I Castaldo
Overview
Explore the profile of I Castaldo including associated specialties, affiliations and a list of published articles.
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Articles
16
Citations
247
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0
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Recent Articles
1.
De Joanna G, De Rosa A, Salvatore E, Castaldo I, De Luca N, Izzo R, et al.
J Neurol Sci
. 2008 Aug;
275(1-2):60-3.
PMID: 18755482
Autonomic nervous system dysfunction is part of the spinocerebellar ataxia (SCA) clinical picture, but few data are available on this topic. The present study is aimed to report a detailed...
2.
Castaldo I, Pinelli M, Monticelli A, Acquaviva F, Giacchetti M, Filla A, et al.
J Med Genet
. 2008 Aug;
45(12):808-12.
PMID: 18697824
Background: The most frequent mutation of Friedreich ataxia (FRDA) is the abnormal expansion of a GAA repeat located within the first intron of FXN gene. It is known that the...
3.
Ragno M, Perretti A, Castaldo I, Scarcella M, Acciarri S, Manganelli F, et al.
Neurol Sci
. 2005 Jul;
26(2):67-71.
PMID: 15995822
The objective was to determine the progression of nervous system involvement in spinocerebellar ataxia type 1 (SCA1). Three presymptomatic members of an Italian SCA1 family underwent molecular analysis and showed...
4.
Maltecca F, Filla A, Castaldo I, Coppola G, Fragassi N, Carella M, et al.
Neurology
. 2003 Nov;
61(10):1441-3.
PMID: 14638975
The authors describe an Italian family with autosomal dominant ataxia, dementia, psychiatric and extrapyramidal features, epilepsy, mild sensorimotor axonal neuropathy, and MRI findings of cerebral and cerebellar atrophy. A child...
5.
Filla A, De Michele G, Cocozza S, Patrignani A, Volpe G, Castaldo I, et al.
Neurology
. 2002 Mar;
58(6):922-8.
PMID: 11914409
Objective: To perform a clinical and molecular study of a large autosomal dominant family with a complex neurologic syndrome that comprises early-onset dementia, extrapyramidal and cerebellar features, and epilepsy. Background:...
6.
Barbieri F, Pellecchia M, Esposito E, Di Stasio E, Castaldo I, Santorelli F, et al.
Neurology
. 2001 May;
56(10):1412-4.
PMID: 11376202
Two brothers presented with late-onset cerebellar ataxia and severe dysphonia. Brain MRI showed vermian and hemispheric cerebellar atrophy. Laringofiberscopy revealed laryngeal abductor paralysis in both patients. Neurophysiologic studies showed a...
7.
Filla A, Mariotti C, Caruso G, Coppola G, Cocozza S, Castaldo I, et al.
Eur Neurol
. 2000 Jul;
44(1):31-6.
PMID: 10894992
Two hundred and forty-eight patients from 116 Italian families with dominant ataxia were studied for CAG expansion within SCA1, 2, 3, 6, 7 (spinocerebellar ataxia) and DRPLA (dentatorubropallidoluysian atrophy) genes....
8.
Filla A, De Michele G, Santoro L, Calabrese O, Castaldo I, Giuffrida S, et al.
J Neurol
. 1999 Aug;
246(6):467-71.
PMID: 10431773
Autosomal dominant cerebellar ataxia type I is the most common form of dominant ataxia. A genetic heterogeneity has been identified with five different loci (SCA1, 2, 3, 4, and 6)....
9.
Trojano L, Chiacchio L, Grossi D, Pisacreta A, Calabrese O, Castaldo I, et al.
J Neurol Sci
. 1998 Jun;
157(2):162-7.
PMID: 9619640
We assessed neuropsychological performances of 22 patients affected by Autosomal Dominant Cerebellar Ataxia type 1. All subjects completed a comprehensive battery of standardized tests requiring a verbal response, without time...
10.
Pianese L, Cavalcanti F, De Michele G, Filla A, Campanella G, Calabrese O, et al.
Am J Hum Genet
. 1997 Feb;
60(2):460-3.
PMID: 9012421
No abstract available.