PD Dr. Sigrun Maier-Wohlfart



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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Unpublished / Preprint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

Protocol for the Phase 2 EDELIFE Trial Investigating the Efficacy and Safety of Intra-Amniotic ER004 Administration to Male Subjects with X-Linked Hypohidrotic Ectodermal Dysplasia (2023) Schneider H, Hadj-Rabia S, Faschingbauer F, Bodemer C, Grange DK, Norton ME, Cavalli R, et al. Journal article Molecular Pathway-Based Classification of Ectodermal Dysplasias: First Five-Yearly Update (2022) Peschel N, Wright JT, Koster MI, Clarke AJ, Tadini G, Fete M, Hadj-Rabia S, et al. Journal article Congenital Nail Disorders among Children with Suspected Ectodermal Dysplasias (2022) Maier-Wohlfart S, Aicher C, Willershausen I, Peschel N, Meißner U, Gölz L, Schneider H Journal article Ectodysplasin A1 Deficiency Leads to Osteopetrosis-like Changes in Bones of the Skull Associated with Diminished Osteoclastic Activity (2022) Schweikl C, Maier-Wohlfart S, Schneider H, Park J Journal article Functional and clinical analysis of five EDA variants associated with ectodermal dysplasia but with a hard-to-predict significance (2022) Goekdere S, Schneider H, Hehr U, Willen L, Schneider P, Maier-Wohlfart S Journal article No evidence for preferential X-chromosome inactivation as the main cause of divergent phenotypes in sisters with X-linked hypohidrotic ectodermal dysplasia (2021) Körber L, Schneider H, Fleischer N, Maier-Wohlfart S Journal article Maternal SARS-CoV-2 infection during pregnancy: possible impact on the infant (2021) Morhart P, Mardin C, Rauh M, Juengert J, Hammersen J, Kehl S, Schuh W, et al. 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 Variants of the ectodysplasin A1 receptor gene underlying homozygous cases of autosomal recessive hypohidrotic ectodermal dysplasia (2019) Wohlfart S, Schneider H 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