Mitochondrial neurogastrointestinal encephalopathy: a clinicopathological mimic of Crohn’s disease-Reference-Cited by-同舟云学术

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Mitochondrial neurogastrointestinal encephalopathy: a clinicopathological mimic of Crohn’s disease

Published:2019-01-15 Issue:1 Volume:19 Page:
ISSN:1471-230X
Container-title:BMC Gastroenterology
language:en
Short-container-title:BMC Gastroenterol

Author:

Patel Ravi,Coulter Lucia Lee,Rimmer Joanna,Parkes Miles,Chinnery Patrick Francis,Swift Oscar

Publisher

Springer Science and Business Media LLC

Subject

Gastroenterology,General Medicine

Link

http://link.springer.com/content/pdf/10.1186/s12876-018-0925-5.pdf

Reference12 articles.

1. Nishino I, Spinazzola A, Hirano M. Thymidine phosphorylase gene mutations in MNGIE, a human mitochondrial disorder. Science. 1999;283(5402):689–92.

2. Giordano C, Sebastiani M, De Giorgio R, et al. Gastrointestinal dysmotility in mitochondrial neurogastrointestinal encephalomyopathy is caused by mitochondrial DNA depletion. Am J Pathol. 2008;173(4):1120–8.

3. Garone C, Tadesse S, Hirano M. Clinical and genetic spectrum of mitochondrial neurogastrointestinal encephalomyopathy. Brain. 2011;134(11):3326–32.

4. Luo Y, de Lange KM, Jostins L, et al. Exploring the genetic architecture of inflammatory bowel disease by whole-genome sequencing identifies association at ADCY7. Nat Genet. 2017;49(2):186–92.

5. Perez-Atayde AR. Diagnosis of mitochondrial neurogastrointestinal encephalopathy disease in gastrointestinal biopsies. Hum Pathol. 2013;44(7):1440–6.

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2. 1,3,4-Oxadiazole: An Emerging Scaffold to Inhibit the Thymidine Phosphorylase as an Anticancer Agent;Current Medicinal Chemistry;2023-07-12

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4. A Novel Mutation in an MNGIE Patient Presenting with More Prominent Neurological Symptoms than GI Symptoms;Neurology India;2023

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