muscle & Nerve|September 1, 1992
Oculopharyngeal muscular dystrophy and mitochondrial abnormalitiesJ Arenas, R A Huertas, Y Campos, et al.
Acta Neurologica Scandinavica|January 1, 1995
Clinical heterogeneity in two pedigrees with the 3243 bp tRNA(Leu(UUR)) mutation of mitochondrial DNAY Campos, J Bautista, E Gutiérrez-Rivas, et al.
American Journal of Human Genetics|October 16, 1999
About the "Pathological" role of the mtDNA T3308C mutationellipsisH Rocha, C Flores, Y Campos, et al.
Electromyography and Clinical Neurophysiology|March 11, 2004
Single fiber electromyography (SFEMG) in mitochondrial diseases (MD)A Cruz-Martínez, J Arpa, S Santiago, et al.
Revista De Neurologia|December 29, 2000
[Benign congenital myopathy associated with a partial deficiency of complexes I and III of the mitochondrial respiratory chain]]M Castro-Gago, J Eirís, E Pintos, et al.
Medicina Clinica|March 29, 2000
[The use of cardiopulmonary exercise test in patients with mitochondrial myopathies]J Fernández, T Montemayor, J Bautista, et al.
Pageof 13