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HIV Medicine|September 22, 2012
End-stage renal disease and dialysis in HIV-positive patients: observations from a long-term cohort study with a follow-up of 22 yearsM Bickel, W Marben, C Betz, et al.Cancer Gene Therapy|May 28, 2021
Whole-exome sequencing in eccrine porocarcinoma indicates promising therapeutic strategiesEvgeniya Denisova, Dana Westphal, Harald M Surowy, et al.Brain : a Journal of Neurology|December 2, 2011
The brain in myotonic dystrophy 1 and 2: evidence for a predominant white matter diseaseMartina Minnerop, Bernd Weber, Jan-Christoph Schoene-Bake, et al.Tissue Antigens|June 16, 2006
Investigation of the p.Ser278Arg polymorphism of the autoimmune regulator (AIRE) gene in alopecia areataJ Pforr, B Blaumeiser, T Becker, et al.International Journal of Immunogenetics|November 23, 2006
Investigation of the functional variant c.-169T > C of the Fc receptor-like 3 (FCRL3) gene in alopecia areataN Schäfer, B Blaumeiser, T Becker, et al.The British Journal of Dermatology|March 13, 2010
Systematic mutation screening of KRT5 supports the hypothesis that Galli-Galli disease is a variant of Dowling-Degos diseaseS Hanneken, A Rütten, S M Pasternack, et al.Frontiers in Immunology|May 4, 2026
Genome-wide association study of atopic and autoimmune comorbidities in alopecia areataMarisol Herrera-Rivero, Yasmina Gossmann, Swapnil Awasthi, et al.The British Journal of Dermatology|November 26, 2005
A non-sense mutation in the corneodesmosin gene in a Mexican family with hypotrichosis simplex of the scalpN O Dávalos, A García-Vargas, J Pforr, et al.Acta Dermato-Venereologica|November 20, 2015
Expanding the Clinical and Genetic Spectrum of KRT1, KRT2 and KRT10 Mutations in Keratinopathic IchthyosisAlrun Hotz, Vinzenz Oji, Emmanuelle Bourrat, et al.Plos One|December 3, 2019
Autosomal-dominant hypotrichosis with woolly hair: Novel gene locus on chromosome 4q35.1-q35.2Annika E Schlaweck, Rachid Tazi-Ahnini, F Buket Ü Basmanav, et al.Pageof 17