Publications by authors named "Sindu Krishna"

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A Novel SUCLA2 Mutation Presenting as a Complex Childhood Movement Disorder.
Caterina Garone, Juliana Gurgel-Giannetti, Simone Sanna-Cherchi, Sindu Krishna, Ali Naini

J Child Neurol· February 2017

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Tissue-specific oxidative stress and loss of mitochondria in CoQ-deficient Pdss2 mutant mice.
Catarina M Quinzii, Caterina Garone, Valentina Emmanuele, Saba Tadesse, Sindu Krishna

FASEB J· February 2013

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Myopathy and parkinsonism in phosphoglycerate kinase deficiency.
Evangelia Sotiriou, Paul Greene, Sindu Krishna, Michio Hirano, Salvatore DiMauro

Muscle Nerve· May 2010

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Myopathic form of phosphoglycerate kinase (PGK) deficiency: a new case and pathogenic considerations.
Ronen Spiegel, Estela Area Gomez, Hasan O Akman, Sindu Krishna, Yoseph Horovitz

Neuromuscul Disord· March 2009

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Respiratory chain dysfunction and oxidative stress correlate with severity of primary CoQ10 deficiency.
Catarina M Quinzii, Luis C López, Jakob Von-Moltke, Ali Naini, Sindu Krishna

FASEB J· June 2008

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The G13513A mutation in the ND5 gene of mitochondrial DNA as a common cause of MELAS or Leigh syndrome: evidence from 12 cases.
Sara Shanske, Jorida Coku, Jiesheng Lu, Jaya Ganesh, Sindu Krishna

Arch Neurol· March 2008

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Mitochondrial myopathy associated with a novel mutation in mtDNA.
Jacklyn Pancrudo, Sara Shanske, Jorida Coku, J Lu, Rebecca Mardach, Sindu Krishna

Neuromuscul Disord· August 2007

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Mitochondrial encephalomyopathy due to a novel mutation in the tRNAGlu of mitochondrial DNA.
Jacklyn Pancrudo, Sara Shanske, Eduardo Bonilla, Mariza Daras, Hasan O Akman, Sindu Krishna

J Child Neurol· July 2007

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Cockayne syndrome in adults: review with clinical and pathologic study of a new case.
Isabelle Rapin, Karen Weidenheim, Yelena Lindenbaum, Pearl Rosenbaum, Saumil N Merchant, Sindu Krishna

J Child Neurol· November 2006

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Clinical spectrum of mitochondrial DNA depletion due to mutations in the thymidine kinase 2 gene.
Maryam Oskoui, Guido Davidzon, Juan Pascual, Ricardo Erazo, Juliana Gurgel-Giannetti, Sindu Krishna

Arch Neurol· August 2006

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Congenital or late-onset myopathy in patients with the T14709C mtDNA mutation.
Michelangelo Mancuso, Silvio Ferraris, Yutaka Nishigaki, Gaetano Azan, Alessandro Mauro, Sindu Krishna

J Neurol Sci· January 2005

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Mitochondrial DNA deletion in a child with megaloblastic anemia and recurrent encephalopathy.
Cigdem Inan Akman, Carolyn M Sue, Sara Shanske, Kurenai Tanji, Eduardo Bonilla, Sindu Krishna

J Child Neurol· April 2004

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Mitochondrial myopathy and complex III deficiency in a patient with a new stop-codon mutation (G339X) in the cytochrome b gene.
Michelangelo Mancuso, Massimiliano Filosto, J Clarke Stevens, Marc Patterson, Sara Shanske, Sindu Krishna

J Neurol Sci· May 2003

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Identical mitochondrial DNA deletion in a woman with ocular myopathy and in her son with pearson syndrome.
Sara Shanske, Yingying Tang, Michio Hirano, Yutaka Nishigaki, Kurenai Tanji, Sindu Krishna

Am J Hum Genet· September 2002

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