Freda MP - Search Results

1

Genetic epidemiology of muscular dystrophies resulting from sarcoglycan gene mutations.

Fanin M, Duggan DJ, Mostacciuolo ML, Martinello F, Freda MP, Sorarù G, Trevisan CP, Hoffman EP, Angelini C. Fanin M, et al. Among authors: freda mp. J Med Genet. 1997 Dec;34(12):973-7. doi: 10.1136/jmg.34.12.973. J Med Genet. 1997. PMID: 9429136 Free PMC article.

2

Clinical-molecular correlation in 104 mild X-linked muscular dystrophy patients: characterization of sub-clinical phenotypes.

Angelini C, Fanin M, Pegoraro E, Freda MP, Cadaldini M, Martinello F. Angelini C, et al. Among authors: freda mp. Neuromuscul Disord. 1994 Jul;4(4):349-58. doi: 10.1016/0960-8966(94)90071-x. Neuromuscul Disord. 1994. PMID: 7981592

3

Homozygous alpha-sarcoglycan mutation in two siblings: one asymptomatic and one steroid-responsive mild limb-girdle muscular dystrophy patient.

Angelini C, Fanin M, Menegazzo E, Freda MP, Duggan DJ, Hoffman EP. Angelini C, et al. Among authors: freda mp. Muscle Nerve. 1998 Jun;21(6):769-75. doi: 10.1002/(sici)1097-4598(199806)21:6<769::aid-mus9>3.0.co;2-5. Muscle Nerve. 1998. PMID: 9585331

4

The clinical spectrum of sarcoglycanopathies.

Angelini C, Fanin M, Freda MP, Duggan DJ, Siciliano G, Hoffman EP. Angelini C, et al. Among authors: freda mp. Neurology. 1999 Jan 1;52(1):176-9. doi: 10.1212/wnl.52.1.176. Neurology. 1999. PMID: 9921870

5

Heart involvement in muscular dystrophies due to sarcoglycan gene mutations.

Melacini P, Fanin M, Duggan DJ, Freda MP, Berardinelli A, Danieli GA, Barchitta A, Hoffman EP, Dalla Volta S, Angelini C. Melacini P, et al. Among authors: freda mp. Muscle Nerve. 1999 Apr;22(4):473-9. doi: 10.1002/(sici)1097-4598(199904)22:4<473::aid-mus8>3.0.co;2-5. Muscle Nerve. 1999. PMID: 10204782

6

Prevalent cardiac involvement in dystrophin Becker type mutation.

Siciliano G, Fanin M, Angelini C, Pollina LE, Miorin M, Saad FA, Freda MP, Muratorio A. Siciliano G, et al. Among authors: freda mp. Neuromuscul Disord. 1994 Jul;4(4):381-6. doi: 10.1016/0960-8966(94)90074-4. Neuromuscul Disord. 1994. PMID: 7981595

7

Duchenne phenotype with in-frame deletion removing major portion of dystrophin rod: threshold effect for deletion size?

Fanin M, Freda MP, Vitiello L, Danieli GA, Pegoraro E, Angelini C. Fanin M, et al. Among authors: freda mp. Muscle Nerve. 1996 Sep;19(9):1154-60. doi: 10.1002/mus.880190902. Muscle Nerve. 1996. PMID: 8761273

8

Prognostic factors in mild dystrophinopathies.

Angelini C, Fanin M, Freda MP, Martinello F, Miorin M, Melacini P, Siciliano G, Pegoraro E, Rosa M, Danieli GA. Angelini C, et al. Among authors: freda mp. J Neurol Sci. 1996 Oct;142(1-2):70-8. doi: 10.1016/0022-510x(96)00144-x. J Neurol Sci. 1996. PMID: 8902723

9

Myocardial involvement is very frequent among patients affected with subclinical Becker's muscular dystrophy.

Melacini P, Fanin M, Danieli GA, Villanova C, Martinello F, Miorin M, Freda MP, Miorelli M, Mostacciuolo ML, Fasoli G, Angelini C, Dalla Volta S. Melacini P, et al. Among authors: freda mp. Circulation. 1996 Dec 15;94(12):3168-75. doi: 10.1161/01.cir.94.12.3168. Circulation. 1996. PMID: 8989125

10

Ataxia and congenital muscular dystrophy: the follow-up of a new specific phenotype.

Trevisan CP, Pastorello E, Tonello S, Armani M, Rigoni MT, Tormene AP, Freda MP, Zortea M, Lombardi S. Trevisan CP, et al. Among authors: freda mp. Brain Dev. 2001 Mar;23(2):108-14. doi: 10.1016/s0387-7604(01)00187-5. Brain Dev. 2001. PMID: 11248459

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