BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

87 related articles for article (PubMed ID: 8548609)

  • 1. [Mitochondrial disease due to the deficit of Q-cytochrome C oxidoreductase coenzyme in the respiratory chain. Report of a new case].
    Roldán S; Lluch MD; Navarro Quesada FJ; Hevia A
    Rev Neurol; 1995; 23(119):139-41. PubMed ID: 8548609
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. [Benign congenital myopathy associated with a partial deficiency of complexes I and III of the mitochondrial respiratory chain]].
    Castro-Gago M; Eirís J; Pintos E; Rodrigo E; Blanco-Barca O; Campos Y; Arenas J
    Rev Neurol; 2000 Nov 1-15; 31(9):838-41. PubMed ID: 11127086
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Mitochondrial DNA depletion in mitochondrial myopathy caused by complex II and IV deficiency of the respiratory chain].
    Arenas Mora J; Campos González Y; Castro-Gago M
    An Esp Pediatr; 1996 Dec; 45(6):656-7. PubMed ID: 9133240
    [No Abstract]   [Full Text] [Related]  

  • 5. [Mitochondrial myopathy caused by complex III and IV deficiency. A familial case].
    Castro-Gago M; Novo-Rodríguez I; García Caballero T; Campos González Y; Huertas Barbero R; Arenas Mora J
    An Esp Pediatr; 1993 Jan; 38(1):82-6. PubMed ID: 8382457
    [No Abstract]   [Full Text] [Related]  

  • 6. A novel gly290asp mitochondrial cytochrome b mutation linked to a complex III deficiency in progressive exercise intolerance.
    Dumoulin R; Sagnol I; Ferlin T; Bozon D; Stepien G; Mousson B
    Mol Cell Probes; 1996 Oct; 10(5):389-91. PubMed ID: 8910895
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Pure mitochondrial myopathy].
    Murakami N; Sakuta R
    Ryoikibetsu Shokogun Shirizu; 2001; (36):186-9. PubMed ID: 11596366
    [No Abstract]   [Full Text] [Related]  

  • 8. Congenital or late-onset myopathy in patients with the T14709C mtDNA mutation.
    Mancuso M; Ferraris S; Nishigaki Y; Azan G; Mauro A; Sammarco P; Krishna S; Tay SK; Bonilla E; Romansky SG; Hirano M; DiMauro S
    J Neurol Sci; 2005 Jan; 228(1):93-7. PubMed ID: 15607216
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mitochondrial myopathy of childhood associated with mitochondrial DNA depletion and a homozygous mutation (T77M) in the TK2 gene.
    Mancuso M; Filosto M; Bonilla E; Hirano M; Shanske S; Vu TH; DiMauro S
    Arch Neurol; 2003 Jul; 60(7):1007-9. PubMed ID: 12873860
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Anesthesia for a patient with mitochondrial respiratory chain complex III deficiency].
    Ortiz-Gómez JR; Souto-Ferro JM
    Rev Esp Anestesiol Reanim; 2006 Nov; 53(9):575-9. PubMed ID: 17297835
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Adult onset mitochondrial myopathy without ophthalmoplegia. Four cases attributable to complex III and IV deficits in the respiratory chain].
    Bautista J; Muñoz-Málaga A; Chinchón I; Segura D; Salazar JA; Bescansa E; Campos Y; Arenas J
    Neurologia; 1995 Oct; 10(8):319-23. PubMed ID: 8554781
    [TBL] [Abstract][Full Text] [Related]  

  • 12. An abnormal exercise test response revealing a respiratory chain complex III deficiency.
    Mousson B; Collombet JM; Dumoulin R; Carrier H; Flocard F; Bouzidi M; Godinot C; Maire I; Mathieu M; Quard S
    Acta Neurol Scand; 1995 Jun; 91(6):488-93. PubMed ID: 7572045
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mitochondrial respiratory chain deficiency revealed by hypothermia.
    Cholley F; Edery P; Ricquier D; Peudenier S; Slama A; Tardieu M
    Neuropediatrics; 2001 Apr; 32(2):104-6. PubMed ID: 11414641
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mitochondrial disease in patients with exercise intolerance.
    Miró O; Grav JM; Casademont J
    N Engl J Med; 2000 Feb; 342(6):439; author reply 439-40. PubMed ID: 10681227
    [No Abstract]   [Full Text] [Related]  

  • 15. Dramatic improvement in mitochondrial cardiomyopathy following treatment with idebenone.
    Lerman-Sagie T; Rustin P; Lev D; Yanoov M; Leshinsky-Silver E; Sagie A; Ben-Gal T; Munnich A
    J Inherit Metab Dis; 2001 Feb; 24(1):28-34. PubMed ID: 11286379
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Systematic evaluation of muscle coenzyme Q10 content in children with mitochondrial respiratory chain enzyme deficiencies.
    Miles MV; Miles L; Tang PH; Horn PS; Steele PE; DeGrauw AJ; Wong BL; Bove KE
    Mitochondrion; 2008 Mar; 8(2):170-80. PubMed ID: 18313367
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Congenital nemaline myopathy with mitochondrial abnormalities. An adult case report].
    Oya Y; Segawa M; Ogawa M; Goto Y; Nonaka I; Kawai M
    Rinsho Shinkeigaku; 2000 May; 40(5):452-8. PubMed ID: 11002727
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The importance of liver biopsy in the investigation of possible mitochondrial respiratory chain disease.
    Panetta J; Gibson K; Kirby DM; Thorburn DR; Boneh A
    Neuropediatrics; 2005 Aug; 36(4):256-9. PubMed ID: 16138250
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Case report of a successful liver transplantation for acute liver failure due to mitochondrial respiratory chain complex III deficiency.
    Iwama I; Baba Y; Kagimoto S; Kishimoto H; Kasahara M; Murayama K; Shimizu K
    Transplant Proc; 2011 Dec; 43(10):4025-8. PubMed ID: 22172894
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Adult onset limb-girdle type mitochondrial myopathy with a mitochondrial DNA np8291 A-to-G substitution.
    Hirata K; Nakagawa M; Higuchi I; Hashimoto K; Hanada K; Takahashi K; Niiyama T; Izumi K; Sakoda S; Yamada H; Osame M
    J Hum Genet; 1999; 44(3):210-4. PubMed ID: 10319590
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.