Similar articles for PMID: 12825077

Year	Number of Results
1983	1
1994	2
1995	1
1996	2
1997	11
1998	5
1999	8
2000	9
2001	11
2002	13
2003	16
2004	13
2005	16
2006	16
2007	7
2008	8
2009	14
2010	19
2011	21
2012	20
2013	14
2014	16
2015	14
2016	14
2017	13
2018	12
2019	11
2020	16
2021	15
2022	14
2023	2
2024	0

1

Novel POLG mutations in progressive external ophthalmoplegia mimicking mitochondrial neurogastrointestinal encephalomyopathy.

Van Goethem G, Schwartz M, Löfgren A, Dermaut B, Van Broeckhoven C, Vissing J. Van Goethem G, et al. Eur J Hum Genet. 2003 Jul;11(7):547-9. doi: 10.1038/sj.ejhg.5201002. Eur J Hum Genet. 2003. PMID: 12825077

2

A very early onset MNGIE-like syndrome with POLG1 mutation and accompanying leukoencephalopathy.

Altuntaş C, Uzunhan TA, Ertürk B, Petmezci MT, Çakar NE, Noyan B, Dokucu Aİ, Önal H. Altuntaş C, et al. Clin Neurol Neurosurg. 2023 Jun;229:107712. doi: 10.1016/j.clineuro.2023.107712. Epub 2023 Apr 7. Clin Neurol Neurosurg. 2023. PMID: 37084649

3

Diagnosing mitochondrial, neurogastrointestinal leukoencephalopathy requires mutations in TYMP1, POLG1, LIG1, or RRM2B.

Finsterer J. Finsterer J. J Med Case Rep. 2023 Apr 14;17(1):162. doi: 10.1186/s13256-023-03916-y. J Med Case Rep. 2023. PMID: 37055871 Free PMC article. No abstract available.

4

Mitochondrial Neurogastrointestinal Encephalomyopathy Causing Fanconi Syndrome.

Razzaq A, Earl W, Levsky S, Rao MK, Seres DS, Hirano M, Rosen RJ. Razzaq A, et al. Kidney Int Rep. 2022 Aug 5;7(11):2534-2536. doi: 10.1016/j.ekir.2022.07.176. eCollection 2022 Nov. Kidney Int Rep. 2022. PMID: 36531873 Free PMC article. No abstract available.

5

Changing faces of mitochondrial disease: autosomal recessive POLG disease mimicking myasthenia gravis and progressive supranuclear palsy.

Elwan M, Schaefer AM, Craig K, Hopton S, Falkous G, Blakely EL, Taylor RW, Warren N. Elwan M, et al. BMJ Neurol Open. 2022 Dec 8;4(2):e000352. doi: 10.1136/bmjno-2022-000352. eCollection 2022. BMJ Neurol Open. 2022. PMID: 36518302 Free PMC article.

6

Case report: A patient with mitochondrial neurogastrointestinal encephalomyopathy and chronic intestinal failure.

Barisic A, Ljubas Kelecic D, Vranesic Bender D, Karas I, Brinar M, Miletic V, Krznaric Z. Barisic A, et al. Front Nutr. 2022 Nov 7;9:983873. doi: 10.3389/fnut.2022.983873. eCollection 2022. Front Nutr. 2022. PMID: 36419558 Free PMC article.

7

Mitochondrial neurogastrointestinal encephalomyopathy in a Pakistani female: a case report.

Khan ZR, Karam A, Ul Haq MA, Aman A, Karam AS. Khan ZR, et al. J Med Case Rep. 2022 Oct 3;16(1):363. doi: 10.1186/s13256-022-03582-6. J Med Case Rep. 2022. PMID: 36192783 Free PMC article.

8

Clinical spectrum of early onset "Mediterranean" (homozygous p.P131L mutation) mitochondrial neurogastrointestinal encephalomyopathy.

Kalkan Uçar S, Yazıcı H, Canda E, Er E, Bulut FD, Eraslan C, Onay H, Bax BE, Çoker M. Kalkan Uçar S, et al. JIMD Rep. 2022 Jul 10;63(5):484-493. doi: 10.1002/jmd2.12315. eCollection 2022 Sep. JIMD Rep. 2022. PMID: 36101829 Free PMC article.

9

Rare pathogenic mutation in the thymidine phosphorylase gene (TYMP) causing mitochondrial neurogastrointestinal encephalomyelopathy.

Shah SAY, Shakeel HA, Hassan WU. Shah SAY, et al. BMJ Neurol Open. 2022 Aug 22;4(2):e000287. doi: 10.1136/bmjno-2022-000287. eCollection 2022. BMJ Neurol Open. 2022. PMID: 36072350 Free PMC article.

10

Anatomical Laser Microdissection of the Ileum Reveals mtDNA Depletion Recovery in A Mitochondrial Neuro-Gastrointestinal Encephalomyopathy (MNGIE) Patient Receiving Liver Transplant.

Boschetti E, Caporali L, D'Angelo R, Malagelada C, Accarino A, Dotti MT, Costa R, Cenacchi G, Pironi L, Rinaldi R, Stanghellini V, Ratti S, Manzoli L, Carelli V, De Giorgio R. Boschetti E, et al. Int J Mol Sci. 2022 Aug 8;23(15):8792. doi: 10.3390/ijms23158792. Int J Mol Sci. 2022. PMID: 35955927 Free PMC article.

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