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The British Journal of Dermatology|July 22, 2014
Loss of desmoglein 1 associated with palmoplantar keratoderma, dermatitis and multiple allergiesC Has, T Jakob, Y He, et al.Der Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete|January 29, 2011
[Epidermolysis bullosa : Diagnosis and therapy]C Has, L Bruckner-TudermanThe British Journal of Dermatology|September 6, 2019
Natural history of growth and anaemia in children with epidermolysis bullosa: a retrospective cohort studyA Reimer, M Hess, A Schwieger-Briel, et al.Der Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete|September 2, 2004
[Hereditary blistering disorders]C Has, J S Kern, L Bruckner-TudermanThe British Journal of Dermatology|March 19, 2013
Phenotypic spectrum of epidermolysis bullosa associated with α6β4 integrin mutationsH Schumann, D Kiritsi, M Pigors, et al.Case Reports in Dermatology|September 11, 2013
Acral peeling skin syndrome resembling epidermolysis bullosa simplex in a 10-month-old boyS Kavaklieva, I Yordanova, L Bruckner-Tuderman, et al.The British Journal of Dermatology|June 21, 2008
Dystrophic epidermolysis bullosa pruriginosa is not associated with frequent FLG gene mutationsH Schumann, C Has, J Kohlhase, et al.The British Journal of Dermatology|January 11, 2012
Conradi-Hünermann-Happle syndrome in males vs. MEND syndrome (male EBP disorder with neurological defects)A W Arnold, L Bruckner-Tuderman, C Has, et al.Giornale Italiano Di Dermatologia E Venereologia : Organo Ufficiale, Societa Italiana Di Dermatologia E Sifilografia|February 15, 2013
Molecular therapies for epidermolysis bullosaC Has, D KiritsiDer Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete|June 6, 2014
[The many facets of inherited skin fragility]C Has, D KiritsiPageof 18