Maria Elena Conidi

Maria Elena Conidi

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Maria Elena Conidi

Maria Elena Conidi

Publications by authors named "Maria Elena Conidi"

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15Publications

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Angela R.: a familial Alzheimer's disease case in the days of Auguste D.

J Neurol 2016 Dec 11;263(12):2494-2498. Epub 2016 Oct 11.

Regional Neurogenetic Centre, Azienda Sanitaria Provinciale Catanzaro, Viale A. Perugini, 88046, Lamezia Terme, CZ, Italy.

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http://dx.doi.org/10.1007/s00415-016-8294-xDOI Listing
December 2016

Frontotemporal dementia and its subtypes: a genome-wide association study.

Authors:
Raffaele Ferrari Dena G Hernandez Michael A Nalls Jonathan D Rohrer Adaikalavan Ramasamy John B J Kwok Carol Dobson-Stone William S Brooks Peter R Schofield Glenda M Halliday John R Hodges Olivier Piguet Lauren Bartley Elizabeth Thompson Eric Haan Isabel Hernández Agustín Ruiz Mercè Boada Barbara Borroni Alessandro Padovani Carlos Cruchaga Nigel J Cairns Luisa Benussi Giuliano Binetti Roberta Ghidoni Gianluigi Forloni Daniela Galimberti Chiara Fenoglio Maria Serpente Elio Scarpini Jordi Clarimón Alberto Lleó Rafael Blesa Maria Landqvist Waldö Karin Nilsson Christer Nilsson Ian R A Mackenzie Ging-Yuek R Hsiung David M A Mann Jordan Grafman Christopher M Morris Johannes Attems Timothy D Griffiths Ian G McKeith Alan J Thomas P Pietrini Edward D Huey Eric M Wassermann Atik Baborie Evelyn Jaros Michael C Tierney Pau Pastor Cristina Razquin Sara Ortega-Cubero Elena Alonso Robert Perneczky Janine Diehl-Schmid Panagiotis Alexopoulos Alexander Kurz Innocenzo Rainero Elisa Rubino Lorenzo Pinessi Ekaterina Rogaeva Peter St George-Hyslop Giacomina Rossi Fabrizio Tagliavini Giorgio Giaccone James B Rowe Johannes C M Schlachetzki James Uphill John Collinge Simon Mead Adrian Danek Vivianna M Van Deerlin Murray Grossman John Q Trojanowski Julie van der Zee William Deschamps Tim Van Langenhove Marc Cruts Christine Van Broeckhoven Stefano F Cappa Isabelle Le Ber Didier Hannequin Véronique Golfier Martine Vercelletto Alexis Brice Benedetta Nacmias Sandro Sorbi Silvia Bagnoli Irene Piaceri Jørgen E Nielsen Lena E Hjermind Matthias Riemenschneider Manuel Mayhaus Bernd Ibach Gilles Gasparoni Sabrina Pichler Wei Gu Martin N Rossor Nick C Fox Jason D Warren Maria Grazia Spillantini Huw R Morris Patrizia Rizzu Peter Heutink Julie S Snowden Sara Rollinson Anna Richardson Alexander Gerhard Amalia C Bruni Raffaele Maletta Francesca Frangipane Chiara Cupidi Livia Bernardi Maria Anfossi Maura Gallo Maria Elena Conidi Nicoletta Smirne Rosa Rademakers Matt Baker Dennis W Dickson Neill R Graff-Radford Ronald C Petersen David Knopman Keith A Josephs Bradley F Boeve Joseph E Parisi William W Seeley Bruce L Miller Anna M Karydas Howard Rosen John C van Swieten Elise G P Dopper Harro Seelaar Yolande A L Pijnenburg Philip Scheltens Giancarlo Logroscino Rosa Capozzo Valeria Novelli Annibale A Puca Massimo Franceschi Alfredo Postiglione Graziella Milan Paolo Sorrentino Mark Kristiansen Huei-Hsin Chiang Caroline Graff Florence Pasquier Adeline Rollin Vincent Deramecourt Florence Lebert Dimitrios Kapogiannis Luigi Ferrucci Stuart Pickering-Brown Andrew B Singleton John Hardy Parastoo Momeni

Lancet Neurol 2014 Jul;13(7):686-99

Laboratory of Neurogenetics, Department of Internal Medicine, Texas Tech University Health Science Center, Lubbock, Texas, USA.

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http://dx.doi.org/10.1016/S1474-4422(14)70065-1DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4112126PMC
July 2014

A new truncating MPZ mutation associated with a very mild CMT1 B phenotype.

Neuromuscul Disord 2010 Dec 17;20(12):817-9. Epub 2010 Sep 17.

Department of Neuroscience, Neurological Clinic, Pisa, Italy.

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http://dx.doi.org/10.1016/j.nmd.2010.08.003DOI Listing
December 2010

Identification of three novel mutations in the CHD7 gene in patients with clinical signs of typical or atypical CHARGE syndrome.

Int J Pediatr Otorhinolaryngol 2010 Dec 12;74(12):1441-4. Epub 2010 Oct 12.

Mother and Child Department, Cytogenetics and Molecular Genetics Unit, University Hospital of Pisa, Pisa, Italy.

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http://dx.doi.org/10.1016/j.ijporl.2010.09.006DOI Listing
December 2010

Novel human pathological mutations. Gene symbol: SPG4. Disease: spastic paraplegia, autosomal dominant.

Hum Genet 2009 Aug;126(2):340

U.O. Citogenetica e Genetica Molecolare: Azienda Ospedaliero Universitaria Pisana, Pisa, Italy.

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August 2009

Gene symbol: JAG1. Disease: Alagille syndrome.

Hum Genet 2008 Oct;124(3):321-2

Azienda Ospedaliero-Universitaria Pisana, U.O.Citogenetica e Genetica Molecolare, Pisa, Roma, 67, 56100 Pisa, Italy.

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October 2008

Gene symbol: JAG1. Disease: Alagille syndrome.

Hum Genet 2008 Oct;124(3):322

Azienda Ospedaliero Universitaria Pisana U.O. Citogenetica e Genetica Molecolare, Pisa, Roma, 67, 56100 Pisa, Italy.

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October 2008

Gene symbol: JAG1. Disease: Alagille syndrome.

Hum Genet 2008 Oct;124(3):322

Azienda Ospedaliero Universitaria Pisana U.O. Citogenetica e Genetica Molecolare, Pisa, Roma, 67, 56100 Pisa, Italy.

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October 2008

Gene symbol: CHD7. Disease: CHARGE syndrome.

Hum Genet 2008 Jun;123(5):549

Azienda Ospedaliera Universitaria Pisana, U.O. Citogenetica e Genetica Molecolare, Pisa, Roma, 67, 56126, Pisa, Italy.

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June 2008