Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Search Results
7 results
Filters applied: . Clear all
Results are displayed in a computed author sort order.
The Results By Year timeline is not available.
Page 1
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.
Genes (Basel). 2023 Jan 6;14(1):153. doi: 10.3390/genes14010153.
Genes (Basel). 2023.
PMID: 36672894
Free PMC article.
Molecular Pathway-Based Classification of Ectodermal Dysplasias: First Five-Yearly Update.
Peschel N, Wright JT, Koster MI, Clarke AJ, Tadini G, Fete M, Hadj-Rabia S, Sybert VP, Norderyd J, Maier-Wohlfart S, Fete TJ, Pagnan N, Visinoni AF, Schneider H.
Peschel N, et al. Among authors: maier wohlfart s.
Genes (Basel). 2022 Dec 10;13(12):2327. doi: 10.3390/genes13122327.
Genes (Basel). 2022.
PMID: 36553593
Free PMC article.
Item in Clipboard
Congenital Nail Disorders among Children with Suspected Ectodermal Dysplasias.
Maier-Wohlfart S, Aicher C, Willershausen I, Peschel N, Meißner U, Gölz L, Schneider H.
Maier-Wohlfart S, et al.
Genes (Basel). 2022 Nov 15;13(11):2119. doi: 10.3390/genes13112119.
Genes (Basel). 2022.
PMID: 36421794
Free PMC article.
Item in Clipboard
Ectodysplasin A1 Deficiency Leads to Osteopetrosis-like Changes in Bones of the Skull Associated with Diminished Osteoclastic Activity.
Schweikl C, Maier-Wohlfart S, Schneider H, Park J.
Schweikl C, et al. Among authors: maier wohlfart s.
Int J Mol Sci. 2022 Oct 13;23(20):12189. doi: 10.3390/ijms232012189.
Int J Mol Sci. 2022.
PMID: 36293046
Free PMC article.
Item in Clipboard
Functional and clinical analysis of five EDA variants associated with ectodermal dysplasia but with a hard-to-predict significance.
Gökdere S, Schneider H, Hehr U, Willen L, Schneider P, Maier-Wohlfart S.
Gökdere S, et al. Among authors: maier wohlfart s.
Front Genet. 2022 Jul 18;13:934395. doi: 10.3389/fgene.2022.934395. eCollection 2022.
Front Genet. 2022.
PMID: 35923710
Free PMC article.
Item in Clipboard
Maternal SARS-CoV-2 infection during pregnancy: possible impact on the infant.
Morhart P, Mardin C, Rauh M, Jüngert J, Hammersen J, Kehl S, Schuh W, Maier-Wohlfart S, Hermes K, Neubert A, Schneider M, Hein A, Woelfle J, Schneider H.
Morhart P, et al. Among authors: maier wohlfart s.
Eur J Pediatr. 2022 Jan;181(1):413-418. doi: 10.1007/s00431-021-04221-w. Epub 2021 Aug 5.
Eur J Pediatr. 2022.
PMID: 34355278
Free PMC article.
Item in Clipboard
No evidence for preferential X-chromosome inactivation as the main cause of divergent phenotypes in sisters with X-linked hypohidrotic ectodermal dysplasia.
Körber L, Schneider H, Fleischer N, Maier-Wohlfart S.
Körber L, et al. Among authors: maier wohlfart s.
Orphanet J Rare Dis. 2021 Feb 23;16(1):98. doi: 10.1186/s13023-021-01735-2.
Orphanet J Rare Dis. 2021.
PMID: 33622384
Free PMC article.
Item in Clipboard
Cite
Cite