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Clinical Chemistry|September 18, 2004
Mutation analysis in Spanish patients with hereditary hemorrhagic telangiectasia: deficient endoglin up-regulation in activated monocytesFrancisco Sanz-Rodriguez, Africa Fernandez-L, Roberto Zarrabeitia, et al.
Immunogenetics|April 11, 2024
Immunoglobulin genes and severity of COVID-19Daniel Vázquez-Coto, Christine Kimball, Guillermo M Albaiceta, et al.
Revista Espanola De Cardiologia|January 20, 2009
[Mutations in sarcomeric genes MYH7, MYBPC3, TNNT2, TNNI3, and TPM1 in patients with hypertrophic cardiomyopathy]Mónica García-Castro, Eliecer Coto, Julián R Reguero, et al.
Coronary Artery Disease|October 24, 2002
Variation in the lipoprotein receptor-related protein, alpha2-macroglobulin and lipoprotein receptor-associated protein genes in relation to plasma lipid levels and risk of early myocardial infarctionPelayo González, Ruth Alvarez, Julián R Reguero, et al.
European Journal of Clinical Investigation|September 20, 2018
Variants in cardiac GATA genes associated with bicuspid aortic valveCristina Alonso-Montes, María Martín, Laura Martínez-Arias, et al.
International Immunopharmacology|November 14, 2015
CDKAL1 gene variants affect the anti-TNF response among Psoriasis patientsPablo Coto-Segura, Ana Batalla, Daniel González-Fernández, et al.
Gene|March 9, 2013
Association between a MYH9 polymorphism (rs3752462) and renal function in the Spanish RENASTUR cohortBeatriz Tavira, Eliecer Coto, Juan Gómez, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|June 24, 2010
Gitelman syndrome in Gypsy paediatric patients carrying the same intron 9 + 1 G>T mutation. Clinical features and impact on quality of lifeJosé David Herrero-Morín, Julián Rodríguez, Eliecer Coto, et al.
Human Immunology|March 31, 2018
Gene variants in the NF-KB pathway (NFKB1, NFKBIA, NFKBIZ) and their association with type 2 diabetes and impaired renal functionEliecer Coto, Carmen Díaz-Corte, Salvador Tranche, et al.
Kidney International|December 17, 2003
A new mutation (intron 9 +1 G>T) in the SLC12A3 gene is linked to Gitelman syndrome in GypsiesEliecer Coto, Julian Rodriguez, Nikola Jeck, et al.
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