174 related articles for article (PubMed ID: 33214395)
21. Allogeneic haematopoietic stem cell transplantation for mitochondrial neurogastrointestinal encephalomyopathy.
Halter JP; Michael W; Schüpbach M; Mandel H; Casali C; Orchard K; Collin M; Valcarcel D; Rovelli A; Filosto M; Dotti MT; Marotta G; Pintos G; Barba P; Accarino A; Ferra C; Illa I; Beguin Y; Bakker JA; Boelens JJ; de Coo IF; Fay K; Sue CM; Nachbaur D; Zoller H; Sobreira C; Pinto Simoes B; Hammans SR; Savage D; Martí R; Chinnery PF; Elhasid R; Gratwohl A; Hirano M
Brain; 2015 Oct; 138(Pt 10):2847-58. PubMed ID: 26264513
[TBL] [Abstract][Full Text] [Related]
22. Brain White Matter Lesions and Presumed Crohn's Disease: Did You Consider MNGIE?
Cousyn L; Boehm V; Shor N; Treton X; Benamouzig R; Gaignard P; Nadjar Y
Can J Neurol Sci; 2020 Jul; 47(4):572-575. PubMed ID: 32122424
[No Abstract] [Full Text] [Related]
23. 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]
24. 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]
25. Thymidine phosphorylase mutations cause instability of mitochondrial DNA.
Hirano M; Lagier-Tourenne C; Valentino ML; Martí R; Nishigaki Y
Gene; 2005 Jul; 354():152-6. PubMed ID: 15975738
[TBL] [Abstract][Full Text] [Related]
26. 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]
27. 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]
28. Large copy number variations in combination with point mutations in the TYMP and SCO2 genes found in two patients with mitochondrial disorders.
Vondráčková A; Veselá K; Kratochvílová H; Kučerová Vidrová V; Vinšová K; Stránecký V; Honzík T; Hansíková H; Zeman J; Tesařová M
Eur J Hum Genet; 2014 Mar; 22(3):431-4. PubMed ID: 23838601
[TBL] [Abstract][Full Text] [Related]
29. 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]
30. Evidence of enteric angiopathy and neuromuscular hypoxia in patients with mitochondrial neurogastrointestinal encephalomyopathy.
Boschetti E; D'Angelo R; Tardio ML; Costa R; Giordano C; Accarino A; Malagelada C; Clavenzani P; Tugnoli V; Caio G; Righi V; Garone C; D'Errico A; Cenacchi G; Dotti MT; Stanghellini V; Sternini C; Pironi L; Rinaldi R; Carelli V; De Giorgio R
Am J Physiol Gastrointest Liver Physiol; 2021 May; 320(5):G768-G779. PubMed ID: 33655764
[TBL] [Abstract][Full Text] [Related]
31. 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]
32. Biochemical abnormalities in a patient with thymidine phosphorylase deficiency with fatal outcome.
Bakker JA; Schlesser P; Smeets HJ; Francois B; Bierau J
J Inherit Metab Dis; 2010 Dec; 33 Suppl 3(Suppl 3):S139-43. PubMed ID: 20151198
[TBL] [Abstract][Full Text] [Related]
33. 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]
34. Intensive nutrition support may benefit patients with a rare mitochondrial disorder.
Kasti A; Nikolaki M; Pyrousis I; Synodinou K; Oikonomopoulos N; Triantafyllou K
Nutr Clin Pract; 2022 Apr; 37(2):361-365. PubMed ID: 34170051
[TBL] [Abstract][Full Text] [Related]
35. Mitochondrial neurogastrointestinal encephalomyopathy treated with peritoneal dialysis and bone marrow transplantation.
Ariaudo C; Daidola G; Ferrero B; Guarena C; Burdese M; Segoloni GP; Biancone L
J Nephrol; 2015 Feb; 28(1):125-7. PubMed ID: 24599829
[TBL] [Abstract][Full Text] [Related]
36. Mitochondrial Neurogastrointestinal Encephalomyopathy Disease in Three Siblings from Pakistan with a Novel Mutation.
Durrani S; Chen BC; Yakob Y; Hian LS; Afroze B
J Pediatr Genet; 2019 Mar; 8(1):15-19. PubMed ID: 30775048
[TBL] [Abstract][Full Text] [Related]
37. 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]
38. Mitochondrial neurogastrointestinal encephalopathy: a clinicopathological mimic of Crohn's disease.
Patel R; Coulter LL; Rimmer J; Parkes M; Chinnery PF; Swift O
BMC Gastroenterol; 2019 Jan; 19(1):11. PubMed ID: 30646848
[TBL] [Abstract][Full Text] [Related]
39. Response to: POLG1 variants can at most cause MNGIE-like but not classic MNGIE phenotypes.
Altuntaş C; Uzunhan TA; Ertürk B; Petmezci MT; Çakar NE; Noyan B; Dokucu Aİ; Önal H
Clin Neurol Neurosurg; 2024 Jan; 236():107893. PubMed ID: 37455189
[No Abstract] [Full Text] [Related]
40.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]