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Year | Number of Results |
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2021 | 2 |
2022 | 5 |
2023 | 1 |
2024 | 0 |
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Page 1
Molecular Pathway-Based Classification of Ectodermal Dysplasias: First Five-Yearly Update.
Genes (Basel). 2022 Dec 10;13(12):2327. doi: 10.3390/genes13122327.
Genes (Basel). 2022.
PMID: 36553593
Free PMC article.
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.
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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.
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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.
Schneider H, Hadj-Rabia S, Faschingbauer F, Bodemer C, Grange DK, Norton ME, Cavalli R, Tadini G, Stepan H, Clarke A, Guillén-Navarro E, Maier-Wohlfart S, Bouroubi A, Porte F.
Schneider H, et al. Among authors: maier wohlfart s.
Genes (Basel). 2023 Jan 6;14(1):153. doi: 10.3390/genes14010153.
Genes (Basel). 2023.
PMID: 36672894
Free PMC article.
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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.
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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.
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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.
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