Casari G - Search Results

1

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

2

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

3

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

4

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

5

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.

6

Haploinsufficiency of AFG3L2, the gene responsible for spinocerebellar ataxia type 28, causes mitochondria-mediated Purkinje cell dark degeneration.

Maltecca F, Magnoni R, Cerri F, Cox GA, Quattrini A, Casari G. Maltecca F, et al. Among authors: casari g. J Neurosci. 2009 Jul 22;29(29):9244-54. doi: 10.1523/JNEUROSCI.1532-09.2009. J Neurosci. 2009. PMID: 19625515 Free PMC article.

7

Novel rat calpastatin mRNA variants.

Servadio A, Casari G. Servadio A, et al. Among authors: casari g. Biochem Mol Biol Int. 1993 Jul;30(4):721-5. Biochem Mol Biol Int. 1993. PMID: 8401330

8

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

9

Benign adult familial myoclonic epilepsy (BAFME): evidence of an extended founder haplotype on chromosome 2p11.1-q12.2 in five Italian families.

Madia F, Striano P, Di Bonaventura C, de Falco A, de Falco FA, Manfredi M, Casari G, Striano S, Minetti C, Zara F. Madia F, et al. Among authors: casari g. Neurogenetics. 2008 May;9(2):139-42. doi: 10.1007/s10048-008-0118-4. Epub 2008 Jan 30. Neurogenetics. 2008. PMID: 18231815

10

The mitochondrial protease AFG3L2 is essential for axonal development.

Maltecca F, Aghaie A, Schroeder DG, Cassina L, Taylor BA, Phillips SJ, Malaguti M, Previtali S, Guénet JL, Quattrini A, Cox GA, Casari G. Maltecca F, et al. Among authors: casari g. J Neurosci. 2008 Mar 12;28(11):2827-36. doi: 10.1523/JNEUROSCI.4677-07.2008. J Neurosci. 2008. PMID: 18337413 Free PMC article.

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