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Novel human pathological mutations. Gene symbol: NOTCH3. Disease: CADASIL.
del Río-Espínola A, Fernández-Cadenas I, Mendióroz M, Gutiérrez-Agullo M, Fernández MT, Fernández-Morales J, Delgado P, Domingues-Montanari S, Solé E, Montaner J. del Río-Espínola A, et al. Hum Genet. 2010 Apr;127(4):473-4. Hum Genet. 2010. PMID: 21488283 No abstract available.
Novel human pathological mutations. Gene symbol: NOTCH3. Disease: CADASIL.
del Río-Espínola A, Fernández-Cadenas I, Mendióroz M, Gutiérrez-Agulló M, Fernández MT, Fernández-Morales J, Maisterra O, Domingues-Montanari S, García-Patos V, Solé E, Montaner J. del Río-Espínola A, et al. Hum Genet. 2010 Apr;127(4):474. Hum Genet. 2010. PMID: 21488300 No abstract available.
CADASIL management or what to do when there is little one can do.
del Río-Espínola A, Mendióroz M, Domingues-Montanari S, Pozo-Rosich P, Solé E, Fernández-Morales J, Fernández-Cadenas I, Montaner J. del Río-Espínola A, et al. Expert Rev Neurother. 2009 Feb;9(2):197-210. doi: 10.1586/14737175.9.2.197. Expert Rev Neurother. 2009. PMID: 19210195 Review.
Update on the Serum Biomarkers and Genetic Factors Associated with Safety and Efficacy of rt-PA Treatment in Acute Stroke Patients.
Nafría C, Fernández-Cadenas I, Mendioroz M, Domingues-Montanari S, Hernández-Guillamón M, Fernández-Morales J, Del Río-Espínola A, Giralt D, Deu L, Delgado P, Rosell A, Montaner J. Nafría C, et al. Stroke Res Treat. 2011;2011:182783. doi: 10.4061/2011/182783. Epub 2011 Jun 9. Stroke Res Treat. 2011. PMID: 21772966 Free PMC article.
KCNK17 genetic variants in ischemic stroke.
Domingues-Montanari S, Fernández-Cadenas I, Del Río-Espinola A, Mendioroz M, Fernandez-Morales J, Corbeto N, Delgado P, Ribó M, Rubiera M, Obach V, Martí-Fàbregas J, Freijo M, Serena J, Montaner J. Domingues-Montanari S, et al. Atherosclerosis. 2010 Jan;208(1):203-9. doi: 10.1016/j.atherosclerosis.2009.07.023. Epub 2009 Jul 31. Atherosclerosis. 2010. PMID: 19647252
Genes involved in hemorrhagic transformations that follow recombinant t-PA treatment in stroke patients.
Fernandez-Cadenas I, Del Rio-Espinola A, Domingues-Montanari S, Mendioroz M, Fernandez-Morales J, Penalba A, Rubiera M, Hernandez-Guillamon M, Rosell A, Delgado P, Chacon P, Ribo M, Alvarez-Sabin J, Molina CA, García-Arumi E, Montaner J. Fernandez-Cadenas I, et al. Pharmacogenomics. 2013 Apr;14(5):495-504. doi: 10.2217/pgs.13.19. Pharmacogenomics. 2013. PMID: 23556447
Candidate-gene association study searching for genetic factors involved in migraine chronification.
Louter MA, Fernandez-Morales J, de Vries B, Winsvold B, Anttila V, Fernandez-Cadenas I, Vila-Pueyo M, Sintas C, van Duijn CM, Cormand B, Álvarez-Sabin J, Montaner J, Ferrari MD, van den Maagdenberg A, Palotie A, Zwart JA, Macaya A, Terwindt GM, Pozo-Rosich P. Louter MA, et al. Cephalalgia. 2015 May;35(6):500-7. doi: 10.1177/0333102414547141. Epub 2014 Aug 28. Cephalalgia. 2015. PMID: 25169732
Association of a genetic variant in the ALOX5AP with higher risk of ischemic stroke: a case-control, meta-analysis and functional study.
Domingues-Montanari S, Fernández-Cadenas I, del Rio-Espinola A, Corbeto N, Krug T, Manso H, Gouveia L, Sobral J, Mendioroz M, Fernández-Morales J, Alvarez-Sabin J, Ribó M, Rubiera M, Obach V, Martí-Fàbregas J, Freijo M, Serena J, Ferro JM, Vicente AM, Oliveira SA, Montaner J. Domingues-Montanari S, et al. Cerebrovasc Dis. 2010;29(6):528-37. doi: 10.1159/000302738. Epub 2010 Mar 30. Cerebrovasc Dis. 2010. PMID: 20357438
48 results