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Cephalalgia : an International Journal of Headache|July 23, 2008
Genetic analysis of 27 Spanish patients with hemiplegic migraine, basilar-type migraine and childhood periodic syndromesE Cuenca-León, R Corominas, N Fernàndez-Castillo, et al.Transplant International : Official Journal of the European Society for Organ Transplantation|January 1, 1995
Post-transplant lymphoma in a liver allograftY Ribas, A Rafecas, J Figueras, et al.Blood|April 15, 1997
Absence of linkage between type III protein S deficiency and the PROS1 and C4BP genes in families carrying the protein S Heerlen alleleY Espinosa-Parrilla, M Morell, J C Souto, et al.Human Genetics|October 1, 1994
Molecular analysis of the (CGG)n expansion in the FMR-1 gene in 59 Spanish fragile X syndrome familiesM Milà, H Kruyer, G Glover, et al.Journal of Medical Genetics|February 9, 1999
High prevalence of the C634Y mutation in the RET proto-oncogene in MEN 2A families in SpainB Sánchez, M Robledo, J Biarnes, et al.Human Molecular Genetics|July 1, 1995
WASP gene mutations in Wiskott-Aldrich syndrome and X-linked thrombocytopeniaJ M Derry, J A Kerns, K I Weinberg, et al.American Journal of Human Genetics|May 1, 1996
Autosomal recessive Wolfram syndrome associated with an 8.5-kb mtDNA single deletionA Barrientos, J Casademont, A Saiz, et al.Proceedings of the National Academy of Sciences of the United States of America|October 10, 1995
Genetic heterogeneity in cystinuria: the SLC3A1 gene is linked to type I but not to type III cystinuriaM J Calonge, V Volpini, L Bisceglia, et al.AIDS (London, England)|May 1, 1993
Effects of zidovudine in 30 patients with mild to end-stage AIDS dementia complexV Tozzi, P Narciso, S Galgani, et al.The Journal of Clinical Investigation|April 1, 1996
A nuclear defect in the 4p16 region predisposes to multiple mitochondrial DNA deletions in families with Wolfram syndromeA Barrientos, V Volpini, J Casademont, et al.Pageof 6