Amalia C Bruni

Amalia C Bruni

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Amalia C Bruni

Amalia C Bruni

Publications by authors named "Amalia C Bruni"

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Mutations in Prion Protein Gene: Pathogenic Mechanisms in C-Terminal vs. N-Terminal Domain, a Review.

Int J Mol Sci 2019 Jul 23;20(14). Epub 2019 Jul 23.

Regional Neurogenetic Centre, ASP Catanzaro, 88046 Lamezia Terme (CZ), Italy.

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http://dx.doi.org/10.3390/ijms20143606DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6678283PMC
July 2019

A C6orf10/LOC101929163 locus is associated with age of onset in C9orf72 carriers.

Brain 2018 10;141(10):2895-2907

Tanz Centre for Research in Neurodegenerative Diseases, University of Toronto, Toronto, ON, Canada.

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http://dx.doi.org/10.1093/brain/awy238DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6158742PMC
October 2018

Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study.

Authors:
Cyril Pottier Xiaolai Zhou Ralph B Perkerson Matt Baker Gregory D Jenkins Daniel J Serie Roberta Ghidoni Luisa Benussi Giuliano Binetti Adolfo López de Munain Miren Zulaica Fermin Moreno Isabelle Le Ber Florence Pasquier Didier Hannequin Raquel Sánchez-Valle Anna Antonell Albert Lladó Tammee M Parsons NiCole A Finch Elizabeth C Finger Carol F Lippa Edward D Huey Manuela Neumann Peter Heutink Matthis Synofzik Carlo Wilke Robert A Rissman Jaroslaw Slawek Emilia Sitek Peter Johannsen Jørgen E Nielsen Yingxue Ren Marka van Blitterswijk Mariely DeJesus-Hernandez Elizabeth Christopher Melissa E Murray Kevin F Bieniek Bret M Evers Camilla Ferrari Sara Rollinson Anna Richardson Elio Scarpini Giorgio G Fumagalli Alessandro Padovani John Hardy Parastoo Momeni Raffaele Ferrari Francesca Frangipane Raffaele Maletta Maria Anfossi Maura Gallo Leonard Petrucelli EunRan Suh Oscar L Lopez Tsz H Wong Jeroen G J van Rooij Harro Seelaar Simon Mead Richard J Caselli Eric M Reiman Marwan Noel Sabbagh Mads Kjolby Anders Nykjaer Anna M Karydas Adam L Boxer Lea T Grinberg Jordan Grafman Salvatore Spina Adrian Oblak M-Marsel Mesulam Sandra Weintraub Changiz Geula John R Hodges Olivier Piguet William S Brooks David J Irwin John Q Trojanowski Edward B Lee Keith A Josephs Joseph E Parisi Nilüfer Ertekin-Taner David S Knopman Benedetta Nacmias Irene Piaceri Silvia Bagnoli Sandro Sorbi Marla Gearing Jonathan Glass Thomas G Beach Sandra E Black Mario Masellis Ekaterina Rogaeva Jean-Paul Vonsattel Lawrence S Honig Julia Kofler Amalia C Bruni Julie Snowden David Mann Stuart Pickering-Brown Janine Diehl-Schmid Juliane Winkelmann Daniela Galimberti Caroline Graff Linn Öijerstedt Claire Troakes Safa Al-Sarraj Carlos Cruchaga Nigel J Cairns Jonathan D Rohrer Glenda M Halliday John B Kwok John C van Swieten Charles L White Bernardino Ghetti Jill R Murell Ian R A Mackenzie Ging-Yuek R Hsiung Barbara Borroni Giacomina Rossi Fabrizio Tagliavini Zbigniew K Wszolek Ronald C Petersen Eileen H Bigio Murray Grossman Vivianna M Van Deerlin William W Seeley Bruce L Miller Neill R Graff-Radford Bradley F Boeve Dennis W Dickson Joanna M Biernacka Rosa Rademakers

Lancet Neurol 2018 06 30;17(6):548-558. Epub 2018 Apr 30.

Department of Neuroscience, Mayo Clinic, Jacksonville, FL, USA. Electronic address:

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http://dx.doi.org/10.1016/S1474-4422(18)30126-1DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6237181PMC
June 2018

Contribution of polymorphic variation of inositol hexakisphosphate kinase 3 (IP6K3) gene promoter to the susceptibility to late onset Alzheimer's disease.

Biochim Biophys Acta 2016 09 21;1862(9):1766-73. Epub 2016 Jun 21.

Department of Biology, Ecology and Earth Science, University of Calabria, Rende, CS, Italy. Electronic address:

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http://dx.doi.org/10.1016/j.bbadis.2016.06.014DOI Listing
September 2016

Influence of controlled encoding and retrieval facilitation on memory performance in patients with different profiles of mild cognitive impairment.

J Neurol 2015 12;262(4):938-48. Epub 2015 Feb 12.

Fondazione IRCCS Santa Lucia, Laboratory of Clinical and Behavioral Neurology, Via Ardeatina 306, 00179, Rome, Italy,

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http://dx.doi.org/10.1007/s00415-015-7662-2DOI Listing
January 2016

Mutation analysis of CHCHD10 in different neurodegenerative diseases.

Brain 2015 Sep 31;138(Pt 9):e380. Epub 2015 Mar 31.

1 Tanz Centre for Research in Neurodegenerative Diseases, University of Toronto, 60 Leonard Street, Toronto, Ontario, Canada, M5T 2S8 8 Department of Medicine, Division of Neurology, University of Toronto, Toronto, Ontario, Canada M5S 1A8

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http://dx.doi.org/10.1093/brain/awv082DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4547051PMC
September 2015

Homozygous carriers of APP A713T mutation in an autosomal dominant Alzheimer disease family.

Neurology 2015 Jun 6;84(22):2266-73. Epub 2015 May 6.

From the Regional Neurogenetic Centre (M.E.C., L.B., G.P., N.S., M.G.M., S.A.M.C., R.C., M.G., M.A., F.F., A. Clodomiro, M.M., F.V., C.C., G.T., R.D.L., R.G.M., A.C.B.), ASP Catanzaro, Lamezia Terme; Department of Cell Biology and Neurosciences (P.P., A. Confaloni), National Institute of Health, Rome; and DINOGMI (P.M.), Università degli studi di Genova, Italy.

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http://www.neurology.org/content/84/22/2266.full.pdf
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http://www.neurology.org/cgi/doi/10.1212/WNL.000000000000164
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http://dx.doi.org/10.1212/WNL.0000000000001648DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4456653PMC
June 2015

Genetics in degenerative dementia: current status and applicability.

Alzheimer Dis Assoc Disord 2014 Jul-Sep;28(3):199-205

Regional Neurogenetic Centre, Lamezia Terme (CZ), Italy.

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https://insights.ovid.com/crossref?an=00002093-201407000-000
Publisher Site
http://dx.doi.org/10.1097/WAD.0000000000000046DOI Listing
April 2015

Hypermethylation of the CpG-island near the C9orf72 G₄C₂-repeat expansion in FTLD patients.

Hum Mol Genet 2014 Nov 6;23(21):5630-7. Epub 2014 Jun 6.

Tanz Centre for Research in Neurodegenerative Diseases, University of Toronto, 60 Leonard Street, Toronto, Ontario, Canada M5T 2S8, Department of Medicine, Division of Neurology, University of Toronto, 1 King's College Circle, Toronto, Ontario, Canada M5S 1A8 and

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http://dx.doi.org/10.1093/hmg/ddu279DOI Listing
November 2014

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

First deep intronic mutation in the NOTCH3 gene in a family with late-onset CADASIL.

Neurobiol Aging 2013 Sep 12;34(9):2234.e9-12. Epub 2013 Apr 12.

Department of Medical, Surgical and Neurological Sciences, University of Siena, Siena, Italy.

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http://dx.doi.org/10.1016/j.neurobiolaging.2013.03.005DOI Listing
September 2013

Chromosome 9p21.3 genotype is associated with vascular dementia and Alzheimer's disease.

Neurobiol Aging 2011 Jul 6;32(7):1231-5. Epub 2009 Aug 6.

Department of Health Sciences, Section of Psychiatry, University of Pavia, Via Bassi 21, Pavia, Italy.

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http://dx.doi.org/10.1016/j.neurobiolaging.2009.07.003DOI Listing
July 2011

APOE polymorphism affects episodic memory among non demented elderly subjects.

Exp Gerontol 2009 Mar 24;44(3):224-7. Epub 2008 Nov 24.

Department of Cell Biology, University of Calabria, Rende, Italy.

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http://dx.doi.org/10.1016/j.exger.2008.11.005DOI Listing
March 2009

The added value of neuropsychologic tests and structural imaging for the etiologic diagnosis of dementia in italian expert centers.

Alzheimer Dis Assoc Disord 2008 Oct-Dec;22(4):309-20

Laboratory of Epidemiology, Neuroimaging and Telemedicine, Scientific Institute for Research and Care (IRCCS) San Giovanni di Dio, FBF, Brescia, Italy.

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February 2009

Association studies between the plasmin genes and late-onset Alzheimer's disease.

Neurobiol Aging 2007 Jul 7;28(7):1041-3. Epub 2006 Jul 7.

Centre for Research in Neurodegenerative Diseases, Department of Medicine, University of Toronto and Toronto Western Hospital Research Institute, Toronto, Ontario, Canada.

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http://dx.doi.org/10.1016/j.neurobiolaging.2006.05.028DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2647723PMC
July 2007

Characterization of nigrostriatal dysfunction in spinocerebellar ataxia 17.

Mov Disord 2006 Jun;21(6):872-5

Department of Neurological Sciences, University of Naples Federico II, Naples, Italy.

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http://dx.doi.org/10.1002/mds.20827DOI Listing
June 2006

Relation of apolipoprotein(a) size to alzheimer's disease and vascular dementia.

Dement Geriatr Cogn Disord 2004 21;18(2):189-96. Epub 2004 Jun 21.

Molecular Medicine Laboratory, IRCCS Policlinico San Matteo, University of Pavia, Pavia, Italy.

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http://dx.doi.org/10.1159/000079200DOI Listing
February 2005

Apolipoprotein(a) null phenotype is related to a delayed age at onset of Alzheimer's disease.

Neurosci Lett 2004 Feb;357(1):45-8

Molecular Medicine Laboratory, IRCCS Policlinico San Matteo, Piazzale Golgi 2, University of Pavia, 27100 Pavia, Italy.

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http://dx.doi.org/10.1016/j.neulet.2003.12.043DOI Listing
February 2004