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 *

178 related articles for article (PubMed ID: 17437622)

  • 1. Cognitive dysfunction and hypogonadotrophic hypogonadism in a Brazilian patient with mitochondrial neurogastrointestinal encephalomyopathy and a novel ECGF1 mutation.
    Carod-Artal FJ; Herrero MD; Lara MC; López-Gallardo E; Ruiz-Pesini E; Martí R; Montoya J
    Eur J Neurol; 2007 May; 14(5):581-5. PubMed ID: 17437622
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A novel ECGF1 mutation in a Thai patient with mitochondrial neurogastrointestinal encephalomyopathy (MNGIE).
    Kintarak J; Liewluck T; Sangruchi T; Hirano M; Kulkantrakorn K; Muengtaweepongsa S
    Clin Neurol Neurosurg; 2007 Sep; 109(7):613-6. PubMed ID: 17544574
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE) in two Mexican brothers harboring a novel mutation in the ECGF1 gene.
    Monroy N; Macías Kauffer LR; Mutchinick OM
    Eur J Med Genet; 2008; 51(3):245-50. PubMed ID: 18280229
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Four novel thymidine phosphorylase gene mutations in mitochondrial neurogastrointestinal encephalomyopathy syndrome (MNGIE) patients.
    Kocaefe YC; Erdem S; Ozgüç M; Tan E
    Eur J Hum Genet; 2003 Jan; 11(1):102-4. PubMed ID: 12529715
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): a disease of two genomes.
    Hirano M; Nishigaki Y; Martí R
    Neurologist; 2004 Jan; 10(1):8-17. PubMed ID: 14720311
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A novel TYMP mutation in a French Canadian patient with mitochondrial neurogastrointestinal encephalomyopathy.
    Laforce R; Valdmanis PN; Dupré N; Rouleau GA; Turgeon AF; Savard M
    Clin Neurol Neurosurg; 2009 Oct; 111(8):691-4. PubMed ID: 19523753
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mitochondrial neurogastrointestinal encephalomyopathy: evidence of mitochondrial DNA depletion in the small intestine.
    Giordano C; Sebastiani M; Plazzi G; Travaglini C; Sale P; Pinti M; Tancredi A; Liguori R; Montagna P; Bellan M; Valentino ML; Cossarizza A; Hirano M; d'Amati G; Carelli V
    Gastroenterology; 2006 Mar; 130(3):893-901. PubMed ID: 16530527
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Thymidine phosphorylase gene mutations in patients with mitochondrial neurogastrointestinal encephalomyopathy syndrome.
    Slama A; Lacroix C; Plante-Bordeneuve V; Lombès A; Conti M; Reimund JM; Auxenfants E; Crenn P; Laforêt P; Joannard A; Seguy D; Pillant H; Joly P; Haut S; Messing B; Said G; Legrand A; Guiochon-Mantel A
    Mol Genet Metab; 2005 Apr; 84(4):326-31. PubMed ID: 15781193
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Characterization of a novel TYMP splice site mutation associated with mitochondrial neurogastrointestinal encephalomyopathy (MNGIE).
    Taanman JW; Daras M; Albrecht J; Davie CA; Mallam EA; Muddle JR; Weatherall M; Warner TT; Schapira AH; Ginsberg L
    Neuromuscul Disord; 2009 Feb; 19(2):151-4. PubMed ID: 19056268
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Thymidine phosphorylase gene mutation is not a primary cause of mitochondrial neurogastrointestinal encephalomyopathy (MNGIE).
    Kumagai Y; Sugiura Y; Sugeno H; Takebayashi Y; Takenoshita S; Yamamoto T
    Intern Med; 2006; 45(7):443-6. PubMed ID: 16679698
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): biochemical features and therapeutic approaches.
    Lara MC; Valentino ML; Torres-Torronteras J; Hirano M; Martí R
    Biosci Rep; 2007 Jun; 27(1-3):151-63. PubMed ID: 17549623
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Thymidine phosphorylase gene mutations cause mitochondrial neurogastrointestinal encephalomyopathy (MNGIE).
    Hirano M; Nishino I; Nishigaki Y; Martí R
    Intern Med; 2006; 45(19):1103. PubMed ID: 17077575
    [No Abstract]   [Full Text] [Related]  

  • 13. Clinical and molecular characterization of a patient with mitochondrial Neurogastrointestinal Encephalomyopathy.
    Habibzadeh P; Silawi M; Dastsooz H; Bahramjahan S; Ezzatzadegan Jahromi S; Ostovan VR; Yavarian M; Mofatteh M; Faghihi MA
    BMC Gastroenterol; 2020 May; 20(1):142. PubMed ID: 32384880
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Increased muscle nucleoside levels associated with a novel frameshift mutation in the thymidine phosphorylase gene in a Spanish patient with MNGIE.
    Blazquez A; Martín MA; Lara MC; Martí R; Campos Y; Cabello A; Garesse R; Bautista J; Andreu AL; Arenas J
    Neuromuscul Disord; 2005 Nov; 15(11):775-8. PubMed ID: 16198108
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Mitochondrial neurogastrointestinal encephalomyopathy and its pathophysiology.
    Kurihara T
    Intern Med; 2006; 45(7):415-6. PubMed ID: 16679693
    [No Abstract]   [Full Text] [Related]  

  • 16. Mitochondrial neurogastrointestinal encephalomyopathy.
    Borhani Haghighi A; Nabavizadeh A; Sass JO; Safari A; Lankarani KB
    Arch Iran Med; 2009 Nov; 12(6):588-90. PubMed ID: 19877753
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Site-specific somatic mitochondrial DNA point mutations in patients with thymidine phosphorylase deficiency.
    Nishigaki Y; Martí R; Copeland WC; Hirano M
    J Clin Invest; 2003 Jun; 111(12):1913-21. PubMed ID: 12813027
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Late-onset MNGIE without peripheral neuropathy due to incomplete loss of thymidine phosphorylase activity.
    Massa R; Tessa A; Margollicci M; Micheli V; Romigi A; Tozzi G; Terracciano C; Piemonte F; Bernardi G; Santorelli FM
    Neuromuscul Disord; 2009 Dec; 19(12):837-40. PubMed ID: 19853446
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Possible toxicity of tuberculostatic agents in a patient with a novel TYMP mutation leading to mitochondrial neurogastrointestinal encephalomyopathy.
    Mihaylova V; Guergueltcheva V; Cherninkova S; Penev L; Georgieva G; Stoyanova K; Todorova A; Tournev I
    J Neurogenet; 2013 Jun; 27(1-2):19-22. PubMed ID: 23590577
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mitochondrial neurogastrointestinal encephalomyopathy: novel pathogenic mutations in thymidine phosphorylase gene in two Italian brothers.
    Libernini L; Lupis C; Mastrangelo M; Carrozzo R; Santorelli FM; Inghilleri M; Leuzzi V
    Neuropediatrics; 2012 Aug; 43(4):201-8. PubMed ID: 22618301
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.