183 related articles for article (PubMed ID: 10937858)
1. Exercise intolerance and the mitochondrial respiratory chain.
DiMauro S
Ital J Neurol Sci; 1999 Dec; 20(6):387-93. PubMed ID: 10937858
[TBL] [Abstract][Full Text] [Related]
2. Mitochondrial myopathies.
DiMauro S
Curr Opin Rheumatol; 2006 Nov; 18(6):636-41. PubMed ID: 17053512
[TBL] [Abstract][Full Text] [Related]
3. Coenzyme Q10 deficiency and isolated myopathy.
Horvath R; Schneiderat P; Schoser BG; Gempel K; Neuen-Jacob E; Plöger H; Müller-Höcker J; Pongratz DE; Naini A; DiMauro S; Lochmüller H
Neurology; 2006 Jan; 66(2):253-5. PubMed ID: 16434667
[TBL] [Abstract][Full Text] [Related]
4. Isolated mitochondrial myopathy associated with muscle coenzyme Q10 deficiency.
Lalani SR; Vladutiu GD; Plunkett K; Lotze TE; Adesina AM; Scaglia F
Arch Neurol; 2005 Feb; 62(2):317-20. PubMed ID: 15710863
[TBL] [Abstract][Full Text] [Related]
5. Mutations in mitochondrial DNA as a cause of exercise intolerance.
DiMauro S; Andreu AL
Ann Med; 2001 Oct; 33(7):472-6. PubMed ID: 11680795
[TBL] [Abstract][Full Text] [Related]
6. Familial cerebellar ataxia with muscle coenzyme Q10 deficiency.
Musumeci O; Naini A; Slonim AE; Skavin N; Hadjigeorgiou GL; Krawiecki N; Weissman BM; Tsao CY; Mendell JR; Shanske S; De Vivo DC; Hirano M; DiMauro S
Neurology; 2001 Apr; 56(7):849-55. PubMed ID: 11294920
[TBL] [Abstract][Full Text] [Related]
7. [Mitochondrial diseases with recurrent myoglobinuria].
Murakami N
Ryoikibetsu Shokogun Shirizu; 2001; (36):183-5. PubMed ID: 11596365
[No Abstract] [Full Text] [Related]
8. Coenzyme Q10 defects may be associated with a deficiency of Q10-independent mitochondrial respiratory chain complexes.
Fragaki K; Chaussenot A; Benoist JF; Ait-El-Mkadem S; Bannwarth S; Rouzier C; Cochaud C; Paquis-Flucklinger V
Biol Res; 2016 Jan; 49():4. PubMed ID: 26742794
[TBL] [Abstract][Full Text] [Related]
9. The dilemma of diagnosing coenzyme Q
Louw R; Smuts I; Wilsenach KL; Jonck LM; Schoonen M; van der Westhuizen FH
Mol Genet Metab; 2018 Sep; 125(1-2):38-43. PubMed ID: 29530532
[TBL] [Abstract][Full Text] [Related]
10. Muscle coenzyme Q deficiency in familial mitochondrial encephalomyopathy.
Ogasahara S; Engel AG; Frens D; Mack D
Proc Natl Acad Sci U S A; 1989 Apr; 86(7):2379-82. PubMed ID: 2928337
[TBL] [Abstract][Full Text] [Related]
11. Human CoQ10 deficiencies.
Quinzii CM; López LC; Naini A; DiMauro S; Hirano M
Biofactors; 2008; 32(1-4):113-8. PubMed ID: 19096106
[TBL] [Abstract][Full Text] [Related]
12. ETFDH mutations as a major cause of riboflavin-responsive multiple acyl-CoA dehydrogenation deficiency.
Olsen RK; Olpin SE; Andresen BS; Miedzybrodzka ZH; Pourfarzam M; Merinero B; Frerman FE; Beresford MW; Dean JC; Cornelius N; Andersen O; Oldfors A; Holme E; Gregersen N; Turnbull DM; Morris AA
Brain; 2007 Aug; 130(Pt 8):2045-54. PubMed ID: 17584774
[TBL] [Abstract][Full Text] [Related]
13. Progression despite replacement of a myopathic form of coenzyme Q10 defect.
Auré K; Benoist JF; Ogier de Baulny H; Romero NB; Rigal O; Lombès A
Neurology; 2004 Aug; 63(4):727-9. PubMed ID: 15326254
[TBL] [Abstract][Full Text] [Related]
14. Neonatal metabolic myopathies.
Tein I
Semin Perinatol; 1999 Apr; 23(2):125-51. PubMed ID: 10331465
[TBL] [Abstract][Full Text] [Related]
15. Missense mutation in the mtDNA cytochrome b gene in a patient with myopathy.
Andreu AL; Bruno C; Shanske S; Shtilbans A; Hirano M; Krishna S; Hayward L; Systrom DS; Brown RH; DiMauro S
Neurology; 1998 Nov; 51(5):1444-7. PubMed ID: 9818877
[TBL] [Abstract][Full Text] [Related]
16. Recurrent myoglobinuria due to a nonsense mutation in the COX I gene of mitochondrial DNA.
Karadimas CL; Greenstein P; Sue CM; Joseph JT; Tanji K; Haller RG; Taivassalo T; Davidson MM; Shanske S; Bonilla E; DiMauro S
Neurology; 2000 Sep; 55(5):644-9. PubMed ID: 10980727
[TBL] [Abstract][Full Text] [Related]
17. Exercise intolerance due to mutations in the cytochrome b gene of mitochondrial DNA.
Andreu AL; Hanna MG; Reichmann H; Bruno C; Penn AS; Tanji K; Pallotti F; Iwata S; Bonilla E; Lach B; Morgan-Hughes J; DiMauro S
N Engl J Med; 1999 Sep; 341(14):1037-44. PubMed ID: 10502593
[TBL] [Abstract][Full Text] [Related]
18. Metabolic and drug-induced muscle disorders.
Scarlato G; Comi GP
Curr Opin Neurol; 2002 Oct; 15(5):533-8. PubMed ID: 12351996
[TBL] [Abstract][Full Text] [Related]
19. Inborn errors of energy metabolism associated with myopathies.
Das AM; Steuerwald U; Illsinger S
J Biomed Biotechnol; 2010; 2010():340849. PubMed ID: 20589068
[TBL] [Abstract][Full Text] [Related]
20. Genetic Rescue of Mitochondrial and Skeletal Muscle Impairment in an Induced Pluripotent Stem Cells Model of Coenzyme Q
Romero-Moya D; Santos-Ocaña C; Castaño J; Garrabou G; Rodríguez-Gómez JA; Ruiz-Bonilla V; Bueno C; González-Rodríguez P; Giorgetti A; Perdiguero E; Prieto C; Moren-Nuñez C; Fernández-Ayala DJ; Victoria Cascajo M; Velasco I; Canals JM; Montero R; Yubero D; Jou C; López-Barneo J; Cardellach F; Muñoz-Cánoves P; Artuch R; Navas P; Menendez P
Stem Cells; 2017 Jul; 35(7):1687-1703. PubMed ID: 28472853
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
