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Extracutaneous manifestations and complications of inherited epidermolysis bullosa: part I. Epithelial associated tissues.
Fine JD, Mellerio JE. Fine JD, et al. Among authors: mellerio je. J Am Acad Dermatol. 2009 Sep;61(3):367-84; quiz 385-6. doi: 10.1016/j.jaad.2009.03.052. J Am Acad Dermatol. 2009. PMID: 19700010 Review.
A recurrent laminin 5 mutation in British patients with lethal (Herlitz) junctional epidermolysis bullosa: evidence for a mutational hotspot rather than propagation of an ancestral allele.
Ashton GH, Mellerio JE, Dunnill MG, Pulkkinen L, Christiano AM, Uitto J, Eady RA, McGrath JA. Ashton GH, et al. Among authors: mellerio je. Br J Dermatol. 1997 May;136(5):674-7. Br J Dermatol. 1997. PMID: 9205497
Recurrent mutations in the type VII collagen gene (COL7A1) in patients with recessive dystrophic epidermolysis bullosa.
Mellerio JE, Dunnill MG, Allison W, Ashton GH, Christiano AM, Uitto J, Eady RA, McGrath JA. Mellerio JE, et al. J Invest Dermatol. 1997 Aug;109(2):246-9. doi: 10.1111/1523-1747.ep12319792. J Invest Dermatol. 1997. PMID: 9242516
Recessive epidermolysis bullosa simplex associated with plectin mutations: infantile respiratory complications in two unrelated cases.
Mellerio JE, Smith FJ, McMillan JR, McLean WH, McGrath JA, Morrison GA, Tierney P, Albert DM, Wiche G, Leigh IM, Geddes JF, Lane EB, Uitto J, Eady RA. Mellerio JE, et al. Br J Dermatol. 1997 Dec;137(6):898-906. Br J Dermatol. 1997. PMID: 9470905
Prognostic implications of determining 180 kDa bullous pemphigoid antigen (BPAG2) gene/protein pathology in neonatal junctional epidermolysis bullosa.
Mellerio JE, Denyer JE, Atherton DJ, Eady RA, McGrath JA. Mellerio JE, et al. Br J Dermatol. 1998 Apr;138(4):661-6. doi: 10.1046/j.1365-2133.1998.02182.x. Br J Dermatol. 1998. PMID: 9640376
E210K mutation in the gene encoding the beta3 chain of laminin-5 (LAMB3) is predictive of a phenotype of generalized atrophic benign epidermolysis bullosa.
Mellerio JE, Eady RA, Atherton DJ, Lake BD, McGrath JA. Mellerio JE, et al. Br J Dermatol. 1998 Aug;139(2):325-31. doi: 10.1046/j.1365-2133.1998.02377.x. Br J Dermatol. 1998. PMID: 9767254
Severe palmo-plantar hyperkeratosis in Dowling-Meara epidermolysis bullosa simplex caused by a mutation in the keratin 14 gene (KRT14).
Shemanko CS, Mellerio JE, Tidman MJ, Lane EB, Eady RA. Shemanko CS, et al. Among authors: mellerio je. J Invest Dermatol. 1998 Nov;111(5):893-5. doi: 10.1046/j.1523-1747.1998.00388.x. J Invest Dermatol. 1998. PMID: 9804355
A recurrent glycine substitution mutation, G2043R, in the type VII collagen gene (COL7A1) in dominant dystrophic epidermolysis bullosa.
Mellerio JE, Salas-Alanis JC, Talamantes ML, Horn H, Tidman MJ, Ashton GH, Eady RA, McGrath JA. Mellerio JE, et al. Br J Dermatol. 1998 Oct;139(4):730-7. doi: 10.1046/j.1365-2133.1998.02496.x. Br J Dermatol. 1998. PMID: 9892921
Pyloric atresia-junctional epidermolysis bullosa syndrome: mutations in the integrin beta4 gene (ITGB4) in two unrelated patients with mild disease.
Mellerio JE, Pulkkinen L, McMillan JR, Lake BD, Horn HM, Tidman MJ, Harper JI, McGrath JA, Uitto J, Eady RA. Mellerio JE, et al. Br J Dermatol. 1998 Nov;139(5):862-71. doi: 10.1046/j.1365-2133.1998.02515.x. Br J Dermatol. 1998. PMID: 9892956
A recurrent frameshift mutation in exon 19 of the type VII collagen gene (COL7A1) in Mexican patients with recessive dystrophic epidermolysis bullosa.
Mellerio JE, Salas-Alanis JC, Amaya-Guerra M, Tamez E, Ashton GH, Mohammedi R, Eady RA, McGrath JA. Mellerio JE, et al. Exp Dermatol. 1999 Feb;8(1):22-9. doi: 10.1111/j.1600-0625.1999.tb00344.x. Exp Dermatol. 1999. PMID: 10206718
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