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Fuencisla Matesanz

Showing results (31-40 of 58) with videos related to

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Neurology|April 30, 2013
TNFRSF1A polymorphisms rs1800693 and rs4149584 in patients with multiple sclerosisManuel Comabella, Ana B Caminero, Sunny Malhotra, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|March 21, 2024
No evidence for association between rs10191329 severity locus and longitudinal disease severity in 1813 relapse-onset multiple sclerosis patients from the MSBase registryMaria Pia Campagna, Eva Kubala Havrdova, Dana Horakova, et al.
Plos One|March 6, 2014
Human endogenous retrovirus HERV-Fc1 association with multiple sclerosis susceptibility: a meta-analysisBelén de la Hera, Jezabel Varadé, Marta García-Montojo, et al.
Human Molecular Genetics|January 28, 2022
Identification of the genetic mechanism that associates L3MBTL3 to multiple sclerosisAntonio Alcina, Maria Fedetz, Isabel Vidal-Cobo, et al.
Retrovirology|January 11, 2014
HERV-W polymorphism in chromosome X is associated with multiple sclerosis risk and with differential expression of MSRVMarta García-Montojo, Belén de la Hera, Jezabel Varadé, et al.
Plos One|August 15, 2015
Influence of the LILRA3 Deletion on Multiple Sclerosis Risk: Original Data and Meta-AnalysisMiguel A Ortiz, Concepción Núñez, David Ordóñez, et al.
Plos One|May 3, 2013
Fine mapping and functional analysis of the multiple sclerosis risk gene CD6Bhairavi Swaminathan, Angélica Cuapio, Iraide Alloza, et al.
Plos One|July 17, 2010
CD40: novel association with Crohn's disease and replication in multiple sclerosis susceptibilityFiona Blanco-Kelly, Fuencisla Matesanz, Antonio Alcina, et al.
Human Mutation|March 21, 2020
Targeted resequencing reveals rare variants enrichment in multiple sclerosis susceptibility genesElia Gil-Varea, Nino Spataro, Luisa María Villar, et al.
Journal of Clinical Medicine|March 1, 2020
A New Risk Variant for Multiple Sclerosis at 11q23.3 <i>Locus</i> Is Associated with Expansion of <i>CXCR5+</i> Circulating Regulatory T CellsElia Gil-Varea, Maria Fedetz, Herena Eixarch, et al.
Pageof 6

Showing results (31-40 of 58) with videos related to

Sort By:
Pageof 6
Neurology|April 30, 2013
TNFRSF1A polymorphisms rs1800693 and rs4149584 in patients with multiple sclerosisManuel Comabella, Ana B Caminero, Sunny Malhotra, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|March 21, 2024
No evidence for association between rs10191329 severity locus and longitudinal disease severity in 1813 relapse-onset multiple sclerosis patients from the MSBase registryMaria Pia Campagna, Eva Kubala Havrdova, Dana Horakova, et al.
Plos One|March 6, 2014
Human endogenous retrovirus HERV-Fc1 association with multiple sclerosis susceptibility: a meta-analysisBelén de la Hera, Jezabel Varadé, Marta García-Montojo, et al.
Human Molecular Genetics|January 28, 2022
Identification of the genetic mechanism that associates L3MBTL3 to multiple sclerosisAntonio Alcina, Maria Fedetz, Isabel Vidal-Cobo, et al.
Retrovirology|January 11, 2014
HERV-W polymorphism in chromosome X is associated with multiple sclerosis risk and with differential expression of MSRVMarta García-Montojo, Belén de la Hera, Jezabel Varadé, et al.
Plos One|August 15, 2015
Influence of the LILRA3 Deletion on Multiple Sclerosis Risk: Original Data and Meta-AnalysisMiguel A Ortiz, Concepción Núñez, David Ordóñez, et al.
Plos One|May 3, 2013
Fine mapping and functional analysis of the multiple sclerosis risk gene CD6Bhairavi Swaminathan, Angélica Cuapio, Iraide Alloza, et al.
Plos One|July 17, 2010
CD40: novel association with Crohn's disease and replication in multiple sclerosis susceptibilityFiona Blanco-Kelly, Fuencisla Matesanz, Antonio Alcina, et al.
Human Mutation|March 21, 2020
Targeted resequencing reveals rare variants enrichment in multiple sclerosis susceptibility genesElia Gil-Varea, Nino Spataro, Luisa María Villar, et al.
Journal of Clinical Medicine|March 1, 2020
A New Risk Variant for Multiple Sclerosis at 11q23.3 <i>Locus</i> Is Associated with Expansion of <i>CXCR5+</i> Circulating Regulatory T CellsElia Gil-Varea, Maria Fedetz, Herena Eixarch, et al.
Pageof 6