Clinical score for early diagnosis and treatment of stroke-like episodes in MELAS syndrome
Author:
Publisher
Springer Science and Business Media LLC
Subject
Neurology (clinical),General Medicine
Link
https://link.springer.com/content/pdf/10.1007/s13760-023-02196-z.pdf
Reference25 articles.
1. Yatsuga S, Povalko N, Nishioka J et al (2012) MELAS: A nationwide prospective cohort study of 96 patients in Japan. Biochim Biophys Acta BBA Gen Subj 1820(5):619–624. https://doi.org/10.1016/j.bbagen.2011.03.015
2. Hirano M, Ricci E, Richard Koenigsberger M et al (1992) MELAS: An original case and clinical criteria for diagnosis. Neuromuscul Disord 2(2):125–135. https://doi.org/10.1016/0960-8966(92)90045-8
3. El-Hattab AW, Emrick LT, Hsu JW et al (2016) Impaired nitric oxide production in children with MELAS syndrome and the effect of arginine and citrulline supplementation. Mol Genet Metab 117(4):407–412. https://doi.org/10.1016/j.ymgme.2016.01.010
4. Zhang J, Guo J, Fang W, Jun Q, Shi K (2015) Clinical features of MELAS and its relation with A3243G gene point mutation. Int J Clin Exp Pathol 8(10):13411–13415
5. Majamaa K, Moilanen JS, Uimonen S et al (1998) Epidemiology of A3243G, the mutation for mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes: prevalence of the mutation in an adult population. Am J Hum Genet 63(2):447–454. https://doi.org/10.1086/301959
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