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Radiologie (Heidelberg, Germany)|July 15, 2026
[Cutaneous and skeletal manifestations of systemic diseases: SKIBO]M Uhl, R Storelli, C Has, et al.American Journal of Ophthalmology|October 12, 2000
Lisch corneal dystrophy is genetically distinct from Meesmann corneal dystrophy and maps to xp22.3W Lisch, A Büttner, F Oeffner, et al.Journal of the European Academy of Dermatology and Venereology : JEADV|September 10, 2014
Epidemiology of inherited epidermolysis bullosa in Romania and genotype-phenotype correlations in patients with dystrophic epidermolysis bullosaS Dănescu, C Has, S Senila, 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.Communications Biology|November 9, 2024
The brain's first "traffic map" through Unified Structural and Functional Connectivity (USFC) modelingArzu C Has Silemek, Haitao Chen, Pascal Sati, et al.The British Journal of Dermatology|July 7, 2019
Skin fragility caused by biallelic KRT10 mutations: an intriguing form of self-improving epidermolytic ichthyosisL Frommherz, J Küsel, A Zimmer, et al.The Biochemical Journal|July 7, 1999
Cloning and characterization of gp36, a human mucin-type glycoprotein preferentially expressed in vascular endotheliumG Zimmer, F Oeffner, V Von Messling, et al.Journal of Cellular and Molecular Medicine|June 18, 2002
Genetic analysis of factor V Leiden in a family with history of thrombosis and venous leg ulcersLucia M. Procopciuc, C. Has, C. Drugan, et al.The British Journal of Dermatology|September 21, 2011
Description of the natural course and clinical manifestations of ichthyosis with confetti caused by a novel KRT10 mutationB Burger, I Spoerri, M Schubert, et al.Journal of Neurology, Neurosurgery, and Psychiatry|September 28, 2007
Frequency of GCH1 deletions in Dopa-responsive dystoniaB Zirn, D Steinberger, C Troidl, et al.Pageof 10