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A Lombes

Showing results (1-10 of 38) with videos related to

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Revue Neurologique|January 1, 1989
Mitochondrial encephalomyopathiesA Lombes, E Bonilla, S Dimauro
Morphologie : Bulletin De L'Association Des Anatomistes|June 24, 2004
[Organization and dynamics of the mitochondrial compartment]F Malka, A Lombes, M Rojo
European Journal of Neurology|August 26, 2006
Task force guidelines handbook: EFNS guidelines on diagnosis and management of fatty acid mitochondrial disordersC Angelini, A Federico, H Reichmann, et al.
Cell Transplantation|January 31, 2009
Myoblast xenotransplantation as a tool to evaluate the appropriateness of nanoparticular versus cellular trackersC Praud, K Vauchez, A Lombes, et al.
Annales De Medecine Interne|January 1, 1987
[Research methods in metabolic myopathies in children]A Lombes, H Ogier, J P Bonnefont, et al.
Neurologic Clinics|August 1, 1990
Mitochondrial encephalomyopathiesS DiMauro, E Bonilla, A Lombes, et al.
American Journal of Human Genetics|March 1, 1990
Transcription and translation of deleted mitochondrial genomes in Kearns-Sayre syndrome: implications for pathogenesisH Nakase, C T Moraes, R Rizzuto, et al.
Neurology|March 1, 1994
Clinical and biochemical features of 10 adult patients with muscle phosphorylase kinase deficiencyD A Wilkinson, P Tonin, S Shanske, et al.
Journal of Inherited Metabolic Disease|January 1, 1986
A new case of methylmalonic aciduria with unexplained negative urinary methylmalonic colorimetric testC Charpentier, M Coude, J L Perignon, et al.
Journal of Bioenergetics and Biomembranes|June 1, 1988
Molecular defects in cytochrome oxidase in mitochondrial diseasesS DiMauro, M Zeviani, R Rizzuto, et al.
Pageof 4

Showing results (1-10 of 38) with videos related to

Sort By:
Pageof 4
Revue Neurologique|January 1, 1989
Mitochondrial encephalomyopathiesA Lombes, E Bonilla, S Dimauro
Morphologie : Bulletin De L'Association Des Anatomistes|June 24, 2004
[Organization and dynamics of the mitochondrial compartment]F Malka, A Lombes, M Rojo
European Journal of Neurology|August 26, 2006
Task force guidelines handbook: EFNS guidelines on diagnosis and management of fatty acid mitochondrial disordersC Angelini, A Federico, H Reichmann, et al.
Cell Transplantation|January 31, 2009
Myoblast xenotransplantation as a tool to evaluate the appropriateness of nanoparticular versus cellular trackersC Praud, K Vauchez, A Lombes, et al.
Annales De Medecine Interne|January 1, 1987
[Research methods in metabolic myopathies in children]A Lombes, H Ogier, J P Bonnefont, et al.
Neurologic Clinics|August 1, 1990
Mitochondrial encephalomyopathiesS DiMauro, E Bonilla, A Lombes, et al.
American Journal of Human Genetics|March 1, 1990
Transcription and translation of deleted mitochondrial genomes in Kearns-Sayre syndrome: implications for pathogenesisH Nakase, C T Moraes, R Rizzuto, et al.
Neurology|March 1, 1994
Clinical and biochemical features of 10 adult patients with muscle phosphorylase kinase deficiencyD A Wilkinson, P Tonin, S Shanske, et al.
Journal of Inherited Metabolic Disease|January 1, 1986
A new case of methylmalonic aciduria with unexplained negative urinary methylmalonic colorimetric testC Charpentier, M Coude, J L Perignon, et al.
Journal of Bioenergetics and Biomembranes|June 1, 1988
Molecular defects in cytochrome oxidase in mitochondrial diseasesS DiMauro, M Zeviani, R Rizzuto, et al.
Pageof 4