Mancuso M - Search Results

1

Congenital or late-onset myopathy in patients with the T14709C mtDNA mutation.

Mancuso M, Ferraris S, Nishigaki Y, Azan G, Mauro A, Sammarco P, Krishna S, Tay SK, Bonilla E, Romansky SG, Hirano M, DiMauro S. Mancuso M, et al. J Neurol Sci. 2005 Jan 15;228(1):93-7. doi: 10.1016/j.jns.2004.10.018. J Neurol Sci. 2005. PMID: 15607216

2

Mitochondrial encephalomyopathies: diagnostic approach.

Dimauro S, Tay S, Mancuso M. Dimauro S, et al. Among authors: mancuso m. Ann N Y Acad Sci. 2004 Apr;1011:217-31. doi: 10.1196/annals.1293.022. Ann N Y Acad Sci. 2004. PMID: 15126299

3

Novel mitochondrial DNA ND5 mutation in a patient with clinical features of MELAS and MERRF.

Naini AB, Lu J, Kaufmann P, Bernstein RA, Mancuso M, Bonilla E, Hirano M, DiMauro S. Naini AB, et al. Among authors: mancuso m. Arch Neurol. 2005 Mar;62(3):473-6. doi: 10.1001/archneur.62.3.473. Arch Neurol. 2005. PMID: 15767514

4

Mitochondrial myopathy and complex III deficiency in a patient with a new stop-codon mutation (G339X) in the cytochrome b gene.

Mancuso M, Filosto M, Stevens JC, Patterson M, Shanske S, Krishna S, DiMauro S. Mancuso M, et al. J Neurol Sci. 2003 May 15;209(1-2):61-3. doi: 10.1016/s0022-510x(02)00462-8. J Neurol Sci. 2003. PMID: 12686403

5

Mitochondrial myopathy of childhood associated with mitochondrial DNA depletion and a homozygous mutation (T77M) in the TK2 gene.

Mancuso M, Filosto M, Bonilla E, Hirano M, Shanske S, Vu TH, DiMauro S. Mancuso M, et al. Arch Neurol. 2003 Jul;60(7):1007-9. doi: 10.1001/archneur.60.7.1007. Arch Neurol. 2003. PMID: 12873860

6

Lack of paternal inheritance of muscle mitochondrial DNA in sporadic mitochondrial myopathies.

Filosto M, Mancuso M, Vives-Bauza C, Vilà MR, Shanske S, Hirano M, Andreu AL, DiMauro S. Filosto M, et al. Among authors: mancuso m. Ann Neurol. 2003 Oct;54(4):524-6. doi: 10.1002/ana.10709. Ann Neurol. 2003. PMID: 14520667

7

Mitochondrial encephalomyopathies: therapeutic approach.

Dimauro S, Mancuso M, Naini A. Dimauro S, et al. Among authors: mancuso m. Ann N Y Acad Sci. 2004 Apr;1011:232-45. doi: 10.1196/annals.1293.023. Ann N Y Acad Sci. 2004. PMID: 15126300

8

A novel polymerase gamma mutation in a family with ophthalmoplegia, neuropathy, and Parkinsonism.

Mancuso M, Filosto M, Oh SJ, DiMauro S. Mancuso M, et al. Arch Neurol. 2004 Nov;61(11):1777-9. doi: 10.1001/archneur.61.11.1777. Arch Neurol. 2004. PMID: 15534189

9

Studies of COX16, COX19, and PET191 in human cytochrome-c oxidase deficiency.

Tay SK, Nesti C, Mancuso M, Schon EA, Shanske S, Bonilla E, Davidson MM, Dimauro S. Tay SK, et al. Among authors: mancuso m. Arch Neurol. 2004 Dec;61(12):1935-7. doi: 10.1001/archneur.61.12.1935. Arch Neurol. 2004. PMID: 15596615

10

New DGK gene mutations in the hepatocerebral form of mitochondrial DNA depletion syndrome.

Mancuso M, Ferraris S, Pancrudo J, Feigenbaum A, Raiman J, Christodoulou J, Thorburn DR, DiMauro S. Mancuso M, et al. Arch Neurol. 2005 May;62(5):745-7. doi: 10.1001/archneur.62.5.745. Arch Neurol. 2005. PMID: 15883261

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