Consensus reclassification of inherited epidermolysis bullosa and other disorders with skin fragility von Has, C., Bauer, J.W., Bodemer, C., Bolling, M.C., Bruckner‐Tuderman, L., Diem, A., Fine, J.‐D., Heagerty, A., Hovnanian, A., Marinkovich, M.P., Martinez, A.E., McGrath, J.A., Moss, C., Murrell, D.F., Palisson, F., Schwieger‐Briel, A., Sprecher, E., Tamai, K., Uitto, J., Woodley, D.T., Zambruno, G., Mellerio, J.E.

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Prevalence, pathophysiology and management of itch in epidermolysis bullosa von Papanikolaou, M., Onoufriadis, A., Mellerio, J.E., Nattkemper, L.A., Yosipovitch, G., Steinhoff, M., McGrath, J.A.

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Understanding the socioeconomic costs of dystrophic epidermolysis bullosa in Europe: a costing and health-related quality of life study von Angelis, A, Mellerio, J. E, Kanavos, P

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Fibroblast cell therapy enhances initial healing in recessive dystrophic epidermolysis bullosa wounds: results of a randomized, vehicle-controlled trial von Petrof, G., Martinez-Queipo, M., Mellerio, J.E., Kemp, P., McGrath, J.A.

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Beta blockers for infantile haemangiomas: where should we go from here? von Mellerio, J. E.

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Enduring support for the case report von Mellerio, J.E.

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Potential therapeutic targeting of inflammation in epidermolysis bullosa simplex von Mellerio, J.E.

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Genotype–phenotype correlation in a large English cohort of patients with autosomal recessive ichthyosis von Simpson, J.K., Martinez‐Queipo, M., Onoufriadis, A., Tso, S., Glass, E., Liu, L., Higashino, T., Scott, W., Tierney, C., Simpson, M.A., Desomchoke, R., Youssefian, L., SaeIdian, A.H, Vahidnezhad, H., Bisquera, A., Ravenscroft, J., Moss, C., O'Toole, E.A., Burrows, N., Leech, S., Jones, E.A., Lim, D., Ilchyshyn, A., Goldstraw, N., Cork, M.J., Darne, S., Uitto, J., Martinez, A.E., Mellerio, J.E., McGrath, J.A.

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Management of cutaneous squamous cell carcinoma in patients with epidermolysis bullosa: best clinical practice guidelines von Mellerio, J.E., Robertson, S.J., Bernardis, C., Diem, A., Fine, J.D., George, R., Goldberg, D., Halmos, G.B., Harries, M., Jonkman, M.F., Lucky, A., Martinez, A.E., Maubec, E., Morris, S., Murrell, D.F., Palisson, F., Pillay, E.I., Robson, A., Salas-Alanis, J.C., McGrath, J.A.

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The psychological functioning of children with epidermolysis bullosa and its relationship with specific aspects of disease von Soon, K., Mason, R., Martinez, A.E., Mellerio, J.E.

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Desmosomal genodermatoses von Petrof, G., Mellerio, J.E., McGrath, J.A.

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Neonatal aggressive systemic mastocytosis von Mellerio, J.E.

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Heterogeneous addiction to transforming growth factor‐beta signalling in recessive dystrophic epidermolysis bullosa‐associated cutaneous squamous cell carcinoma von Dayal, J.H.S., Mason, S.M., Salas‐Alanis, J.C., McGrath, J.A., Taylor, R.G., Mellerio, J.E., Blyth, K., South, A.P., Inman, G.J.

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EBGene trial: patient preselection outcomes for the European GENEGRAFT ex vivo phase I/II gene therapy trial for recessive dystrophic epidermolysis bullosa von Gaucher, S., Lwin, S.M., Titeux, M., Abdul‐Wahab, A., Pironon, N., Izmiryan, A., Miskinyte, S., Ganier, C., Duchatelet, S., Mellerio, J.E., Bourrat, E., McGrath, J.A., Hovnanian, A.

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Recommendations on pregnancy, childbirth and aftercare in epidermolysis bullosa: a consensus‐based guideline von Greenblatt, D.T., Pillay, E., Snelson, K., Saad, R., Torres Pradilla, M., Widhiati, S., Diem, A., Knight, C., Thompson, K., Azzopardi, N., Werkentoft, M., Moore, Z., Patton, D., Mayre‐Chilton, K.M., Murrell, D.F., Mellerio, J.E.

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Wound healing in epidermolysis bullosa von Bruckner‐Tuderman, L., Mellerio, J.E.

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Clinical features and WNT10A mutations in seven unrelated cases of Schöpf-Schulz-Passarge syndrome von Tziotzios, C., Petrof, G., Liu, L., Verma, A., Wedgeworth, E.K., Mellerio, J.E., McGrath, J.A.

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Practical management of epidermolysis bullosa: consensus clinical position statement from the European Reference Network for Rare Skin Diseases von Has, C., El Hachem, M., Bučková, H., Fischer, P., Friedová, M., Greco, C., Nevoránková, P., Salavastru, C., Mellerio, J.E., Zambruno, G., Bodemer, C.

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Foot care in epidermolysis bullosa: evidence‐based guideline von Khan, M.T., O'Sullivan, M., Faitli, B., Mellerio, J.E., Fawkes, R., Wood, M., Hubbard, L.D., Harris, A.G., Iacobaccio, L., Vlahovic, T., James, L., Brains, L., Fitzpatrick, M., Mayre‐Chilton, K.

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Under-recognition of acral peeling skin syndrome: 59 new cases with 15 novel mutations von Szczecinska, W., Nesteruk, D., Wertheim-Tysarowska, K., Greenblatt, D.T., Baty, D., Browne, F., Liu, L., Ozoemena, L., Terron-Kwiatkowski, A., McGrath, J.A., Mellerio, J.E., Morton, J., Woźniak, K., Kowalewski, C., Has, C., Moss, C.

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