These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

131 related articles for article (PubMed ID: 23704442)

  • 1. Persistent hyperlactacidaemia: about a clinical case.
    Oliveira AR; Valente R; Ramos J; Ventura L
    BMJ Case Rep; 2013 May; 2013():. PubMed ID: 23704442
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Leigh syndrome: pyruvate dehydrogenase defect. A case with peripheral neuropathy.
    Chabrol B; Mancini J; Benelli C; Gire C; Munnich A
    J Child Neurol; 1994 Jan; 9(1):52-5. PubMed ID: 8151084
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Proton spectroscopy in patients with Leigh's disease and mitochondrial enzyme deficiency.
    Kruse B; Hanefeld F; Holzbach U; Wilichowski E; Christen HJ; Merboldt KD; Hänicke W; Frahm J
    Dev Med Child Neurol; 1994 Sep; 36(9):839-43. PubMed ID: 7926334
    [No Abstract]   [Full Text] [Related]  

  • 4. Outcome of thiamine treatment in a child with Leigh disease due to thiamine-responsive pyruvate dehydrogenase deficiency.
    Di Rocco M; Lamba LD; Minniti G; Caruso U; Naito E
    Eur J Paediatr Neurol; 2000; 4(3):115-7. PubMed ID: 10872106
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Clinical, pathological and radiological survey of patients with Leigh syndrome.
    Yis U; Hiz Kurul S; Dirik E; Cakmakçi H; Ozer E
    Minerva Pediatr; 2009 Aug; 61(4):371-8. PubMed ID: 19752846
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Leigh disease (subacute necrotizing encephalomyelopathy): report of one case.
    Wu TS; Lee CC; Lin JT; Hsu HH; Lin ST; Jong YJ; Shen EY
    Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi; 1993; 34(4):301-7. PubMed ID: 8213161
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Leigh syndrome associated with a deficiency of the pyruvate dehydrogenase complex: results of treatment with a ketogenic diet.
    Wijburg FA; Barth PG; Bindoff LA; Birch-Machin MA; van der Blij JF; Ruitenbeek W; Turnbull DM; Schutgens RB
    Neuropediatrics; 1992 Jun; 23(3):147-52. PubMed ID: 1641082
    [TBL] [Abstract][Full Text] [Related]  

  • 8. LIPT1 deficiency presenting as early infantile epileptic encephalopathy, Leigh disease, and secondary pyruvate dehydrogenase complex deficiency.
    Stowe RC; Sun Q; Elsea SH; Scaglia F
    Am J Med Genet A; 2018 May; 176(5):1184-1189. PubMed ID: 29681092
    [TBL] [Abstract][Full Text] [Related]  

  • 9. MR findings in patients with subacute necrotizing encephalomyelopathy (Leigh syndrome): correlation with biochemical defect.
    Medina L; Chi TL; DeVivo DC; Hilal SK
    AJNR Am J Neuroradiol; 1990; 11(2):379-84. PubMed ID: 2156413
    [TBL] [Abstract][Full Text] [Related]  

  • 10. MR findings in patients with subacute necrotizing encephalomyelopathy (Leigh syndrome): correlation with biochemical defect.
    Medina L; Chi TL; DeVivo DC; Hilal SK
    AJR Am J Roentgenol; 1990 Jun; 154(6):1269-74. PubMed ID: 2159689
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Clinical and laboratory survey of 65 Chinese patients with Leigh syndrome.
    Yang YL; Sun F; Zhang Y; Qian N; Yuan Y; Wang ZX; Qi Y; Xiao JX; Wang XY; Qi ZY; Zhang YH; Jiang YW; Bao XH; Qin J; Wu XR
    Chin Med J (Engl); 2006 Mar; 119(5):373-7. PubMed ID: 16542579
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Leigh syndrome due to mitochondrial respiratory chain complex II deficiency].
    Ma YY; Wu TF; Liu YP; Wang Q; Song JQ; Xiao JX; Jiang YW; Yang YL
    Zhongguo Dang Dai Er Ke Za Zhi; 2011 Jul; 13(7):569-72. PubMed ID: 21752325
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Leigh syndrome presenting with dystonia: report of one case.
    Huang WY; Chi CS; Mak SC; Wu HM; Yang MT
    Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi; 1995; 36(5):378-81. PubMed ID: 8607367
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Assessment and therapy monitoring of Leigh disease by MRI and proton spectroscopy.
    Krägeloh-Mann I; Grodd W; Niemann G; Haas G; Ruitenbeek W
    Pediatr Neurol; 1992; 8(1):60-4. PubMed ID: 1558578
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A rare mitochondrial disorder: Leigh syndrome--a case report.
    Shrikhande DY; Kalakoti P; Syed MM; Ahya K; Singh G
    Ital J Pediatr; 2010 Sep; 36():62. PubMed ID: 20843336
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Spectrum of neurological and survival outcomes in pyruvate dehydrogenase complex (PDC) deficiency: lack of correlation with genotype.
    DeBrosse SD; Okajima K; Zhang S; Nakouzi G; Schmotzer CL; Lusk-Kopp M; Frohnapfel MB; Grahame G; Kerr DS
    Mol Genet Metab; 2012 Nov; 107(3):394-402. PubMed ID: 23021068
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Leigh disease in a 3-year-old girl].
    Kałuza J; Krauze M; Marszał E; Wojczańska-Stanek K; Jamroz E; Szwed-Białozyt B
    Neurol Neurochir Pol; 1991; 25(4):497-500. PubMed ID: 1803261
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [The molecular background of Leigh syndrome].
    Piekutowska-Abramczuk D
    Neurol Neurochir Pol; 2008; 42(3):238-50. PubMed ID: 18651330
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Case of methylmalonic acidemia presenting clinically Leigh encephalopathy].
    Ito H; Mori K; Ito M; Naito E; Yokota I; Kuroda Y
    No To Hattatsu; 2004 Jul; 36(4):324-9. PubMed ID: 15272617
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Leigh syndrome: a heterogeneous disease].
    Arenas J
    Neurologia; 2003 Jun; 18(5):239-40. PubMed ID: 12768508
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.