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DiMauro

Showing results (331-340 of 942) with videos related to

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JAMA Neurology|September 11, 2013
Longitudinal clinical follow-up of a large family with the R357P Twinkle mutationCarmen Paradas, Pilar Camaño, David Otaegui, et al.
Journal of Dairy Science|February 26, 2019
Genomic selection of milk fatty acid composition in Sarda dairy sheep: Effect of different phenotypes and relationship matrices on heritability and breeding value accuracyA Cesarani, G Gaspa, F Correddu, 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.
Optics Letters|October 30, 2009
Aberration-free stretcher design for ultrashort-pulse amplificationG Cheriaux, P Rousseau, F Salin, et al.
Molecular and Cellular Biology|March 1, 1991
Replication-competent human mitochondrial DNA lacking the heavy-strand promoter regionC T Moraes, F Andreetta, E Bonilla, et al.
Neurology|July 17, 1999
Phenotypic analysis of autosomal dominant hereditary spastic paraplegia linked to chromosome 8qP Hedera, S DiMauro, E Bonilla, et al.
Brain : a Journal of Neurology|January 23, 2003
The spectrum of exercise tolerance in mitochondrial myopathies: a study of 40 patientsTanja Taivassalo, Tina Dysgaard Jensen, Nancy Kennaway, et al.
Nature Genetics|July 1, 1993
A mitochondrial tRNA anticodon swap associated with a muscle diseaseC T Moraes, F Ciacci, E Bonilla, et al.
The Journal of Pediatrics|January 15, 1998
Infantile phosphofructokinase deficiency with arthrogryposis: clinical benefit of a ketogenic dietK J Swoboda, L Specht, H R Jones, et al.
Lancet (London, England)|March 2, 1991
Depletion of muscle mitochondrial DNA in AIDS patients with zidovudine-induced myopathyE Arnaudo, M Dalakas, S Shanske, et al.
Pageof 95

Showing results (331-340 of 942) with videos related to

Sort By:
Pageof 95
JAMA Neurology|September 11, 2013
Longitudinal clinical follow-up of a large family with the R357P Twinkle mutationCarmen Paradas, Pilar Camaño, David Otaegui, et al.
Journal of Dairy Science|February 26, 2019
Genomic selection of milk fatty acid composition in Sarda dairy sheep: Effect of different phenotypes and relationship matrices on heritability and breeding value accuracyA Cesarani, G Gaspa, F Correddu, 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.
Optics Letters|October 30, 2009
Aberration-free stretcher design for ultrashort-pulse amplificationG Cheriaux, P Rousseau, F Salin, et al.
Molecular and Cellular Biology|March 1, 1991
Replication-competent human mitochondrial DNA lacking the heavy-strand promoter regionC T Moraes, F Andreetta, E Bonilla, et al.
Neurology|July 17, 1999
Phenotypic analysis of autosomal dominant hereditary spastic paraplegia linked to chromosome 8qP Hedera, S DiMauro, E Bonilla, et al.
Brain : a Journal of Neurology|January 23, 2003
The spectrum of exercise tolerance in mitochondrial myopathies: a study of 40 patientsTanja Taivassalo, Tina Dysgaard Jensen, Nancy Kennaway, et al.
Nature Genetics|July 1, 1993
A mitochondrial tRNA anticodon swap associated with a muscle diseaseC T Moraes, F Ciacci, E Bonilla, et al.
The Journal of Pediatrics|January 15, 1998
Infantile phosphofructokinase deficiency with arthrogryposis: clinical benefit of a ketogenic dietK J Swoboda, L Specht, H R Jones, et al.
Lancet (London, England)|March 2, 1991
Depletion of muscle mitochondrial DNA in AIDS patients with zidovudine-induced myopathyE Arnaudo, M Dalakas, S Shanske, et al.
Pageof 95