Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Andrea Molari"'
Autor:
Maria Livia Fantini, Giovanni Cossu, Andrea Molari, Monia Cabinio, Ozlem Uyanik, Roberto Cilia, Maurizio Melis, Angelo Antonini, Luigi Ferini-Strambi
Publikováno v:
Parkinson's Disease, Vol 2010 (2010)
Pantothenate kinase-associated neurodegeneration (PKAN) is a familial or sporadic disease characterized by extrapyramidal and corticospinal signs with dementia. Patients show iron accumulation in the basal ganglia, with neuronal loss and gliosis. A m
Externí odkaz:
https://doaj.org/article/fb98f779843947ac89aaadce1c9b5f50
Autor:
Anna Ladogana, Sandro Orru, Marta Melis, Sarah Vascellari, Giovanni Defazio, Giovanni Cossu, Piero Parchi, Anna Poleggi, Gianluca Floris, Andrea Molari, Luisa Balestrino, Maurizio Melis
Publikováno v:
neurogenetics. 21:251-257
In genetic prion diseases (gPrD), five genetic variants (E200K, V210I, V180I, P102L, and D178N) are responsible for about 85% of cases. The R208H is one of the several additional rare mutations and to date, only 16 cases carrying this mutation have b
Autor:
Giovanni Cossu, Paolo Contu, Maurizio Melis, Alessandra Mereu, Marcello Deriu, Daniela Murgia, Davide Manca, Paola Ferrigno, Andrea Molari
Publikováno v:
Movement Disorders. 24:697-701
The aim of our study was to explore restless legs syndrome (RLS) frequency in multiple sclerosis (MS)-patients and establish whether RLS could be a symptom of MS. Over a period of 1 year, we consecutively enrolled 202 MS-patients and 212 healthy cont
Autor:
Alessio Di Fonzo, Marcello Deriu, Maurizio Melis, Giovanni Cossu, Marina van Doeselaar, Andrea Molari, Ben A. Oostra, Vincenzo Bonifati
Publikováno v:
Parkinsonism & Related Disorders, 13(1), 17-21. Elsevier
The Leucine-Rich Repeat Kinase 2 (LRRK2) Gly2019Ser mutation is frequent among Parkinson's disease (PD) patients from the Arab, Jewish, and Iberian populations, while another mutation, Arg1441Gly, is common in the Basque population. We studied the pr
Autor:
Gianfranco Sau, Laura Minafra, Giannina Melis, Alessandra Mereu, Giovanni Cossu, Maria Giovanna Marrosu, Marcello Deriu, Miriana Fresu, Tiziana Pisano, Isidoro Cesare Giuseppe Aiello, Maurizio Melis, Enzo Ortu, Carlo Cianchetti, Andrea Molari, Paolo Contu
Publikováno v:
Movement Disorders. 21:2005-2008
We performed a service-based epidemiological study of primary blepharospasm in the island of Sardinia (Italy). Due to its favorable geographical location, we are confident we will provide reliable data from patients seeking botulinum toxin treatment.
Publikováno v:
Movement Disorders. 19:1109-1111
We report on a patient with persistent abnormal shoulder posture associated with isolated neurogenic hypertrophy of the trapezius muscle due to accessory nerve injury. The patient complained of marked difficulty in shoulder elevation and abduction. O
Autor:
Andrea Molari, Paola Ferrigno, L. Pinna, Maurizio Melis, Giannina Melis, Andrea Spissu, F. Zonza, Giovanni Cossu
Publikováno v:
Neurological Sciences. 24:138-140
Hashimoto's encephalopathy and Creutzfeldt-Jakob disease (CJD) often have similar clinical features and may be confused, especially at onset. A 61-year-old woman developed rapidly progressive ataxia, myoclonus and dementia, with abnormalities seen on
Autor:
Andrea, Molari, Carlo, Carcassi
Publikováno v:
Journal of sleep research. 19(4)
Autor:
Andrea Molari, Giovanni Cossu, Maria Livia Fantini, Maurizio Melis, Monia Cabinio, Luigi Ferini-Strambi, Ozlem Uyanik, Roberto Cilia, Angelo Antonini
Publikováno v:
Parkinson's Disease, Vol 2010 (2010)
Parkinson's Disease
Parkinson's Disease
Pantothenate kinase-associated neurodegeneration (PKAN) is a familial or sporadic disease characterized by extrapyramidal and corticospinal signs with dementia. Patients show iron accumulation in the basal ganglia, with neuronal loss and gliosis. A m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::809c383281a7b8b471b3df9ae76f41c4
http://hdl.handle.net/11577/3263725
http://hdl.handle.net/11577/3263725
Autor:
Maurizio Melis, Giovanni Cossu, Davide Manca, Daniela Murgia, Paola Ferrigno, Andrea Molari, Emanuele Marcia
Publikováno v:
Movement Disorders. 24:2293-2294