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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2021 | 2 |
2022 | 2 |
2023 | 1 |
2024 | 1 |
Search Results
5 results
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Page 1
Enterokinase deficiency with novel TMPRSS15 gene mutation masquerading as acrodermatitis enteropathica.
Pediatr Dermatol. 2023 Mar;40(2):389-391. doi: 10.1111/pde.15197. Epub 2022 Nov 21.
Pediatr Dermatol. 2023.
PMID: 36410965
Secondary acrodermatitis enteropathica-like skin findings in a case of methylmalonic acidemia.
Chen Y, Li Z, Liu C, Wang S.
Chen Y, et al.
Pediatr Dermatol. 2022 Nov;39(6):987-989. doi: 10.1111/pde.15051. Epub 2022 Jun 11.
Pediatr Dermatol. 2022.
PMID: 35689470
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IL36RN mutations in Chinese patients with acute generalized exanthematous pustulosis.
Li Z, He Y, Wang S.
Li Z, et al.
Int J Dermatol. 2024 Apr 22. doi: 10.1111/ijd.17213. Online ahead of print.
Int J Dermatol. 2024.
PMID: 38647146
No abstract available.
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Novel deletion of the POFUT1 gene associated with multiple seborrheic keratosis Dowling-Degos disease.
Chen Y, Li Z, Song D, Wang S.
Chen Y, et al.
J Dermatol. 2021 Dec;48(12):e591-e593. doi: 10.1111/1346-8138.16154. Epub 2021 Sep 15.
J Dermatol. 2021.
PMID: 34524711
No abstract available.
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Recurrent c.459 C>A mutation of the PERP gene results in severe Olmsted syndrome with congenital hypotrichosis, atopic dermatitis, and growth retardation.
Song D, Ran X, Chen Y, Li Z, Li F, Lan Y, Wang S.
Song D, et al.
J Dermatol. 2021 Oct;48(10):E508-E509. doi: 10.1111/1346-8138.16060. Epub 2021 Jul 15.
J Dermatol. 2021.
PMID: 34265120
No abstract available.
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