Ataxia-telangiectasia (A-T) is a rare neurodegenerative disease, due to A-T mutated (ATM) gene mutations, which typically presents with signs of progressive neurological dysfunction, cerebellar ataxia and uncoordinated movements. A-T severely affects patients' quality of life. Successful treatment options are still not available. The aim of this multicenter study, performed with a blind evaluation procedure, was to define the minimal effective dosage of oral betamethasone, thus preventing the occurrence of side effects.

Minimum effective betamethasone dosage on the neurological phenotype in patients with ataxia-telangiectasia: a multicenter observer-blind study

DEL GIUDICE, ERIKA;
2018-01-01

Abstract

Ataxia-telangiectasia (A-T) is a rare neurodegenerative disease, due to A-T mutated (ATM) gene mutations, which typically presents with signs of progressive neurological dysfunction, cerebellar ataxia and uncoordinated movements. A-T severely affects patients' quality of life. Successful treatment options are still not available. The aim of this multicenter study, performed with a blind evaluation procedure, was to define the minimal effective dosage of oral betamethasone, thus preventing the occurrence of side effects.
2018
2018
Altra università italiana
LS5_11 Neurological disorders (e.g. Alzheimer's disease, Huntington's disease, Parkinson's disease)
Esperti anonimi
Inglese
Internazionale
ELETTRONICO
SARA scale; ataxia and gait disorders; ataxia-telangiectasia; betamethasone; primary immunodeficiency
Ateneo di appartenenza
12
info:eu-repo/semantics/article
262
Cirillo, E; DEL GIUDICE, Erika; Micheli, R; Cappellari, A M; Soresina, A; Dellepiane, R M; Pietrogrande, M C; Dell'Era, L; Specchia, F; Pession, A; Pl...espandi
1 Contributo su Rivista::1.1 Articolo in rivista
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11379/507345
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