Pianese L - Search Results

1

Determinants of onset age in Friedreich's ataxia.

De Michele G, Filla A, Criscuolo C, Scarano V, Cavalcanti F, Pianese L, Monticelli A, Cocozza S. De Michele G, et al. Among authors: pianese l. J Neurol. 1998 Mar;245(3):166-8. doi: 10.1007/s004150050198. J Neurol. 1998. PMID: 9553847

2

Identification of a novel transcript of X25, the human gene involved in Friedreich ataxia.

Pianese L, Tammaro A, Turano M, De Biase I, Monticelli A, Cocozza S. Pianese L, et al. Neurosci Lett. 2002 Mar 8;320(3):137-40. doi: 10.1016/s0304-3940(02)00048-4. Neurosci Lett. 2002. PMID: 11852181

3

Up-regulation of c-Jun N-terminal kinase pathway in Friedreich's ataxia cells.

Pianese L, Busino L, De Biase I, De Cristofaro T, Lo Casale MS, Giuliano P, Monticelli A, Turano M, Criscuolo C, Filla A, Varrone S, Cocozza S. Pianese L, et al. Hum Mol Genet. 2002 Nov 1;11(23):2989-96. doi: 10.1093/hmg/11.23.2989. Hum Mol Genet. 2002. PMID: 12393810

4

New clues on the origin of the Friedreich ataxia expanded alleles from the analysis of new polymorphisms closely linked to the mutation.

Monticelli A, Giacchetti M, De Biase I, Pianese L, Turano M, Pandolfo M, Cocozza S. Monticelli A, et al. Among authors: pianese l. Hum Genet. 2004 Apr;114(5):458-63. doi: 10.1007/s00439-004-1089-7. Epub 2004 Feb 7. Hum Genet. 2004. PMID: 14767759

5

Friedreich's disease. A linkage study in southern and central Italy.

Cavalcanti F, Cocozza S, Filla A, De Michele G, Pianese L, Porcellini A, Monticelli A, Pandolfo M, Banfi S, Varrone S, et al. Cavalcanti F, et al. Among authors: pianese l. Acta Neurol (Napoli). 1992 Aug-Dec;14(4-6):519-23. Acta Neurol (Napoli). 1992. PMID: 1363458

6

Has spinocerebellar ataxia type 2 a distinct phenotype? Genetic and clinical study of an Italian family.

Filla A, De Michele G, Banfi S, Santoro L, Perretti A, Cavalcanti F, Pianese L, Castaldo I, Barbieri F, Campanella G, et al. Filla A, et al. Among authors: pianese l. Neurology. 1995 Apr;45(4):793-6. doi: 10.1212/wnl.45.4.793. Neurology. 1995. PMID: 7723972

7

Late onset Friedreich's disease: clinical features and mapping of mutation to the FRDA locus.

De Michele G, Filla A, Cavalcanti F, Di Maio L, Pianese L, Castaldo I, Calabrese O, Monticelli A, Varrone S, Campanella G, et al. De Michele G, et al. Among authors: pianese l. J Neurol Neurosurg Psychiatry. 1994 Aug;57(8):977-9. doi: 10.1136/jnnp.57.8.977. J Neurol Neurosurg Psychiatry. 1994. PMID: 8057123 Free PMC article.

8

Evidence of a genetic marker associated with early onset in Friedreich's ataxia.

Cocozza S, Antonelli A, Campanella G, Cavalcanti F, De Michele G, Di Donato S, Filla A, Monticelli A, Pianese L, Piccinelli A, et al. Cocozza S, et al. Among authors: pianese l. J Neurol. 1993;240(4):254-6. doi: 10.1007/BF00818715. J Neurol. 1993. PMID: 8496716

9

The relationship between trinucleotide (GAA) repeat length and clinical features in Friedreich ataxia.

Filla A, De Michele G, Cavalcanti F, Pianese L, Monticelli A, Campanella G, Cocozza S. Filla A, et al. Among authors: pianese l. Am J Hum Genet. 1996 Sep;59(3):554-60. Am J Hum Genet. 1996. PMID: 8751856 Free PMC article.

10

Broadened Friedreich's ataxia phenotype after gene cloning. Minimal GAA expansion causes late-onset spastic ataxia.

Ragno M, De Michele G, Cavalcanti F, Pianese L, Monticelli A, Curatola L, Bollettini F, Cocozza S, Caruso G, Santoro L, Filla A. Ragno M, et al. Among authors: pianese l. Neurology. 1997 Dec;49(6):1617-20. doi: 10.1212/wnl.49.6.1617. Neurology. 1997. PMID: 9409356

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