BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

181 related articles for article (PubMed ID: 8781089)

  • 1. Cardiac mitochondrial dysfunction in Leigh syndrome.
    Marin-Garcia J; Ananthakrishnan R; Korson M; Goldenthal MJ; Perez-Atayde A
    Pediatr Cardiol; 1996; 17(6):387-9. PubMed ID: 8781089
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Adult Leigh syndrome with mitochondrial DNA mutation at 8993.
    Nagashima T; Mori M; Katayama K; Nunomura M; Nishihara H; Hiraga H; Tanaka S; Goto Y; Nagashima K
    Acta Neuropathol; 1999 Apr; 97(4):416-22. PubMed ID: 10208283
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mitochondrial DNA 8993T>G mutation in a child with ornithine transcarbamylase deficiency and leigh syndrome: an unexpected association.
    Henriques M; Diogo L; Garcia P; Pratas J; Simões M; Grazina M
    J Child Neurol; 2012 Aug; 27(8):1059-61. PubMed ID: 22241703
    [TBL] [Abstract][Full Text] [Related]  

  • 4. De novo mtDNA nt 8993 (T-->G) mutation resulting in Leigh syndrome.
    Takahashi S; Makita Y; Oki J; Miyamoto A; Yanagawa J; Naito E; Goto Y; Okuno A
    Am J Hum Genet; 1998 Mar; 62(3):717-9. PubMed ID: 9556461
    [No Abstract]   [Full Text] [Related]  

  • 5. The mutation at nt 8993 of mitochondrial DNA is a common cause of Leigh's syndrome.
    Santorelli FM; Shanske S; Macaya A; DeVivo DC; DiMauro S
    Ann Neurol; 1993 Dec; 34(6):827-34. PubMed ID: 8250532
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mitochondrial DNA mutations in Leigh syndrome and their phylogenetic implications.
    Makino M; Horai S; Goto Y; Nonaka I
    J Hum Genet; 2000; 45(2):69-75. PubMed ID: 10721666
    [TBL] [Abstract][Full Text] [Related]  

  • 7. G8363A mutation in the mitochondrial DNA transfer ribonucleic acidLys gene: another cause of Leigh syndrome.
    Shtilbans A; Shanske S; Goodman S; Sue CM; Bruno C; Johnson TL; Lava NS; Waheed N; DiMauro S
    J Child Neurol; 2000 Nov; 15(11):759-61. PubMed ID: 11108511
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Two mtDNA mutations 14487T>C (M63V, ND6) and 12297T>C (tRNA Leu) in a Leigh syndrome family.
    Wang J; Brautbar A; Chan AK; Dzwiniel T; Li FY; Waters PJ; Graham BH; Wong LJ
    Mol Genet Metab; 2009 Feb; 96(2):59-65. PubMed ID: 19062322
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A case of sporadic infantile histiocytoid cardiomyopathy caused by the A8344G (MERRF) mitochondrial DNA mutation.
    Vallance HD; Jeven G; Wallace DC; Brown MD
    Pediatr Cardiol; 2004; 25(5):538-40. PubMed ID: 15164143
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Clinical heterogeneity associated with mitochondrial DNA A8344G point mutation].
    Zhao J; Zhao DH; Zhang W; Lü H; Yuan Y; Qi Y; Wang ZX
    Zhonghua Yi Xue Za Zhi; 2012 Oct; 92(40):2835-8. PubMed ID: 23290212
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A second missense mutation in the mitochondrial ATPase 6 gene in Leigh's syndrome.
    de Vries DD; van Engelen BG; Gabreëls FJ; Ruitenbeek W; van Oost BA
    Ann Neurol; 1993 Sep; 34(3):410-2. PubMed ID: 8395787
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Leigh syndrome caused by mitochondrial DNA G13513A mutation: frequency and clinical features in Japan.
    Sudo A; Honzawa S; Nonaka I; Goto YI
    J Hum Genet; 2004; 49(2):92-96. PubMed ID: 14730434
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mutation of mitochondrial DNA G13513A presenting with Leigh syndrome, Wolff-Parkinson-White syndrome and cardiomyopathy.
    Wang SB; Weng WC; Lee NC; Hwu WL; Fan PC; Lee WT
    Pediatr Neonatol; 2008 Aug; 49(4):145-9. PubMed ID: 19054921
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Unusual findings in Leigh syndrome caused by T8993C mutation.
    Yiş U; Seneca S; Dirik E; Kurul SH; Ozer E; Cakmakçi H; De Meirleir L
    Eur J Paediatr Neurol; 2009 Nov; 13(6):550-2. PubMed ID: 19046652
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Mitochondrial DNA point mutation T9176C in Leigh syndrome.
    Wilson CJ; Wood NW; Leonard JV; Surtees R; Rahman S
    J Child Neurol; 2000 Dec; 15(12):830-3. PubMed ID: 11198506
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Mitochondrial DNA mutations and cardiomyopathy].
    Ozawa T; Sugiyama S; Tanaka M
    Nihon Rinsho; 1991 Jan; 49(1):204-10. PubMed ID: 2002603
    [No Abstract]   [Full Text] [Related]  

  • 17. Leigh syndrome resulting from de novo mutation at position 8993 of mitochondrial DNA.
    Seller A; Kennedy CR; Temple IK; Brown GK
    J Inherit Metab Dis; 1997 Mar; 20(1):102-3. PubMed ID: 9061574
    [No Abstract]   [Full Text] [Related]  

  • 18. [Mitochondrial dysfunction and brain development disorders].
    Goto Y
    No To Shinkei; 2001 May; 53(5):421-6. PubMed ID: 11424352
    [No Abstract]   [Full Text] [Related]  

  • 19. Phenotypic differences between T-->C and T-->G mutations at nt 8993 of mitochondrial DNA in Leigh syndrome.
    Fujii T; Hattori H; Higuchi Y; Tsuji M; Mitsuyoshi I
    Pediatr Neurol; 1998 Mar; 18(3):275-7. PubMed ID: 9568930
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Clinical heterogeneity associated with the mitochondrial DNA T8993C point mutation.
    Santorelli FM; Mak SC; Vazquez-Memije ME; Shanske S; Kranz-Eble P; Jain KD; Bluestone DL; De Vivo DC; DiMauro S
    Pediatr Res; 1996 May; 39(5):914-7. PubMed ID: 8726250
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.