Kennaway NG - Search Results

1

Treatment of mitochondrial myopathy due to complex III deficiency with vitamins K3 and C: A 31P-NMR follow-up study.

Argov Z, Bank WJ, Maris J, Eleff S, Kennaway NG, Olson RE, Chance B. Argov Z, et al. Among authors: kennaway ng. Ann Neurol. 1986 Jun;19(6):598-602. doi: 10.1002/ana.410190615. Ann Neurol. 1986. PMID: 3014998

2

Aerobic conditioning in patients with mitochondrial myopathies: physiological, biochemical, and genetic effects.

Taivassalo T, Shoubridge EA, Chen J, Kennaway NG, DiMauro S, Arnold DL, Haller RG. Taivassalo T, et al. Among authors: kennaway ng. Ann Neurol. 2001 Aug;50(2):133-41. doi: 10.1002/ana.1050. Ann Neurol. 2001. PMID: 11506394

3

MELAS syndrome with mitochondrial tRNA(Leu)(UUR) mutation: correlation of clinical state, nerve conduction, and muscle 31P magnetic resonance spectroscopy during treatment with nicotinamide and riboflavin.

Penn AM, Lee JW, Thuillier P, Wagner M, Maclure KM, Menard MR, Hall LD, Kennaway NG. Penn AM, et al. Among authors: kennaway ng. Neurology. 1992 Nov;42(11):2147-52. doi: 10.1212/wnl.42.11.2147. Neurology. 1992. PMID: 1436526

4

Mitochondrial myopathy: tissue-specific expression of a defect in ubiquinol-cytochrome c reductase.

Darley-Usmar VM, Watanabe M, Uchiyama Y, Kondo I, Kennaway NG, Gronke L, Hamaguchi H. Darley-Usmar VM, et al. Among authors: kennaway ng. Clin Chim Acta. 1986 Aug 15;158(3):253-61. doi: 10.1016/0009-8981(86)90289-5. Clin Chim Acta. 1986. PMID: 3021360

5

Lactic acidosis and mitochondrial myopathy associated with deficiency of several components of complex III of the respiratory chain.

Kennaway NG, Buist NR, Darley-Usmar VM, Papadimitriou A, Dimauro S, Kelley RI, Capaldi RA, Blank NK, D'Agostino A. Kennaway NG, et al. Pediatr Res. 1984 Oct;18(10):991-9. doi: 10.1203/00006450-198410000-00017. Pediatr Res. 1984. PMID: 6093035

6

31P NMR study of improvement in oxidative phosphorylation by vitamins K3 and C in a patient with a defect in electron transport at complex III in skeletal muscle.

Eleff S, Kennaway NG, Buist NR, Darley-Usmar VM, Capaldi RA, Bank WJ, Chance B. Eleff S, et al. Among authors: kennaway ng. Proc Natl Acad Sci U S A. 1984 Jun;81(11):3529-33. doi: 10.1073/pnas.81.11.3529. Proc Natl Acad Sci U S A. 1984. PMID: 6587367 Free PMC article.

7

Mitochondrial myopathies involving the respiratory chain: a biochemical analysis.

Takamiya S, Yanamura W, Capaldi RA, Kennaway NG, Bart R, Sengers RC, Trijbels JM, Ruitenbeek W. Takamiya S, et al. Among authors: kennaway ng. Ann N Y Acad Sci. 1986;488:33-43. doi: 10.1111/j.1749-6632.1986.tb46546.x. Ann N Y Acad Sci. 1986. PMID: 3034117 Review. No abstract available.

8

Deficiency in ubiquinone cytochrome c reductase in a patient with mitochondrial myopathy and lactic acidosis.

Darley-Usmar VM, Kennaway NG, Buist NR, Capaldi RA. Darley-Usmar VM, et al. Among authors: kennaway ng. Proc Natl Acad Sci U S A. 1983 Aug;80(16):5103-6. doi: 10.1073/pnas.80.16.5103. Proc Natl Acad Sci U S A. 1983. PMID: 6308671 Free PMC article.

9

Defects in the cytochrome bc1 complex in mitochondrial diseases.

Kennaway NG. Kennaway NG. J Bioenerg Biomembr. 1988 Jun;20(3):325-52. doi: 10.1007/BF00769636. J Bioenerg Biomembr. 1988. PMID: 2841308

10

Remarkable improvement in adult Leigh syndrome with partial cytochrome c oxidase deficiency.

Goldenberg PC, Steiner RD, Merkens LS, Dunaway T, Egan RA, Zimmerman EA, Nesbit G, Robinson B, Kennaway NG. Goldenberg PC, et al. Among authors: kennaway ng. Neurology. 2003 Mar 11;60(5):865-8. doi: 10.1212/01.wnl.0000049460.72439.7f. Neurology. 2003. PMID: 12629249

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