Giuseppe Lucente
Overview
Explore the profile of Giuseppe Lucente 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
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Articles
25
Citations
85
Followers
0
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Recent Articles
11.
Alvarez M, Lucente G, Martinez L, Almendrote M, Ramos A, Broto J, et al.
Ann Vasc Surg
. 2020 Sep;
70:569.e1-569.e4.
PMID: 32927034
Ischemic lumbosacral plexopathy secondary to an acute aortic dissection is a rare condition that is usually unilateral and frequently accompanied by a simultaneous spinal cord infarction. The functional prognosis relies...
12.
Ballester-Lopez A, Nunez-Manchon J, Koehorst E, Linares-Pardo I, Almendrote M, Lucente G, et al.
Neurol Genet
. 2020 Aug;
6(4):e484.
PMID: 32802949
Objective: We aimed to determine whether 3D imaging reconstruction allows identifying molecular:clinical associations in myotonic dystrophy type 1 (DM1). Methods: We obtained myoblasts from 6 patients with DM1 and 6...
13.
Ballester-Lopez A, Linares-Pardo I, Koehorst E, Nunez-Manchon J, Pintos-Morell G, Coll-Canti J, et al.
Genes (Basel)
. 2020 Jul;
11(7).
PMID: 32645888
The number of cytosine-thymine-guanine (CTG) repeats ('CTG expansion size') in the 3'untranslated region (UTR) region of the -protein kinase () gene is a hallmark of myotonic dystrophy type 1 (DM1),...
14.
Lucente G, Martinez-Barenys C, Ramos-Fransi A, Almendrote-Munoz M, Lopez de Castro P, Deletis V, et al.
J Clin Neurophysiol
. 2020 Jan;
38(3):226-230.
PMID: 31895134
Introduction: The phrenic nerve could be easily injured during cardiothoracic surgeries because of its anatomical relationships. The aim of this study is to describe a new, feasible, and reproducible methodology...
15.
Lucente G, Valls-Sole J, Murillo N, Rothwell J, Coll J, Davalos A, et al.
Neuromodulation
. 2019 Nov;
23(3):312-323.
PMID: 31725939
Objective: Hemispatial neglect is a frequent condition usually following nondominant hemispheric brain injury. It strongly affects rehabilitation strategies and everyday life activities. It is associated with behavioral and cognitive disability...
16.
Ballester-Lopez A, Koehorst E, Almendrote M, Martinez-Pineiro A, Lucente G, Linares-Pardo I, et al.
Hum Mutat
. 2019 Oct;
41(2):420-431.
PMID: 31608518
Carriage of interruptions in CTG repeats of the myotonic dystrophy protein kinase gene has been associated with a broad spectrum of myotonic dystrophy type 1 (DM1) phenotypes, mostly mild. However,...
17.
Lam S, Lucente G, Schneider H, Picht T
Acta Neurochir (Wien)
. 2019 Mar;
161(5):995-1002.
PMID: 30927156
Objective: Navigated transcranial magnetic stimulation (nTMS) has found widespread usage across many clinical centers as part of their surgical planning routines. NTMS offers a non-invasive approach to delineation of the...
18.
Lucente G, Almendrote M, Ramos-Fransi A, Martinez-Pineiro A, Camano P, Ballester-Lopez A, et al.
J Neurol Sci
. 2018 Aug;
391:112-113.
PMID: 30103957
No abstract available.
19.
Nunez-Manchon J, Ballester-Lopez A, Koehorst E, Linares-Pardo I, Coenen D, Ara I, et al.
J Inherit Metab Dis
. 2018 Jul;
41(6):1295.
PMID: 30030676
Unfortunately the name of one of the authors was spelled incorrectly in the published original article. The correct name is Alejandro Santos-Lozano. The original article got updated.
20.
Nunez-Manchon J, Ballester-Lopez A, Koehorst E, Linares-Pardo I, Coenen D, Ara I, et al.
J Inherit Metab Dis
. 2018 Jun;
41(6):1027-1035.
PMID: 29926259
McArdle disease is an autosomal recessive condition caused by deficiency of the PYGM gene-encoded muscle isoform of glycogen phosphorylase. Some cases of "manifesting" heterozygotes or carriers (i.e., patients who show...