Angelini C - Search Results

1

Correlations between clinical severity, genotype and muscle pathology in limb girdle muscular dystrophy type 2A.

Fanin M, Nardetto L, Nascimbeni AC, Tasca E, Spinazzi M, Padoan R, Angelini C. Fanin M, et al. Among authors: angelini c. J Med Genet. 2007 Oct;44(10):609-14. doi: 10.1136/jmg.2007.050328. Epub 2007 May 25. J Med Genet. 2007. PMID: 17526799 Free PMC article.

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

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.

4

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

5

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

6

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

7

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

8

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: angelini c. Neuromuscul Disord. 1994 Jul;4(4):381-6. doi: 10.1016/0960-8966(94)90074-4. Neuromuscul Disord. 1994. PMID: 7981595

9

Absence of dystrophin and spectrin in regenerating muscle fibers from Becker dystrophy patients.

Fanin M, Pegoraro E, Angelini C. Fanin M, et al. Among authors: angelini c. J Neurol Sci. 1994 May;123(1-2):88-94. doi: 10.1016/0022-510x(94)90208-9. J Neurol Sci. 1994. PMID: 8064327

10

Occurrence of two different intragenic deletions in two male relatives affected with Duchenne muscular dystrophy.

Mostacciuolo ML, Miorin M, Vitiello L, Rampazzo A, Fanin M, Angelini C, Danieli GA. Mostacciuolo ML, et al. Among authors: angelini c. Am J Med Genet. 1994 Mar 1;50(1):84-6. doi: 10.1002/ajmg.1320500118. Am J Med Genet. 1994. PMID: 8160758

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