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Y Campos

Showing results (11-20 of 121) with videos related to

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Annals of the Rheumatic Diseases|June 1, 1995
Respiratory chain enzyme defects in patients with idiopathic inflammatory myopathyY Campos, J Arenas, A Cabello, et al.
Actas Dermo-Sifiliograficas|January 24, 2017
Congenital Melanocytic Nevus Syndrome: A Case SeriesA Recio, A I Sánchez-Moya, V Félix, et al.
Insect Biochemistry and Molecular Biology|August 1, 1997
Evidence for two distinct members of the amylase gene family in the yellow fever mosquito, Aedes aegyptiG L Grossman, Y Campos, D W Severson, et al.
Neurology|October 1, 1996
Single large-scale mitochondrial DNA deletion in a patient with mitochondrial myopathy associated with multiple symmetric lipomatosisY Campos, M A Martín, C Navarro, et al.
Molecular Genetics and Metabolism|August 5, 2000
The pathogenic role of point mutations affecting the translational initiation codon of mitochondrial genesM A Fernández-Moreno, B Bornstein, Y Campos, et al.
Brain & Development|June 17, 1998
Congenital ocular motor apraxia associated with myopathy, external hydrocephalus and NADH dehydrogenase deficiencyJ E Puñal, E Rodríguez, E Pintos, et al.
Experimental Parasitology|March 21, 1998
Leishmania sp.: growth and survival are impaired by ion channel blockersA Ponte-Sucre, Y Campos, M Fernandez, et al.
Neuromuscular Disorders : NMD|March 14, 2000
A missense mutation T487N in the myophosphorylase gene in a Spanish patient with McArdle's diseaseJ C Rubio, M A Martín, Y Campos, et al.
Pediatric Neurology|November 21, 1997
Syndrome of encephalopathy, petechiae, and ethylmalonic aciduriaM T García-Silva, A Ribes, Y Campos, et al.
Memorias Do Instituto Oswaldo Cruz|May 5, 1998
Sensitivity of Leishmania spp. to glibenclamide and 4-aminopyridine: a tool for the study of drug resistance developmentA Ponte-Sucre, Y Campos, J Vázquez, et al.
Pageof 13

Showing results (11-20 of 121) with videos related to

Sort By:
Pageof 13
Annals of the Rheumatic Diseases|June 1, 1995
Respiratory chain enzyme defects in patients with idiopathic inflammatory myopathyY Campos, J Arenas, A Cabello, et al.
Actas Dermo-Sifiliograficas|January 24, 2017
Congenital Melanocytic Nevus Syndrome: A Case SeriesA Recio, A I Sánchez-Moya, V Félix, et al.
Insect Biochemistry and Molecular Biology|August 1, 1997
Evidence for two distinct members of the amylase gene family in the yellow fever mosquito, Aedes aegyptiG L Grossman, Y Campos, D W Severson, et al.
Neurology|October 1, 1996
Single large-scale mitochondrial DNA deletion in a patient with mitochondrial myopathy associated with multiple symmetric lipomatosisY Campos, M A Martín, C Navarro, et al.
Molecular Genetics and Metabolism|August 5, 2000
The pathogenic role of point mutations affecting the translational initiation codon of mitochondrial genesM A Fernández-Moreno, B Bornstein, Y Campos, et al.
Brain & Development|June 17, 1998
Congenital ocular motor apraxia associated with myopathy, external hydrocephalus and NADH dehydrogenase deficiencyJ E Puñal, E Rodríguez, E Pintos, et al.
Experimental Parasitology|March 21, 1998
Leishmania sp.: growth and survival are impaired by ion channel blockersA Ponte-Sucre, Y Campos, M Fernandez, et al.
Neuromuscular Disorders : NMD|March 14, 2000
A missense mutation T487N in the myophosphorylase gene in a Spanish patient with McArdle's diseaseJ C Rubio, M A Martín, Y Campos, et al.
Pediatric Neurology|November 21, 1997
Syndrome of encephalopathy, petechiae, and ethylmalonic aciduriaM T García-Silva, A Ribes, Y Campos, et al.
Memorias Do Instituto Oswaldo Cruz|May 5, 1998
Sensitivity of Leishmania spp. to glibenclamide and 4-aminopyridine: a tool for the study of drug resistance developmentA Ponte-Sucre, Y Campos, J Vázquez, et al.
Pageof 13