Angelini C - Search Results

1

Calpain-3 and dysferlin protein screening in patients with limb-girdle dystrophy and myopathy.

Fanin M, Pegoraro E, Matsuda-Asada C, Brown RH Jr, Angelini C. Fanin M, et al. Among authors: angelini c. Neurology. 2001 Mar 13;56(5):660-5. doi: 10.1212/wnl.56.5.660. Neurology. 2001. PMID: 11245721

2

Prevalence of dystrophin-positive fibers in 85 Duchenne muscular dystrophy patients.

Fanin M, Danieli GA, Vitiello L, Senter L, Angelini C. Fanin M, et al. Among authors: angelini c. Neuromuscul Disord. 1992;2(1):41-5. doi: 10.1016/0960-8966(92)90025-2. Neuromuscul Disord. 1992. PMID: 1525557

3

Is the carboxyl-terminus of dystrophin required for membrane association? A novel, severe case of Duchenne muscular dystrophy.

Hoffman EP, Garcia CA, Chamberlain JS, Angelini C, Lupski JR, Fenwick R. Hoffman EP, et al. Among authors: angelini c. Ann Neurol. 1991 Oct;30(4):605-10. doi: 10.1002/ana.410300414. Ann Neurol. 1991. PMID: 1789686

4

Congenital muscular dystrophy: brain alterations in an unselected series of Western patients.

Trevisan CP, Carollo C, Segalla P, Angelini C, Drigo P, Giordano R. Trevisan CP, et al. Among authors: angelini c. J Neurol Neurosurg Psychiatry. 1991 Apr;54(4):330-4. doi: 10.1136/jnnp.54.4.330. J Neurol Neurosurg Psychiatry. 1991. PMID: 1905345 Free PMC article.

5

Enormous dystrophin in a patient with Becker muscular dystrophy.

Angelini C, Beggs AH, Hoffman EP, Fanin M, Kunkel LM. Angelini C, et al. Neurology. 1990 May;40(5):808-12. doi: 10.1212/wnl.40.5.808. Neurology. 1990. PMID: 2158637

6

Liver fatty acid-binding protein in two cases of human lipid storage.

Vergani L, Fanin M, Martinuzzi A, Galassi A, Appi A, Carrozzo R, Rosa M, Angelini C. Vergani L, et al. Among authors: angelini c. Mol Cell Biochem. 1990 Oct 15-Nov 8;98(1-2):225-30. doi: 10.1007/BF00231388. Mol Cell Biochem. 1990. PMID: 2266963

7

Improved diagnosis of Becker muscular dystrophy by dystrophin testing.

Hoffman EP, Kunkel LM, Angelini C, Clarke A, Johnson M, Harris JB. Hoffman EP, et al. Among authors: angelini c. Neurology. 1989 Aug;39(8):1011-7. doi: 10.1212/wnl.39.8.1011. Neurology. 1989. PMID: 2668783

8

Myotonic dystrophy: evidence for a possible dominant-negative RNA mutation.

Wang J, Pegoraro E, Menegazzo E, Gennarelli M, Hoop RC, Angelini C, Hoffman EP. Wang J, et al. Among authors: angelini c. Hum Mol Genet. 1995 Apr;4(4):599-606. doi: 10.1093/hmg/4.4.599. Hum Mol Genet. 1995. PMID: 7543316

9

Dystrophin-positive fibers in Duchenne dystrophy: origin and correlation to clinical course.

Fanin M, Danieli GA, Cadaldini M, Miorin M, Vitiello L, Angelini C. Fanin M, et al. Among authors: angelini c. Muscle Nerve. 1995 Oct;18(10):1115-20. doi: 10.1002/mus.880181007. Muscle Nerve. 1995. PMID: 7659105

10

Genetic and biochemical normalization in female carriers of Duchenne muscular dystrophy: evidence for failure of dystrophin production in dystrophin-competent myonuclei.

Pegoraro E, Schimke RN, Garcia C, Stern H, Cadaldini M, Angelini C, Barbosa E, Carroll J, Marks WA, Neville HE, Marks H, Appleton S, Toriello H, Wessel HB, Donnelly J, Bernes SM, Taber JW, Weiss L, Hoffman EP. Pegoraro E, et al. Among authors: angelini c. Neurology. 1995 Apr;45(4):677-90. doi: 10.1212/wnl.45.4.677. Neurology. 1995. PMID: 7723955

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