BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

143 related articles for article (PubMed ID: 8170674)

  • 1. [Specific enzyme diagnosis in mitochondrial myopathies and encephalomyopathies].
    László A; Sümegi B; Alkonyi I; Horváth E; Sztriha L; Várkonyi A; Zombori J
    Orv Hetil; 1994 Apr; 135(14):747-50. PubMed ID: 8170674
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Morphological methods in the diagnosis of mitochondrial encephalomyopathies: the role of electron microscopy.
    Kyriacou K; Hadjisavvas A; Zenios A; Papacharalambous R; Kyriakides T
    Ultrastruct Pathol; 2005; 29(3-4):169-74. PubMed ID: 16036873
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Mitochondrial myopathy and mitochondrial encephalomyopathy].
    Song D; Liu C; Lu Q; Shi J; Chen J; Zhang H; Zhang Y; Wang H; Zhang W; Li G
    Zhonghua Yi Xue Za Zhi; 2002 Feb; 82(3):158-60. PubMed ID: 11953149
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Diagnosis and therapy of mitochondriopathies].
    Sperl W
    Wien Klin Wochenschr; 1997 Feb; 109(3):93-9. PubMed ID: 9139466
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Biochemical investigations and immunoblot analyses of two unrelated patients with an isolated deficiency in complex II of the mitochondrial respiratory chain.
    Birch-Machin MA; Marsac C; Ponsot G; Parfait B; Taylor RW; Rustin P; Munnich A
    Biochem Biophys Res Commun; 1996 Mar; 220(1):57-62. PubMed ID: 8602857
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Inhibition of mitochondrial complex IV leads to secondary loss complex II-III activity: implications for the pathogenesis and treatment of mitochondrial encephalomyopathies.
    Hargreaves IP; Duncan AJ; Wu L; Agrawal A; Land JM; Heales SJ
    Mitochondrion; 2007 Jul; 7(4):284-7. PubMed ID: 17395552
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Early mitochondrial encephalomyopathy due to complex IV deficiency consistent with Alpers-Huttenlocher syndrome: report of two cases].
    Castro-Gago M; González-Conde V; Fernández-Seara MJ; Rodrigo-Sáez E; Fernández-Cebrián S; Alonso-Martín A; Campos Y; Arenas J; Eirís-Puñal J
    Rev Neurol; 1999 Nov 16-30; 29(10):912-7. PubMed ID: 10637838
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Cytochrome c oxidase activity in single muscle fibers: assay techniques and diagnostic applications.
    Johnson MA; Bindoff LA; Turnbull DM
    Ann Neurol; 1993 Jan; 33(1):28-35. PubMed ID: 8388186
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [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]  

  • 11. Automated analysis of mitochondrial enzymes in cultured skin fibroblasts.
    Williams AJ; Coakley J; Christodoulou J
    Anal Biochem; 1998 Jun; 259(2):176-80. PubMed ID: 9618194
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Mitochondrial diseases].
    Nagel JD; Haverkamp F; Lentze MJ
    Klin Padiatr; 1997; 209(6):345-56. PubMed ID: 9445918
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Long-term outcome and clinical spectrum of 73 pediatric patients with mitochondrial diseases.
    Debray FG; Lambert M; Chevalier I; Robitaille Y; Decarie JC; Shoubridge EA; Robinson BH; Mitchell GA
    Pediatrics; 2007 Apr; 119(4):722-33. PubMed ID: 17403843
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Apoptosis in mitochondrial myopathies is linked to mitochondrial proliferation.
    Auré K; Fayet G; Leroy JP; Lacène E; Romero NB; Lombès A
    Brain; 2006 May; 129(Pt 5):1249-59. PubMed ID: 16537564
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. An overview of a cohort of South African patients with mitochondrial disorders.
    Smuts I; Louw R; du Toit H; Klopper B; Mienie LJ; van der Westhuizen FH
    J Inherit Metab Dis; 2010 Dec; 33 Suppl 3():S95-104. PubMed ID: 20135231
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Benign infantile mitochondrial myopathy].
    Sakuta R
    Ryoikibetsu Shokogun Shirizu; 2001; (36):181-2. PubMed ID: 11596364
    [No Abstract]   [Full Text] [Related]  

  • 18. Diagnostic yield muscle biopsy in patients with clinical evidence of mitochondrial cytopathy.
    Rollins S; Prayson RA; McMahon JT; Cohen BH
    Am J Clin Pathol; 2001 Sep; 116(3):326-30. PubMed ID: 11554158
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Activities of respiratory chain complexes and pyruvate dehydrogenase in isolated muscle mitochondria in premature neonates.
    Honzik T; Wenchich L; Böhm M; Hansikova H; Pejznochova M; Zapadlo M; Plavka R; Zeman J
    Early Hum Dev; 2008 Apr; 84(4):269-76. PubMed ID: 17698302
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Investigation of children for mitochondriopathy confirms need for strict patient selection, improved morphological criteria, and better laboratory methods.
    Miles L; Wong BL; Dinopoulos A; Morehart PJ; Hofmann IA; Bove KE
    Hum Pathol; 2006 Feb; 37(2):173-84. PubMed ID: 16426917
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.