Publications by authors named "Maria Anfossi"

Claim this Profile
G
Genetic variation in APOE, GRN, and TP53 are phenotype modifiers in frontotemporal dementia.
Irene Rosas, Carmen Martínez, Eliecer Coto, Jordi Clarimón, Alberto Lleó, Maria Anfossi

Neurobiol Aging· March 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
,
, age at onset, and ancestry help discriminate behavioral from language variants in FTLD cohorts.
Beatrice Costa, Claudia Manzoni, Manuel Bernal-Quiros, Demis A Kia, Miquel Aguilar, Maria Anfossi

Neurology· December 2020

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
R
Role for ATXN1, ATXN2, and HTT intermediate repeats in frontotemporal dementia and Alzheimer's disease.
Irene Rosas, Carmen Martínez, Jordi Clarimón, Alberto Lleó, Ignacio Illán-Gala, Maria Anfossi

Neurobiol Aging· March 2020

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
F
Frequency of Cardiovascular Genetic Risk Factors in a Calabrian Population and Their Effects on Dementia.
Raffaele Maletta, Nicoletta Smirne, Livia Bernardi, Maria Anfossi, Maura Gallo

J Alzheimers Dis· January 2019

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study.
Cyril Pottier, Xiaolai Zhou, Ralph B Perkerson, Matt Baker, Gregory D Jenkins, Maria Anfossi

Lancet Neurol· June 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
R
Role of Niemann-Pick Type C Disease Mutations in Dementia.
Chiara Cupidi, Francesca Frangipane, Maura Gallo, Alessandra Clodomiro, Rosanna Colao, Maria Anfossi

J Alzheimers Dis· February 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
The novel PSEN1 M84V mutation associated to frontal dysexecutive syndrome, spastic paraparesis, and cerebellar atrophy in a dominant Alzheimer's disease family.
Maura Gallo, Francesca Frangipane, Chiara Cupidi, Matteo De Bartolo, Sabina Turone, Maria Anfossi

Neurobiol Aging· August 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
The Genetic Variability of UCP4 Affects the Individual Susceptibility to Late-Onset Alzheimer's Disease and Modifies the Disease's Risk in APOE-ɛ4 Carriers.
Alberto Montesanto, Paolina Crocco, Maria Anfossi, Nicoletta Smirne, Gianfranco Puccio

J Alzheimers Dis· December 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
Angela R.: a familial Alzheimer's disease case in the days of Auguste D.
Laura Borrello, Chiara Cupidi, Valentina Laganà, Maria Anfossi, Maria Elena Conidi

J Neurol· December 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
H
Homozygous carriers of APP A713T mutation in an autosomal dominant Alzheimer disease family.
Maria E Conidi, Livia Bernardi, Gianfranco Puccio, Nicoletta Smirne, Maria G Muraca, Maria Anfossi

Neurology· June 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
E
Estimating the inheritance of frontotemporal lobar degeneration in the Italian population.
Barbara Borroni, Mario Grassi, Marta Bianchi, Amalia Cecilia Bruni, Raffaele Giovanni Maletta, Maria Anfossi

J Alzheimers Dis· February 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
Association of the variant Cys139Arg at GRN gene to the clinical spectrum of frontotemporal lobar degeneration.
Irene Piaceri, Silvia Pradella, Chiara Cupidi, Serena Nannucci, Cristina Polito, Maria Anfossi

J Alzheimers Dis· December 2014

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
N
Novel N-terminal domain mutation in prion protein detected in 2 patients diagnosed with frontotemporal lobar degeneration syndrome.
Livia Bernardi, Chiara Cupidi, Francesca Frangipane, Maria Anfossi, Maura Gallo

Neurobiol Aging· November 2014

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
F
Frontotemporal dementia and its subtypes: a genome-wide association study.
Raffaele Ferrari, Dena G Hernandez, Michael A Nalls, Jonathan D Rohrer, Adaikalavan Ramasamy, Maria Anfossi

Lancet Neurol· July 2014

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Identification of three novel LRRK2 mutations associated with Parkinson's disease in a Calabrian population.
Maria Anfossi, Rosanna Colao, Maura Gallo, Livia Bernardi, M Elena Conidi

J Alzheimers Dis· June 2014

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
R
Role of TOMM40 rs10524523 polymorphism in onset of alzheimer's disease caused by the PSEN1 M146L mutation.
Livia Bernardi, Maura Gallo, Maria Anfossi, Maria Elena Conidi, Rosanna Colao

J Alzheimers Dis· April 2014

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
Autosomal dominant frontotemporal lobar degeneration due to the C9ORF72 hexanucleotide repeat expansion: late-onset psychotic clinical presentation.
Daniela Galimberti, Chiara Fenoglio, Maria Serpente, Chiara Villa, Rossana Bonsi, Maria Anfossi

Biol Psychiatry· September 2013

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
E
Epidemiology and genetics of frontotemporal dementia: a door-to-door survey in southern Italy.
Livia Bernardi, Francesca Frangipane, Nicoletta Smirne, Rosanna Colao, Gianfranco Puccio, Maria Anfossi

Neurobiol Aging· December 2012

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A novel pathogenic PSEN1 mutation in a family with Alzheimer's disease: phenotypical and neuropathological features.
Maura Gallo, Norina Marcello, Sabrina A M Curcio, Rosanna Colao, Silvana Geracitano, Maria Anfossi

J Alzheimers Dis· November 2011

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
PSEN1 and PRNP gene mutations: co-occurrence makes onset very early in a family with FTD phenotype.
Livia Bernardi, Maria Anfossi, Maura Gallo, Silvana Geracitano, Rosanna Cola

J Alzheimers Dis· September 2011

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
MAPT V363I variation in a sporadic case of frontotemporal dementia: variable penetrant mutation or rare polymorphism?
Maria Anfossi, Livia Bernardi, Maura Gallo, Silvana Geracitano, Rosanna Colao

Alzheimer Dis Assoc Disord· June 2011

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Compound heterozygosity of 2 novel MAPT mutations in frontotemporal dementia.
Maria Anfossi, Romina Vuono, Raffaele Maletta, Kanwar Virdee, Maria Mirabelli

Neurobiol Aging· April 2011

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
N
Novel MAPT Val75Ala mutation and PSEN2 Arg62Hys in two siblings with frontotemporal dementia.
Maura Gallo, Carmine Tomaino, Gianfranco Puccio, Francesca Frangipane, Sabrina A M Curcio, Maria Anfossi

Neurol Sci· February 2010

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
AbetaPP A713T mutation in late onset Alzheimer's disease with cerebrovascular lesions.
Livia Bernardi, Silvana Geracitano, Rosanna Colao, Gianfranco Puccio, Maura Gallo, Maria Anfossi

J Alzheimers Dis· December 2009

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
L
Late onset familial Alzheimer's disease: novel presenilin 2 mutation and PS1 E318G polymorphism.
Livia Bernardi, Carmine Tomaino, Maria Anfossi, Maura Gallo, Silvana Geracitano

J Neurol· April 2008

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis