Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Aaron E Boyce"'
Publikováno v:
The Australasian journal of dermatologyReferences. 62(3)
Purpureocillium lilacinum, previously classified as Paecilomyces lilacinus, is a ubiquitous hyaline hyphomycete considered to be an emerging opportunistic human pathogen that is resistant to traditional antifungal agents. This case report describes w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ca1df77324419a85e295ada59be17088
https://pubmed.ncbi.nlm.nih.gov/34170516
https://pubmed.ncbi.nlm.nih.gov/34170516
Publikováno v:
Contact Dermatitis. 83:161-162
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::70247d78575c4306120625b88a5aaa07
https://doi.org/10.1111/cod.13590
https://doi.org/10.1111/cod.13590
Autor:
Tanasit Techanukul, Chung Wo Chow, Lesley M McGregor, Lachlan Warren, Dedee F. Murrell, Aaron E Boyce, John A. McGrath
Publikováno v:
Australasian Journal of Dermatology. 53:61-65
Ectodermal dysplasia-skin fragility syndrome (ED-SFS) is a rare autosomal recessive genodermatosis resulting from mutations in the PKP1 gene, encoding the desmosomal plaque protein plakophilin-1 (PKP1). Mutations in PKP1 may manifest with skin fragil
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2ae93595013f30d74a5e4fbb7de4fa50
https://doi.org/10.1111/j.1440-0960.2011.00846.x
https://doi.org/10.1111/j.1440-0960.2011.00846.x
Publikováno v:
Australasian Journal of Dermatology. 50:190-193
Erosive mucosal lichen planus (LP) is a well-established variant of LP characterized by the formation of ulcerative lesions predominantly involving the oral and genital mucosae. Less commonly, this condition may involve oesophageal and/or ocular muco
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2046bbc54a712831fcc76a6e4ab3dce7
https://doi.org/10.1111/j.1440-0960.2009.00536.x
https://doi.org/10.1111/j.1440-0960.2009.00536.x
Autor:
Aaron E, Boyce, John A, McGrath, Tanasit, Techanukul, Dédée F, Murrell, Chung Wo, Chow, Lesley, McGregor, Lachlan J, Warren
Publikováno v:
The Australasian journal of dermatology. 53(1)
Ectodermal dysplasia-skin fragility syndrome (ED-SFS) is a rare autosomal recessive genodermatosis resulting from mutations in the PKP1 gene, encoding the desmosomal plaque protein plakophilin-1 (PKP1). Mutations in PKP1 may manifest with skin fragil
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1b3a0bb51834aee6aebd6200746a8428
https://pubmed.ncbi.nlm.nih.gov/22309335
https://pubmed.ncbi.nlm.nih.gov/22309335