Browsing by Author Fernández-Burriel, M.

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TitleAuthor(s)???itemlist.dc.contributor.advisor??????itemlist.dc.contributor.editor??????itemlist.dc.contributor.titulacion???Issue Date???itemlist.dc.identifier.doi??????itemlist.dc.source??????itemlist.dc.description.sjr??????itemlist.dc.description.sjrq??????itemlist.dc.description.jcr??????itemlist.dc.description.jcrq???TypePreview
Paroxysmal stereotypy-tic-dystonia syndromeCabrera-López, J. C.; Martí-Herrero, M.; Fernández-Burriel, M.; Toledo Bravo de Laguna, L. ; Domínguez-Ramírez, S., et al2003Revista de Neurologia[ISSN 0210-0010],v. 36, p. 729-7340,201Q4Artículo
The R608del mutation in the acid sphingomyelinase gene (SMPD1) is the most prevalent among patients from Gran Canaria Island with Niemann-Pick disease type B [2]Fernández-Burriel, M.; Peña, L. ; Ramos, J. C.; Cabrera, J. C.; Marti, M., et al200310.1034/j.1399-0004.2003.00025.xClinical Genetics[ISSN 0009-9163],v. 63, p. 235-2362,025Q3Comentario
Molecular diagnosis of adult dominant polycystic kidney disease in the Canary IslandsTorres, M. J.; Rodriguez Perez, J. C. ; Hernández Socorro, C. R. ; Anabitarte, A.; Caballero, A., et al2006Nefrologia[ISSN 0211-6995],v. 26 (6), p. 666-6720,609Q4Artículo