C.54/TI_/Telethon/Italy[Grants and Funding] - Search Results

Year	Number of Results
1994	1
1998	3
1999	3
2000	4
2001	5
2004	3
2005	1
2006	1
2024	0

1

Limb-girdle muscular dystrophies: heterogeneity of clinical phenotypes and pathogenetic mechanisms.

Angelini C. Angelini C. Acta Myol. 2004 Dec;23(3):130-6. Acta Myol. 2004. PMID: 15938568 Review.

2

Cognitive impairment and (CTG)n expansion in myotonic dystrophy patients.

Perini GI, Menegazzo E, Ermani M, Zara M, Gemma A, Ferruzza E, Gennarelli M, Angelini C. Perini GI, et al. Biol Psychiatry. 1999 Aug 1;46(3):425-31. doi: 10.1016/s0006-3223(99)00016-5. Biol Psychiatry. 1999. PMID: 10435210

3

Epidemiology of myotonic dystrophy in Italy: re-apprisal after genetic diagnosis.

Siciliano G, Manca M, Gennarelli M, Angelini C, Rocchi A, Iudice A, Miorin M, Mostacciuolo M. Siciliano G, et al. Clin Genet. 2001 May;59(5):344-9. doi: 10.1034/j.1399-0004.2001.590508.x. Clin Genet. 2001. PMID: 11359466

4

Calpain-3 and dysferlin protein screening in patients with limb-girdle dystrophy and myopathy.

Fanin M, Pegoraro E, Matsuda-Asada C, Brown RH Jr, Angelini C. Fanin M, et al. Neurology. 2001 Mar 13;56(5):660-5. doi: 10.1212/wnl.56.5.660. Neurology. 2001. PMID: 11245721

5

The role of botulinum toxin injection and upper esophageal sphincter myotomy in treating oropharyngeal dysphagia.

Zaninotto G, Marchese Ragona R, Briani C, Costantini M, Rizzetto C, Portale G, Zanetti L, Masiero S, Costantino M, Nicoletti L, Polidoro A, Feltrin G, Angelini C, Ancona E, Guidolin D, Parenti AR. Zaninotto G, et al. J Gastrointest Surg. 2004 Dec;8(8):997-1006. doi: 10.1016/j.gassur.2004.09.037. J Gastrointest Surg. 2004. PMID: 15585387

6

Acute quadriplegic myopathy in a 17-month-old boy.

Salviati L, Laverda AM, Zancan L, Fanin M, Angelini C, Meznaric-Petrusa M. Salviati L, et al. J Child Neurol. 2000 Jan;15(1):63-6. doi: 10.1177/088307380001500115. J Child Neurol. 2000. PMID: 10641615

7

Laminin alpha2 muscular dystrophy: genotype/phenotype studies of 22 patients.

Pegoraro E, Marks H, Garcia CA, Crawford T, Mancias P, Connolly AM, Fanin M, Martinello F, Trevisan CP, Angelini C, Stella A, Scavina M, Munk RL, Servidei S, Bönnemann CC, Bertorini T, Acsadi G, Thompson CE, Gagnon D, Hoganson G, Carver V, Zimmerman RA, Hoffman EP. Pegoraro E, et al. Neurology. 1998 Jul;51(1):101-10. doi: 10.1212/wnl.51.1.101. Neurology. 1998. PMID: 9674786

8

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. 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

9

Private beta- and gamma-sarcoglycan gene mutations: evidence of a founder effect in Northern Italy.

Fanin M, Hoffman EP, Angelini C, Pegoraro E. Fanin M, et al. Hum Mutat. 2000;16(1):13-7. doi: 10.1002/1098-1004(200007)16:1<13::AID-HUMU3>3.0.CO;2-V. Hum Mutat. 2000. PMID: 10874299

10

Radiological evidence of subclinical dysphagia in motor neuron disease.

Briani C, Marcon M, Ermani M, Costantini M, Bottin R, Iurilli V, Zaninotto G, Primon D, Feltrin G, Angelini C. Briani C, et al. J Neurol. 1998 Apr;245(4):211-6. doi: 10.1007/s004150050207. J Neurol. 1998. PMID: 9591222

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