Pegoraro E - Search Results

1

Brain involvement in myotonic dystrophies: neuroimaging and neuropsychological comparative study in DM1 and DM2.

Romeo V, Pegoraro E, Ferrati C, Squarzanti F, Sorarù G, Palmieri A, Zucchetta P, Antunovic L, Bonifazi E, Novelli G, Trevisan CP, Ermani M, Manara R, Angelini C. Romeo V, et al. Among authors: pegoraro e. J Neurol. 2010 Aug;257(8):1246-55. doi: 10.1007/s00415-010-5498-3. Epub 2010 Mar 11. J Neurol. 2010. PMID: 20221771

2

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: pegoraro e. Hum Mol Genet. 1995 Apr;4(4):599-606. doi: 10.1093/hmg/4.4.599. Hum Mol Genet. 1995. PMID: 7543316

3

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. Neurology. 1995 Apr;45(4):677-90. doi: 10.1212/wnl.45.4.677. Neurology. 1995. PMID: 7723955

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

5

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: pegoraro e. J Neurol Sci. 1994 May;123(1-2):88-94. doi: 10.1016/0022-510x(94)90208-9. J Neurol Sci. 1994. PMID: 8064327

6

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. Among authors: pegoraro e. Muscle Nerve. 1994 Apr;17(4):386-91. doi: 10.1002/mus.880170405. Muscle Nerve. 1994. PMID: 8170484 Clinical Trial.

7

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: pegoraro e. Neuroepidemiology. 1993;12(6):326-30. doi: 10.1159/000110334. Neuroepidemiology. 1993. PMID: 8309507

8

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: pegoraro e. Muscle Nerve. 1996 Sep;19(9):1154-60. doi: 10.1002/mus.880190902. Muscle Nerve. 1996. PMID: 8761273

9

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: pegoraro e. Neuroepidemiology. 1996;15(4):173-9. doi: 10.1159/000109905. Neuroepidemiology. 1996. PMID: 8817499

10

Myotonia and the muscle chloride channel: dominant mutations show variable penetrance and founder effect.

Koty PP, Pegoraro E, Hobson G, Marks HG, Turel A, Flagler D, Cadaldini M, Angelini C, Hoffman EP. Koty PP, et al. Among authors: pegoraro e. Neurology. 1996 Oct;47(4):963-8. doi: 10.1212/wnl.47.4.963. Neurology. 1996. PMID: 8857727

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