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Page 1
MELAS: clinical features, biochemistry, and molecular genetics.
Ciafaloni E, Ricci E, Shanske S, Moraes CT, Silvestri G, Hirano M, Simonetti S, Angelini C, Donati MA, Garcia C, et al. Ciafaloni E, et al. Ann Neurol. 1992 Apr;31(4):391-8. doi: 10.1002/ana.410310408. Ann Neurol. 1992. PMID: 1586140
Correlation between clinical and molecular features in two MELAS families.
Martinuzzi A, Bartolomei L, Carrozzo R, Mostacciuolo M, Carbonin C, Toso V, Ciafaloni E, Shanske S, DiMauro S, Angelini C. Martinuzzi A, et al. Among authors: ciafaloni e. J Neurol Sci. 1992 Dec;113(2):222-9. doi: 10.1016/0022-510x(92)90250-o. J Neurol Sci. 1992. PMID: 1487758
Maternally inherited Leigh syndrome.
Ciafaloni E, Santorelli FM, Shanske S, Deonna T, Roulet E, Janzer C, Pescia G, DiMauro S. Ciafaloni E, et al. J Pediatr. 1993 Mar;122(3):419-22. doi: 10.1016/s0022-3476(05)83431-6. J Pediatr. 1993. PMID: 8095070
Fat embolism syndrome in patients with Duchenne muscular dystrophy.
Medeiros MO, Behrend C, King W, Sanders J, Kissel J, Ciafaloni E. Medeiros MO, et al. Among authors: ciafaloni e. Neurology. 2013 Apr 2;80(14):1350-2. doi: 10.1212/WNL.0b013e31828ab313. Epub 2013 Mar 20. Neurology. 2013. PMID: 23516314 No abstract available.
130 results