Works by Krishna, Sindu

Results: 8

Mitochondrial Encephalomyopathy Due to a Novel Mutation in the tRNA<sup>Glu</sup> of Mitochondrial DNA.

Published in:

Journal of Child Neurology, 2007, v. 22, n. 7, p. 858, doi. 10.1177/0883073807304199

By:

Pancrudo, Jacklyn;
Shanske, Sara;
Bonilla, Eduardo;
Daras, Mariza;
Akman, Hasan O.;
Krishna, Sindu;
Malkin, Elfrida;
Dimauro, Salvatore

Publication type:

Article

Cockayne Syndrome in Adults: Review With Clinical and Pathologic Study of a New Case.

Published in:

Journal of Child Neurology, 2006, v. 21, n. 11, p. 991, doi. 10.1177/08830738060210110101

By:

Rapin, Isabelle;
Weidenheim, Karen;
Lindenbaum, Yelena;
Rosenbaum, Pearl;
Merchant, Saumil N.;
Krishna, Sindu;
Dickson, Dennis W.

Publication type:

Article

Mitochondrial DNA Deletion in a Child With Megaloblastic Anemia and Recurrent Encephalopathy.

Published in:

Journal of Child Neurology, 2004, v. 19, n. 4, p. 258, doi. 10.1177/088307380401900403

By:

Akman, Cigdem Inan;
Sue, Carolyn M.;
Shanske, Sara;
Tanji, Kurenai;
Bonilla, Eduardo;
Ojaimi, Joceline;
Krishna, Sindu;
Schubert, Romaine;
DiMauro, Salvatore

Publication type:

Article

Respiratory chain dysfunction and oxidative stress correlate with severity of primary CoQ<sub>10</sub> deficiency.

Published in:

FASEB Journal, 2008, v. 22, n. 6, p. 1874, doi. 10.1096/fj.07-100149

By:

Quinzii, Catarina M.;
López, Luis C.;
Von-Moltke, Jakob;
Naini, Ali;
Krishna, Sindu;
Schuelke, Markus;
Salviati, Leonardo;
Navas, Plácido;
DiMauro, Salvatore;
Hirano, Michio

Publication type:

Article

Fatal infantile cardioencephalomyopathy with COX deficiency and mutations in SCO2, a COX assembly gene.

Published in:

Nature Genetics, 1999, v. 23, n. 3, p. 333, doi. 10.1038/15513

By:

Papadopoulou, Lefkothea C.;
Sue, Carolyn M.;
Davidson, Mercy M.;
Tanji, Kurenai;
Nishino, Ichizo;
Sadlock, James E.;
Krishna, Sindu;
Walker, Winsome;
Selby, Jeanette;
Glerum, D. Moira;
Coster, Rudy Van;
Lyon, Gilles;
Scalais, Emmanuel;
Lebel, Roger;
Kaplan, Paige;
Shanske, Sara;
De Vivo, Darryl C.;
Bonilla, Eduardo;
Hirano, Michio

Publication type:

Article

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

Published in:

Journal of Child Neurology, 2017, v. 32, n. 2, p. 246, doi. 10.1177/0883073816666221

By:

Garone, Caterina;
Gurgel-Giannetti, Juliana;
Sanna-Cherchi, Simone;
Krishna, Sindu;
Naini, Ali;
Quinzii, Catarina M.;
Hirano, Michio

Publication type:

Article

Myopathy and parkinsonism in phosphoglycerate kinase deficiency.

Published in:

Muscle & Nerve, 2010, v. 41, n. 5, p. 707, doi. 10.1002/mus.21612

By:

Sotiriou, Evangelia;
Greene, Paul;
Krishna, Sindu;
Hirano, Michio;
DiMauro, Salvatore

Publication type:

Article

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

Published in:

FASEB Journal, 2013, v. 27, n. 2, p. 612, doi. 10.1096/fj.12-209361

By:

Quinzii, Catarina M.;
Garone, Caterina;
Emmanuele, Valentina;
Tadesse, Saba;
Krishna, Sindu;
Dorado, Beatriz;
Hirano, Michio

Publication type:

Article