Casari G - Search Results

1

Charcot-Marie-Tooth disease type 2C: a distinct genetic entity. Clinical and molecular characterization of the first European family.

Santoro L, Manganelli F, Di Maio L, Barbieri F, Carella M, D'Adamo P, Casari G. Santoro L, et al. Among authors: casari g. Neuromuscul Disord. 2002 May;12(4):399-404. doi: 10.1016/s0960-8966(01)00305-4. Neuromuscul Disord. 2002. PMID: 12062259

2

Dementia, ataxia, extrapyramidal features, and epilepsy: phenotype spectrum in two Italian families with spinocerebellar ataxia type 17.

De Michele G, Maltecca F, Carella M, Volpe G, Orio M, De Falco A, Gombia S, Servadio A, Casari G, Filla A, Bruni A. De Michele G, et al. Among authors: casari g. Neurol Sci. 2003 Oct;24(3):166-7. doi: 10.1007/s10072-003-0112-4. Neurol Sci. 2003. PMID: 14598069

3

Intergenerational instability and marked anticipation in SCA-17.

Maltecca F, Filla A, Castaldo I, Coppola G, Fragassi NA, Carella M, Bruni A, Cocozza S, Casari G, Servadio A, De Michele G. Maltecca F, et al. Among authors: casari g. Neurology. 2003 Nov 25;61(10):1441-3. doi: 10.1212/01.wnl.0000094123.09098.a0. Neurology. 2003. PMID: 14638975

4

Behavioral disorder, dementia, ataxia, and rigidity in a large family with TATA box-binding protein mutation.

Bruni AC, Takahashi-Fujigasaki J, Maltecca F, Foncin JF, Servadio A, Casari G, D'Adamo P, Maletta R, Curcio SA, De Michele G, Filla A, El Hachimi KH, Duyckaerts C. Bruni AC, et al. Among authors: casari g. Arch Neurol. 2004 Aug;61(8):1314-20. doi: 10.1001/archneur.61.8.1314. Arch Neurol. 2004. PMID: 15313853

5

A new benign adult familial myoclonic epilepsy (BAFME) pedigree suggesting linkage to chromosome 2p11.1-q12.2.

Striano P, Chifari R, Striano S, de Fusco M, Elia M, Guerrini R, Casari G, Canevini MP. Striano P, et al. Among authors: casari g. Epilepsia. 2004 Feb;45(2):190-2. doi: 10.1111/j.0013-9580.2004.39903.x. Epilepsia. 2004. PMID: 14738428 Free article.

6

A new locus for autosomal recessive hereditary spastic paraplegia maps to chromosome 16q24.3.

De Michele G, De Fusco M, Cavalcanti F, Filla A, Marconi R, Volpe G, Monticelli A, Ballabio A, Casari G, Cocozza S. De Michele G, et al. Among authors: casari g. Am J Hum Genet. 1998 Jul;63(1):135-9. doi: 10.1086/301930. Am J Hum Genet. 1998. PMID: 9634528 Free PMC article.

7

Existence of a genetic risk factor on chromosome 5q in Italian coeliac disease families.

Greco L, Babron MC, Corazza GR, Percopo S, Sica R, Clot F, Fulchignoni-Lataud MC, Zavattari P, Momigliano-Richiardi P, Casari G, Gasparini P, Tosi R, Mantovani V, De Virgiliis S, Iacono G, D'Alfonso A, Selinger-Leneman H, Lemainque A, Serre JL, Clerget-Darpoux F. Greco L, et al. Among authors: casari g. Ann Hum Genet. 2001 Jan;65(Pt 1):35-41. doi: 10.1046/j.1469-1809.2001.6510035.x. Ann Hum Genet. 2001. PMID: 11415521

8

Early onset autosomal dominant dementia with ataxia, extrapyramidal features, and epilepsy.

Filla A, De Michele G, Cocozza S, Patrignani A, Volpe G, Castaldo I, Ruggiero G, Bonavita V, Masters C, Casari G, Bruni A. Filla A, et al. Among authors: casari g. Neurology. 2002 Mar 26;58(6):922-8. doi: 10.1212/wnl.58.6.922. Neurology. 2002. PMID: 11914409

9

Further evidence of genetic heterogeneity in familial essential tremor.

Aridon P, Ragonese P, De Fusco M, Salemi G, Casari G, Savettieri G. Aridon P, et al. Among authors: casari g. Parkinsonism Relat Disord. 2008;14(1):15-8. doi: 10.1016/j.parkreldis.2007.05.002. Epub 2007 Aug 20. Parkinsonism Relat Disord. 2008. PMID: 17703985

10

Axonal degeneration in paraplegin-deficient mice is associated with abnormal mitochondria and impairment of axonal transport.

Ferreirinha F, Quattrini A, Pirozzi M, Valsecchi V, Dina G, Broccoli V, Auricchio A, Piemonte F, Tozzi G, Gaeta L, Casari G, Ballabio A, Rugarli EI. Ferreirinha F, et al. Among authors: casari g. J Clin Invest. 2004 Jan;113(2):231-42. doi: 10.1172/JCI20138. J Clin Invest. 2004. PMID: 14722615 Free PMC article.

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