Krishna S - Search Results

1

Respiratory chain dysfunction and oxidative stress correlate with severity of primary CoQ10 deficiency.

Quinzii CM, López LC, Von-Moltke J, Naini A, Krishna S, Schuelke M, Salviati L, Navas P, DiMauro S, Hirano M. Quinzii CM, et al. Among authors: krishna s. FASEB J. 2008 Jun;22(6):1874-85. doi: 10.1096/fj.07-100149. Epub 2008 Jan 29. FASEB J. 2008. PMID: 18230681 Free PMC article.

2

Tissue-specific oxidative stress and loss of mitochondria in CoQ-deficient Pdss2 mutant mice.

Quinzii CM, Garone C, Emmanuele V, Tadesse S, Krishna S, Dorado B, Hirano M. Quinzii CM, et al. Among authors: krishna s. FASEB J. 2013 Feb;27(2):612-21. doi: 10.1096/fj.12-209361. Epub 2012 Nov 12. FASEB J. 2013. PMID: 23150520 Free PMC article.

3

The G13513A mutation in the ND5 gene of mitochondrial DNA as a common cause of MELAS or Leigh syndrome: evidence from 12 cases.

Shanske S, Coku J, Lu J, Ganesh J, Krishna S, Tanji K, Bonilla E, Naini AB, Hirano M, DiMauro S. Shanske S, et al. Among authors: krishna s. Arch Neurol. 2008 Mar;65(3):368-72. doi: 10.1001/archneurol.2007.67. Arch Neurol. 2008. PMID: 18332249

4

A Novel SUCLA2 Mutation Presenting as a Complex Childhood Movement Disorder.

Garone C, Gurgel-Giannetti J, Sanna-Cherchi S, Krishna S, Naini A, Quinzii CM, Hirano M. Garone C, et al. Among authors: krishna s. J Child Neurol. 2017 Feb;32(2):246-250. doi: 10.1177/0883073816666221. Epub 2016 Sep 28. J Child Neurol. 2017. PMID: 27651038 Free PMC article.

5

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. Among authors: krishna s. J Neurol Sci. 2005 Jan 15;228(1):93-7. doi: 10.1016/j.jns.2004.10.018. J Neurol Sci. 2005. PMID: 15607216

6

Myopathy and parkinsonism in phosphoglycerate kinase deficiency.

Sotiriou E, Greene P, Krishna S, Hirano M, DiMauro S. Sotiriou E, et al. Among authors: krishna s. Muscle Nerve. 2010 May;41(5):707-10. doi: 10.1002/mus.21612. Muscle Nerve. 2010. PMID: 20151463 Free PMC article.

7

Missense mutation in the mtDNA cytochrome b gene in a patient with myopathy.

Andreu AL, Bruno C, Shanske S, Shtilbans A, Hirano M, Krishna S, Hayward L, Systrom DS, Brown RH Jr, DiMauro S. Andreu AL, et al. Among authors: krishna s. Neurology. 1998 Nov;51(5):1444-7. doi: 10.1212/wnl.51.5.1444. Neurology. 1998. PMID: 9818877

8

Identical mitochondrial DNA deletion in a woman with ocular myopathy and in her son with pearson syndrome.

Shanske S, Tang Y, Hirano M, Nishigaki Y, Tanji K, Bonilla E, Sue C, Krishna S, Carlo JR, Willner J, Schon EA, DiMauro S. Shanske S, et al. Among authors: krishna s. Am J Hum Genet. 2002 Sep;71(3):679-83. doi: 10.1086/342482. Epub 2002 Jul 31. Am J Hum Genet. 2002. PMID: 12152148 Free PMC article.

9

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. Among authors: krishna s. 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

10

Mitochondrial encephalomyopathy due to a novel mutation in the tRNAGlu of mitochondrial DNA.

Pancrudo J, Shanske S, Bonilla E, Daras M, Akman HO, Krishna S, Malkin E, DiMauro S. Pancrudo J, et al. Among authors: krishna s. J Child Neurol. 2007 Jul;22(7):858-62. doi: 10.1177/0883073807304199. J Child Neurol. 2007. PMID: 17715279

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