DiMauro S - Search Results

1

[Mitochondrial encephalopathies: where are we going?].

DiMauro S, Andreu AL, Bonilla E. DiMauro S, et al. Rev Neurol. 1999 Jan 16-31;28(2):164-8. Rev Neurol. 1999. PMID: 10101786 Review. Spanish.

2

A new mutation associated with MELAS is located in a mitochondrial DNA polypeptide-coding gene.

Manfredi G, Schon EA, Moraes CT, Bonilla E, Berry GT, Sladky JT, DiMauro S. Manfredi G, et al. Among authors: dimauro s. Neuromuscul Disord. 1995 Sep;5(5):391-8. doi: 10.1016/0960-8966(94)00079-o. Neuromuscul Disord. 1995. PMID: 7496173 Free article.

3

Multiple mitochondrial DNA deletions in sporadic inclusion body myositis: a study of 56 patients.

Santorelli FM, Sciacco M, Tanji K, Shanske S, Vu TH, Golzi V, Griggs RC, Mendell JR, Hays AP, Bertorini TE, Pestronk A, Bonilla E, DiMauro S. Santorelli FM, et al. Among authors: dimauro s. Ann Neurol. 1996 Jun;39(6):789-95. doi: 10.1002/ana.410390615. Ann Neurol. 1996. PMID: 8651651

4

Mitochondrial encephalomyopathy with coenzyme Q10 deficiency.

Sobreira C, Hirano M, Shanske S, Keller RK, Haller RG, Davidson E, Santorelli FM, Miranda AF, Bonilla E, Mojon DS, Barreira AA, King MP, DiMauro S. Sobreira C, et al. Among authors: dimauro s. Neurology. 1997 May;48(5):1238-43. doi: 10.1212/wnl.48.5.1238. Neurology. 1997. PMID: 9153450

5

Clinical manifestations of mitochondrial DNA depletion.

Vu TH, Sciacco M, Tanji K, Nichter C, Bonilla E, Chatkupt S, Maertens P, Shanske S, Mendell J, Koenigsberger MR, Sharer L, Schon EA, DiMauro S, DeVivo DC. Vu TH, et al. Among authors: dimauro s. Neurology. 1998 Jun;50(6):1783-90. doi: 10.1212/wnl.50.6.1783. Neurology. 1998. PMID: 9633728

6

Mitochondria in neuromuscular disorders.

DiMauro S, Bonilla E, Davidson M, Hirano M, Schon EA. DiMauro S, et al. Biochim Biophys Acta. 1998 Aug 10;1366(1-2):199-210. doi: 10.1016/s0005-2728(98)00113-3. Biochim Biophys Acta. 1998. PMID: 9714805 Free article. Review.

7

A nonsense mutation (G15059A) in the cytochrome b gene in a patient with exercise intolerance and myoglobinuria.

Andreu AL, Bruno C, Dunne TC, Tanji K, Shanske S, Sue CM, Krishna S, Hadjigeorgiou GM, Shtilbans A, Bonilla E, DiMauro S. Andreu AL, et al. Among authors: dimauro s. Ann Neurol. 1999 Jan;45(1):127-30. doi: 10.1002/1531-8249(199901)45:1<127::aid-art20>3.0.co;2-y. Ann Neurol. 1999. PMID: 9894887

8

Mitochondrial involvement in Alzheimer's disease.

Bonilla E, Tanji K, Hirano M, Vu TH, DiMauro S, Schon EA. Bonilla E, et al. Among authors: dimauro s. Biochim Biophys Acta. 1999 Feb 9;1410(2):171-82. doi: 10.1016/s0005-2728(98)00165-0. Biochim Biophys Acta. 1999. PMID: 10076025 Free article. Review.

9

Exercise intolerance due to a nonsense mutation in the mtDNA ND4 gene.

Andreu AL, Tanji K, Bruno C, Hadjigeorgiou GM, Sue CM, Jay C, Ohnishi T, Shanske S, Bonilla E, DiMauro S. Andreu AL, et al. Among authors: dimauro s. Ann Neurol. 1999 Jun;45(6):820-3. doi: 10.1002/1531-8249(199906)45:6<820::aid-ana22>3.0.co;2-w. Ann Neurol. 1999. PMID: 10360780

10

A new mitochondrial DNA mutation (A3288G) in the tRNA(Leu(UUR)) gene associated with familial myopathy.

Hadjigeorgiou GM, Kim SH, Fischbeck KH, Andreu AL, Berry GT, Bingham P, Shanske S, Bonilla E, DiMauro S. Hadjigeorgiou GM, et al. Among authors: dimauro s. J Neurol Sci. 1999 Apr 1;164(2):153-7. doi: 10.1016/s0022-510x(99)00062-3. J Neurol Sci. 1999. PMID: 10402027

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