Prof. Dr. Holm Schneider



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Types of publications

Journal article
Book chapter / Article in edited volumes
Authored book
Translation
Thesis
Edited Volume
Conference contribution
Other publication type
Unpublished / Preprint

Publication year

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To

Abstract

Journal

T Cell Impairment Is Predictive for a Severe Clinical Course in NEMO Deficiency (2020) Heller S, Kölsch U, Magg T, Krüger R, Scheuern A, Schneider H, Eichinger A, et al. Journal article 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
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