Leena Bruckner-Tuderman

Conradi–Hünermann–Happle syndrome in males vs. MEND syndrome (male EBP disorder with neurological defects)

R. Happle, C. Has, L. Bruckner-Tuderman, 2012, The British journal of dermatology.

Some epidermolysis bullosa acquisita sera react with epitopes within the triple‐helical collagenous domain as indicated by immunoelectron microscopy

T. Hashimoto, L. Bruckner-Tuderman, N. Ishii, 2009, The British journal of dermatology.

Injury-Driven Stiffening of the Dermis Expedites Skin Carcinoma Progression.

W. Römer, L. Bruckner-Tuderman, J. Madl, 2016, Cancer research.

Phenotypic spectrum of epidermolysis bullosa associated with α6β4 integrin mutations

A. Sieron, C. Has, J. Kohlhase, 2013, The British journal of dermatology.

Identification of novel and known KRT5 and KRT14 mutations in 53 patients with epidermolysis bullosa simplex: correlation between genotype and phenotype

T. Krieg, C. Has, L. Bruckner-Tuderman, 2010, The British journal of dermatology.

Kindlin-1 Is required for RhoGTPase-mediated lamellipodia formation in keratinocytes.

C. Has, Yinghong He, Zhigang Zhang, 2009, The American journal of pathology.

STAT3 targeting in dystrophic epidermolysis bullosa

C. Gretzmeier, C. Gaggioli, L. Bruckner-Tuderman, 2019, The British journal of dermatology.

Combined anti‐inflammatory and low‐dose antiproliferative therapy for squamous cell carcinomas in recessive dystrophic epidermolysis bullosa

C. Has, A. Reimer, L. Bruckner-Tuderman, 2020, Journal of the European Academy of Dermatology and Venereology : JEADV.