Angelini C - Search Results

1

Expression profiling characterization of laminin alpha-2 positive MDC.

Millino C, Bellin M, Fanin M, Romualdi C, Pegoraro E, Angelini C, Lanfranchi G. Millino C, et al. Among authors: angelini c. Biochem Biophys Res Commun. 2006 Nov 17;350(2):345-51. doi: 10.1016/j.bbrc.2006.09.063. Epub 2006 Sep 25. Biochem Biophys Res Commun. 2006. PMID: 17010933

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

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

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

5

Survival motor neuron gene transcript analysis in muscles from spinal muscular atrophy patients.

Gennarelli M, Lucarelli M, Capon F, Pizzuti A, Merlini L, Angelini C, Novelli G, Dallapiccola B. Gennarelli M, et al. Among authors: angelini c. Biochem Biophys Res Commun. 1995 Aug 4;213(1):342-8. doi: 10.1006/bbrc.1995.2135. Biochem Biophys Res Commun. 1995. PMID: 7639755

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

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

8

MtDNA mutations associated with Leber's hereditary optic neuropathy: studies on cytoplasmic hybrid (cybrid) cells.

Vergani L, Martinuzzi A, Carelli V, Cortelli P, Montagna P, Schievano G, Carrozzo R, Angelini C, Lugaresi E. Vergani L, et al. Among authors: angelini c. Biochem Biophys Res Commun. 1995 May 25;210(3):880-8. doi: 10.1006/bbrc.1995.1740. Biochem Biophys Res Commun. 1995. PMID: 7763260

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

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

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