CARECCHIO, MIRYAM

CARECCHIO, MIRYAM  

Dipartimento di Neuroscienze - DNS  

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Risultati 1 - 20 di 72 (tempo di esecuzione: 0.03 secondi).
Titolo Data di pubblicazione Autori Rivista Serie Titolo libro
Adult diagnosis of Cockayne syndrome 2019 Carecchio M. + NEUROLOGY - -
An adult patient with 3-methylglutaconic aciduria type 1 and movement disorders 2022 Lerjefors, LBonato, GBertolin, CSalviati, LCarecchio, M + JOURNAL OF NEUROLOGY - -
Adult-Onset Focal Chorea in Fahr's Disease Resulting From SLC20A2 Mutation: A Novel Phenotype 2015 Carecchio M. + MOVEMENT DISORDERS CLINICAL PRACTICE - -
ATP1A3-related disorders: An update 2018 Carecchio M. + EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY - -
Atypical Parkinsonism with apraxia and supranuclear gaze abnormalities in type 1 Gaucher disease. Expanding the spectrum: Case report and literature review 2010 Carecchio M. + MOVEMENT DISORDERS - -
C2orf37 mutational spectrum in Woodhouse-Sakati syndrome patients 2010 Carecchio M. + CLINICAL GENETICS - -
The CACNA1B R1389H variant is not associated with myoclonus-dystonia in a large European multicentric cohort 2015 Carecchio M. + HUMAN MOLECULAR GENETICS - -
CANS: Childhood acute neuropsychiatric syndromes 2018 Carecchio M + EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY - -
Cerebellar and cortical hypometabolism in progressive stimulus-sensitive limb myoclonus in celiac disease 2021 Mozzetta S.Carecchio M.Gazzola G.Cecchin D.Cagnin A. NEUROLOGICAL SCIENCES - -
Cerebellar and cortical hypometabolism in progressive stimulus-sensitive limb myoclonus in celiac disease (Apr, 10.1007/s10072-021-05264-5, 2021) 2021 Mozzetta, SCarecchio, MGazzola, GCecchin, DCagnin, A NEUROLOGICAL SCIENCES - -
Cerebrospinal fluid biomarkers in progranulin mutations carriers 2011 Carecchio M. + JOURNAL OF ALZHEIMER'S DISEASE - -
Complex movement disorders in primary antiphospholipid syndrome: A case report 2009 Carecchio M. + JOURNAL OF THE NEUROLOGICAL SCIENCES - -
Corrigendum to “Restless legs syndrome in NKX2-1-related chorea: An expansion of the disease spectrum” (Brain and Development (2019) 41(3) (250–256), (S0387760418304959), (10.1016/j.braindev.2018.10.001)) 2019 Carecchio M.Fusco C. + BRAIN & DEVELOPMENT - -
Defective Fas-mediated T-cell apoptosis predicts acute onset CIDP 2009 Carecchio M. + JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM - -
Defining the epsilon-sarcoglycan (SGCE) gene phenotypic signature in myoclonus-dystonia: A reappraisal of genetic testing criteria 2013 Carecchio M. + MOVEMENT DISORDERS - -
Diagnosis and treatment of pediatric onset isolated dystonia 2018 Carecchio M. + EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY - -
DYT2 screening in early-onset isolated dystonia 2017 Carecchio M. + EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY - -
Early onset frontotemporal dementia with psychiatric presentation due to the C9ORF72 hexanucleotide repeat expansion: A case report 2014 Carecchio M. + BMC NEUROLOGY - -
Effect of Intensive Rehabilitation Program in Thermal Water on a Group of People with Parkinson’s Disease: A Retrospective Longitudinal Study 2022 Di Marco, RobertoPistonesi, FrancescaCianci, ValeriaBiundo, RobertaWeis, LucaTognolo, LucreziaBaba, AlfoncRubega, MariaGentile, GiovanniTedesco, ChiaraCarecchio, MiryamAntonini, AngeloMasiero, Stefano HEALTHCARE - -
EIF2AK2 Missense Variants Associated with Early Onset Generalized Dystonia 2020 Carecchio M.Garavaglia B. + ANNALS OF NEUROLOGY - -