FAU.de
Deutsch
Login
Home
Publications
Research Grants
Inventions & Patents
Awards
Additional Research Activities
Faculties & Institutions
Research Areas
Professur für Kinderheilkunde/Experimentelle Perinatalmedizin
Friedrich-Alexander-Universität Erlangen-Nürnberg
Medizinische Fakultät
Einrichtungen, die zum Universitätsklinikum Erlangen gehören
Department of Paediatrics and Adolescent Medicine
Lehrstuhl für Kinder- und Jugendmedizin
Overview
Publications
(92)
Research Grants
(7)
Types of publications
Toggle all
Journal article
Journal article
Book chapter / Article in edited volumes
Book chapter / Article in edited volumes
Authored book
Authored book
Translation
Translation
Thesis
Thesis
Edited Volume
Edited Volume
Conference contribution
Conference contribution
Other publication type
Other publication type
Unpublished / Preprint
Unpublished / Preprint
Publication year
From
To
Abstract
Journal
Filters (inactive)
Fetal and Maternal Safety Considerations for In Utero Therapy Clinical Trials: iFeTiS Consensus Statement (2020)
Sagar R, Almeida-Porada G, Blakemore K, Chan JK, Choolani M, Götherström C, Jaulent A, et al.
Journal article, Review article
Aberrant splicing as potential modifier of the phenotype of junctional epidermolysis bullosa (2020)
Mittwollen R, Wohlfart S, Park J, Grosch E, Has C, Hohenester E, Schneider H, Hammersen J
Journal article
Safety and immunogenicity of Fc-EDA, a recombinant ectodysplasin A1 replacement protein, in human subjects (2020)
Körber I, Klein OD, Morhart P, Faschingbauer F, Grange DK, Clarke A, Bodemer C, et al.
Journal article
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
‹
1
2
3
4
5
6
...
10
›