Melas syndrome
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pediatrics, Perinatology and Child Health
Link
http://link.springer.com/content/pdf/10.1007/BF02727181.pdf
Reference23 articles.
1. Pavlakis SG, Phillips PC, Dimauros S, Devivo DC, Rowland LP Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke like eposide: A distinctive clinical syndrome.Ann Neurol 1984; 16 : 481–88.
2. Driscoll PF, Larsen PD, Gruber AB. MELAS syndrome involving a mother and two children.Arch Neurol 1987; 44: 971–73.
3. Kishnani PS, Van Hove JLK, Shoffner JS, Kaufman A, Bossen EH, Kahler SG. Acute pancreatitis in an infant with lactic acidosis and a mutation at nucleotide 3243 in the mitochondrial DNA tRNALeu (uur) Gene.Eur J Pediatr 1996; 155: 898–903.
4. Ciafaloni E, Ricci E, Shanske Set al. MELAS: Clincal features, biochemistry and molecular genetics.Ann Neurol 1992; 31: 391–98.
5. Fujii T, Okuno T, Ito Net al. MELAS of infantile onset : mitochondrial angiopathy or cytopathy?J Neurol Scie. 1991 :37–41.
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