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Results: 1 to 20 of 31

1.

Progressive cerebral vascular degeneration with mitochondrial encephalopathy.

Longo N, Schrijver I, Vogel H, Pique LM, Cowan TM, Pasquali M, Steinberg GK, Hedlund GL, Ernst SL, Gallagher RC, Enns GM.

Am J Med Genet A. 2008 Feb 1;146(3):361-7. doi: 10.1002/ajmg.a.31841.

PMID:
18203188
[PubMed - indexed for MEDLINE]
2.

Heteroplasmic mitochondrial DNA mutation in a patient with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes.

Chiang LM, Jong YJ, Huang SC, Tsai JL, Pang CY, Lee HC, Wei YH.

J Formos Med Assoc. 1995 Jan-Feb;94(1-2):42-7. Review.

PMID:
7613232
[PubMed - indexed for MEDLINE]
3.

The mitochondrial myopathy encephalopathy, lactic acidosis with stroke-like episodes (MELAS) syndrome: a review of treatment options.

Scaglia F, Northrop JL.

CNS Drugs. 2006;20(6):443-64. Review. Erratum in: CNS Drugs. 2008;22(1):81.

PMID:
16734497
[PubMed - indexed for MEDLINE]
4.

Diagnosis and management of MELAS.

Thambisetty M, Newman NJ.

Expert Rev Mol Diagn. 2004 Sep;4(5):631-44. Review.

PMID:
15347257
[PubMed - indexed for MEDLINE]
5.

[Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) with chronic renal failure: report of mother-child cases].

Ihara M, Tanaka H, Yashiro M, Nishimura Y.

Rinsho Shinkeigaku. 1996 Sep;36(9):1069-73. Review. Japanese.

PMID:
8976130
[PubMed - indexed for MEDLINE]
6.

A case of mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes associated with diabetes mellitus and hypothalamo-pituitary dysfunction.

Joko T, Iwashige K, Hashimoto T, Ono Y, Kobayashi K, Sekiguchi N, Kuroki T, Yanase T, Takayanagi R, Umeda F, Nawata H.

Endocr J. 1997 Dec;44(6):805-9. Review.

PMID:
9622295
[PubMed - indexed for MEDLINE]
Free Article
7.

[MELAS syndrome as a differential diagnosis of ischemic stroke].

Finsterer J.

Fortschr Neurol Psychiatr. 2009 Jan;77(1):25-31. doi: 10.1055/s-2008-1100821. Epub 2008 Nov 14. Review. German.

PMID:
19012224
[PubMed - indexed for MEDLINE]
8.

[MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes)].

Goto Y.

Ryoikibetsu Shokogun Shirizu. 2001;(36):146-9. Review. Japanese. No abstract available.

PMID:
11596349
[PubMed - indexed for MEDLINE]
9.

Mitochondrial encephalomyopathy with elderly onset of stroke-like episodes.

Minamoto H, Kawabata K, Okuda B, Shibuya N, Tachibana H, Sugita M, Goto Y, Nishino I, Nonaka I.

Intern Med. 1996 Dec;35(12):991-5. Review.

PMID:
9031002
[PubMed - indexed for MEDLINE]
Free Article
10.

Genetic, pathogenetic, and phenotypic implications of the mitochondrial A3243G tRNALeu(UUR) mutation.

Finsterer J.

Acta Neurol Scand. 2007 Jul;116(1):1-14. Review.

PMID:
17587249
[PubMed - indexed for MEDLINE]
11.

[Mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS) associated with hypothalamo-pituitary hypofunction--a case report].

Ishii A, Watanabe S, Ohkoshi N, Mizusawa H, Kanazawa I.

Rinsho Shinkeigaku. 1991 Feb;31(2):179-83. Review. Japanese.

PMID:
2060243
[PubMed - indexed for MEDLINE]
12.

MELAS syndrome: peripheral neuropathy and cytochrome C-oxidase deficiency: a case report and review of the literature.

Barak Y, Arnon S, Wolach B, Raz Y, Ashkenasi A, Glick B, Shapira Y.

Isr J Med Sci. 1995 Apr;31(4):224-9. Review.

PMID:
7721560
[PubMed - indexed for MEDLINE]
13.

[Maternally inherited diabetes mellitus, deafness, chronic progressive external ophthalmoplegia and myopathy as the result of A3243G mutation of mtDNA].

Gál A, Szabó A, Pentelényi K, Pál Z.

Orv Hetil. 2008 Aug 24;149(34):1593-8. doi: 10.1556/OH.2008.28398. Review. Hungarian.

PMID:
18708313
[PubMed - indexed for MEDLINE]
14.

Mitochondrial encephalopathy, lactic acidosis, and strokelike episodes: basic concepts, clinical phenotype, and therapeutic management of MELAS syndrome.

Sproule DM, Kaufmann P.

Ann N Y Acad Sci. 2008 Oct;1142:133-58. doi: 10.1196/annals.1444.011. Review. Erratum in: Ann N Y Acad Sci. 2009 Apr;1161:601.

PMID:
18990125
[PubMed - indexed for MEDLINE]
15.

Pathogenesis of stroke-like episodes in MELAS: analysis of neurovascular cellular mechanisms.

Iizuka T, Sakai F.

Curr Neurovasc Res. 2005 Jan;2(1):29-45. Review.

PMID:
16181098
[PubMed - indexed for MEDLINE]
16.

Newborn screening for medium-chain acyl-CoA dehydrogenase deficiency: a global perspective.

Rhead WJ.

J Inherit Metab Dis. 2006 Apr-Jun;29(2-3):370-7. Review.

PMID:
16763904
[PubMed - indexed for MEDLINE]
17.

[Pathogenesis and treatment of stroke-like episodes in MELAS].

Iizuka T.

Rinsho Shinkeigaku. 2008 Nov;48(11):1006-9. Review. Japanese.

PMID:
19198146
[PubMed - indexed for MEDLINE]
18.

[Mitochondrial myopathy. Encephalopathy with lactic acidosis and cerebral infarction].

Destée A, Martin JJ, Muller JP, Scholte HR, Verier A, Largillière C, Warot P.

Rev Neurol (Paris). 1989;145(1):37-48. Review. French.

PMID:
2646681
[PubMed - indexed for MEDLINE]
19.

Mitochondrial encephalomyopathy with lactic acidosis and stroke (MELAS).

Matsumoto J, Saver JL, Brennan KC, Ringman JM.

Rev Neurol Dis. 2005 Winter;2(1):30-4. Review.

PMID:
16400302
[PubMed - indexed for MEDLINE]
20.

[Pathomechanism and clinical presentation of neurobehavioral disturbances in a patient with MELAS syndrome].

Pachalska M, DiMauro S, MacQueen BD, Tłokiński W, Jeleńska-Szyguła I.

Neurol Neurochir Pol. 2001 Jul-Aug;35(4):681-93. Review. Polish.

PMID:
11783410
[PubMed - indexed for MEDLINE]

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