Similar articles for PMID: 19667227

Year	Number of Results
1994	1
1996	1
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2001	2
2002	1
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2007	6
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2009	14
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2012	4
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2020	5
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2023	4
2024	0

1

Mitochondrial neurogastrointestinal encephalopathy due to mutations in RRM2B.

Shaibani A, Shchelochkov OA, Zhang S, Katsonis P, Lichtarge O, Wong LJ, Shinawi M. Shaibani A, et al. Arch Neurol. 2009 Aug;66(8):1028-32. doi: 10.1001/archneurol.2009.139. Arch Neurol. 2009. PMID: 19667227 Free PMC article.

2

Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE)-like phenotype: an expanded clinical spectrum of POLG1 mutations.

Tang S, Dimberg EL, Milone M, Wong LJ. Tang S, et al. J Neurol. 2012 May;259(5):862-8. doi: 10.1007/s00415-011-6268-6. Epub 2011 Oct 13. J Neurol. 2012. PMID: 21993618

3

Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): a disease of two genomes.

Hirano M, Nishigaki Y, Martí R. Hirano M, et al. Neurologist. 2004 Jan;10(1):8-17. doi: 10.1097/01.nrl.0000106919.06469.04. Neurologist. 2004. PMID: 14720311 Review.

4

Mitochondrial DNA depletion syndrome due to mutations in the RRM2B gene.

Bornstein B, Area E, Flanigan KM, Ganesh J, Jayakar P, Swoboda KJ, Coku J, Naini A, Shanske S, Tanji K, Hirano M, DiMauro S. Bornstein B, et al. Neuromuscul Disord. 2008 Jun;18(6):453-9. doi: 10.1016/j.nmd.2008.04.006. Epub 2008 May 27. Neuromuscul Disord. 2008. PMID: 18504129 Free PMC article.

5

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. Giordano C, et al. Gastroenterology. 2006 Mar;130(3):893-901. doi: 10.1053/j.gastro.2006.01.004. Gastroenterology. 2006. PMID: 16530527

6

MNGIE: from nuclear DNA to mitochondrial DNA.

Nishino I, Spinazzola A, Hirano M. Nishino I, et al. Neuromuscul Disord. 2001 Jan;11(1):7-10. doi: 10.1016/s0960-8966(00)00159-0. Neuromuscul Disord. 2001. PMID: 11166160 Review.

7

Mitochondrial neurogastrointestinal encephalomyopathy mimicking anorexia nervosa.

Feddersen B, DE LA Fontaine L, Sass JO, Lutz J, Abicht A, Klopstock T, Verma IC, Meisenzahl E, Pogarell O. Feddersen B, et al. Am J Psychiatry. 2009 Apr;166(4):494-5. doi: 10.1176/appi.ajp.2008.08101525. Am J Psychiatry. 2009. PMID: 19339372 No abstract available.

8

A novel thymidine phosphorylase mutation in a family with Mitochondrial Neurogastrointestinal Encephalomyopathy (MNGIE): Molecular docking, dynamic simulation and computational investigations.

Ammar M, Safi W, Tlili A, Alila-Fersi O, Frikha F, Chouchen J, Mnif F, Kharrat M, Maalej M, Felhi R, Abid M, Mnif-Feki M, Kacem FH, Fakhfakh F, Mkaouar-Rebai E. Ammar M, et al. Int J Dev Neurosci. 2022 Nov;82(7):626-638. doi: 10.1002/jdn.10215. Epub 2022 Jul 25. Int J Dev Neurosci. 2022. PMID: 35841120

9

Four novel thymidine phosphorylase gene mutations in mitochondrial neurogastrointestinal encephalomyopathy syndrome (MNGIE) patients.

Kocaefe YC, Erdem S, Ozgüç M, Tan E. Kocaefe YC, et al. Eur J Hum Genet. 2003 Jan;11(1):102-4. doi: 10.1038/sj.ejhg.5200908. Eur J Hum Genet. 2003. PMID: 12529715

10

[Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE)].

Honzík T, Tesarová M, Hansíková H, Krijt J, Benes P, Zámecník J, Wenchich L, Zeman J. Honzík T, et al. Cas Lek Cesk. 2006;145(8):665-70. Cas Lek Cesk. 2006. PMID: 16995425 Czech.

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