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Results: 1-9 |
Results: 9
Mitochondrial DNA depletion associated with partial complex II and IV deficiencies and 3-methylglutaconic aciduria
Authors: Scaglia, F Sutton, VR Bodamer, OAF Vogel, H Shapira, SK Naviaux, RK Vladutiu, GD
Citation: F. Scaglia et al., Mitochondrial DNA depletion associated with partial complex II and IV deficiencies and 3-methylglutaconic aciduria, J CHILD NEU, 16(2), 2001, pp. 136-138
Nerve conduction changes in patients with mitochondrial diseases treated with dichloroacetate
Authors: Spruijt, L Naviaux, RK McGowan, KA Nyhan, WL Sheean, G Haas, RH Barshop, BA
Citation: L. Spruijt et al., Nerve conduction changes in patients with mitochondrial diseases treated with dichloroacetate, MUSCLE NERV, 24(7), 2001, pp. 916-924
Need for public debate about fertility treatments - Manipulations of the mitochondrial germ line must be openly debated and followed up.
Authors: Naviaux, RK Singh, KK
Citation: Rk. Naviaux et Kk. Singh, Need for public debate about fertility treatments - Manipulations of the mitochondrial germ line must be openly debated and followed up., NATURE, 413(6854), 2001, pp. 347-347
Medium-chain acyl coenzyme a dehydrogenase deficiency - Occurrence in an infant and his father
Authors: Bodman, M Smith, D Nyhan, WL Naviaux, RK
Citation: M. Bodman et al., Medium-chain acyl coenzyme a dehydrogenase deficiency - Occurrence in an infant and his father, ARCH NEUROL, 58(5), 2001, pp. 811-814
Kearns-Sayre syndrome presenting as 2-oxoadipic aciduria
Authors: Barshop, BA Nyhan, WL Naviaux, RK McGowan, KA Friedlander, M Haas, RH
Citation: Ba. Barshop et al., Kearns-Sayre syndrome presenting as 2-oxoadipic aciduria, MOL GEN MET, 69(1), 2000, pp. 64-68
Autism associated with the mitochondrial DNA G8363A transfer RNA(Lys) mutation
Authors: Graf, WD Marin-Garcia, J Gao, HG Pizzo, S Naviaux, RK Markusic, D Barshop, BA Courchesne, E Haas, RH
Citation: Wd. Graf et al., Autism associated with the mitochondrial DNA G8363A transfer RNA(Lys) mutation, J CHILD NEU, 15(6), 2000, pp. 357-361
Mitochondrial DNA disorders
Authors: Naviaux, RK
Citation: Rk. Naviaux, Mitochondrial DNA disorders, EUR J PED, 159, 2000, pp. S219-S226
Mitochondrial DNA polymerase gamma deficiency and mtDNA depletion in a child with Alpers' syndrome
Authors: Naviaux, RK Nyhan, WL Barshop, BA Poulton, J Markusic, D Karpinski, NC Haas, RH
Citation: Rk. Naviaux et al., Mitochondrial DNA polymerase gamma deficiency and mtDNA depletion in a child with Alpers' syndrome, ANN NEUROL, 45(1), 1999, pp. 54-58
Sensitive assay for mitochondrial DNA polymerase gamma
Authors: Naviaux, RK Markusic, D Barshop, BA Nyhan, WL Haas, RH
Citation: Rk. Naviaux et al., Sensitive assay for mitochondrial DNA polymerase gamma, CLIN CHEM, 45(10), 1999, pp. 1725-1733
Risultati: 1-9 |