Consensus reclassification of inherited epidermolysis bullosa and other disorders with skin fragility
Cristina Has(University of Freiburg), Jemima E. Mellerio(Great Ormond Street Hospital), Adrian Heagerty(Heart of England NHS Foundation Trust), David T. Woodley(University of Southern California), Giovanna Zambruno(Bambino Gesù Children's Hospital), Johann Bauer(Universität Innsbruck), Agnes Schwieger‐Briel(University Children's Hospital Zurich), Alain Hovnanian(Inserm), Anna E. Martinez(National Health Service), Leena Bruckner‐Tuderman(University Medical Center Freiburg), Jouni Uitto(Thomas Jefferson University), Jo‐David Fine(Vanderbilt University), Eli Sprecher(Boston Children's Hospital), M. Peter Marinkovich(Stanford University), Christine Bodemer(Hôpital Necker-Enfants Malades), Maria C. Bolling(University Medical Center Groningen), Anja Diem(Paracelsus Medical University), Celia Moss(Birmingham Dental Hospital), John A. McGrath(King's College London), Francis Palisson(Universidad del Desarrollo), Katsuto Tamai(The University of Osaka), Dédée F. Murrell(Sutherland Hospital)
Cited by 778
Related Papers
TLR3 Deficiency in Patients with Herpes Simplex Encephalitis
|Science|2007|1.1k
Inherited epidermolysis bullosa: Updated recommendations on diagnosis and classification
|Journal of the American Academy of Dermatology|2014|933
The classification of inherited epidermolysis bullosa (EB): Report of the Third International Consensus Meeting on Diagnosis and Classification of EB
|Journal of the American Academy of Dermatology|2008|933
X-linked anhidrotic ectodermal dysplasia with immunodeficiency is caused by impaired NF-κB signaling
|Nature Genetics|2001|819
Gain-of-function human <i>STAT1</i> mutations impair IL-17 immunity and underlie chronic mucocutaneous candidiasis
|The Journal of Experimental Medicine|2011|797