FACULTAD DE CIENCIAS
Facultad
Hospital Universitario La Fe
Valencia, EspañaPublicaciones en colaboración con investigadores/as de Hospital Universitario La Fe (27)
2023
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Use of sera cell free DNA (cfDNA) and exovesicle-DNA for the molecular diagnosis of chronic Chagas disease
PloS one, Vol. 18, Núm. 9, pp. e0282814
2022
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Common Variation in the PIN1 Locus Increases the Genetic Risk to Suffer from Sertoli Cell-Only Syndrome
Journal of Personalized Medicine, Vol. 12, Núm. 6
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Common genetic variation in KATNAL1 non-coding regions is involved in the susceptibility to severe phenotypes of male infertility
Andrology, Vol. 10, Núm. 7, pp. 1339-1350
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Contribution of TEX15 genetic variants to the risk of developing severe non-obstructive oligozoospermia
Frontiers in Cell and Developmental Biology, Vol. 10
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Immune and spermatogenesis-related loci are involved in the development of extreme patterns of male infertility
Communications Biology, Vol. 5, Núm. 1
2021
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Effect and in silico characterization of genetic variants associated with severe spermatogenic disorders in a large Iberian cohort
Andrology, Vol. 9, Núm. 4, pp. 1151-1165
2020
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Correlation between short-term air pollution exposure and unprovoked lung embolism. Prospective observational (Contamina-TEP Group)
Thrombosis Research, Vol. 192, pp. 134-140
2019
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GWAS for systemic sclerosis identifies multiple risk loci and highlights fibrotic and vasculopathy pathways
Nature Communications, Vol. 10, Núm. 1
2018
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Air density dependence of the soft X-ray PTW 34013 ionization chamber
Physica Medica, Vol. 46, pp. 109-113
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Gene-level association analysis of systemic sclerosis: A comparison of African-Americans and White populations
PLoS ONE, Vol. 13, Núm. 1
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Sex Differences in Patients With Occult Cancer After Venous Thromboembolism
Clinical and Applied Thrombosis/Hemostasis, Vol. 24, Núm. 3, pp. 489-495
2017
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Air density dependence of the response of the PTW SourceCheck 4pi ionization chamber for 125I brachytherapy seeds
Physica Medica, Vol. 38, pp. 93-97
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Analysis of ATP8B4 F436L Missense Variant in a Large Systemic Sclerosis Cohort
Arthritis and Rheumatology, Vol. 69, Núm. 6, pp. 1337-1338
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Regulation of Fn14 receptor and NF-κB underlies inflammation in Meniere's disease
Frontiers in Immunology, Vol. 8, Núm. DEC
2016
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In vitro antileishmanial activity of aza-scorpiand macrocycles. Inhibition of the antioxidant enzyme iron superoxide dismutase
RSC Advances, Vol. 6, Núm. 21, pp. 17446-17455
2015
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Characterization of the PTW SourceCheck ionization chamber with the Valencia lodgment for 125I seed verification
Physica Medica, Vol. 31, Núm. 8, pp. 922-928
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PTGER4 gene variant rs76523431 is a candidate risk factor for radiological joint damage in rheumatoid arthritis patients: A genetic study of six cohorts
Arthritis Research and Therapy, Vol. 17, Núm. 1
2014
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A genome-wide association study follow-up suggests a possible role for PPARG in systemic sclerosis susceptibility
Arthritis Research and Therapy, Vol. 16, Núm. 1
2013
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Bioavailability of antihypertensive lactoferricin B-derived peptides: Transepithelial transport and resistance to intestinal and plasma peptidases
International Dairy Journal, Vol. 32, Núm. 2, pp. 169-174
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Confirmation of TNIP1 but not RHOB and PSORS1C1 as systemic sclerosis risk factors in a large independent replication study
Annals of the Rheumatic Diseases, Vol. 72, Núm. 4, pp. 602-607