Angelini C - Search Results

1

Cardiomyopathy in patients with POMT1-related congenital and limb-girdle muscular dystrophy.

Bello L, Melacini P, Pezzani R, D'Amico A, Piva L, Leonardi E, Torella A, Soraru G, Palmieri A, Smaniotto G, Gavassini BF, Vianello A, Nigro V, Bertini E, Angelini C, Tosatto SC, Pegoraro E. Bello L, et al. Among authors: angelini c. Eur J Hum Genet. 2012 Dec;20(12):1234-9. doi: 10.1038/ejhg.2012.71. Epub 2012 May 2. Eur J Hum Genet. 2012. PMID: 22549409 Free PMC article.

2

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.

3

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

4

Evolution of cardiac involvement in progressive ophthalmoplegia with deleted mitochondrial DNA.

Melacini P, Angelini C, Buja G, Micaglio G, Valente ML. Melacini P, et al. Among authors: angelini c. Jpn Heart J. 1990 Jan;31(1):115-20. doi: 10.1536/ihj.31.115. Jpn Heart J. 1990. PMID: 2335842

5

The natural history of cardiac involvement in myotonic dystrophy: an eight-year follow-up in 17 patients.

Melacini P, Buja G, Fasoli G, Angelini C, Armani M, Scognamiglio R, Dalla Volta S. Melacini P, et al. Among authors: angelini c. Clin Cardiol. 1988 Apr;11(4):231-8. doi: 10.1002/clc.4960110407. Clin Cardiol. 1988. PMID: 3365873 Free article.

6

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

7

Divergence of central nervous system involvement in 2 Italian sisters with congenital muscular dystrophy: a clinical and neuroradiological follow-up.

Trevisan CP, Martinello F, Ferruzza E, Angelini C. Trevisan CP, et al. Among authors: angelini c. Eur Neurol. 1995;35(4):230-5. doi: 10.1159/000117134. Eur Neurol. 1995. PMID: 7671985

8

Correlation between cardiac involvement and CTG trinucleotide repeat length in myotonic dystrophy.

Melacini P, Villanova C, Menegazzo E, Novelli G, Danieli G, Rizzoli G, Fasoli G, Angelini C, Buja G, Miorelli M, et al. Melacini P, et al. Among authors: angelini c. J Am Coll Cardiol. 1995 Jan;25(1):239-45. doi: 10.1016/0735-1097(94)00351-p. J Am Coll Cardiol. 1995. PMID: 7798509 Free article.

9

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. Neuromuscul Disord. 1994 Jul;4(4):349-58. doi: 10.1016/0960-8966(94)90071-x. Neuromuscul Disord. 1994. PMID: 7981592

10

A study on duplications of the dystrophin gene: evidence of a geographical difference in the distribution of breakpoints by intron.

Galvagni F, Saad FA, Danieli GA, Miorin M, Vitiello L, Mostacciuolo ML, Angelini C. Galvagni F, et al. Among authors: angelini c. Hum Genet. 1994 Jul;94(1):83-7. doi: 10.1007/BF02272848. Hum Genet. 1994. PMID: 8034300

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