Brown MD - Search Results

1

The role of the ND5 gene in LHON: characterization of a new, heteroplasmic LHON mutation.

Mayorov V, Biousse V, Newman NJ, Brown MD. Mayorov V, et al. Among authors: brown md. Ann Neurol. 2005 Nov;58(5):807-11. doi: 10.1002/ana.20669. Ann Neurol. 2005. PMID: 16240359

2

Mitochondrial oxidative phosphorylation in autosomal dominant optic atrophy.

Mayorov VI, Lowrey AJ, Biousse V, Newman NJ, Cline SD, Brown MD. Mayorov VI, et al. Among authors: brown md. BMC Biochem. 2008 Sep 10;9:22. doi: 10.1186/1471-2091-9-22. BMC Biochem. 2008. PMID: 18783614 Free PMC article.

3

The role of mtDNA background in disease expression: a new primary LHON mutation associated with Western Eurasian haplogroup J.

Brown MD, Starikovskaya E, Derbeneva O, Hosseini S, Allen JC, Mikhailovskaya IE, Sukernik RI, Wallace DC. Brown MD, et al. Hum Genet. 2002 Feb;110(2):130-8. doi: 10.1007/s00439-001-0660-8. Epub 2002 Jan 24. Hum Genet. 2002. PMID: 11935318

4

A novel recurrent mitochondrial DNA mutation in ND3 gene is associated with isolated complex I deficiency causing Leigh syndrome and dystonia.

Sarzi E, Brown MD, Lebon S, Chretien D, Munnich A, Rotig A, Procaccio V. Sarzi E, et al. Among authors: brown md. Am J Med Genet A. 2007 Jan 1;143A(1):33-41. doi: 10.1002/ajmg.a.31565. Am J Med Genet A. 2007. PMID: 17152068

5

OPA1 mutations and mitochondrial DNA haplotypes in autosomal dominant optic atrophy.

Han J, Thompson-Lowrey AJ, Reiss A, Mayorov V, Jia H, Biousse V, Newman NJ, Brown MD. Han J, et al. Among authors: brown md. Genet Med. 2006 Apr;8(4):217-25. doi: 10.1097/01.gim.0000214299.61930.c0. Genet Med. 2006. PMID: 16617242 Free article.

6

Complete mitochondrial DNA sequence analysis in a family with early-onset dystonia and optic atrophy.

Brown MD, Hosseini S, Steiner I, Wallace DC, Korn-Lubetzki I. Brown MD, et al. Mov Disord. 2004 Feb;19(2):235-7. doi: 10.1002/mds.10646. Mov Disord. 2004. PMID: 14978686

7

Cuban optic neuropathy.

Newman NJ, Torroni A, Brown MD, Lott MT, Wallace DC, Philen R, Roman GC. Newman NJ, et al. Among authors: brown md. Neurology. 1995 Feb;45(2):397. doi: 10.1212/wnl.45.2.397. Neurology. 1995. PMID: 7710535 No abstract available.

8

A mitochondrial DNA mutation at nucleotide pair 14459 of the NADH dehydrogenase subunit 6 gene associated with maternally inherited Leber hereditary optic neuropathy and dystonia.

Jun AS, Brown MD, Wallace DC. Jun AS, et al. Among authors: brown md. Proc Natl Acad Sci U S A. 1994 Jun 21;91(13):6206-10. doi: 10.1073/pnas.91.13.6206. Proc Natl Acad Sci U S A. 1994. PMID: 8016139 Free PMC article.

9

Diseases resulting from mitochondrial DNA point mutations.

Wallace DC, Lott MT, Shoffner JM, Brown MD. Wallace DC, et al. Among authors: brown md. J Inherit Metab Dis. 1992;15(4):472-9. doi: 10.1007/BF01799605. J Inherit Metab Dis. 1992. PMID: 1528007 Review.

10

A mitochondrial DNA variant, identified in Leber hereditary optic neuropathy patients, which extends the amino acid sequence of cytochrome c oxidase subunit I.

Brown MD, Yang CC, Trounce I, Torroni A, Lott MT, Wallace DC. Brown MD, et al. Am J Hum Genet. 1992 Aug;51(2):378-85. Am J Hum Genet. 1992. PMID: 1322638 Free PMC article.

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