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Novel and recurrent COL7A1 mutations in Chilean patients with dystrophic epidermolysis bullosa.
Rodríguez FA, Gana MJ, Yubero MJ, Zillmann G, Krämer SM, Catalán J, Rubio-Astudillo J, González S, Liu L, Ozoemena L, Mellerio JE, McGrath JA, Palisson F, Conget P. Rodríguez FA, et al. Among authors: mcgrath ja. J Dermatol Sci. 2012 Feb;65(2):149-52. doi: 10.1016/j.jdermsci.2011.11.010. Epub 2011 Dec 13. J Dermatol Sci. 2012. PMID: 22209565 No abstract available.
Neonatal diagnosis of Kindler syndrome.
Fassihi H, Wessagowit V, Jones C, Dopping-Hepenstal P, Denyer J, Mellerio JE, Clark S, McGrath JA. Fassihi H, et al. Among authors: mcgrath ja. J Dermatol Sci. 2005 Sep;39(3):183-5. doi: 10.1016/j.jdermsci.2005.05.007. J Dermatol Sci. 2005. PMID: 16051467 No abstract available.
Prenatal diagnosis of epidermolysis bullosa.
Fassihi H, McGrath JA. Fassihi H, et al. Among authors: mcgrath ja. Dermatol Clin. 2010 Apr;28(2):231-7, viii. doi: 10.1016/j.det.2010.02.001. Dermatol Clin. 2010. PMID: 20447485 Review.
Potential of fibroblast cell therapy for recessive dystrophic epidermolysis bullosa.
Wong T, Gammon L, Liu L, Mellerio JE, Dopping-Hepenstal PJ, Pacy J, Elia G, Jeffery R, Leigh IM, Navsaria H, McGrath JA. Wong T, et al. Among authors: mcgrath ja. J Invest Dermatol. 2008 Sep;128(9):2179-89. doi: 10.1038/jid.2008.78. Epub 2008 Apr 3. J Invest Dermatol. 2008. PMID: 18385758 Free article. Clinical Trial.
A homozygous nonsense mutation within the dystonin gene coding for the coiled-coil domain of the epithelial isoform of BPAG1 underlies a new subtype of autosomal recessive epidermolysis bullosa simplex.
Groves RW, Liu L, Dopping-Hepenstal PJ, Markus HS, Lovell PA, Ozoemena L, Lai-Cheong JE, Gawler J, Owaribe K, Hashimoto T, Mellerio JE, Mee JB, McGrath JA. Groves RW, et al. Among authors: mcgrath ja. J Invest Dermatol. 2010 Jun;130(6):1551-7. doi: 10.1038/jid.2010.19. Epub 2010 Feb 18. J Invest Dermatol. 2010. PMID: 20164846 Free article.
695 results