Imma Castaldo
Imma Castaldo
Dipartimento di Biologia e Patologia Cellulare e Molecolare UniversitÓ "Federico II" di Napoli
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Mitochondrial AKAP121 links cAMP and src signaling to oxidative metabolism
A Livigni, A Scorziello, S Agnese, A Adornetto, A Carlucci, C Garbi, ...
Molecular biology of the cell 17 (1), 263-271, 2006
Late onset Friedreich's disease: clinical features and mapping of mutation to the FRDA locus.
G De Michele, A Filla, F Cavalcanti, L Di Maio, L Pianese, I Castaldo, ...
Journal of Neurology, Neurosurgery & Psychiatry 57 (8), 977-979, 1994
DNA methylation in intron 1 of the frataxin gene is related to GAA repeat length and age of onset in Friedreich ataxia patients
I Castaldo, M Pinelli, A Monticelli, F Acquaviva, M Giacchetti, A Filla, ...
Journal of medical genetics 45 (12), 808-812, 2008
Intergenerational instability and marked anticipation in SCA-17
F Maltecca, A Filla, I Castaldo, G Coppola, NA Fragassi, M Carella, ...
Neurology 61 (10), 1441-1443, 2003
Somatic mosaicism in sperm is associated with intergenerational (CAG) n changes in Huntington disease
H Telenius, E Almqvist, B Kremer, N Spence, F Squitieri, K Nichol, ...
Human molecular genetics 4 (2), 189-195, 1995
The effect of parental gender on the GAA dynamic mutation in the FRDA gene.
L Pianese, F Cavalcanti, G De Michele, A Filla, G Campanella, ...
American journal of human genetics 60 (2), 460, 1997
Relative frequencies of CAG expansions in spinocerebellar ataxia and dentatorubropallidoluysian atrophy in 116 Italian families
A Filla, C Mariotti, G Caruso, G Coppola, S Cocozza, I Castaldo, ...
European neurology 44 (1), 31-36, 2000
Spinocerebellar ataxia type 2 in southern Italy: a clinical and molecular study of 30 families
A Filla, G De Michele, L Santoro, O Calabrese, I Castaldo, S Giuffrida, ...
Journal of neurology 246, 467-471, 1999
Recombinant human erythropoietin increases frataxin protein expression without increasing mRNA expression
F Acquaviva, I Castaldo, A Filla, M Giacchetti, D Marmolino, A Monticelli, ...
The Cerebellum 7, 360-365, 2008
PPAR-γ agonist azelaoyl PAF increases frataxin protein and mRNA expression. New implications for the friedreich’s ataxia therapy
D Marmolino, F Acquaviva, M Pinelli, A Monticelli, I Castaldo, A Filla, ...
The Cerebellum 8, 98-103, 2009
Pro12Ala polymorphism of the PPARγ2 locus modulates the relationship between energy intake and body weight in type 2 diabetic patients
O Vaccaro, E Lapice, A Monticelli, M Giacchetti, I Castaldo, R Galasso, ...
Diabetes care 30 (5), 1156-1161, 2007
Reduced striatal [123I]FP‐CIT binding in SCA2 patients without parkinsonism
A Varrone, E Salvatore, G De Michele, P Barone, V Sansone, ...
Annals of Neurology: Official Journal of the American Neurologicalá…, 2004
Has spinocerebellar ataxia type 2 a distinct phenotype? Genetic and clinical study of an Italian family
A Filla, G De Michele, S Banfi, L Santoro, A Perretti, F Cavalcanti, ...
Neurology 45 (4), 793-796, 1995
Autosomal dominant cerebellar ataxia type I. Clinical and molecular study in 36 Italian families including a comparison between SCA1 and SCA2 phenotypes
A Filla, G De Michele, G Campanella, A Perretti, L Santoro, L Serlenga, ...
Journal of the neurological sciences 142 (1-2), 140-147, 1996
DNA damage signatures in peripheral blood cells as biomarkers in prodromal huntington disease
I Castaldo, M De Rosa, A Romano, C Zuchegna, F Squitieri, R Mechelli, ...
Annals of neurology 85 (2), 296-301, 2019
Autonomic nervous system abnormalities in spinocerebellar ataxia type 2: a cardiovascular neurophysiologic study
G De Joanna, A De Rosa, E Salvatore, I Castaldo, N De Luca, R Izzo, ...
Journal of the neurological sciences 275 (1-2), 60-63, 2008
Predictors of survival in a Huntington's disease population from southern Italy
C Rinaldi, E Salvatore, I Giordano, S De Matteis, T Tucci, VR Cinzia, ...
Canadian journal of neurological sciences 39 (1), 48-51, 2012
Analysis of (CAG) n size heterogeneity in somatic and sperm cell DNA from intermediate and expanded Huntington disease gene carriers
B Giovannone, G Sabbadini, L Di Maio, O Calabrese, I Castaldo, ...
Human Mutation 10 (6), 458-464, 1997
Early onset autosomal dominant dementia with ataxia, extrapyramidal features, and epilepsy
A Filla, G De Michele, S Cocozza, A Patrignani, G Volpe, I Castaldo, ...
Neurology 58 (6), 922-928, 2002
Multimodal electrophysiologic follow-up study in 3 mutated but presymptomatic members of a spinocerebellar ataxia type 1 (SCA1) family
M Ragno, AC Perretti, I Castaldo, M Scarcella, S Acciarri, F Manganelli, ...
Neurological Sciences 26, 67-71, 2005
Il sistema al momento non pu˛ eseguire l'operazione. Riprova pi¨ tardi.
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