E Fabrizio
Overview
Explore the profile of E Fabrizio including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
21
Citations
632
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Azaza M, Tanougast C, Fabrizio E, Mami A
ISA Trans
. 2016 Jan;
61:297-307.
PMID: 26749556
Greenhouse climate control is complicated procedure since the number of variables involved on it and which are dependent on each other. This paper presents a contribution to integrate greenhouse inside...
2.
Goldwurm S, Di Fonzo A, Simons E, Rohe C, Zini M, Canesi M, et al.
J Med Genet
. 2005 Nov;
42(11):e65.
PMID: 16272257
Background: Mutations in the gene Leucine-Rich Repeat Kinase 2 (LRRK2) were recently identified as the cause of PARK8 linked autosomal dominant Parkinson's disease. Objective: To study recurrent LRRK2 mutations in...
3.
Bonifati V, Rohe C, Breedveld G, Fabrizio E, De Mari M, Tassorelli C, et al.
Neurology
. 2005 Jul;
65(1):87-95.
PMID: 16009891
Objective: To assess the prevalence, nature, and associated phenotypes of PINK1 gene mutations in a large series of patients with early-onset (<50 years) parkinsonism. Methods: The authors studied 134 patients...
4.
Meco G, Fabrizio E, Epifanio A, Di Raimondo G, Vanacore N, Morgante L
Clin Neuropharmacol
. 2005 Mar;
28(2):102-3.
PMID: 15795556
No abstract available.
5.
Bonifati V, Lucking C, Fabrizio E, Periquet M, Meco G, Brice A
J Neurol Neurosurg Psychiatry
. 2001 Sep;
71(4):531-4.
PMID: 11561042
The objective was to describe a family with autosomal recessive, early onset parkinsonism, with affected siblings carrying three different exon rearrangements in the parkin gene. The living affected siblings were...
6.
Bonifati V, De Michele G, Lucking C, Durr A, Fabrizio E, Ambrosio G, et al.
Neurol Sci
. 2001 Aug;
22(1):51-2.
PMID: 11487197
Mutations of the parkin gene on chromosome 6 cause autosomal recessive, early onset parkinsonism. This is the most frequent form of monogenic parkinsonism so far identified. The associated phenotypical spectrum...
7.
Gasparini M, Bonifati V, Fabrizio E, Fabbrini G, Brusa L, Lenzi G, et al.
J Neurol
. 2001 Jul;
248(5):399-402.
PMID: 11437162
27 patients with essential tremor (ET) were studied to determine the cognitive feature of this condition. 15 familial cases and 12 cases with a family history Parkinson's disease (PD) were...
8.
Abbas N, Lucking C, Ricard S, Durr A, Bonifati V, De Michele G, et al.
Hum Mol Genet
. 1999 Mar;
8(4):567-74.
PMID: 10072423
Autosomal recessive juvenile parkinsonism (AR-JP, PARK2; OMIM 602544), one of the monogenic forms of Parkinson's disease (PD), was initially described in Japan. It is characterized by early onset (before age...
9.
Vaughan J, Durr A, Tassin J, Bereznai B, Gasser T, Bonifati V, et al.
Ann Neurol
. 1998 Aug;
44(2):270-3.
PMID: 9708553
We report the results of a screen of 230 European familial index cases of Parkinson's disease for the recently described Ala53Thr mutation in the alpha-synuclein gene in an autosomal dominant...
10.
Gasser T, Muller-Myhsok B, Wszolek Z, Oehlmann R, Calne D, Bonifati V, et al.
Nat Genet
. 1998 Mar;
18(3):262-5.
PMID: 9500549
Parkinson's disease (PD) is a common degenerative neurologic disorder, which is pathologically characterized by a selective degeneration of dopaminergic neurons of the substantia nigra pars compacta, and the presence of...