Ragno M - Search Results

1

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy, genetic homogeneity, and mapping of the locus within a 2-cM interval.

Ducros A, Nagy T, Alamowitch S, Nibbio A, Joutel A, Vahedi K, Chabriat H, Iba-Zizen MT, Julien J, Davous P, Goas JY, Lyon-Caen O, Dubois B, Ducrocq X, Salsa F, Ragno M, Burkhard P, Bassetti C, Hutchinson M, Vérin M, Viader F, Chapon F, Levasseur M, Mas JL, Delrieu O, et al. Ducros A, et al. Among authors: ragno m. Am J Hum Genet. 1996 Jan;58(1):171-81. Am J Hum Genet. 1996. PMID: 8554054 Free PMC article.

2

An Italian kindred with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL).

Ragno M, Tournier-Lasserve E, Fiori MG, Manca A, Patrosso MC, Ferlini A, Sirocchi G, Trojano L, Chabriat H, Salvi F. Ragno M, et al. Ann Neurol. 1995 Aug;38(2):231-6. doi: 10.1002/ana.410380216. Ann Neurol. 1995. PMID: 7654071

3

A kindred affected by cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL). A 2-year neuropsychological follow-up.

Trojano L, Ragno M, Manca A, Caruso G. Trojano L, et al. Among authors: ragno m. J Neurol. 1998 Apr;245(4):217-22. doi: 10.1007/s004150050208. J Neurol. 1998. PMID: 9591223

4

Charcot-Marie-Tooth disease: molecular characterization of patients from central and southern Italy.

Guzzetta V, Santoro L, Gasparo-Rippa P, Ragno M, Vita G, Caruso G, Andria G. Guzzetta V, et al. Among authors: ragno m. Clin Genet. 1995 Jan;47(1):27-32. doi: 10.1111/j.1399-0004.1995.tb03917.x. Clin Genet. 1995. PMID: 7774040

5

High recurrence of the R1006C NOTCH3 mutation in central Italian patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL).

Cappelli A, Ragno M, Cacchiò G, Scarcella M, Staffolani P, Pianese L. Cappelli A, et al. Among authors: ragno m. Neurosci Lett. 2009 Sep 22;462(2):176-8. doi: 10.1016/j.neulet.2009.06.087. Epub 2009 Jul 2. Neurosci Lett. 2009. PMID: 19576955

6

Androgen receptor gene (CAG)n repeat analysis in the differential diagnosis between Kennedy disease and other motoneuron disorders.

Ferlini A, Patrosso MC, Guidetti D, Merlini L, Uncini A, Ragno M, Plasmati R, Fini S, Repetto M, Vezzoni P, et al. Ferlini A, et al. Among authors: ragno m. Am J Med Genet. 1995 Jan 2;55(1):105-11. doi: 10.1002/ajmg.1320550125. Am J Med Genet. 1995. PMID: 7702080

7

Genome-wide genotyping demonstrates a polygenic risk score associated with white matter hyperintensity volume in CADASIL.

Opherk C, Gonik M, Duering M, Malik R, Jouvent E, Hervé D, Adib-Samii P, Bevan S, Pianese L, Silvestri S, Dotti MT, De Stefano N, Liem M, Boon EM, Pescini F, Pachai C, Bracoud L, Müller-Myhsok B, Meitinger T, Rost N, Pantoni L, Lesnik Oberstein S, Federico A, Ragno M, Markus HS, Tournier-Lasserve E, Rosand J, Chabriat H, Dichgans M. Opherk C, et al. Among authors: ragno m. Stroke. 2014 Apr;45(4):968-72. doi: 10.1161/STROKEAHA.113.004461. Epub 2014 Feb 27. Stroke. 2014. PMID: 24578207 Free article.

8

Two novel Italian CADASIL families from Central Italy with mutation CGC-TGC at codon 1006 in the exon 19 Notch3 gene.

Ragno M, Fabrizi GM, Cacchiò G, Scarcella M, Sirocchi G, Selvaggio F, Taioli F, Ferrarini M, Trojano L. Ragno M, et al. Neurol Sci. 2006 Sep;27(4):252-6. doi: 10.1007/s10072-006-0679-7. Neurol Sci. 2006. PMID: 16998728

9

Renal involvement in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL): report of a case with a six-year follow-up.

Ragno M, Trojano L, Pianese L, Boni MV, Silvestri S, Mambelli V, Lorenzi T, Scarpelli M, Morroni M. Ragno M, et al. Histol Histopathol. 2012 Oct;27(10):1307-14. doi: 10.14670/HH-27.1307. Histol Histopathol. 2012. PMID: 22936449

10

"CADASIL coma" in an Italian homozygous CADASIL patient: comparison with clinical and MRI findings in age-matched heterozygous patients with the same G528C NOTCH3 mutation.

Ragno M, Pianese L, Morroni M, Cacchiò G, Manca A, Di Marzio F, Silvestri S, Miceli C, Scarcella M, Onofrj M, Trojano L. Ragno M, et al. Neurol Sci. 2013 Nov;34(11):1947-53. doi: 10.1007/s10072-013-1418-5. Epub 2013 Apr 10. Neurol Sci. 2013. PMID: 23572112

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