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Items: 8

1.

Renal amino acid transport in adults with oxidative phosphorylation diseases.

Shoffner JM, Voljavec AS, Dixon J, Kaufman A, Wallace DC, Mitch WE.

Kidney Int. 1995 Apr;47(4):1101-7.

2.

Leber's hereditary optic neuropathy: a model for mitochondrial neurodegenerative diseases.

Brown MD, Voljavec AS, Lott MT, MacDonald I, Wallace DC.

FASEB J. 1992 Jul;6(10):2791-9. Review.

PMID:
1634041
3.

Mitochondrial DNA complex I and III mutations associated with Leber's hereditary optic neuropathy.

Brown MD, Voljavec AS, Lott MT, Torroni A, Yang CC, Wallace DC.

Genetics. 1992 Jan;130(1):163-73.

4.

Mitochondrial DNA mutations associated with neuromuscular diseases: analysis and diagnosis using the polymerase chain reaction.

Wallace DC, Lott MT, Lezza AM, Seibel P, Voljavec AS, Shoffner JM.

Pediatr Res. 1990 Nov;28(5):525-8.

PMID:
2123980
5.

Evaluation of procedures for assaying oxidative phosphorylation enzyme activities in mitochondrial myopathy muscle biopsies.

Zheng XX, Shoffner JM, Voljavec AS, Wallace DC.

Biochim Biophys Acta. 1990 Aug 9;1019(1):1-10. Review.

PMID:
2168748
6.

Variable genotype of Leber's hereditary optic neuropathy patients.

Lott MT, Voljavec AS, Wallace DC.

Am J Ophthalmol. 1990 Jun 15;109(6):625-31.

PMID:
2346190
7.

Spontaneous Kearns-Sayre/chronic external ophthalmoplegia plus syndrome associated with a mitochondrial DNA deletion: a slip-replication model and metabolic therapy.

Shoffner JM, Lott MT, Voljavec AS, Soueidan SA, Costigan DA, Wallace DC.

Proc Natl Acad Sci U S A. 1989 Oct;86(20):7952-6.

8.

Evidence in a lethal infantile mitochondrial disease for a nuclear mutation affecting respiratory complexes I and IV.

Zheng X, Shoffner JM, Lott MT, Voljavec AS, Krawiecki NS, Winn K, Wallace DC.

Neurology. 1989 Sep;39(9):1203-9.

PMID:
2549452

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