Striate palmoplantar keratoderma resulting from a missense mutation in DSG1

por Vodo, D., O’Toole, E.A., Malchin, N., Lahav, A., Adir, N., Sarig, O., Green, K., Smith, F. J.D., Sprecher, E.
Publicado en Br J Dermatol (2018)

The molecular genetic analysis of the expanding pachyonychia congenita case collection

por Wilson, NJ, O'Toole, EA, Milstone, LM, Hansen, CD, Shepherd, AA, Al-Asadi, E, Schwartz, ME, McLean, WHI, Sprecher, E, Smith, FJD
Publicado en Br J Dermatol (2014)

Loss of function desmoplakin I and II mutations underlie dominant arrhythmogenic cardiomyopathy with a hair and skin phenotype

por Maruthappu, T., Posafalvi, A., Castelletti, S., Delaney, P.J., Syrris, P., O’Toole, E.A., Green, K.J., Elliott, P.M., Lambiase, P.D., Tinker, A., McKenna, W.J., Kelsell, D.P.
Publicado en Br J Dermatol (2019)

Distinctive clinical and histological characteristics of atrophic and hypertrophic facial photoageing

por Langton, A.K., Ayer, J., Griffiths, T.W., Rashdan, E., Naidoo, K., Caley, M.P., Birch‐Machin, M.A., O'Toole, E.A., Watson, R.E.B., Griffiths, C.E.M.
Publicado en J Eur Acad Dermatol Venereol (2020)