Ferrone M - Search Results

1

Mutations in the POLG1 gene are not a relevant cause of cerebellar ataxia in Italy.

Cagnoli C, Brussino A, Di Gregorio E, Caroppo P, Stola S, Dragone E, Ferrone M, Padovan S, Migone N, Orsi L, Brusco A. Cagnoli C, et al. Among authors: ferrone m. J Neurol. 2008 Jul;255(7):1079-80. doi: 10.1007/s00415-008-0772-3. Epub 2008 May 5. J Neurol. 2008. PMID: 18446310 No abstract available.

2

Spinocerebellar ataxia type 12 identified in two Italian families may mimic sporadic ataxia.

Brussino A, Graziano C, Giobbe D, Ferrone M, Dragone E, Arduino C, Lodi R, Tonon C, Gabellini A, Rinaldi R, Miccoli S, Grosso E, Bellati MC, Orsi L, Migone N, Brusco A. Brussino A, et al. Among authors: ferrone m. Mov Disord. 2010 Jul 15;25(9):1269-73. doi: 10.1002/mds.22835. Mov Disord. 2010. PMID: 20629122

3

Spinocerebellar Ataxia Tethering PCR: A Rapid Genetic Test for the Diagnosis of Spinocerebellar Ataxia Types 1, 2, 3, 6, and 7 by PCR and Capillary Electrophoresis.

Cagnoli C, Brussino A, Mancini C, Ferrone M, Orsi L, Salmin P, Pappi P, Giorgio E, Pozzi E, Cavalieri S, Di Gregorio E, Ferrero M, Filla A, De Michele G, Gellera C, Mariotti C, Nethisinghe S, Giunti P, Stevanin G, Brusco A. Cagnoli C, et al. Among authors: ferrone m. J Mol Diagn. 2018 May;20(3):289-297. doi: 10.1016/j.jmoldx.2017.12.006. Epub 2018 Feb 17. J Mol Diagn. 2018. PMID: 29462666 Free article.

4

ATXN2 intermediate repeat expansions influence the clinical phenotype in frontotemporal dementia.

Rubino E, Mancini C, Boschi S, Ferrero P, Ferrone M, Bianca S, Zucca M, Orsi L, Pinessi L, Govone F, Vacca A, Gai A, Giordana MT, Brusco A, Rainero I. Rubino E, et al. Among authors: ferrone m. Neurobiol Aging. 2019 Jan;73:231.e7-231.e9. doi: 10.1016/j.neurobiolaging.2018.09.009. Epub 2018 Sep 22. Neurobiol Aging. 2019. PMID: 30342763 Free article.

5

Molecular genetic analysis of von Hippel-Lindau disease by denaturing high-performance liquid chromatography.

Menegatti E, Ferrone M, Gallone S, Mameli M, Grosso E, Migone N. Menegatti E, et al. Among authors: ferrone m. Contrib Nephrol. 2001;(136):306-11. doi: 10.1159/000060206. Contrib Nephrol. 2001. PMID: 11688398 No abstract available.

6

Congenital bilateral absence of vas deferens with a new missense mutation (P499A) in the CFTR gene.

Arduino C, Ferrone M, Brusco A, Garnerone S, Fontana D, Rolle L, Carbonara AO. Arduino C, et al. Among authors: ferrone m. Clin Genet. 1998 Mar;53(3):202-4. doi: 10.1111/j.1399-0004.1998.tb02677.x. Clin Genet. 1998. PMID: 9630075

7

Polyvariant mutant CFTR genes in patients with chronic pancreatitis.

Arduino C, Gallo M, Brusco A, Garnerone S, Piana MR, Di Maggio S, Gerbino Promis G, Ferrone M, Angeli A, Gaia E. Arduino C, et al. Among authors: ferrone m. Clin Genet. 1999 Nov;56(5):400-4. doi: 10.1034/j.1399-0004.1999.560509.x. Clin Genet. 1999. PMID: 10668931

8

Exercise intolerance and recurrent myoglobinuria as the only expression of Xp21 Becker type muscular dystrophy.

Doriguzzi C, Palmucci L, Mongini T, Chiadò-Piat L, Restagno G, Ferrone M. Doriguzzi C, et al. Among authors: ferrone m. J Neurol. 1993 May;240(5):269-71. doi: 10.1007/BF00838159. J Neurol. 1993. PMID: 8326329

9

Juvenile renal cell carcinoma as first manifestation of von Hippel-Lindau disease.

Granata A, Sessa A, Righetti M, Cordaro S, Leone G, Figura M, Fatuzzo P, Rapisarda F, Di Maria E, Ciotti P, Mandich P, Nardo A, Ferrone M, Gallone S, Liuzzo G. Granata A, et al. Among authors: ferrone m. J Nephrol. 2004 Mar-Apr;17(2):306-10. J Nephrol. 2004. PMID: 15293534

10

A polymorphism of the hypocretin receptor 2 gene is associated with cluster headache.

Rainero I, Gallone S, Valfrè W, Ferrero M, Angilella G, Rivoiro C, Rubino E, De Martino P, Savi L, Ferrone M, Pinessi L. Rainero I, et al. Among authors: ferrone m. Neurology. 2004 Oct 12;63(7):1286-8. doi: 10.1212/01.wnl.0000142424.65251.db. Neurology. 2004. PMID: 15477554

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