Ricci E - Search Results

1

Congenital muscular dystrophies with cognitive impairment. A population study.

Messina S, Bruno C, Moroni I, Pegoraro E, D'Amico A, Biancheri R, Berardinelli A, Boffi P, Cassandrini D, Farina L, Minetti C, Moggio M, Mongini T, Mottarelli E, Pane M, Pantaleoni C, Pichiecchio A, Pini A, Ricci E, Saredi S, Sframeli M, Tortorella G, Toscano A, Trevisan CP, Uggetti C, Vasco G, Comi GP, Santorelli FM, Bertini E, Mercuri E. Messina S, et al. Among authors: ricci e. Neurology. 2010 Sep 7;75(10):898-903. doi: 10.1212/WNL.0b013e3181f11dd5. Neurology. 2010. PMID: 20820001

2

Peripheral neuropathy with giant axons and cardiomyopathy associated with desmin type intermediate filaments in skeletal muscle.

Sabatelli M, Bertini E, Ricci E, Salviati G, Magi S, Papacci M, Tonali P. Sabatelli M, et al. Among authors: ricci e. J Neurol Sci. 1992 May;109(1):1-10. doi: 10.1016/0022-510x(92)90086-z. J Neurol Sci. 1992. PMID: 1517757 Review.

3

Progressive depletion of fast alpha-actinin-positive muscle fibers in Duchenne muscular dystrophy.

Minetti C, Ricci E, Bonilla E. Minetti C, et al. Among authors: ricci e. Neurology. 1991 Dec;41(12):1977-81. doi: 10.1212/wnl.41.12.1977. Neurology. 1991. PMID: 1745358

4

Dominantly inherited mitochondrial myopathy with multiple deletions of mitochondrial DNA: clinical, morphologic, and biochemical studies.

Servidei S, Zeviani M, Manfredi G, Ricci E, Silvestri G, Bertini E, Gellera C, Di Mauro S, Di Donato S, Tonali P. Servidei S, et al. Among authors: ricci e. Neurology. 1991 Jul;41(7):1053-9. doi: 10.1212/wnl.41.7.1053. Neurology. 1991. PMID: 2067633

5

Distal infantile spinal muscular atrophy associated with paralysis of the diaphragm: a variant of infantile spinal muscular atrophy.

Bertini E, Gadisseux JL, Palmieri G, Ricci E, Di Capua M, Ferriere G, Lyon G. Bertini E, et al. Among authors: ricci e. Am J Med Genet. 1989 Jul;33(3):328-35. doi: 10.1002/ajmg.1320330309. Am J Med Genet. 1989. PMID: 2801766

6

Late onset scleroatonic familial myopathy (Ullrich disease): a study of two sibs.

Ricci E, Bertini E, Boldrini R, Sabatelli M, Servidei S, Mazziotta MR, Bosman C, Tonali P. Ricci E, et al. Am J Med Genet. 1988 Dec;31(4):933-42. doi: 10.1002/ajmg.1320310428. Am J Med Genet. 1988. PMID: 3239582

7

Autosomal recessive hypermyelinating neuropathy.

Sabatelli M, Mignogna T, Lippi G, Servidei S, Manfredi G, Ricci E, Bertini E, Lo Monaco M, Tonali P. Sabatelli M, et al. Among authors: ricci e. Acta Neuropathol. 1994;87(4):337-42. doi: 10.1007/BF00313601. Acta Neuropathol. 1994. PMID: 8017168

8

Reducing body myopathy and desmin storage in skeletal muscle: morphological and biochemical findings.

Bertini E, Salviati G, Apollo F, Ricci E, Servidei S, Broccolini A, Papacci M, Tonali P. Bertini E, et al. Among authors: ricci e. Acta Neuropathol. 1994;87(1):106-12. doi: 10.1007/BF00386261. Acta Neuropathol. 1994. PMID: 8140891

9

Cardiomyopathy may be the only clinical manifestation in female carriers of Duchenne muscular dystrophy.

Mirabella M, Servidei S, Manfredi G, Ricci E, Frustaci A, Bertini E, Rana M, Tonali P. Mirabella M, et al. Among authors: ricci e. Neurology. 1993 Nov;43(11):2342-5. doi: 10.1212/wnl.43.11.2342. Neurology. 1993. PMID: 8232953

10

Manifesting heterozygotes in McArdle's disease: clinical, morphological and biochemical studies in a family.

Manfredi G, Silvestri G, Servidei S, Ricci E, Mirabella M, Bertini E, Papacci M, Rana M, Tonali P. Manfredi G, et al. Among authors: ricci e. J Neurol Sci. 1993 Mar;115(1):91-4. doi: 10.1016/0022-510x(93)90071-6. J Neurol Sci. 1993. PMID: 8468596

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