Listar Investigación por autor "Lopez-Trascasa, Margarita"
Mostrando ítems 1-4 de 4
-
Detection of C1 inhibitor (SERPING1/C1NH) mutations in exon 8 in patients with hereditary angioedema: evidence for 10 novel mutations
Blanch, Álvaro; Roche, Olga; López-Granados, Eduardo; Fontán, Gumersindo; López-Trascasa, Margarita (2002)article -
First case of homozygous C1 inhibitor deficiency
Blanch, Alvaro; Roche, Olga; Urrutia, Ignacio; Gamboa, Pedro; Fontán, Gumersindo; [et al.] (2006)article -
Hereditary angioedema due to C1 inhibitor deficiency: patient registry and approach to the prevalence in Spain
Roche, Olga; Blanch, Alvaro; Caballero, Teresa; Sastre, Noelia; Callejo, Daniel; [et al.] (2005-04)article -
Hereditary angioedema: the mutation spectrum of SERPING1/C1NH in a large Spanish cohort
Roche, Olga; Blanch, Álvaro; Duponchel, Christiane; Fontán, Gumersindo; Tosi, Mario; [et al.] (2005)article