Related Articles by Review for PMID: 32310383

Year	Number of Results
1993	3
1995	1
2003	1
2008	1
2009	1
2010	1
2014	1
2016	1
2017	1
2019	1
2021	1
2023	3
2025	1

1

Myoclonic Epilepsy and Ragged Red Fibers.

Hameed S, Tadi P. Hameed S, et al. 2023 Jul 16. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2025 Jan–. 2023 Jul 16. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2025 Jan–. PMID: 32310383 Free Books & Documents.

2

MERRF.

Velez-Bartolomei F, Lee C, Enns G. Velez-Bartolomei F, et al. 2003 Jun 3 [updated 2021 Jan 7]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews^® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025. 2003 Jun 3 [updated 2021 Jan 7]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews^® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025. PMID: 20301693 Free Books & Documents. Review.

3

When should MERRF (myoclonus epilepsy associated with ragged-red fibers) be the diagnosis?

Lorenzoni PJ, Scola RH, Kay CS, Silvado CE, Werneck LC. Lorenzoni PJ, et al. Arq Neuropsiquiatr. 2014 Oct;72(10):803-11. doi: 10.1590/0004-282x20140124. Arq Neuropsiquiatr. 2014. PMID: 25337734 Free article. Review.

4

[Fukuhara disease].

Fukuhara N. Fukuhara N. Brain Nerve. 2008 Jan;60(1):53-8. Brain Nerve. 2008. PMID: 18232333 Review. Japanese.

5

Pharmacotherapeutic management of epilepsy in MERRF syndrome.

Finsterer J. Finsterer J. Expert Opin Pharmacother. 2019 Jul;20(10):1289-1297. doi: 10.1080/14656566.2019.1609941. Epub 2019 May 7. Expert Opin Pharmacother. 2019. PMID: 31063406 Review.

6

Mitochondrial DNA mutation-elicited oxidative stress, oxidative damage, and altered gene expression in cultured cells of patients with MERRF syndrome.

Wu SB, Ma YS, Wu YT, Chen YC, Wei YH. Wu SB, et al. Mol Neurobiol. 2010 Jun;41(2-3):256-66. doi: 10.1007/s12035-010-8123-7. Epub 2010 Apr 23. Mol Neurobiol. 2010. PMID: 20411357 Review.

7

Identification of new variants in MTRNR1 and MTRNR2 genes using whole mitochondrial genome sequencing in a Taiwanese family with MERRF (myoclonic epilepsy with ragged-red fibers) syndrome.

Wu YT, Huang SC, Shiao YM, Syu WC, Wei YH, Hsu YC. Wu YT, et al. Hear Res. 2023 Oct;438:108876. doi: 10.1016/j.heares.2023.108876. Epub 2023 Aug 22. Hear Res. 2023. PMID: 37683310 Review.

8

[Molecular genetic analysis for myoclonus epilepsy associated with ragged-red fibers (MERRF)].

Tanno Y, Yoneda M, Tanaka K, Tsuji S. Tanno Y, et al. Nihon Rinsho. 1993 Sep;51(9):2379-85. Nihon Rinsho. 1993. PMID: 8411716 Review. Japanese.

9

Myoclonus epilepsy in mitochondrial disorders.

Lamperti C, Zeviani M. Lamperti C, et al. Epileptic Disord. 2016 Sep 1;18(S2):94-102. doi: 10.1684/epd.2016.0846. Epileptic Disord. 2016. PMID: 27618766 Review.

10

The Mitochondrial tRNA^Ser(UCN) Gene: A Novel m.7484A>G Mutation Associated with Mitochondrial Encephalomyopathy and Literature Review.

Borgione E, Lo Giudice M, Santa Paola S, Giuliano M, Di Blasi FD, Di Stefano V, Lupica A, Brighina F, Pettinato R, Romano C, Scuderi C. Borgione E, et al. Life (Basel). 2023 Feb 16;13(2):554. doi: 10.3390/life13020554. Life (Basel). 2023. PMID: 36836911 Free PMC article. Review.

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