Monticelli A - Search Results

1

Serum transferrin receptor levels in Friedreich's and other degenerative ataxias.

Scarano V, de Cristofaro T, De Michele G, Salvatore E, De Biase I, Monticelli A, Filla A, Cocozza S. Scarano V, et al. Among authors: monticelli a. Neurology. 2001 Jul 10;57(1):159-60. doi: 10.1212/wnl.57.1.159. Neurology. 2001. PMID: 11445653 No abstract available.

2

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: monticelli a. 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.

3

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: monticelli a. J Neurol. 1993;240(4):254-6. doi: 10.1007/BF00818715. J Neurol. 1993. PMID: 8496716

4

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: monticelli a. Neurology. 1997 Dec;49(6):1617-20. doi: 10.1212/wnl.49.6.1617. Neurology. 1997. PMID: 9409356

5

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: monticelli a. J Neurol. 1998 Mar;245(3):166-8. doi: 10.1007/s004150050198. J Neurol. 1998. PMID: 9553847

6

Relation between trinucleotide GAA repeat length and sensory neuropathy in Friedreich's ataxia.

Santoro L, De Michele G, Perretti A, Crisci C, Cocozza S, Cavalcanti F, Ragno M, Monticelli A, Filla A, Caruso G. Santoro L, et al. Among authors: monticelli a. J Neurol Neurosurg Psychiatry. 1999 Jan;66(1):93-6. doi: 10.1136/jnnp.66.1.93. J Neurol Neurosurg Psychiatry. 1999. PMID: 9886462 Free PMC article.

7

Atypical Friedreich ataxia phenotype associated with a novel missense mutation in the X25 gene.

De Michele G, Filla A, Cavalcanti F, Tammaro A, Monticelli A, Pianese L, Di Salle F, Perreti A, Santoro L, Caruso G, Cocozza S. De Michele G, et al. Among authors: monticelli a. Neurology. 2000 Jan 25;54(2):496-9. doi: 10.1212/wnl.54.2.496. Neurology. 2000. PMID: 10668723

8

A novel mutation in SACS gene in a family from southern Italy.

Criscuolo C, Banfi S, Orio M, Gasparini P, Monticelli A, Scarano V, Santorelli FM, Perretti A, Santoro L, De Michele G, Filla A. Criscuolo C, et al. Among authors: monticelli a. Neurology. 2004 Jan 13;62(1):100-2. doi: 10.1212/wnl.62.1.100. Neurology. 2004. PMID: 14718706 Free article.

9

Real time PCR quantification of frataxin mRNA in the peripheral blood leucocytes of Friedreich ataxia patients and carriers.

Pianese L, Turano M, Lo Casale MS, De Biase I, Giacchetti M, Monticelli A, Criscuolo C, Filla A, Cocozza S. Pianese L, et al. Among authors: monticelli a. J Neurol Neurosurg Psychiatry. 2004 Jul;75(7):1061-3. doi: 10.1136/jnnp.2003.028605. J Neurol Neurosurg Psychiatry. 2004. PMID: 15201375 Free PMC article.

10

Ataxia with oculomotor apraxia type 1 in Southern Italy: late onset and variable phenotype.

Criscuolo C, Mancini P, Saccà F, De Michele G, Monticelli A, Santoro L, Scarano V, Banfi S, Filla A. Criscuolo C, et al. Among authors: monticelli a. Neurology. 2004 Dec 14;63(11):2173-5. doi: 10.1212/01.wnl.0000145604.57000.36. Neurology. 2004. PMID: 15596775

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