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R Van Coster

Showing results (31-40 of 46) with videos related to

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Journal of the Neurological Sciences|July 1, 1991
Cytochrome c oxidase-associated Leigh syndrome: phenotypic features and pathogenetic speculationsR Van Coster, A Lombres, D C De Vivo, et al.
European Journal of Neurology|October 25, 2007
Infantile presentation of the mitochondrial A8344G mutationE Scalais, C Nuttin, S Seneca, et al.
Human Reproduction (Oxford, England)|July 3, 2020
Germline nuclear transfer in mice may rescue poor embryo development associated with advanced maternal age and early embryo arrestM Tang, M Popovic, P Stamatiadis, et al.
Neuropediatrics|August 23, 2007
Ethylmalonic encephalopathy: clinical and biochemical observationsD I Zafeiriou, P Augoustides-Savvopoulou, D Haas, et al.
Pediatric Research|October 20, 2001
Blue native polyacrylamide gel electrophoresis: a powerful tool in diagnosis of oxidative phosphorylation defectsR Van Coster, J Smet, E George, et al.
Genetic Counseling (Geneva, Switzerland)|February 28, 2018
Mitochondrial Neurogastrointestinal Encephalopathy: Clinical, Biochemical and Molecular Study in Three Egyptian PatientsL Selim, R Van Coster, D Mehaney, et al.
Biochemical and Biophysical Research Communications|August 17, 2000
Combined enzymatic complex I and III deficiency associated with mutations in the nuclear encoded NDUFS4 geneS M Budde, L P van den Heuvel, A J Janssen, et al.
AJNR. American Journal of Neuroradiology|March 10, 2001
Alexander disease: diagnosis with MR imagingM S van der Knaap, S Naidu, S N Breiter, et al.
Annals of Neurology|May 11, 2000
Differential features of patients with mutations in two COX assembly genes, SURF-1 and SCO2C M Sue, C Karadimas, N Checcarelli, et al.
Molecular Human Reproduction|October 26, 2019
Comparative analysis of different nuclear transfer techniques to prevent the transmission of mitochondrial DNA variantsM Tang, R R Guggilla, Y Gansemans, et al.
Pageof 5

Showing results (31-40 of 46) with videos related to

Sort By:
Pageof 5
Journal of the Neurological Sciences|July 1, 1991
Cytochrome c oxidase-associated Leigh syndrome: phenotypic features and pathogenetic speculationsR Van Coster, A Lombres, D C De Vivo, et al.
European Journal of Neurology|October 25, 2007
Infantile presentation of the mitochondrial A8344G mutationE Scalais, C Nuttin, S Seneca, et al.
Human Reproduction (Oxford, England)|July 3, 2020
Germline nuclear transfer in mice may rescue poor embryo development associated with advanced maternal age and early embryo arrestM Tang, M Popovic, P Stamatiadis, et al.
Neuropediatrics|August 23, 2007
Ethylmalonic encephalopathy: clinical and biochemical observationsD I Zafeiriou, P Augoustides-Savvopoulou, D Haas, et al.
Pediatric Research|October 20, 2001
Blue native polyacrylamide gel electrophoresis: a powerful tool in diagnosis of oxidative phosphorylation defectsR Van Coster, J Smet, E George, et al.
Genetic Counseling (Geneva, Switzerland)|February 28, 2018
Mitochondrial Neurogastrointestinal Encephalopathy: Clinical, Biochemical and Molecular Study in Three Egyptian PatientsL Selim, R Van Coster, D Mehaney, et al.
Biochemical and Biophysical Research Communications|August 17, 2000
Combined enzymatic complex I and III deficiency associated with mutations in the nuclear encoded NDUFS4 geneS M Budde, L P van den Heuvel, A J Janssen, et al.
AJNR. American Journal of Neuroradiology|March 10, 2001
Alexander disease: diagnosis with MR imagingM S van der Knaap, S Naidu, S N Breiter, et al.
Annals of Neurology|May 11, 2000
Differential features of patients with mutations in two COX assembly genes, SURF-1 and SCO2C M Sue, C Karadimas, N Checcarelli, et al.
Molecular Human Reproduction|October 26, 2019
Comparative analysis of different nuclear transfer techniques to prevent the transmission of mitochondrial DNA variantsM Tang, R R Guggilla, Y Gansemans, et al.
Pageof 5