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Sindu Krishna

Fatal infantile cardioencephalomyopathy with COX deficiency and mutations in SCO2, a COX assembly gene
1999 · Lefkothea C. Papadopoulou, Carolyn M. Sue, et al. · Nature Genetics · 571
Respiratory chain dysfunction and oxidative stress correlate with severity of primary CoQ 10 deficiency
2008 · Catarina M. Quinzii, Luis C. López, et al. · The FASEB Journal · 168
Maternally inherited hearing loss in a large kindred with a novel T7511C mutation in the mitochondrial DNA tRNA Ser(UCN) gene
1999 · C.M. Sue, K. Tanji, et al. · Neurology · 164
Subcellular distribution of daunorubicin in P-glycoprotein-positive and -negative drug-resistant cell lines using laser-assisted confocal microscopy.
1991 · J E Gervasoni, S Z Fields, et al. · PubMed · 156
Intracellular distribution and pharmacokinetics of daunorubicin in anthracycline-sensitive and -resistant HL-60 cells.
1989 · A A Hindenburg, J E Gervasoni, et al. · PubMed · 129
Clinical Spectrum of Mitochondrial DNA Depletion Due to Mutations in the Thymidine Kinase 2 Gene
2006 · Maryam Oskoui, Guido Davidzon, et al. · Archives of Neurology · 125
Cockayne Syndrome in Adults: Review With Clinical and Pathologic Study of a New Case
2006 · Isabelle Rapin, Karen Weidenheim, et al. · Journal of Child Neurology · 124
The G13513A mutation in the ND5 gene of mitochondrial DNA as a common cause of MELAS or Leigh syndrome: evidence from 12 cases.
2008 · Sara Shanske, Jorida Coku, et al. · PubMed · 123
A nonsense mutation (G15059A) in the cytochromeb gene in a patient with exercise intolerance and myoglobinuria
1999 · A. L. Andreu, C. Bruno, et al. · Annals of Neurology · 117
Maternally Inherited Cardiomyopathy: An Atypical Presentation of the mtDNA 12S rRNA Gene A1555G Mutation
1999 · Filippo M. Santorelli, Kurenai Tanji, et al. · The American Journal of Human Genetics · 110
Role of glutathione and dependent enzymes in anthracycline-resistant HL60/AR cells.
1989 · J Lutzky, M B Astor, et al. · PubMed · 95
Identical Mitochondrial DNA Deletion in a Woman with Ocular Myopathy and in Her Son with Pearson Syndrome
2002 · Sara Shanske, Yingying Tang, et al. · The American Journal of Human Genetics · 87
Missense mutation in the mtDNA cytochrome b gene in a patient with myopathy
1998 · A. L. Andreu, C. Bruno, et al. · Neurology · 84
Tissue‐specific oxidative stress and loss of mitochondria in CoQ‐deficient Pdss2 mutant mice
2012 · Catarina M. Quinzii, Caterina Garone, et al. · The FASEB Journal · 66
Myopathy and parkinsonism in phosphoglycerate kinase deficiency
2010 · Evangelia Sotiriou, Paul Greene, et al. · Muscle & Nerve · 49
A Splice Junction Mutation in the αMGene of Phosphorylase Kinase in a Patient with Myopathy
1998 · Claudio Bruno, Giovanni Manfredi, et al. · Biochemical and Biophysical Research Communications · 44
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Myopathic form of phosphoglycerate kinase (PGK) deficiency: A new case and pathogenic considerations
2009 · Ronen Spiegel, Estela Area Gomez, et al. · Neuromuscular Disorders · 43
Mitochondrial myopathy and complex III deficiency in a patient with a new stop-codon mutation (G339X) in the cytochrome b gene
2003 · Michelangelo Mancuso, Massimiliano Filosto, et al. · Journal of the Neurological Sciences · 40
The mitochondrial DNA A8344G mutation in leigh syndrome revealed by analysis in paraffin‐embedded sections: Revisiting the past
1998 · F. M. Santorelli, K. Tanji, et al. · Annals of Neurology · 31
Mitochondrial myopathy associated with a novel mutation in mtDNA
2007 · Jacklyn Pancrudo, Sara Shanske, et al. · Neuromuscular Disorders · 22
A5814G Mutation in Mitochondrial DNA Can Cause Mitochondrial Myopathy and Cardiomyopathy
2001 · Charalampos Karadimas, Kurenai Tanji, et al. · Journal of Child Neurology · 18
Congenital or late-onset myopathy in patients with the T14709C mtDNA mutation
2004 · Michelangelo Mancuso, Silvio Ferraris, et al. · Journal of the Neurological Sciences · 17
A Novel SUCLA2 Mutation Presenting as a Complex Childhood Movement Disorder
2016 · Caterina Garone, Juliana Gurgel-Giannetti, et al. · Journal of Child Neurology · 15
Mitochondrial DNA Deletion in a Child Mitochondrial DNA Deletion in a Child With Megaloblastic Anemia and Recurrent Encephalopathy
2004 · Cigdem Inan Akman, Carolyn M. Sue, et al. · Journal of Child Neurology · 15
Membrane glycoprotein changes associated with anthracycline resistance in HL-60 cells
1991 · James E. Gervasoni, Robert N. Taub, et al. · Cancer Chemotherapy and Pharmacology · 9
Works count: 36
Citation count: 2,437
H-index: 20
I10-index: 24
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