Angelini C - Search Results

1

Cardiac involvement in Becker muscular dystrophy.

Melacini P, Fanin M, Danieli GA, Fasoli G, Villanova C, Angelini C, Vitiello L, Miorelli M, Buja GF, Mostacciuolo ML, et al. Melacini P, et al. Among authors: angelini c. J Am Coll Cardiol. 1993 Dec;22(7):1927-34. doi: 10.1016/0735-1097(93)90781-u. J Am Coll Cardiol. 1993. PMID: 8245351 Free article.

2

Letter: Duchenne carrier detection.

Danieli GA, Angelini C. Danieli GA, et al. Among authors: angelini c. Lancet. 1976 Jul 10;2(7976):90. doi: 10.1016/s0140-6736(76)92301-1. Lancet. 1976. PMID: 59163 No abstract available.

3

Duchenne muscular dystrophy. A population study.

Danieli GA, Mostacciuolo ML, Bonfante A, Angelini C. Danieli GA, et al. Among authors: angelini c. Hum Genet. 1977 Feb 11;35(2):225-31. doi: 10.1007/BF00393974. Hum Genet. 1977. PMID: 844870

4

Further evidence of a duplication in 17p11.2 in families with recurrence of HMSN Ia (Charcot-Marie-Tooth neuropathy type Ia).

Müller E, Mostacciuolo ML, Micaglio G, Angelini C, Danieli GA. Müller E, et al. Among authors: angelini c. Hum Genet. 1992 Nov;90(3):231-4. doi: 10.1007/BF00220067. Hum Genet. 1992. PMID: 1487234

5

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: angelini c. J Neurol Sci. 1992 Dec;113(2):222-9. doi: 10.1016/0022-510x(92)90250-o. J Neurol Sci. 1992. PMID: 1487758

6

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

7

Epidemiology of spinal muscular atrophies in a sample of the Italian population.

Mostacciuolo ML, Danieli GA, Trevisan C, Müller E, Angelini C. Mostacciuolo ML, et al. Among authors: angelini c. Neuroepidemiology. 1992;11(1):34-8. doi: 10.1159/000110905. Neuroepidemiology. 1992. PMID: 1608493

8

Screening for mutations in the muscle promoter region and for exonic deletions in a series of 115 DMD and BMD patients.

Vitiello L, Mostacciuolo ML, Oliviero S, Schiavon F, Nicoletti L, Angelini C, Danieli GA. Vitiello L, et al. Among authors: angelini c. J Med Genet. 1992 Feb;29(2):127-30. doi: 10.1136/jmg.29.2.127. J Med Genet. 1992. PMID: 1613762 Free PMC article.

9

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.

10

Exploring the molecular basis for variability among patients with Becker muscular dystrophy: dystrophin gene and protein studies.

Beggs AH, Hoffman EP, Snyder JR, Arahata K, Specht L, Shapiro F, Angelini C, Sugita H, Kunkel LM. Beggs AH, et al. Among authors: angelini c. Am J Hum Genet. 1991 Jul;49(1):54-67. Am J Hum Genet. 1991. PMID: 2063877 Free PMC article.

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