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The acute porphyrias.
Elder GH, Hift RJ, Meissner PN. Elder GH, et al. Lancet. 1997 May 31;349(9065):1613-7. doi: 10.1016/S0140-6736(96)09070-8. Lancet. 1997. PMID: 9174571 Review. No abstract available.
Molecular epidemiology of erythropoietic protoporphyria in the U.K.
Whatley SD, Mason NG, Holme SA, Anstey AV, Elder GH, Badminton MN. Whatley SD, et al. Among authors: elder gh. Br J Dermatol. 2010 Mar;162(3):642-6. doi: 10.1111/j.1365-2133.2010.09631.x. Epub 2010 Jan 22. Br J Dermatol. 2010. PMID: 20105171
The incidence of inherited porphyrias in Europe.
Elder G, Harper P, Badminton M, Sandberg S, Deybach JC. Elder G, et al. J Inherit Metab Dis. 2013 Sep;36(5):849-57. doi: 10.1007/s10545-012-9544-4. Epub 2012 Nov 1. J Inherit Metab Dis. 2013. PMID: 23114748
C-terminal deletions in the ALAS2 gene lead to gain of function and cause X-linked dominant protoporphyria without anemia or iron overload.
Whatley SD, Ducamp S, Gouya L, Grandchamp B, Beaumont C, Badminton MN, Elder GH, Holme SA, Anstey AV, Parker M, Corrigall AV, Meissner PN, Hift RJ, Marsden JT, Ma Y, Mieli-Vergani G, Deybach JC, Puy H. Whatley SD, et al. Among authors: elder gh. Am J Hum Genet. 2008 Sep;83(3):408-14. doi: 10.1016/j.ajhg.2008.08.003. Epub 2008 Sep 4. Am J Hum Genet. 2008. PMID: 18760763 Free PMC article.
Photosensitivity and acute liver injury in myeloproliferative disorder secondary to late-onset protoporphyria caused by deletion of a ferrochelatase gene in hematopoietic cells.
Goodwin RG, Kell WJ, Laidler P, Long CC, Whatley SD, McKinley M, Badminton MN, Burnett AK, Williams GT, Elder GH. Goodwin RG, et al. Among authors: elder gh. Blood. 2006 Jan 1;107(1):60-2. doi: 10.1182/blood-2004-12-4939. Epub 2005 Sep 8. Blood. 2006. PMID: 16150949 Free article.
223 results