BONATO, GIULIA

BONATO, GIULIA  

Università di Padova  

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Risultati 1 - 13 di 13 (tempo di esecuzione: 0.033 secondi).
Titolo Data di pubblicazione Autori Rivista Serie Titolo libro
An adult patient with 3-methylglutaconic aciduria type 1 and movement disorders 2022 Lerjefors, LBonato, GBertolin, CSalviati, LCarecchio, M + JOURNAL OF NEUROLOGY - -
Antiphospholipid-Related Chorea: Two Case Reports and Role of Metabolic Imaging 2022 Lerjefors, LisaAndretta, SilviaBonato, GiuliaMainardi, MicheleCarecchio, MiryamAntonini, Angelo MOVEMENT DISORDERS CLINICAL PRACTICE - -
Correction to: Frontotemporal dementia phenotype in late-onset Huntington disease without chorea (Neurological Sciences, (2023), 44, 9, (3327-3329), 10.1007/s10072-023-06823-8) 2023 Bonato G.Cecchin D.Cagnin A. + NEUROLOGICAL SCIENCES - -
Deep brain stimulation of globus pallidus internus and subthalamic nucleus in Parkinson’s disease: a multicenter, retrospective study of efficacy and safety 2023 Bonato G.Weis L.Biundo R.Ferreri F.Landi A.Guerra A.Antonini A. + NEUROLOGICAL SCIENCES - -
Deep brain stimulation of globus pallidus internus and subthalamic nucleus in Parkinson’s disease: a multicenter, retrospective study of efficacy and safety 2024 Bonato G.Weis L.Biundo R.Ferreri F.Landi A.Guerra A.Antonini A. + NEUROLOGICAL SCIENCES - -
Dominant VPS16 Pathogenic Variants: Not Only Isolated Dystonia 2023 Bonato G.Carecchio M. + MOVEMENT DISORDERS CLINICAL PRACTICE - -
Expanding the genetics and phenotypic spectrum of Lysine-specific demethylase 5C (KDM5C): a report of 13 novel mutations 2023 Emanuela LeonardiMaria Cristina AspromonteElisa BettellaRoberta PolliGiulia BonatoSerena PellegrinMiryam CarecchioAlessandra Murgia + EUROPEAN JOURNAL OF HUMAN GENETICS - -
Frontotemporal dementia phenotype in late-onset Huntington disease without chorea 2023 Giulia, BonatoDiego, CecchinAnnachiara, Cagnin + NEUROLOGICAL SCIENCES - -
Genetic mutations in Parkinson’s disease: screening of a selected population from North-Eastern Italy 2024 Bonato, GiuliaAntonini, AngeloCampagnolo, MartaGuerra, AndreaBiundo, RobertaSalviati, LeonardoCarecchio, Miryam + NEUROLOGICAL SCIENCES - -
Increased glucosylsphingosine levels and Gaucher disease in GBA1-associated Parkinson's disease 2024 Carecchio M.Bonato G. + PARKINSONISM & RELATED DISORDERS - -
Non-Motor Symptoms in Primary Familial Brain Calcification 2024 Bonato G.Salviati L.Carecchio M. + JOURNAL OF CLINICAL MEDICINE - -
Rapidly progressive multiple system atrophy in a patient carrying LRRK2 G2019S mutation 2023 Bonato, GiuliaEmmi, AronCampagnolo, MartaMusso, GiuliaCarecchio, MiryamAntonini, Angelo + NEUROLOGICAL SCIENCES - -
The clinical and genetic spectrum of primary familial brain calcification 2023 Carecchio, MiryamBonato, Giulia + JOURNAL OF NEUROLOGY - -