Miguel Lucas
Overview
Explore the profile of Miguel Lucas including associated specialties, affiliations and a list of published articles.
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Articles
30
Citations
631
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0
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Recent Articles
1.
De Beir J, Lucas M, Jesus A, Gata L, Finn A, Rodrigues F
Pediatr Infect Dis J
. 2024 Jan;
43(3):e106-e108.
PMID: 38241651
An increase in invasive group A Streptococcus infections was reported in 2022, associated with intense respiratory virus circulation. We describe a marked increase of noninvasive group A Streptococcus infections. Although...
2.
Relvas M, Xara J, Lucas M, Coelho S, Coutinho I, Cardoso J, et al.
J Paediatr Child Health
. 2023 Jan;
59(3):573-576.
PMID: 36718585
No abstract available.
3.
Tristan-Clavijo E, Scholl F, Macaya A, Iglesias G, Rojas A, Lucas M, et al.
Mov Disord
. 2016 Aug;
31(11):1743-1748.
PMID: 27477325
Background: Episodic ataxia type 1 is a rare autosomal dominant neurological disorder caused by mutations in the KCNA1 gene that encodes the α subunit of voltage-gated potassium channel Kv1.1. The...
4.
Matesanz F, Potenciano V, Fedetz M, Ramos-Mozo P, Abad-Grau M, Karaky M, et al.
Hum Mol Genet
. 2015 Jul;
24(19):5619-27.
PMID: 26152201
Several variants in strong linkage disequilibrium (LD) at the SP140 locus have been associated with multiple sclerosis (MS), Crohn's disease (CD) and chronic lymphocytic leukemia (CLL). To determine the causal...
5.
Delgado-Garcia M, Matesanz F, Alcina A, Fedetz M, Garcia-Sanchez M, Ruiz-Pena J, et al.
Mult Scler
. 2014 Nov;
21(9):1104-11.
PMID: 25392328
Background: Recent findings have shown a correlation between the intrathecal IgG index and variants at the immunoglobulin heavy chain (IGHC) locus in patients with multiple sclerosis (MS). Objectives: The objective...
6.
Mondejar R, Solano F, Rubio R, Delgado M, Perez-Sempere A, Gonzalez-Meneses A, et al.
PLoS One
. 2014 Jan;
9(1):e86286.
PMID: 24466005
Objective: To study the molecular genetic and clinical features of cerebral cavernous malformations (CCM) in a cohort of Spanish patients. Methods: We analyzed the CCM1, CCM2, and CCM3 genes by...
7.
Mondejar R, Garcia-Moreno J, Rubio R, Solano F, Delgado M, Garcia-Bravo B, et al.
J Clin Neurol
. 2014 Jan;
10(1):64-8.
PMID: 24465266
Background: Lipoid proteinosis (LP) is a rare autosomal recessive disorder characterized by a hoarse voice, variable scarring, and infiltration of the skin and mucosa. This disease is associated with mutations...
8.
Garcia-Montojo M, de la Hera B, Varade J, de la Encarnacion A, Camacho I, Dominguez-Mozo M, et al.
Retrovirology
. 2014 Jan;
11:2.
PMID: 24405691
Background: Multiple Sclerosis (MS) is an autoimmune demyelinating disease that occurs more frequently in women than in men. Multiple Sclerosis Associated Retrovirus (MSRV) is a member of HERV-W, a multicopy...
9.
Swaminathan B, Cuapio A, Alloza I, Matesanz F, Alcina A, Garcia-Barcina M, et al.
PLoS One
. 2013 May;
8(4):e62376.
PMID: 23638056
CD6 has recently been identified and validated as risk gene for multiple sclerosis (MS), based on the association of a single nucleotide polymorphism (SNP), rs17824933, located in intron 1. CD6...
10.
Alcina A, Fedetz M, Fernandez O, Saiz A, Izquierdo G, Lucas M, et al.
J Med Genet
. 2012 Nov;
50(1):25-33.
PMID: 23160276
Background And Aim: Several studies have highlighted the association of the 12q13.3-12q14.1 region with coeliac disease, type 1 diabetes, rheumatoid arthritis and multiple sclerosis (MS); however, the causal variants underlying...