Zobrazeno 1 - 8
of 8
pro vyhledávání: '"F. David Carmona"'
Autor:
Sandra Sousa, Susana Seixas, Patrícia Isabel Marques, Olga López-Rodrigo, João Gonçalves, Lluís Bassas, Alberto Pacheco, Alberto Barros, M. Fernanda Peraza, Carlos Calhaz-Jorge, F. David Carmona, Josvany Sánchez-Curbelo, Gema Romeu, Cristina Gonzalez, Miriam Cerván-Martín, Iris Pereira-Caetano, S.C. Correia, Joaquim Nunes, Rocio Rivera-Egea, M. Irene Suazo-Sánchez, Samuel Santos-Ribeiro, Rogelio Palomino-Morales, José A. Castilla, Sara Larriba, Rafael Jiménez, Nicolás Garrido, Vicente Maldonado, David Amoros, Alexandra M. Lopes, Francisco J. Barrionuevo, Susana Gómez, Maria Graça Pinto, Miguel Burgos, Filipa Carvalho, Ana Aguiar, Fernando Quintana, M. Carmen Gonzalvo, Saturnino Luján, J. Aguilar, F. Javier Vicente, Ana Clavero
Objective: To evaluate whether SOHLH2 intronic variation contributes to the genetic predisposition to male infertility traits, including severe oligospermia (SO) and different nonobstructive azoospermia (NOA) clinical phenotypes. Design: Genetic asso
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e760c0e15d688af86f0dda15218b0cfe
https://hdl.handle.net/10400.18/7351
https://hdl.handle.net/10400.18/7351
Autor:
Trinitario Pina Murcia, Mark Little, F. David Carmona, Ricardo Blanco, Miguel Gonzalez-Gay, Sandosh Padmanabhan, Norberto Ortego-Centeno, Javier Llorca, Raquel Rios-Fernández, David Jayne, Olga Sanchez Pernaute, Laura Tío Barrera, Ann Morgan, Nurullah Akkoç, Patrick Coit, Javier Martin, ALEIDA MARTÍNEZ ZAPICO, Juan Jose Alegre Sancho, Kenneth Smith, Antonio Fernandez-Nebro, Lourdes Ortiz-Fernández
ObjetiveSystemic vasculitides represent a heterogeneous group of rare complex diseases of the blood vessels with a poorly understood aetiology. To investigate the shared genetic component underlying their predisposition, we performed the first cross-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e7d12d120178e910348b5417c1ef03e2
https://hdl.handle.net/10668/12055
https://hdl.handle.net/10668/12055
Autor:
Gema Robledo, Amr H. Sawalha, Haner Direskeneli, Sule Yavuz, Tamara Fernández-Aranguren, F. David Carmona, Alberto Serrano-Fernández, Javier Martín, Ahmet Mesut Onat
Publikováno v:
The Journal of rheumatology. 43(7)
Objective.To evaluate the genetic background of systemic sclerosis (SSc) in the Turkish population.Methods.There were 354 cases and 718 unaffected controls from Turkey genotyped for the most relevant SSc genetic markers (IRF5-rs10488631, STAT4-rs3821
Autor:
F. David Carmona, Javier Martín
Publikováno v:
Systemic Vasculitides: Current Status and Perspectives ISBN: 9783319401348
Giant cell arteritis (GCA) is a complex condition in which many loci across the genome may be involved in its susceptibility and phenotypic expression. However, recent large-scale genetic data has shown that the HLA system exerts most of the genetic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9a952757e9a64a5de2996a394e63acee
https://doi.org/10.1007/978-3-319-40136-2_9
https://doi.org/10.1007/978-3-319-40136-2_9
Autor:
F David Carmona, Jose-Ezequiel Martin, Lorenzo Beretta, Carmen P Simeón, Patricia E Carreira, José Luis Callejas, Mónica Fernández-Castro, Luis Sáez-Comet, Emma Beltrán, María Teresa Camps, María Victoria Egurbide, Spanish Scleroderma Group, Paolo Airó, Raffaella Scorza, Claudio Lunardi, Nicolas Hunzelmann, Gabriela Riemekasten, Torsten Witte, Alexander Kreuter, Jörg H W Distler, Rajan Madhok, Paul Shiels, Jacob M van Laar, Carmen Fonseca, Christopher Denton, Ariane Herrick, Jane Worthington, Annemie J Schuerwegh, Madelon C Vonk, Alexandre E Voskuyl, Timothy R D J Radstake, Javier Martín
Publikováno v:
PLoS ONE, Vol 8, Iss 1, p e54419 (2013)
PLoS One, 8
PLoS One, 8, 1
PLoS ONE, 8(1):e54419. Public Library of Science
Carmona, F D, Martin, J E, Beretta, L, Simeon, C P, Carreira, P E, Callejas, J L, Fernandez-Castro, M, Saez-Comet, L, Beltran, E, Camps, M T, Egurbide, M V, Airo, P, Scorza, R, Lunardi, C, Hunzelmann, N, Riemekasten, G, Witte, T, Kreuter, A, Distler, J H W, Madhok, R, Shiels, P, van Laar, J M, Fonseca, C, Denton, C, Herrick, A, Worthington, J, Schuerwegh, A J, Vonk, M C, Voskuyl, A E, Radstake, T R D J & Martin, J 2013, ' The Systemic Lupus Erythematosus IRF5 Risk Haplotype Is Associated with Systemic Sclerosis ', PLoS ONE, vol. 8, no. 1, e54419 . https://doi.org/10.1371/journal.pone.0054419
PLoS ONE
PLoS One, 8
PLoS One, 8, 1
PLoS ONE, 8(1):e54419. Public Library of Science
Carmona, F D, Martin, J E, Beretta, L, Simeon, C P, Carreira, P E, Callejas, J L, Fernandez-Castro, M, Saez-Comet, L, Beltran, E, Camps, M T, Egurbide, M V, Airo, P, Scorza, R, Lunardi, C, Hunzelmann, N, Riemekasten, G, Witte, T, Kreuter, A, Distler, J H W, Madhok, R, Shiels, P, van Laar, J M, Fonseca, C, Denton, C, Herrick, A, Worthington, J, Schuerwegh, A J, Vonk, M C, Voskuyl, A E, Radstake, T R D J & Martin, J 2013, ' The Systemic Lupus Erythematosus IRF5 Risk Haplotype Is Associated with Systemic Sclerosis ', PLoS ONE, vol. 8, no. 1, e54419 . https://doi.org/10.1371/journal.pone.0054419
PLoS ONE
Systemic sclerosis (SSc) is a fibrotic autoimmune disease in which the genetic component plays an important role. One of the strongest SSc association signals outside the human leukocyte antigen (HLA) region corresponds to interferon (IFN) regulatory
Autor:
Jose Luis Andreu Sanchez, Eugenio De Miguel, F. David Carmona, Patricia E Carreira, Ricardo Blanco, Luis Rodriguez-Rodriguez, José Luis Andreu, Miguel Gonzalez-Gay, Luis Sáez Comet, Norberto Ortego-Centeno, Ivan Castellvi, Monica Rodriguez Carballeira, Federico Diaz-Gonzalez, Jose luis Callejas, Benjamin Fernandez-Gutierrez, MA Aguirre, Javier Narvaez, Emma Beltrán Catalán, Javier Martin, Antonio Fernandez-Nebro, Francisco J Blanco Garcia
Publikováno v:
The Journal of rheumatology. 39(6)
Objective.We evaluated whether a single-nucleotide polymorphism (SNP) of theTRAF6gene previously associated with systemic lupus erythematosus and rheumatoid arthritis may be a common risk factor for systemic sclerosis (SSc) and giant cell arteritis (
Autor:
Aurora, Serrano, F David, Carmona, José A, Miranda-Filloy, Santos, Castañeda, Luis, Rodríguez-Rodríguez, Inmaculada C, Morado, Carmen, Gómez-Vaquero, Roser, Solans, Bernardo, Sopeña, Ricardo, Blanco, Ainhoa, Unzurrunzaga, Norberto, Ortego-Centeno, Begoña, Marí-Alfonso, Eugenio, de Miguel, Ana, Hidalgo-Conde, Javier, Martín, Miguel A, González-Gay
Publikováno v:
Clinical and experimental rheumatology. 30(1 Suppl 70)
CD226 genetic variants have been associated with a number of autoimmune diseases. The aim of this study was to investigate the potential implication of the CD226 loci in the susceptibility to and main clinical manifestations of giant cell arteritis (
Autor:
Serrano A, F. David Carmona, Castañeda S, Ja, Miranda-Filloy, Ic, Morado, Gomez-Vaquero C, Solans R, Sopeña B, Blanco R, Unzurrunzaga A, Ortego-Centeno N, Marí-Alfonso B, Hidalgo-Conde A, Hernández-Rodríguez J, Mc, Cid, Martín J, Ma, Gonzalez-Gay
Publikováno v:
Scopus-Elsevier
ResearcherID
CIÊNCIAVITAE
Europe PubMed Central
ResearcherID
CIÊNCIAVITAE
Europe PubMed Central
Polymorphisms of the CC chemokine receptor 6 (CCR6) gene have been recently reported to be associated with a number of autoimmune diseases. We aimed to investigate the possible influence of CCR6 rs3093024 gene variant in the susceptibility to and cli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::93e481669285964839cc868b9f5cc3fa
http://www.scopus.com/inward/record.url?eid=2-s2.0-84878385030&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-84878385030&partnerID=MN8TOARS