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

Academic Article
Publication Date:
2018
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.
CRIS type:
1.1 Articolo in rivista
Keywords:
SARA scale; ataxia and gait disorders; ataxia-telangiectasia; betamethasone; primary immunodeficiency
List of contributors:
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; Plebani, A; Pignata, C
Handle:
https://iris.unibs.it/handle/11379/507345
Published in:
EUROPEAN JOURNAL OF NEUROLOGY
Journal
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