V Bonifati
Overview
Explore the profile of V Bonifati including associated specialties, affiliations and a list of published articles.
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Snapshot
Articles
78
Citations
2985
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0
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Recent Articles
1.
Geut H, Vergouw L, Galis Y, Ingrassia A, de Jong F, Quadri M, et al.
Parkinsonism Relat Disord
. 2019 Feb;
63:162-168.
PMID: 30777654
Introduction: The disease course of dementia with Lewy bodies (DLB) can be rapidly progressive, clinically resembling Creutzfeldt-Jakob's disease (CJD). To better understand factors contributing to this rapidly progressive disease course,...
2.
Obeso J, Stamelou M, Goetz C, Poewe W, Lang A, Weintraub D, et al.
Mov Disord
. 2017 Sep;
32(9):1264-1310.
PMID: 28887905
This article reviews and summarizes 200 years of Parkinson's disease. It comprises a relevant history of Dr. James Parkinson's himself and what he described accurately and what he missed from...
3.
De Rosa A, Pellegrino T, Pappata S, Lieto M, Bonifati V, Palma V, et al.
Parkinsonism Relat Disord
. 2016 Jan;
23:102-5.
PMID: 26725142
Introduction: PARK20 is a rare autosomal recessive parkinsonism related to the SYNJ1 gene and characterized by early-onset of disease and atypical signs such as supranuclear vertical gaze palsy, dementia, dystonia,...
4.
Lewthwaite A, Lambert T, Rolfe E, Olgiati S, Quadri M, Simons E, et al.
Parkinsonism Relat Disord
. 2015 Jan;
21(4):394-7.
PMID: 25634433
Background: GTP cyclohydrolase I (GCH1) mutations are the commonest cause of Dopa-responsive dystonia (DRD). Clinical phenotypes can be broad, even within a single family. Methods: We present clinical, genetic and...
5.
Di Toro Mammarella L, Mignarri A, Battisti C, Monti L, Bonifati V, Rasi F, et al.
J Neurol
. 2013 Nov;
261(1):227-8.
PMID: 24276520
No abstract available.
6.
Berardelli A, Wenning G, Antonini A, Berg D, Bloem B, Bonifati V, et al.
Eur J Neurol
. 2013 Jan;
20(1):16-34.
PMID: 23279440
Background: A Task Force was convened by the EFNS/MDS-ES Scientist Panel on Parkinson's disease (PD) and other movement disorders to systemically review relevant publications on the diagnosis of PD. Methods:...
7.
Correia Guedes L, Ferreira J, Rosa M, Coelho M, Bonifati V, Sampaio C
Parkinsonism Relat Disord
. 2009 Dec;
16(4):237-42.
PMID: 19945904
Background: The LRRK2 G2019S mutation is the most frequent known cause of familial and sporadic Parkinson's disease. Knowledge of its worldwide frequency distribution is essential for clinical and molecular research...
8.
Di Fonzo A, Dekker M, Montagna P, Baruzzi A, Yonova E, Correia Guedes L, et al.
Neurology
. 2008 Nov;
72(3):240-5.
PMID: 19038853
Background: The combination of early-onset, progressive parkinsonism with pyramidal tract signs has been known as pallido-pyramidal or parkinsonian-pyramidal syndrome since the first description by Davison in 1954. Very recently, a...
9.
Silveira-Moriyama L, Guedes L, Kingsbury A, Ayling H, Shaw K, Barbosa E, et al.
Neurology
. 2008 Sep;
71(13):1021-6.
PMID: 18809839
Background: Mutations in PARK8 (LRRK2) are associated with autosomal dominant parkinsonism and Parkinson disease (PD). Hyposmia is present in at least 80% of patients with PD and an accumulation of...
10.
Bonifati V, Wu-Chou Y, Schweiger D, Di Fonzo A, Lu C, Oostra B
Neurology
. 2008 Jun;
70(24):2348.
PMID: 18541891
No abstract available.