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Page 1
Myopathological findings in progressive myoclonus epilepsy.
Pierobon-Bormioli S, Angelini C, Armani M, Testa GF. Pierobon-Bormioli S, et al. Among authors: armani m. Acta Neuropathol Suppl. 1981;7:334-7. doi: 10.1007/978-3-642-81553-9_96. Acta Neuropathol Suppl. 1981. PMID: 6261519
Genetic epidemiology of myotonic dystrophy.
Mostacciuolo ML, Barbujani G, Armani M, Danieli GA, Angelini C. Mostacciuolo ML, et al. Among authors: armani m. Genet Epidemiol. 1987;4(4):289-98. doi: 10.1002/gepi.1370040407. Genet Epidemiol. 1987. PMID: 3666435
Familial neuromuscular disease with tubular aggregates.
Pierobon-Bormioli S, Armani M, Ringel SP, Angelini C, Vergani L, Betto R, Salviati G. Pierobon-Bormioli S, et al. Among authors: armani m. Muscle Nerve. 1985 May;8(4):291-8. doi: 10.1002/mus.880080405. Muscle Nerve. 1985. PMID: 16758595
A childhood case of hypokalemic periodic paralysis.
Gobbi G, Armani M, Pierobon Bormioli S, Giovanardi Rossi P, Angelini C. Gobbi G, et al. Among authors: armani m. Acta Neurol (Napoli). 1984 Apr;6(2):147-51. Acta Neurol (Napoli). 1984. PMID: 6741656 No abstract available.
70 results