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 *

260 related articles for article (PubMed ID: 21794876)

  • 1. Mitochondrial neurogastrointestinal encephalopathy in an Indian family with possible manifesting carriers of heterozygous TYMP mutation.
    Nalini A; Gayathri N
    J Neurol Sci; 2011 Oct; 309(1-2):131-5. PubMed ID: 21794876
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A novel thymidine phosphorylase mutation in a Chinese MNGIE patient.
    Wang HF; Wang J; Wang YL; Fan JJ; Mo GL; Gong FY; Chai ZM; Zhang J; Meng HX; Li CX; Guo JH; Pu CQ
    Acta Neurol Belg; 2017 Mar; 117(1):259-267. PubMed ID: 27709505
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. Clinical and genetic spectrum of mitochondrial neurogastrointestinal encephalomyopathy.
    Garone C; Tadesse S; Hirano M
    Brain; 2011 Nov; 134(Pt 11):3326-32. PubMed ID: 21933806
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): case report with a new mutation.
    Bariş Z; Eminoğlu T; Dalgiç B; Tümer L; Hasanoğlu A
    Eur J Pediatr; 2010 Nov; 169(11):1375-8. PubMed ID: 20585803
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A mitochondrial neurogastrointestinal encephalomyopathy with intestinal pseudo-obstruction resulted from a novel splice site mutation.
    Erdogan MA; Seckin Y; Harputluoglu MM; Karincaoglu M; Aladag M; Caliskan AR; Bilgic Y; Yildirim O; Cagin YF; Atayan Y; Cengiz AN; Emul C; Esener Z; Erbay MF; Tekedereli I
    Clin Dysmorphol; 2019 Jan; 28(1):22-25. PubMed ID: 30407211
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE)].
    Honzík T; Tesarová M; Hansíková H; Krijt J; Benes P; Zámecník J; Wenchich L; Zeman J
    Cas Lek Cesk; 2006; 145(8):665-70. PubMed ID: 16995425
    [TBL] [Abstract][Full Text] [Related]  

  • 9. MNGIE with lack of skeletal muscle involvement and a novel TP splice site mutation.
    Szigeti K; Wong LJ; Perng CL; Saifi GM; Eldin K; Adesina AM; Cass DL; Hirano M; Lupski JR; Scaglia F
    J Med Genet; 2004 Feb; 41(2):125-9. PubMed ID: 14757860
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Mitochondrial Neurogastrointestinal Encephalopathy: Clinical, Biochemical and Molecular Study in Three Egyptian Patients.
    Selim L; Van Coster R; Mehaney D; Hassan F; Vanlander A; Smet J; De Latter E; Vandemeulebroecke K; Mohamed Abdou D; Nakhla G; Mostafa M; Habets D; Bakker J; Abdel Bary A
    Genet Couns; 2016; 27(2):193-205. PubMed ID: 29485812
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mitochondrial neurogastrointestinal encephalomyopathy in a Pakistani female: a case report.
    Khan ZR; Karam A; Ul Haq MA; Aman A; Karam AS
    J Med Case Rep; 2022 Oct; 16(1):363. PubMed ID: 36192783
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Compound heterozygous mutations of TYMP as underlying causes of mitochondrial neurogastrointestinal encephalomyopathy (MNGIE).
    Suh BC; Jeong HN; Yoon BS; Park JH; Kim HJ; Park SW; Hwang JH; Choi BO; Chung KW
    Mol Med Rep; 2013 Jul; 8(1):17-22. PubMed ID: 23685548
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mitochondrial neurogastrointestinal encephalomyopathy: an autosomal recessive disorder due to thymidine phosphorylase mutations.
    Nishino I; Spinazzola A; Papadimitriou A; Hammans S; Steiner I; Hahn CD; Connolly AM; Verloes A; Guimarães J; Maillard I; Hamano H; Donati MA; Semrad CE; Russell JA; Andreu AL; Hadjigeorgiou GM; Vu TH; Tadesse S; Nygaard TG; Nonaka I; Hirano I; Bonilla E; Rowland LP; DiMauro S; Hirano M
    Ann Neurol; 2000 Jun; 47(6):792-800. PubMed ID: 10852545
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Mitochondrial Neuro-Gastro-Intestinal Encephalopathy (MNGIE): When and how to suspect it in front of an atypical anorexia nervosa?].
    Danjou M; Guardia D; Geoffroy PA; Seguy D; Cottencin O
    Encephale; 2016 Dec; 42(6):574-579. PubMed ID: 27371119
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A Novel Mutation in an MNGIE Patient Presenting with More Prominent Neurological Symptoms than GI Symptoms.
    Chen X; Xiong X; Liu S; Duan C; Xu R; Yang Q
    Neurol India; 2023; 71(2):323-325. PubMed ID: 37148061
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Transient clinical improvement of a mitochondrial neurogastrointestinal encephalomyopathy-like syndrome after allogeneic haematopoietic stem cell transplantation.
    Baker MK; Schutte CM; Ranchhod N; Brittain D; van Rensburg JE
    BMJ Case Rep; 2017 Aug; 2017():. PubMed ID: 28765176
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. 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]  

  • 20. Leukoencephalopathy with a case of heterozygous POLG mutation mimicking mitochondrial neurogastrointestinal encephalomyopathy (MNGIE).
    Yasuda K; Murase N; Yoshinaga K; Ohtani R; Goto YI; Takahashi R; Nakamura M
    J Clin Neurosci; 2019 Mar; 61():302-304. PubMed ID: 30385167
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.