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1.

Otological complications in inversa type recessive dystrophic epidermolysis bullosa.

Robertson, S J; Prodinger, C; Liu, L; Skilbeck, C; Petrof, G; Martinez, A E; Mellerio, J E; Greenblatt, D T.

Clin Exp Dermatol; 47(4): 717-723, 2022 Apr.

Artículo en Inglés | MEDLINE | ID: mdl-34826142

2.

Prevalence, pathophysiology and management of itch in epidermolysis bullosa.

Papanikolaou, M; Onoufriadis, A; Mellerio, J E; Nattkemper, L A; Yosipovitch, G; Steinhoff, M; McGrath, J A.

Br J Dermatol; 184(5): 816-825, 2021 05.

Artículo en Inglés | MEDLINE | ID: mdl-32810291

3.

Heterogeneous addiction to transforming growth factor-beta signalling in recessive dystrophic epidermolysis bullosa-associated cutaneous squamous cell carcinoma.

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.

Br J Dermatol; 184(4): 697-708, 2021 04.

Artículo en Inglés | MEDLINE | ID: mdl-32726455

4.

Practical management of epidermolysis bullosa: consensus clinical position statement from the European Reference Network for Rare Skin Diseases.

Has, C; El Hachem, M; Bucková, H; Fischer, P; Friedová, M; Greco, C; Nevoránková, P; Salavastru, C; Mellerio, J E; Zambruno, G; Bodemer, C.

J Eur Acad Dermatol Venereol; 35(12): 2349-2360, 2021 Dec.

Artículo en Inglés | MEDLINE | ID: mdl-34545960

5.

Creating new guidelines on how best to treat foot symptoms in people with EB.

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.

Br J Dermatol; 182(3): e89-e114, 2020 03.

Artículo en Inglés | MEDLINE | ID: mdl-32107777

6.

Foot care in epidermolysis bullosa: evidence-based guideline.

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.

Br J Dermatol; 182(3): 593-604, 2020 03.

Artículo en Inglés | MEDLINE | ID: mdl-31397882

7.

Consensus reclassification of inherited epidermolysis bullosa and other disorders with skin fragility.

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.

Br J Dermatol; 183(4): 614-627, 2020 10.

Artículo en Inglés | MEDLINE | ID: mdl-32017015

8.

Genotype-phenotype correlation in a large English cohort of patients with autosomal recessive ichthyosis.

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.

Br J Dermatol; 182(3): 729-737, 2020 03.

Artículo en Inglés | MEDLINE | ID: mdl-31168818

9.

Recommendations on pregnancy, childbirth and aftercare in epidermolysis bullosa: a consensus-based guideline.

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.

Br J Dermatol; 186(4): 620-632, 2022 04.

Artículo en Inglés | MEDLINE | ID: mdl-34687549

10.

Management of cutaneous squamous cell carcinoma in patients with epidermolysis bullosa: best clinical practice guidelines.

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.

Br J Dermatol; 174(1): 56-67, 2016 Jan.

Artículo en Inglés | MEDLINE | ID: mdl-26302137

11.

Characteristics of children with Netherton syndrome: a review of 21 patients.

Prodinger, C; Yerlett, N; MacDonald, C; Subhanitthaya, C; Laimer, M; Goh, L; Du Toit, G; Mellerio, J E; Petrof, G; Martinez, A E.

J Eur Acad Dermatol Venereol; 35(7): e466-e469, 2021 Jul.

Artículo en Inglés | MEDLINE | ID: mdl-33725371

12.

The psychological functioning of children with epidermolysis bullosa and its relationship with specific aspects of disease.

Soon, K; Mason, R; Martinez, A E; Mellerio, J E.

Br J Dermatol; 182(3): 789-790, 2020 03.

Artículo en Inglés | MEDLINE | ID: mdl-31587254

13.

EBGene trial: patient preselection outcomes for the European GENEGRAFT ex vivo phase I/II gene therapy trial for recessive dystrophic epidermolysis bullosa.

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.

Br J Dermatol; 182(3): 794-797, 2020 03.

Artículo en Inglés | MEDLINE | ID: mdl-31557321

14.

Whole-exome sequencing improves mutation detection in a diagnostic epidermolysis bullosa laboratory.

Takeichi, T; Liu, L; Fong, K; Ozoemena, L; McMillan, J R; Salam, A; Campbell, P; Akiyama, M; Mellerio, J E; McLean, W H I; Simpson, M A; McGrath, J A.

Br J Dermatol; 172(1): 94-100, 2015 Jan.

Artículo en Inglés | MEDLINE | ID: mdl-24947307

15.

PLACK syndrome: the penny dropped.

O'Sullivan, S; Ozoemena, L; Liu, L; McGrath, J A; Mellerio, J E; Martinez, A E.

Clin Exp Dermatol; 45(8): 1091-1092, 2020 Dec.

Artículo en Inglés | MEDLINE | ID: mdl-32918489

16.

Enduring support for the case report.

Mellerio, J E.

Br J Dermatol; 181(3): 429-430, 2019 09.

Artículo en Inglés | MEDLINE | ID: mdl-31475346

17.

Beta blockers for infantile haemangiomas: where should we go from here?

Mellerio, J E.

Br J Dermatol; 180(3): 450-451, 2019 03.

Artículo en Inglés | MEDLINE | ID: mdl-30821386

18.

Potential therapeutic targeting of inflammation in epidermolysis bullosa simplex.

Mellerio, J E.

Br J Dermatol; 180(2): 258-260, 2019 02.

Artículo en Inglés | MEDLINE | ID: mdl-30714107

19.

Clinical features and WNT10A mutations in seven unrelated cases of Schöpf-Schulz-Passarge syndrome.

Tziotzios, C; Petrof, G; Liu, L; Verma, A; Wedgeworth, E K; Mellerio, J E; McGrath, J A.

Br J Dermatol; 171(5): 1211-4, 2014 Nov.

Artículo en Inglés | MEDLINE | ID: mdl-24902757

20.

Mutations in EXPH5 result in autosomal recessive inherited skin fragility.

Liu, L; Mellerio, J E; Martinez, A E; McMillan, J R; Aristodemou, S; Parsons, M; McGrath, J A.

Br J Dermatol; 170(1): 196-9, 2014 Jan.

Artículo en Inglés | MEDLINE | ID: mdl-24443915

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Otological complications in inversa type recessive dystrophic epidermolysis bullosa.

Prevalence, pathophysiology and management of itch in epidermolysis bullosa.

Heterogeneous addiction to transforming growth factor-beta signalling in recessive dystrophic epidermolysis bullosa-associated cutaneous squamous cell carcinoma.

Practical management of epidermolysis bullosa: consensus clinical position statement from the European Reference Network for Rare Skin Diseases.

Creating new guidelines on how best to treat foot symptoms in people with EB.

Foot care in epidermolysis bullosa: evidence-based guideline.

Consensus reclassification of inherited epidermolysis bullosa and other disorders with skin fragility.

Genotype-phenotype correlation in a large English cohort of patients with autosomal recessive ichthyosis.

Recommendations on pregnancy, childbirth and aftercare in epidermolysis bullosa: a consensus-based guideline.

Management of cutaneous squamous cell carcinoma in patients with epidermolysis bullosa: best clinical practice guidelines.

Characteristics of children with Netherton syndrome: a review of 21 patients.

The psychological functioning of children with epidermolysis bullosa and its relationship with specific aspects of disease.

EBGene trial: patient preselection outcomes for the European GENEGRAFT ex vivo phase I/II gene therapy trial for recessive dystrophic epidermolysis bullosa.

Whole-exome sequencing improves mutation detection in a diagnostic epidermolysis bullosa laboratory.

PLACK syndrome: the penny dropped.

Enduring support for the case report.

Beta blockers for infantile haemangiomas: where should we go from here?

Potential therapeutic targeting of inflammation in epidermolysis bullosa simplex.

Clinical features and WNT10A mutations in seven unrelated cases of Schöpf-Schulz-Passarge syndrome.

Mutations in EXPH5 result in autosomal recessive inherited skin fragility.