Imaging counterpart of postural instability and vertical ocular dysfunction in patients with PSP: A multimodal MRI study

Autor: Andrea Quattrone a, Maria Eugenia Caligiuri b, c, Maurizio Morelli a, Salvatore Nigro c, Basilio Vescio d, Gennarina Arabia a, Giuseppe Nicoletti c, Rita Nisticò c, Maria Salsone c, Fabiana Novellino c, Gaetano Barbagallo a, Maria Grazia Vaccaro c, Umberto Sabatini e, Virginia Vescio e, Carlo Stanà e, Federico Rocca c, Manuela Caracciolo c, Aldo Quattrone b

Publikováno v: Parkinsonism & related disorders 63 (2019): 124–130. doi:10.1016/j.parkreldis.2019.02.022
info:cnr-pdr/source/autori:Andrea Quattrone a, Maria Eugenia Caligiuri b,c, Maurizio Morelli a,c, Salvatore Nigro c, Basilio Vescio d, Gennarina Arabia a,c, Giuseppe Nicoletti c, Rita Nisticò c, Maria Salsone c, Fabiana Novellino c, Gaetano Barbagallo a, Maria Grazia Vaccaro c, Umberto Sabatini e, Virginia Vescio e, Carlo Stanà e, Federico Rocca c, Manuela Caracciolo c, Aldo Quattrone b,c/titolo:Imaging counterpart of postural instability and vertical ocular dysfunction in patients with PSP: A multimodal MRI study/doi:10.1016%2Fj.parkreldis.2019.02.022/rivista:Parkinsonism & related disorders/anno:2019/pagina_da:124/pagina_a:130/intervallo_pagine:124–130/volume:63

Introduction We investigated the imaging counterpart of two functional domains (ocular motor dysfunction and postural instability) in progressive supranuclear palsy (PSP) patients classified according to the new clinical diagnostic criteria. Methods

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b845a07df8b8e650306ce2e30163016f
https://doi.org/10.1016/j.parkreldis.2019.02.022

Development and Validation of a New Wearable Mobile Device for the Automated Detection of Resting Tremor in Parkinson's Disease and Essential Tremor.

Autor: Vescio, Basilio¹ (AUTHOR) basilio.vescio@biotecnomed.it, Nisticò, Rita² (AUTHOR) rita.nistico@cnr.it, Augimeri, Antonio¹ (AUTHOR) antonio.augimeri@biotecnomed.it, Quattrone, Andrea³ (AUTHOR) an.quattrone@hotmail.it, Crasà, Marianna⁴ (AUTHOR) marianna.crasa@gmail.com, Quattrone, Aldo^2,4 (AUTHOR) quattrone@unicz.it, Fassina, Giorgio (AUTHOR)

Publikováno v: Diagnostics (2075-4418). Feb2021, Vol. 11 Issue 2, p200-200. 1p.

Further evidence of genetic heterogeneity in autosomal dominant distal motor neuronopathy

Autor: Aldo Quattrone, M Muglia, G. Peluso, Rosalucia Mazzei, Francesca Luisa Conforti, A. L. Gabriele, Michele Bellesi, Manuela Caracciolo, Emanuele Medici, Francesco Logullo, Leandro Provinciali, Angela Magariello, Luca Passamonti, Alessandra Patitucci, Teresa Sprovieri

Publikováno v: Neuromuscular disorders 14 (2004): 705–710. doi:10.1016/j.nmd.2004.07.004
info:cnr-pdr/source/autori:Luca Passamonti a; Maria Muglia b; Angela Magariello b; Michele Bellesi a; Francesca Luisa Conforti b; Rosalucia Mazzei b; Alessandra Patitucci b; Anna Lia Gabriele b; Teresa Sprovieri b; Giuseppina Peluso b; Manuela Caracciolo b; Emanuele Medici a; Francesco Logullo a; Leandro Provinciali a; Aldo Quattrone b, c/titolo:Further evidence of genetic heterogeneity in autosomal dominant distal motor neuronopathy./doi:10.1016%2Fj.nmd.2004.07.004/rivista:Neuromuscular disorders/anno:2004/pagina_da:705/pagina_a:710/intervallo_pagine:705–710/volume:14

Distal hereditary motor neuronopathy is a genetically and clinically heterogeneous disorder. To date, five loci, and their relative genes, have been mapped on chromosomes 7p14, 7q11, 9q34, 11q12 and 12q24, respectively. We describe an Italian family

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f06149a443e5cba04968e593c086353f
https://doi.org/10.1111/j.1085-9489.2004.009209bp.x