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Results: 1 to 20 of 23

Related Articles by Review for PubMed (Select 17200493)

1.

Parkinson syndrome, neuropathy, and myopathy caused by the mutation A8344G (MERRF) in tRNALys.

Horvath R, Kley RA, Lochmüller H, Vorgerd M.

Neurology. 2007 Jan 2;68(1):56-8.

PMID:
17200493
2.

Pathogenetic aspects of the A8344G mutation of mitochondrial DNA associated with MERRF syndrome and multiple symmetric lipomas.

Larsson NG, Tulinius MH, Holme E, Oldfors A.

Muscle Nerve Suppl. 1995;3:S102-6. Review.

PMID:
7603509
3.

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

Tanno Y, Yoneda M, Tanaka K, Tsuji S.

Nihon Rinsho. 1993 Sep;51(9):2379-85. Review. Japanese.

PMID:
8411716
4.

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.

Mol Neurobiol. 2010 Jun;41(2-3):256-66. doi: 10.1007/s12035-010-8123-7. Epub 2010 Apr 23. Review.

PMID:
20411357
5.

[MERRF (myoclonus epilepsy associated with ragged-red fibers)].

Goto Y.

Ryoikibetsu Shokogun Shirizu. 2001;(36):150-2. Review. Japanese. No abstract available.

PMID:
11596350
6.

Mitochondrial DNA G8363A mutation in the tRNA Lys gene: clinical, biochemical and pathological study.

Virgilio R, Ronchi D, Bordoni A, Fassone E, Bonato S, Donadoni C, Torgano G, Moggio M, Corti S, Bresolin N, Comi GP.

J Neurol Sci. 2009 Jun 15;281(1-2):85-92. doi: 10.1016/j.jns.2009.01.025. Epub 2009 Mar 10. Review.

PMID:
19278689
7.

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

Lorenzoni PJ, Scola RH, Kay CS, Silvado CE, Werneck LC.

Arq Neuropsiquiatr. 2014 Oct;72(10):803-11. Review.

8.

[Fukuhara disease].

Fukuhara N.

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

PMID:
18232333
9.

MERRF: a model disease for understanding the principles of mitochondrial genetics.

Shoffner JM, Lott MT, Wallace DC.

Rev Neurol (Paris). 1991;147(6-7):431-5. Review.

PMID:
1962048
10.

[MERRF/MELAS overlap syndrome].

Goto Y.

Ryoikibetsu Shokogun Shirizu. 2001;(36):159. Review. Japanese. No abstract available.

PMID:
11596353
11.

[MERRF/MELAS overlap syndrome].

Goto Y.

Nihon Rinsho. 2002 Apr;60 Suppl 4:296-7. Review. Japanese. No abstract available.

PMID:
12013869
12.

[MERRF].

Goto Y.

Nihon Rinsho. 2002 Apr;60 Suppl 4:292-5. Review. Japanese. No abstract available.

PMID:
12013868
13.
14.

[MERRF].

Yoneda M.

Ryoikibetsu Shokogun Shirizu. 2002;(37 Pt 6):262-4. Review. Japanese. No abstract available.

PMID:
12483877
15.

Hereditary myosin myopathies.

Oldfors A.

Neuromuscul Disord. 2007 May;17(5):355-67. Epub 2007 Apr 16. Review.

PMID:
17434305
16.

Clinical features and genetics of myoclonic epilepsy with ragged red fibers.

DiMauro S, Hirano M, Kaufmann P, Tanji K, Sano M, Shungu DC, Bonilla E, DeVivo DC.

Adv Neurol. 2002;89:217-29. Review. No abstract available.

PMID:
11968448
17.
18.

Clinical and morphological phenotype of the filamin myopathy: a study of 31 German patients.

Kley RA, Hellenbroich Y, van der Ven PF, Fürst DO, Huebner A, Bruchertseifer V, Peters SA, Heyer CM, Kirschner J, Schröder R, Fischer D, Müller K, Tolksdorf K, Eger K, Germing A, Brodherr T, Reum C, Walter MC, Lochmüller H, Ketelsen UP, Vorgerd M.

Brain. 2007 Dec;130(Pt 12):3250-64. Review.

19.

Hematological manifestations of primary mitochondrial disorders.

Finsterer J.

Acta Haematol. 2007;118(2):88-98. Epub 2007 Jul 18. Review.

PMID:
17637511
20.

[Myoclonus epilepsy].

Higashi T, Kikuchi S, Tashiro K.

Nihon Rinsho. 2002 Apr;60 Suppl 4:515-8. Review. Japanese. No abstract available.

PMID:
12013929
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