Prof. Dr. Holm Schneider

Professur für Kinderheilkunde/Experimentelle Perinatalmedizin

BAFF 60-mer, and Differential BAFF 60-mer Dissociating Activities in Human Serum, Cord Blood and Cerebrospinal Fluid (2020) Eslami M, Meinl E, Eibel H, Willen L, Donzé O, Distl O, Schneider H, et al. Journal article Erythroderma and Hypernatraemic Dehydration in Newborn - A Case report of Netherton Syndrome (2020) Anneser V, Mueller F, Wild F, Metze D, Schneider H, Steinhoff M, Seeliger S Journal article Natural history of X-linked hypohidrotic ectodermal dysplasia: a 5-year follow-up study (2020) Wohlfart S, Meiller R, Hammersen J, Park J, Menzel-Severing J, Melichar VO, Huttner K, et al. Journal article 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