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Published in Molecular biology of the cell (01.01.2006)
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DNA damage signatures in peripheral blood cells as biomarkers in prodromal huntington disease
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Autosomal dominant cerebellar ataxia type I. Clinical and molecular study in 36 Italian families including a comparison between SCA1 and SCA2 phenotypes
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Published in Journal of the neurological sciences (01.10.1996)
Published in Journal of the neurological sciences (01.10.1996)
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Can telomere shortening in human peripheral blood leukocytes serve as a disease biomarker of Friedreich's ataxia?
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Published in Antioxidants & redox signaling (10.04.2013)
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PPAR-γ Agonist Azelaoyl PAF Increases Frataxin Protein and mRNA Expression. New Implications for the Friedreich’s Ataxia Therapy
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Published in Cerebellum (London, England) (01.06.2009)
Published in Cerebellum (London, England) (01.06.2009)
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Recombinant Human Erythropoietin Increases Frataxin Protein Expression Without Increasing mRNA Expression
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Published in Cerebellum (London, England) (01.09.2008)
Published in Cerebellum (London, England) (01.09.2008)
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Shorter telomeres in patients with cerebral autosomal dominant arteriopathy and leukoencephalopathy (CADASIL)
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Published in Neurogenetics (01.11.2011)
Published in Neurogenetics (01.11.2011)
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Reduced striatal [123I]FP-CIT binding in SCA2 patients without parkinsonism
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Published in Annals of neurology (01.03.2004)
Published in Annals of neurology (01.03.2004)
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PPAR-[gamma] Agonist Azelaoyl PAF Increases Frataxin Protein and mRNA Expression. New Implications for the Friedreich's Ataxia Therapy
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Published in Cerebellum (London, England) (01.06.2009)
Published in Cerebellum (London, England) (01.06.2009)
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Analysis of DTC nutrigenetic services in Italy: state of the art, agreement to the ESHG statement and future outlooks
Cocozza, Sergio, Pinelli, Michele, Cinque, Vincenzo, Acquaviva, Fabio, Vergara, Paola, Cianflone, Alessandra, Castaldo, Imma, Monticelli, Antonella
Published in Nature precedings (03.04.2012)
Published in Nature precedings (03.04.2012)
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Pro 12Ala polymorphism of the PPARγ2 locus modulates the relationship between energy intake and body weight in type 2 diabetic patients
VACCARO, Olga, LAPICE, Emanuela, RICCARDI, Gabriele, MONTICELLI, Antonella, GIACCHETTI, Manuela, CASTALDO, Imma, GALASSO, Rocco, PINELLI, Michele, DONNARUMMA, Giovanna, RIVELLESE, Angela A, COCOZZA, Sergio
Published in Diabetes care (01.05.2007)
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Published in Diabetes care (01.05.2007)
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Pro12Ala polymorphism of the PPARgamma2 locus modulates the relationship between energy intake and body weight in type 2 diabetic patients
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Published in Diabetes care (01.05.2007)
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Published in Diabetes care (01.05.2007)
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Analysis of (CAG)n size heterogeneity in somatic and sperm cell DNA from intermediate and expanded Huntington disease gene carriers
Giovannone, Barbara, Sabbadini, Guglielmo, Di Maio, Luigi, Calabrese, Olga, Castaldo, Imma, Frontali, Marina, Novelletto, Andrea, Squitieri, Ferdinando
Published in Human mutation (1997)
Published in Human mutation (1997)
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Determinants of cognitive disorders in Autosomal Dominant Cerebellar Ataxia type 1
Trojano, Luigi, Chiacchio, Laura, Grossi, Dario, Pisacreta, Anna Italia, Calabrese, Olga, Castaldo, Imma, De Michele, Giuseppe, Filla, Alessandro
Published in Journal of the neurological sciences (07.05.1998)
Published in Journal of the neurological sciences (07.05.1998)
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Linkage disequilibrium between FD1-D9S202 haplotypes and the Friedreich's ataxia locus in a central-southern Italian population
Pianese, L, Cocozza, S, Campanella, G, Castaldo, I, Cavalcanti, F, De Michele, G, Filla, A, Monticelli, A, Munaro, M, Redolfi, E
Published in Journal of medical genetics (01.02.1994)
Published in Journal of medical genetics (01.02.1994)
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Conference Proceeding
Cerebellar vermis aplasia: Patient report and exclusion of the candidate genes EN2 and ZIC1
Titomanlio, Luigi, Pierri, Nicola Brunetti, Romano, Alfonso, Imperati, Floriana, Borrelli, Melissa, Barletta, Valentina, Diano, Alvaro Antonio, Castaldo, Imma, Santoro, Lucio, Del Giudice, Ennio
Published in American Journal of Medical Genetics Part A (15.07.2005)
Published in American Journal of Medical Genetics Part A (15.07.2005)
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