1. Expanding the clinical spectrum of hereditary fibrosing poikiloderma with tendon contractures, myopathy and pulmonary fibrosis due to FAM111B mutations. Issue 1 (December 2015) Authors: Mercier, Sandra; Küry, Sébastien; Salort-Campana, Emmanuelle; Magot, Armelle; Agbim, Uchenna; Besnard, Thomas; Bodak, Nathalie; Bou-Hanna, Chantal; Bréhéret, Flora; Brunelle, Perrine; Caillon, Florence; Chabrol, Brigitte; Cormier-Daire, Valérie; David, Albert; Eymard, Bruno; Faivre, Laurence; Fig... Journal: Orphanet journal of rare diseases Issue: Volume 9:Issue 1(2014) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Identification of translational dermatology research priorities in the U.K.: results of an electronic Delphi exercise. (1st November 2015) Authors: Healy, E.; Brown, S.J.; Langan, S.M.; Nicholls, S.G.; Shams, K.; Reynolds, N.J.; Ardern‐Jones, Mike; Benham, Marilyn; Jaega, Mike; Leigh, Irene; McLean, Irwin; Rush, Emma; Walton, Shernaz; Griffiths, Chris Journal: British journal of dermatology Issue: Volume 173:Number 5(2015:Nov.) Page Start: 1191 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗