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J M Shoffner

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Clinical Neuroscience (New York, N.Y.)|January 1, 1995
Oxidative phosphorylation diseases and cerebellar ataxiaJ M Shoffner, A Kaufman, D Koontz, et al.
Pediatric Research|November 1, 1990
Mitochondrial DNA mutations associated with neuromuscular diseases: analysis and diagnosis using the polymerase chain reactionD C Wallace, M T Lott, A M Lezza, et al.
Nature Genetics|December 1, 1992
Mitochondrial DNA deletions in human brain: regional variability and increase with advanced ageM Corral-Debrinski, T Horton, M T Lott, et al.
Cell|June 15, 1990
Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutationJ M Shoffner, M T Lott, A M Lezza, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|November 1, 1993
Variable retinal and neurologic manifestations in patients harboring the mitochondrial DNA 8993 mutationR G Ortiz, N J Newman, J M Shoffner, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 1, 1989
Spontaneous Kearns-Sayre/chronic external ophthalmoplegia plus syndrome associated with a mitochondrial DNA deletion: a slip-replication model and metabolic therapyJ M Shoffner, M T Lott, A S Voljavec, et al.
Annals of Neurology|October 1, 1993
Oxidative damage to mitochondrial DNA shows marked age-dependent increases in human brainP Mecocci, U MacGarvey, A E Kaufman, et al.
Neurology|September 1, 1989
Evidence in a lethal infantile mitochondrial disease for a nuclear mutation affecting respiratory complexes I and IVX Zheng, J M Shoffner, M T Lott, et al.
Neurology|February 1, 1995
Mitochondrial encephalomyopathy associated with a single nucleotide pair deletion in the mitochondrial tRNALeu(UUR) geneJ M Shoffner, M G Bialer, S G Pavlakis, et al.
Nature Genetics|April 1, 1992
Maternally transmitted diabetes and deafness associated with a 10.4 kb mitochondrial DNA deletionS W Ballinger, J M Shoffner, E V Hedaya, et al.
Pageof 5

Showing results (31-40 of 50) with videos related to

Sort By:
Pageof 5
Clinical Neuroscience (New York, N.Y.)|January 1, 1995
Oxidative phosphorylation diseases and cerebellar ataxiaJ M Shoffner, A Kaufman, D Koontz, et al.
Pediatric Research|November 1, 1990
Mitochondrial DNA mutations associated with neuromuscular diseases: analysis and diagnosis using the polymerase chain reactionD C Wallace, M T Lott, A M Lezza, et al.
Nature Genetics|December 1, 1992
Mitochondrial DNA deletions in human brain: regional variability and increase with advanced ageM Corral-Debrinski, T Horton, M T Lott, et al.
Cell|June 15, 1990
Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutationJ M Shoffner, M T Lott, A M Lezza, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|November 1, 1993
Variable retinal and neurologic manifestations in patients harboring the mitochondrial DNA 8993 mutationR G Ortiz, N J Newman, J M Shoffner, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 1, 1989
Spontaneous Kearns-Sayre/chronic external ophthalmoplegia plus syndrome associated with a mitochondrial DNA deletion: a slip-replication model and metabolic therapyJ M Shoffner, M T Lott, A S Voljavec, et al.
Annals of Neurology|October 1, 1993
Oxidative damage to mitochondrial DNA shows marked age-dependent increases in human brainP Mecocci, U MacGarvey, A E Kaufman, et al.
Neurology|September 1, 1989
Evidence in a lethal infantile mitochondrial disease for a nuclear mutation affecting respiratory complexes I and IVX Zheng, J M Shoffner, M T Lott, et al.
Neurology|February 1, 1995
Mitochondrial encephalomyopathy associated with a single nucleotide pair deletion in the mitochondrial tRNALeu(UUR) geneJ M Shoffner, M G Bialer, S G Pavlakis, et al.
Nature Genetics|April 1, 1992
Maternally transmitted diabetes and deafness associated with a 10.4 kb mitochondrial DNA deletionS W Ballinger, J M Shoffner, E V Hedaya, et al.
Pageof 5