Page 169 - MEMOCiberer014

Publicaciones científicas más relevantes
• lópez-lera a, m torres-canizales J, GarriDo s, morales a, lópez-trascasa m. rotHmunD-tHomson syndrome and glomerulonephritis in a homozygous C1q-deficient patient due to a Gly164Ser C1qC mutation . J Invest Dermatol; 2014 Apr . 134(4):1152-4 . PMID: 24157463 Doi: 10 .1038/jid .2013 .444
• sáncHez cHincHilla D, pinto s, Hoppe b, aDraGna m, lopez l, Justa rolDan ml, peña a, lopez trascasa m, sáncHez-corral p, roDríGuez De córDoba s. Complement mutations in diacylglycerol kinase-e-associa- ted atypical hemolytic uremic syndrome . Clin J Am Soc Nephrol; 2014 Sep 5 . 9(9):1611-9 . PMID: 25135762 Doi: 10 .2215/CJN .01640214
• cicarDi m, aberer W, banerJi a, bas m, bernstein Ja, borK K, caballero t, FarKas H, GrumacH a, Kaplan ap, rieDl ma, triGGiani m, zanicHelli a, zuraW b. Classification, diagnosis, and approach to treatment for angioedema: consensus report from the Hereditary Angioedema International Working Group . Allergy; 2014 May . 69(5):602-16 . PMID: 24673465 Doi: 10 .1111/all .12380
• aberer W, maurer m, resHeF a, lonGHurst H, KiVity s, byGum a, caballero t, bloom b, nair n, malbrán a. Open-label, multicenter study of self-administered icatibant for attacks of hereditary angioedema . Allergy; 2014 Mar . 69(3):305-14 . PMID: 24438203 Doi: 10 .1111/all .12303
• cHariGnon D, GHannam a, DeFenDi F, ponarD D, monnier n, lópez trascasa m, launay D, caballero t, DJe- nouHat K, Fain o, cicHon s, martin l, Drouet c. Hereditary angioedema with F12 mutation: factors modifying the clinical phenotype . Allergy; 2014 Dec . 69(12):1659-65 . PMID: 25134986 Doi: 10 .1111/ all .12515
Institución: Servicio Madrileño de Salud Contacto: Hospital La Paz · Paseo de la Castellana, 261 . 28046 MADRID Teléfono: (+34) 91 207 14 63 · E .mail: mltrascasa@salud .madrid .org
www .ciberer .es 169