1. First report of a FXII gene mutation in a Brazilian family with hereditary angio‐oedema with normal C1 inhibitor. (1st October 2015) Authors: Stieber, C.; Grumach, A.S.; Cordeiro, E.; Constantino‐Silva, R.N.; Barth, S.; Hoffmann, P.; Pesquero, J.B.; Renné, T.; Nöthen, M.M.; Cichon, S. Journal: British journal of dermatology Issue: Volume 173:Number 4(2015:Oct.) Page Start: 1102 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. First report of a FXII gene mutation in a Brazilian family with hereditary angio‐oedema with normal C1 inhibitor. (1st September 2015) Authors: Stieber, C.; Grumach, A.S.; Cordeiro, E.; Constantino‐Silva, R.N.; Barth, S.; Hoffmann, P.; Pesquero, J.B.; Renné, T.; Nöthen, M.M.; Cichon, S. Journal: British journal of dermatology Issue: Volume 173:Number 4(2015:Oct.) Page Start: 1102 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Hereditary angioedema: first report of the Brazilian registry and challenges. (7th August 2012) Authors: Grumach, A.S.; Valle, S.O.R.; Toledo, E.; de Moraes Vasconcelos, D.; Villela, M.M.S.; Mansour, E.; Pinto, J.A.; Campos, R.A.; França, A.T. Journal: Journal of the European Academy of Dermatology and Venereology Issue: Volume 27:Number 3(2013:Mar.) Page Start: e338 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Variability of disease activity in patients with hereditary angioedema type 1/2: longitudinal data from the Icatibant Outcome Survey. (5th October 2021) Authors: Maurer, M.; Caballero, T.; Aberer, W.; Zanichelli, A.; Bouillet, L.; Bygum, A.; Grumach, A.S.; Botha, J.; Andresen, I.; Longhurst, H.J. Journal: Journal of the European Academy of Dermatology and Venereology Issue: Volume 35:Number 12(2021) Page Start: 2421 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗