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Skin Health and Disease|June 6, 2022
Rothmund-Thomson syndrome type 1 caused by biallelic ANAPC1 gene mutationsB Zirn, U Bernbeck, K Alt, et al.Journal of the European Academy of Dermatology and Venereology : JEADV|July 17, 2021
High rate of self-improving phenotypes in children with non-syndromic congenital ichthyosis: case series from south-western GermanyL Frommherz, A Krause, J Kopp, et al.Der Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete|June 18, 2009
[Kindler syndrome. A new bullous dermatosis]C HasThe Journal of General Virology|March 12, 1999
The cytoplasmic tail of the influenza C virus glycoprotein HEF negatively affects transport to the cell surfaceF Oeffner, H D Klenk, G HerrlerJournal of Liposome Research|September 28, 2019
A comprehensive review on recent preparation techniques of liposomesC Has, P SuntharEuropean Journal of Dermatology : EJD|September 12, 2000
The Conradi-Hünermann-Happle syndrome is caused by mutations in the gene that encodes a 8- 7 sterol isomerase and is biochemically related to the CHILD syndromeH Traupe, C HasGiornale Italiano Di Dermatologia E Venereologia : Organo Ufficiale, Societa Italiana Di Dermatologia E Sifilografia|February 15, 2013
Molecular therapies for epidermolysis bullosaC Has, D KiritsiKlinische Wochenschrift|September 15, 1987
Hereditary angioedema and aortitisU Hoffmann, J Buss, V Voigtlaender, et al.Der Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete|June 6, 2014
[The many facets of inherited skin fragility]C Has, D KiritsiDer Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete|June 15, 2019
[Syndromes with skin fragility]A Reimer, C HasPageof 10