Angelini C - Search Results

1

Psychopathological features and suicidal ideation in amyotrophic lateral sclerosis patients.

Palmieri A, Sorarù G, Albertini E, Semenza C, Vottero-Ris F, D'Ascenzo C, Querin G, Zennaro A, Pegoraro E, Angelini C. Palmieri A, et al. Among authors: angelini c. Neurol Sci. 2010 Dec;31(6):735-40. doi: 10.1007/s10072-010-0332-3. Epub 2010 Jun 3. Neurol Sci. 2010. PMID: 20521074

2

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

3

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

4

Deflazacort in Duchenne dystrophy: study of long-term effect.

Angelini C, Pegoraro E, Turella E, Intino MT, Pini A, Costa C. Angelini C, et al. Muscle Nerve. 1994 Apr;17(4):386-91. doi: 10.1002/mus.880170405. Muscle Nerve. 1994. PMID: 8170484 Clinical Trial.

5

Reappraisal of the incidence rate of Duchenne and Becker muscular dystrophies on the basis of molecular diagnosis.

Mostacciuolo ML, Miorin M, Pegoraro E, Fanin M, Schiavon F, Vitiello L, Saad FA, Angelini C, Danieli GA. Mostacciuolo ML, et al. Among authors: angelini c. Neuroepidemiology. 1993;12(6):326-30. doi: 10.1159/000110334. Neuroepidemiology. 1993. PMID: 8309507

6

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

7

Motor neuron disease in the Padua district of Italy: an epidemiological study.

Briani C, Marcon M, Dam M, Beghi E, Pegoraro E, Angelini C. Briani C, et al. Among authors: angelini c. Neuroepidemiology. 1996;15(4):173-9. doi: 10.1159/000109905. Neuroepidemiology. 1996. PMID: 8817499

8

alpha-Sarcoglycan (adhalin) deficiency: complete deficiency patients are 5% of childhood-onset dystrophin-normal muscular dystrophy and most partial deficiency patients do not have gene mutations.

Duggan DJ, Fanin M, Pegoraro E, Angelini C, Hoffman EP. Duggan DJ, et al. Among authors: angelini c. J Neurol Sci. 1996 Sep 1;140(1-2):30-9. doi: 10.1016/0022-510x(96)00028-7. J Neurol Sci. 1996. PMID: 8866424

9

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

10

Genetic epidemiology of muscular dystrophies resulting from sarcoglycan gene mutations.

Fanin M, Duggan DJ, Mostacciuolo ML, Martinello F, Freda MP, Sorarù G, Trevisan CP, Hoffman EP, Angelini C. Fanin M, et al. Among authors: angelini c. J Med Genet. 1997 Dec;34(12):973-7. doi: 10.1136/jmg.34.12.973. J Med Genet. 1997. PMID: 9429136 Free PMC article.

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