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Items: 1 to 20 of 31

1.

A novel mitochondrial tRNAPhe mutation causes MERRF syndrome.

Mancuso M, Filosto M, Mootha VK, Rocchi A, Pistolesi S, Murri L, DiMauro S, Siciliano G.

Neurology. 2004 Jun 8;62(11):2119-21.

PMID:
15184630
2.

[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
3.

A new mitochondrial point mutation in the transfer RNA(Leu) gene in a patient with a clinical phenotype resembling Kearns-Sayre syndrome.

Seneca S, Verhelst H, De Meirleir L, Meire F, Ceuterick-De Groote C, Lissens W, Van Coster R.

Arch Neurol. 2001 Jul;58(7):1113-8. Review.

PMID:
11448301
4.

[Fukuhara disease].

Fukuhara N.

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

PMID:
18232333
5.

Mitochondrial DNA mutation and muscle pathology in mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes.

Mita S, Tokunaga M, Kumamoto T, Uchino M, Nonaka I, Ando M.

Muscle Nerve Suppl. 1995;3:S113-8. Review.

PMID:
7603511
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.

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

PMID:
20411357
7.

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
8.
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.

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. Review.

PMID:
19278689
11.

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

Goto Y.

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

PMID:
11596350
12.

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.

13.

Update in molecular genetics: mitochondrial energy transduction disorders.

Marzuki S, Sudoyo H, Lertrit P.

Southeast Asian J Trop Med Public Health. 1995;26 Suppl 1:155-61. Review. No abstract available.

PMID:
8629096
14.
15.

Mitochondrial disorders. Methods and specimen selection for diagnostic molecular pathology.

Kiechle FL, Kaul KL, Farkas DH.

Arch Pathol Lab Med. 1996 Jun;120(6):597-603. Review.

PMID:
8651866
16.

Mitochondrial cytopathies.

Schmiedel J, Jackson S, Schäfer J, Reichmann H.

J Neurol. 2003 Mar;250(3):267-77. Review.

PMID:
12638015
17.

Transmission of the human mitochondrial genome.

Howell N, Chinnery PF, Ghosh SS, Fahy E, Turnbull DM.

Hum Reprod. 2000 Jul;15 Suppl 2:235-45. Review.

PMID:
11041529
18.

[MERRF].

Yoneda M.

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

PMID:
12483877
19.

Role of taurine in the pathologies of MELAS and MERRF.

Schaffer SW, Jong CJ, Ito T, Azuma J.

Amino Acids. 2014 Jan;46(1):47-56. doi: 10.1007/s00726-012-1414-8. Review.

PMID:
23179085
20.

Mitochondrial abnormalities in inclusion-body myositis.

Oldfors A, Moslemi AR, Jonasson L, Ohlsson M, Kollberg G, Lindberg C.

Neurology. 2006 Jan 24;66(2 Suppl 1):S49-55. Review.

PMID:
16432145

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