Zobrazeno 1 - 10
of 13
pro vyhledávání: '"S. T. Holden"'
Publikováno v:
Clinical and Experimental Dermatology. 45:518-520
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::08715f94e31f7a4a4ac9098e3cc27b67
https://doi.org/10.1111/ced.14177
https://doi.org/10.1111/ced.14177
Publikováno v:
Clinical and experimental dermatologyReferences. 46(8)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f9d5f7145e9a050845b5da1c9121ec99
https://pubmed.ncbi.nlm.nih.gov/34435384
https://pubmed.ncbi.nlm.nih.gov/34435384
Publikováno v:
The British journal of dermatologyReferences. 184(2)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fbb8a0c53fb07a99027eecda2338c741
https://pubmed.ncbi.nlm.nih.gov/32696461
https://pubmed.ncbi.nlm.nih.gov/32696461
Publikováno v:
Clinical and experimental dermatology. 42(4)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::99b6f77d65a040eb31331de145213957
https://pubmed.ncbi.nlm.nih.gov/28397289
https://pubmed.ncbi.nlm.nih.gov/28397289
Autor:
Suzanne E. Clements, S. T. Holden, Jemima E. Mellerio, Huw Dorkins, F. Escande, John A. McGrath, Tanasit Techanukul
Publikováno v:
British Journal of Dermatology. 163:624-629
Summary Background Rapp–Hodgkin syndrome (RHS) and Hay–Wells [also known as ankyloblepharon–ectodermal defects–cleft lip/palate (AEC)] syndrome have been designated as distinct ectodermal dysplasia syndromes despite both disorders having over
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::efad7e3753db8c25352757697172b4de
https://doi.org/10.1111/j.1365-2133.2010.09859.x
https://doi.org/10.1111/j.1365-2133.2010.09859.x
Publikováno v:
British Journal of Dermatology. 160:1103-1109
Summary Focal dermal hypoplasia (FDH) is an X-linked dominant disorder featuring developmental abnormalities of ectodermal and mesodermal tissues. Pathogenic mutations in the PORCN gene (locus Xp11.23) were identified in 2007 and thus far 27 differen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c3cbd1f3f81b8d6b27a5cb2ad53d9217
https://doi.org/10.1111/j.1365-2133.2009.09048.x
https://doi.org/10.1111/j.1365-2133.2009.09048.x
Publikováno v:
Clinical and Experimental Dermatology. 40:99-100
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6b6b91e646e01893b70dfc4c9cbf4e9d
https://doi.org/10.1111/ced.12521
https://doi.org/10.1111/ced.12521
Autor:
Jemima E. Mellerio, Charu Deshpande, Elizabeth Wraige, S. T. Holden, V. A. E. Pinder, A. M. Powell, Ata Siddiqui
Publikováno v:
Clinical and experimental dermatology. 38(7)
Summary Variegate porphyria is an autosomal dominant disorder that usually presents with photosensitivity and acute neurological crises in adulthood. It is caused by heterozygous mutations in the protoporphyrinogen oxidase gene (PPOX). A rarer varian
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c734fdd4d827ed59cc638cde1d072963
https://pubmed.ncbi.nlm.nih.gov/24073655
https://pubmed.ncbi.nlm.nih.gov/24073655
Autor:
S E, Clements, T, Techanukul, S T, Holden, J E, Mellerio, H, Dorkins, F, Escande, J A, McGrath
Publikováno v:
The British journal of dermatology. 163(3)
Rapp-Hodgkin syndrome (RHS) and Hay-Wells [also known as ankyloblepharon-ectodermal defects-cleft lip/palate (AEC)] syndrome have been designated as distinct ectodermal dysplasia syndromes despite both disorders having overlapping clinical features a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::45305a073e0c0c42debfdd6ab0fcdbd3
https://pubmed.ncbi.nlm.nih.gov/20491771
https://pubmed.ncbi.nlm.nih.gov/20491771
Autor:
S T Holden, B Shiferaw
This chapter illustrates how a multiperiod bioeconomic household-level model, in which changes in resource quality have feedback effects on future land productivity, can be used to explore the economic and environmental impacts of natural resource ma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cae068f8f81b59655826e81facb69311
https://doi.org/10.1079/9780851998282.0269
https://doi.org/10.1079/9780851998282.0269
