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Links from PubMed

Items: 5

1.

A specific point mutation in the mitochondrial genome of Caucasians with MELAS.

Enter C, Müller-Höcker J, Zierz S, Kurlemann G, Pongratz D, Förster C, Obermaier-Kusser B, Gerbitz KD.

Hum Genet. 1991 Dec;88(2):233-6.

PMID:
1684568
3.

MELAS syndrome: Clinical manifestations, pathogenesis, and treatment options.

El-Hattab AW, Adesina AM, Jones J, Scaglia F.

Mol Genet Metab. 2015 Sep-Oct;116(1-2):4-12. doi: 10.1016/j.ymgme.2015.06.004. Epub 2015 Jun 15. Review.

PMID:
26095523
4.

[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
5.

Morphological studies of skeletal muscle in lactic acidosis.

Romero NB, Lombès A, Touati G, Rigal O, Frachon P, Cheval MA, Giraud M, Possekel S, Fardeau M, Ogier de Baulny H.

J Inherit Metab Dis. 1996;19(4):528-34. Review.

PMID:
8884576

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