Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Gennarina Arabia b"'
Autor:
Salvatore Nigro a, Gaetano Barbagallo b, Maria Giovanna Bianco c, Maurizio Morelli b, Gennarina Arabia b, Andrea Quattrone b, Sara Gasparini b, e, Giuseppe Lucio Cascini d, Aldo Quattrone f, g
Publikováno v:
Parkinsonism & related disorders 69 (2019): 23–29. doi:10.1016/j.parkreldis.2019.10.020
info:cnr-pdr/source/autori:Salvatore Nigro a, Gaetano Barbagallo b, Maria Giovanna Bianco c, Maurizio Morelli b, Gennarina Arabia b, Andrea Quattrone b, Sara Gasparini b,e, Giuseppe Lucio Cascini d, Aldo Quattrone f,g/titolo:Track density imaging: A reliable method to assess white matter changes in Progressive Supranuclear Palsy with predominant parkinsonism/doi:10.1016%2Fj.parkreldis.2019.10.020/rivista:Parkinsonism & related disorders/anno:2019/pagina_da:23/pagina_a:29/intervallo_pagine:23–29/volume:69
info:cnr-pdr/source/autori:Salvatore Nigro a, Gaetano Barbagallo b, Maria Giovanna Bianco c, Maurizio Morelli b, Gennarina Arabia b, Andrea Quattrone b, Sara Gasparini b,e, Giuseppe Lucio Cascini d, Aldo Quattrone f,g/titolo:Track density imaging: A reliable method to assess white matter changes in Progressive Supranuclear Palsy with predominant parkinsonism/doi:10.1016%2Fj.parkreldis.2019.10.020/rivista:Parkinsonism & related disorders/anno:2019/pagina_da:23/pagina_a:29/intervallo_pagine:23–29/volume:69
Introduction Track density imaging (TDI) has been proven to be a useful approach able to investigate white matter (WM) anatomical integrity in several neurodegenerative conditions, such as Parkinson's disease (PD) and classical phenotype of Progressi
Autor:
Maria Salsone a, Rita Nistico' a, Basilio Vescio a, Fabiana Novellino a, Maurizio Morelli b, Angela Lupo b, Gennarina Arabia b, Aldo Quattrone a, b
Publikováno v:
Parkinsonism & related disorders 33 (2016): 134–137. doi:10.1016/j.parkreldis.2016.09.027
info:cnr-pdr/source/autori:Maria Salsone a, Rita Nistico' a, Basilio Vescio a, Fabiana Novellino a, Maurizio Morelli b, Angela Lupo b, Gennarina Arabia b, Aldo Quattrone a,b/titolo:Heart rate variability in patients with essential tremor: A cross sectional study./doi:10.1016%2Fj.parkreldis.2016.09.027/rivista:Parkinsonism & related disorders/anno:2016/pagina_da:134/pagina_a:137/intervallo_pagine:134–137/volume:33
info:cnr-pdr/source/autori:Maria Salsone a, Rita Nistico' a, Basilio Vescio a, Fabiana Novellino a, Maurizio Morelli b, Angela Lupo b, Gennarina Arabia b, Aldo Quattrone a,b/titolo:Heart rate variability in patients with essential tremor: A cross sectional study./doi:10.1016%2Fj.parkreldis.2016.09.027/rivista:Parkinsonism & related disorders/anno:2016/pagina_da:134/pagina_a:137/intervallo_pagine:134–137/volume:33
Objective To investigate heart rate variability (HRV) in patients with Essential Tremor (ET) in comparison with patients with Parkinson's Disease (PD). Methods This is a cross sectional control study including 10 patients with ET, 10 patients with PD
Autor:
Monica Gagliardi a, Gennarina Arabia b, Rita Nisticò a, Grazia Iannello a, Radha Procopio a, b, Lucia Manfredini b, Grazia Annesi a, Aldo Quattrone a, c
Publikováno v:
Journal of the neurological sciences 390 (2018): 209–211. doi:10.1016/j.jns.2018.04.043
info:cnr-pdr/source/autori:Monica Gagliardi a, Gennarina Arabia b, Rita Nisticò a, Grazia Iannello a, Radha Procopio a,b, Lucia Manfredini b, Grazia Annesi a, Aldo Quattrone a,c/titolo:Mutational analysis of TARDBP gene in patients affected by Parkinson's disease from Calabria./doi:10.1016%2Fj.jns.2018.04.043/rivista:Journal of the neurological sciences/anno:2018/pagina_da:209/pagina_a:211/intervallo_pagine:209–211/volume:390
info:cnr-pdr/source/autori:Monica Gagliardi a, Gennarina Arabia b, Rita Nisticò a, Grazia Iannello a, Radha Procopio a,b, Lucia Manfredini b, Grazia Annesi a, Aldo Quattrone a,c/titolo:Mutational analysis of TARDBP gene in patients affected by Parkinson's disease from Calabria./doi:10.1016%2Fj.jns.2018.04.043/rivista:Journal of the neurological sciences/anno:2018/pagina_da:209/pagina_a:211/intervallo_pagine:209–211/volume:390
Objective Neurodegenerative diseases are often characterized by the presence of intracellular or extracellular protein aggregates in the central nervous system. Mutations of TARDBP gene have been shown to cause Amyotrophic Lateral Sclerosis and have