Neurociències Clíniques
2014 SGR 1418
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Hospital Universitario Central de Asturias
Oviedo, EspañaPublicaciones en colaboración con investigadores/as de Hospital Universitario Central de Asturias (10)
2021
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CYP24A1 and KL polymorphisms are associated with the extent of vascular calcification but do not improve prediction of cardiovascular events
Nephrology Dialysis Transplantation, Vol. 36, Núm. 11, pp. 2076-2083
2020
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Association of a single nucleotide polymorphism combination pattern of the Klotho gene with non-cardiovascular death in patients with chronic kidney disease
Clinical Kidney Journal, Vol. 13, Núm. 6, pp. 1017-1024
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Genome-Wide Association Study of VKORC1 and CYP2C9 on acenocoumarol dose, stroke recurrence and intracranial haemorrhage in Spain
Scientific Reports, Vol. 10, Núm. 1
2019
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Association of candidate gene polymorphisms with chronic kidney disease: Results of a case-control analysis in the NEFRONA cohort
Frontiers in Genetics, Vol. 10, Núm. FEB
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The rs1126616 single nucleotide polymorphism of the osteopontin gene is independently associated with cardiovascular events in a chronic kidney disease cohort
Journal of Clinical Medicine, Vol. 8, Núm. 5
2018
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Prognostic factors and analysis of mortality due to brain haemorrhages associated with vitamin K antagonist oral anticoagulants. Results from the TAC registry
Neurologia, Vol. 33, Núm. 7, pp. 419-426
2014
2011
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Plan de asistencia sanitaria al ICTUS II. 2010
Neurologia, Vol. 26, Núm. 7, pp. 383-396
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Recursos asistenciales en ictus en España 2010: análisis de una encuesta nacional del Grupo de Estudio de Enfermedades Cerebrovasculares
Neurologia, Vol. 26, Núm. 8, pp. 449-454
2009
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Prevalencia de enfermedad arterial periférica asintomática en pacientes con ictus isquémico no cardioembólico
Neurologia, Vol. 24, Núm. 6, pp. 366-372