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European Journal of Medical Genetics|May 21, 2009
C329X in KRIT1 is a founder mutation among CCM patients in SardiniaMilena Cau, Mario Loi, Maurizio Melis, et al.
Parkinsonism & Related Disorders|October 27, 2006
LRRK2 mutations and Parkinson's disease in Sardinia--A Mediterranean genetic isolateGiovanni Cossu, Marina van Doeselaar, Marcello Deriu, et al.
Parkinson'S Disease|October 27, 2010
Sleep in genetically confirmed pantothenate kinase-associated neurodegeneration: a video-polysomnographic studyMaria Livia Fantini, Giovanni Cossu, Andrea Molari, et al.
Neurogenetics|June 14, 2011
Broadening the phenotype of TARDBP mutations: the TARDBP Ala382Thr mutation and Parkinson's disease in SardiniaMarialuisa Quadri, Giovanni Cossu, Valeria Saddi, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|April 28, 2016
Parkinsonism and dementia are negative prognostic factors for the outcome of subdural hematomaRoberta Arca, Valeria Ricchi, Daniela Murgia, et al.
Therapeutics and Clinical Risk Management|October 13, 2018
A multicentric pharmacovigilance study: collection and analysis of adverse drug reactions in relapsing-remitting multiple sclerosis patientsAgnese Gugliandolo, Federica Longo, Maria Giovanna Marrosu, et al.
Haematologica|July 28, 2011
A pilot trial of deferiprone for neurodegeneration with brain iron accumulationGiovanni Abbruzzese, Giovanni Cossu, Manuela Balocco, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|February 27, 2017
Use of rivaroxaban in patients with strokeDanilo Toni, Antonio Carolei, Valeria Caso, et al.
Journal of the Neurological Sciences|September 17, 2022
Relationship between CSF tau biomarkers and structural brain MRI measures in frontotemporal lobar degenerationGiuseppe Fenu, Valentina Oppo, Giulia Serra, et al.
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