Angelini C - Search Results

1

A standardized clinical evaluation of patients affected by facioscapulohumeral muscular dystrophy: The FSHD clinical score.

Lamperti C, Fabbri G, Vercelli L, D'Amico R, Frusciante R, Bonifazi E, Fiorillo C, Borsato C, Cao M, Servida M, Greco F, Di Leo R, Volpi L, Manzoli C, Cudia P, Pastorello E, Ricciardi L, Siciliano G, Galluzzi G, Rodolico C, Santoro L, Tomelleri G, Angelini C, Ricci E, Palmucci L, Moggio M, Tupler R. Lamperti C, et al. Among authors: angelini c. Muscle Nerve. 2010 Aug;42(2):213-7. doi: 10.1002/mus.21671. Muscle Nerve. 2010. PMID: 20544930

2

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

3

Myophosphorylase deficiency affects muscle mitochondrial respiration as shown by 31P-MR spectroscopy in a case with associated multifocal encephalopathy.

Siciliano G, Rossi B, Martini A, Angelini C, Martinuzzi A, Lodi R, Zaniol P, Barbiroli B, Muratorio A. Siciliano G, et al. Among authors: angelini c. J Neurol Sci. 1995 Jan;128(1):84-91. doi: 10.1016/0022-510x(94)00207-5. J Neurol Sci. 1995. PMID: 7722538

4

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

5

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

6

Residual muscle cytochrome c oxidase activity accounts for submaximal exercise lactate threshold in chronic progressive external ophthalmoplegia.

Siciliano G, Rossi B, Manca L, Angelini C, Tessa A, Vergani L, Martinuzzi A, Muratorio A. Siciliano G, et al. Among authors: angelini c. Muscle Nerve. 1996 Mar;19(3):342-9. doi: 10.1002/(SICI)1097-4598(199603)19:3<342::AID-MUS10>3.0.CO;2-U. Muscle Nerve. 1996. PMID: 8606699

7

Duchenne phenotype with in-frame deletion removing major portion of dystrophin rod: threshold effect for deletion size?

Fanin M, Freda MP, Vitiello L, Danieli GA, Pegoraro E, Angelini C. Fanin M, et al. Among authors: angelini c. Muscle Nerve. 1996 Sep;19(9):1154-60. doi: 10.1002/mus.880190902. Muscle Nerve. 1996. PMID: 8761273

8

Prognostic factors in mild dystrophinopathies.

Angelini C, Fanin M, Freda MP, Martinello F, Miorin M, Melacini P, Siciliano G, Pegoraro E, Rosa M, Danieli GA. Angelini C, et al. J Neurol Sci. 1996 Oct;142(1-2):70-8. doi: 10.1016/0022-510x(96)00144-x. J Neurol Sci. 1996. PMID: 8902723

9

Homozygous alpha-sarcoglycan mutation in two siblings: one asymptomatic and one steroid-responsive mild limb-girdle muscular dystrophy patient.

Angelini C, Fanin M, Menegazzo E, Freda MP, Duggan DJ, Hoffman EP. Angelini C, et al. Muscle Nerve. 1998 Jun;21(6):769-75. doi: 10.1002/(sici)1097-4598(199806)21:6<769::aid-mus9>3.0.co;2-5. Muscle Nerve. 1998. PMID: 9585331

10

The clinical spectrum of sarcoglycanopathies.

Angelini C, Fanin M, Freda MP, Duggan DJ, Siciliano G, Hoffman EP. Angelini C, et al. Neurology. 1999 Jan 1;52(1):176-9. doi: 10.1212/wnl.52.1.176. Neurology. 1999. PMID: 9921870

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