126 related articles for article (PubMed ID: 1658240)
21. Early-onset cerebellar ataxia, myoclonus and hypogonadism in a case of mitochondrial complex III deficiency treated with vitamins K3 and C.
Toscano A; Fazio MC; Vita G; Cannavó S; Bresolin N; Bet L; Prelle A; Barbiroli B; Iotti S; Zaniol P
J Neurol; 1995 Mar; 242(4):203-9. PubMed ID: 7798118
[TBL] [Abstract][Full Text] [Related]
22. Increased mitochondrial DNA deletions in the skeletal muscle of myotonic dystrophy.
Sahashi K; Tanaka M; Tashiro M; Ohno K; Ibi T; Takahashi A; Ozawa T
Gerontology; 1992; 38(1-2):18-29. PubMed ID: 1319380
[TBL] [Abstract][Full Text] [Related]
23. Cytoplasmic body and mitochondrial DNA deletion.
Sahashi K; Ohno K; Tanaka M; Ibi T; Yamamoto T; Tashiro M; Sato W; Takahashi A; Ozawa T
J Neurol Sci; 1990 Nov; 99(2-3):291-300. PubMed ID: 1964959
[TBL] [Abstract][Full Text] [Related]
24. The mitochondrial DNA transfer RNALeu(UUR) A-->G(3243) mutation. A clinical and genetic study.
Hammans SR; Sweeney MG; Hanna MG; Brockington M; Morgan-Hughes JA; Harding AE
Brain; 1995 Jun; 118 ( Pt 3)():721-34. PubMed ID: 7600089
[TBL] [Abstract][Full Text] [Related]
25. Lipoic (thioctic) acid increases brain energy availability and skeletal muscle performance as shown by in vivo 31P-MRS in a patient with mitochondrial cytopathy.
Barbiroli B; Medori R; Tritschler HJ; Klopstock T; Seibel P; Reichmann H; Iotti S; Lodi R; Zaniol P
J Neurol; 1995 Jul; 242(7):472-7. PubMed ID: 7595680
[TBL] [Abstract][Full Text] [Related]
26. A novel mutation in the mitochondrial DNA tRNA Leu (UUR) gene associated with late-onset ocular myopathy.
Maeso E; Rueda A; Jiménez S; Del Hoyo P; Martín R; Cabello A; Mendoza LM; Arenas J; Campos Y
Neuromuscul Disord; 2007 May; 17(5):415-8. PubMed ID: 17363246
[TBL] [Abstract][Full Text] [Related]
27. Preliminary observations on brain energy metabolism in migraine studied by in vivo phosphorus 31 NMR spectroscopy.
Welch KM; Levine SR; D'Andrea G; Schultz LR; Helpern JA
Neurology; 1989 Apr; 39(4):538-41. PubMed ID: 2927679
[TBL] [Abstract][Full Text] [Related]
28. A new mitochondrial point mutation in the transfer RNA(Leu) gene in a patient with a clinical phenotype resembling Kearns-Sayre syndrome.
Seneca S; Verhelst H; De Meirleir L; Meire F; Ceuterick-De Groote C; Lissens W; Van Coster R
Arch Neurol; 2001 Jul; 58(7):1113-8. PubMed ID: 11448301
[TBL] [Abstract][Full Text] [Related]
29. Sporadic MERRF/MELAS overlap syndrome associated with the 3243 tRNA(Leu(UUR)) mutation of mitochondrial DNA.
Campos Y; Martin MA; Lorenzo G; Aparicio M; Cabello A; Arenas J
Muscle Nerve; 1996 Feb; 19(2):187-90. PubMed ID: 8559168
[TBL] [Abstract][Full Text] [Related]
30. [31P-NMR spectroscopy of mitochondrial myopathies: the relation between abnormal energy metabolism and muscle biopsy findings].
Kawai M; Itoh M; Okazawa H; Kamakura K
Rinsho Shinkeigaku; 1989 Feb; 29(2):167-71. PubMed ID: 2546706
[TBL] [Abstract][Full Text] [Related]
31. A new mitochondrial DNA mutation (A3288G) in the tRNA(Leu(UUR)) gene associated with familial myopathy.
Hadjigeorgiou GM; Kim SH; Fischbeck KH; Andreu AL; Berry GT; Bingham P; Shanske S; Bonilla E; DiMauro S
J Neurol Sci; 1999 Apr; 164(2):153-7. PubMed ID: 10402027
[TBL] [Abstract][Full Text] [Related]
32. Mitochondrial dysfunction in migraine.
Yorns WR; Hardison HH
Semin Pediatr Neurol; 2013 Sep; 20(3):188-93. PubMed ID: 24331360
[TBL] [Abstract][Full Text] [Related]
33. Mitochondrial DNA and RNA processing in MELAS.
Kaufmann P; Koga Y; Shanske S; Hirano M; DiMauro S; King MP; Schon EA
Ann Neurol; 1996 Aug; 40(2):172-80. PubMed ID: 8773598
[TBL] [Abstract][Full Text] [Related]
34. Quantitative analysis of skeletal muscle bioenergetics and proton efflux in migraine and cluster headache.
Lodi R; Kemp GJ; Montagna P; Pierangeli G; Cortelli P; Iotti S; Radda GK; Barbiroli B
J Neurol Sci; 1997 Feb; 146(1):73-80. PubMed ID: 9077499
[TBL] [Abstract][Full Text] [Related]
35. Deletions of mitochondrial DNA in Kearns-Sayre syndrome and ocular myopathies: genetic, biochemical and morphological studies.
Degoul F; Nelson I; Lestienne P; Francois D; Romero N; Duboc D; Eymard B; Fardeau M; Ponsot G; Paturneau-Jouas M
J Neurol Sci; 1991 Feb; 101(2):168-77. PubMed ID: 1851820
[TBL] [Abstract][Full Text] [Related]
36. Phosphorus magnetic resonance spectroscopy (31P MRS) in neuromuscular disorders.
Argov Z; Bank WJ
Ann Neurol; 1991 Jul; 30(1):90-7. PubMed ID: 1834009
[TBL] [Abstract][Full Text] [Related]
37. [Mitochondrial tRNA(leu(UUR)) gene mutation and the decreased activity of cytochrome C oxidase in preeclampsia].
Zhang G; Wang Z; Lin M
Zhonghua Fu Chan Ke Za Zhi; 1999 Jul; 34(7):403-5. PubMed ID: 11360649
[TBL] [Abstract][Full Text] [Related]
38. [Comparison of clinical pictures of mitochondrial encephalomyopathy with tRNA(Leu(UUR)) mutation in 3243 with that in 3254].
Mitsuoka T; Kawarai T; Watanabe C; Katayama S; Nakamura S
No To Shinkei; 1998 Dec; 50(12):1089-92. PubMed ID: 9989353
[TBL] [Abstract][Full Text] [Related]
39. Detection of "deleted" mitochondrial genomes in cytochrome-c oxidase-deficient muscle fibers of a patient with Kearns-Sayre syndrome.
Mita S; Schmidt B; Schon EA; DiMauro S; Bonilla E
Proc Natl Acad Sci U S A; 1989 Dec; 86(23):9509-13. PubMed ID: 2556715
[TBL] [Abstract][Full Text] [Related]
40. In vivo 31P nuclear magnetic resonance spectroscopy of skeletal muscle energetics in endotoxemic rats: a prospective, randomized study.
Gilles RJ; D'Orio V; Ciancabilla F; Carlier PG
Crit Care Med; 1994 Mar; 22(3):499-505. PubMed ID: 8125002
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]