Publicaciones en colaboración con investigadores/as de Centro de Investigación Biomédica en Red sobre Enfermedades Raras (10)

2024

  1. Further Evidence of Cerebellar Cognitive Affective/Schmahmann Syndrome in RFC1-Related Syndrome

    Movement Disorders

  2. Relationship between sex, APOE genotype, endocannabinoids and cognitive change in older adults with metabolic syndrome during a 3-year Mediterranean diet intervention

    Nutrition Journal, Vol. 23, Núm. 1

2016

  1. CHK1 expression in Gastric Cancer is modulated by p53 and RB1/E2F1: Implications in chemo/radiotherapy response

    Scientific Reports, Vol. 6

2015

  1. Semantic verbal fluency pattern, dementia rating scores and adaptive behavior correlate with plasma Aβ42concentrations in down syndrome young adults

    Frontiers in Behavioral Neuroscience, Vol. 9, Núm. NOVEMBER

2010

  1. Involvement of ERK1/2, p38 and PI3K in megakaryocytic differentiation of K562 cells

    European Journal of Haematology, Vol. 84, Núm. 5, pp. 430-440

  2. L718P mutation in the membrane-proximal cytoplasmic tail of β3 promotes abnormal αIIbβ3 clustering and lipid microdomain coalescence, and associates with a thrombasthenia-like phenotype

    Haematologica, Vol. 95, Núm. 7, pp. 1158-1166

2009

  1. New insights into the expression and role of platelet factor XIII-A

    Journal of Thrombosis and Haemostasis, Vol. 7, Núm. 7, pp. 1184-1191

  2. Possible role for cellular FXIII in monocyte-derived dendritic cell motility

    European Journal of Cell Biology, Vol. 88, Núm. 8, pp. 423-431

  3. The second wind phenomenon in very young McArdle's patients

    Neuromuscular Disorders, Vol. 19, Núm. 6, pp. 403-405

2008

  1. The / allele of the ACE gene is associated with improved exercise capacity in women with McArdle disease

    British Journal of Sports Medicine, Vol. 42, Núm. 2, pp. 134-140