Professur für Kinderheilkunde/Experimentelle Perinatalmedizin

Homozygous Biallelic KRT5 Mutations in Epidermolysis Bullosa Simplex, Including a Complete Human Keratin 5 "Knock-Out", in Families with Extensive Consanguinity (2019) Vahidnezhad H, Youssefian L, Daneshpazhooh M, Mahmoudi H, Kariminejad A, Fischer J, Christiansen J, et al. Conference contribution Deficiency of Fhl2 leads to delayed neuronal cell migration and premature astrocyte differentiation (2019) Kim SY, Ludwig S, Schneider H, Wixler V, Park J, Völkl S Journal article Variants of the ectodysplasin A1 receptor gene underlying homozygous cases of autosomal recessive hypohidrotic ectodermal dysplasia (2019) Wohlfart S, Schneider H Journal article Ectodermal dysplasias: Classification and organization by phenotype, genotype and molecular pathway (2019) Wright JT, Fete M, Schneider H, Zinser M, Koster MI, Clarke AJ, Hadj-Rabia S, et al. Journal article Prenatal treatment of X-linked hypohidrotic ectodermal dysplasia using recombinant ectodysplasin in a canine model (2019) Margolis CA, Schneider P, Huttner K, Kirby N, Houser TP, Wildman L, Grove GL, et al. Journal article Conditional Alox12b Knockout: Degradation of the Corneocyte Lipid Envelope in a Mouse Model of Autosomal Recessive Congenital Ichthyoses (2019) Krieg P, Dick A, Latzko S, Rosenberger S, Meyer J, Crumrine D, Hielscher T, et al. Journal article Reliability of prenatal detection of X-linked hypohidrotic ectodermal dysplasia by tooth germ sonography (2019) Hammersen J, Wohlfart S, Goecke TW, Köninger A, Stepan H, Gallinat R, Morris S, et al. Journal article Biallelic KRT5 mutations in autosomal recessive epidermolysis bullosa simplex, including a complete human keratin 5 “knock-out” (2019) Vahidnezhad H, Youssefian L, Daneshpazhooh M, Mahmoudi H, Kariminejad A, Fischer J, Christiansen J, et al. Journal article Attenuation of Severe Generalized Junctional Epidermolysis Bullosa by Systemic Treatment with Gentamicin (2019) Hammersen J, Neuner A, Wild F, Schneider H Journal article Sweating ability of patients with p63-associated syndromes (2018) Ferstl P, Wohlfart S, Schneider H Journal article