Shoubridge EA - Search Results

1

Cytochrome c oxidase deficiency.

Shoubridge EA. Shoubridge EA. Am J Med Genet. 2001 Spring;106(1):46-52. doi: 10.1002/ajmg.1378. Am J Med Genet. 2001. PMID: 11579424 Review.

2

Distribution and threshold expression of the tRNA(Lys) mutation in skeletal muscle of patients with myoclonic epilepsy and ragged-red fibers (MERRF).

Boulet L, Karpati G, Shoubridge EA. Boulet L, et al. Among authors: shoubridge ea. Am J Hum Genet. 1992 Dec;51(6):1187-200. Am J Hum Genet. 1992. PMID: 1334369 Free PMC article.

3

Mitochondrial dysfunction in multiple symmetrical lipomatosis.

Berkovic SF, Andermann F, Shoubridge EA, Carpenter S, Robitaille Y, Andermann E, Melmed C, Karpati G. Berkovic SF, et al. Among authors: shoubridge ea. Ann Neurol. 1991 May;29(5):566-9. doi: 10.1002/ana.410290519. Ann Neurol. 1991. PMID: 1650162

4

Correlative multidisciplinary approach to the study of mitochondrial encephalomyopathies.

Karpati G, Arnold D, Matthews P, Carpenter S, Andermann F, Shoubridge E. Karpati G, et al. Rev Neurol (Paris). 1991;147(6-7):455-61. Rev Neurol (Paris). 1991. PMID: 1962050 Review.

5

Deletion mutants are functionally dominant over wild-type mitochondrial genomes in skeletal muscle fiber segments in mitochondrial disease.

Shoubridge EA, Karpati G, Hastings KE. Shoubridge EA, et al. Cell. 1990 Jul 13;62(1):43-9. doi: 10.1016/0092-8674(90)90238-a. Cell. 1990. PMID: 2163769

6

Segregation of mitochondrial DNAs carrying a pathogenic point mutation (tRNA(leu3243)) in cybrid cells.

Shoubridge EA. Shoubridge EA. Biochem Biophys Res Commun. 1995 Aug 4;213(1):189-95. doi: 10.1006/bbrc.1995.2115. Biochem Biophys Res Commun. 1995. PMID: 7639735

7

Familial myopathy with conspicuous depletion of mitochondria in muscle fibers: a morphologically distinct disease.

Genge A, Karpati G, Arnold D, Shoubridge EA, Carpenter S. Genge A, et al. Among authors: shoubridge ea. Neuromuscul Disord. 1995 Mar;5(2):139-44. doi: 10.1016/0960-8966(94)00039-c. Neuromuscul Disord. 1995. PMID: 7767093

8

Late-onset mitochondrial myopathy.

Johnston W, Karpati G, Carpenter S, Arnold D, Shoubridge EA. Johnston W, et al. Among authors: shoubridge ea. Ann Neurol. 1995 Jan;37(1):16-23. doi: 10.1002/ana.410370106. Ann Neurol. 1995. PMID: 7818252

9

Mitochondrial DNA diseases: histological and cellular studies.

Shoubridge EA. Shoubridge EA. J Bioenerg Biomembr. 1994 Jun;26(3):301-10. doi: 10.1007/BF00763101. J Bioenerg Biomembr. 1994. PMID: 8077183 Review.

10

Mitochondrial DNA depletion: prevalence in a pediatric population referred for neurologic evaluation.

Macmillan CJ, Shoubridge EA. Macmillan CJ, et al. Among authors: shoubridge ea. Pediatr Neurol. 1996 Apr;14(3):203-10. doi: 10.1016/0887-8994(96)00018-5. Pediatr Neurol. 1996. PMID: 8736403

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

Search Page

Search Results