Striate palmoplantar keratoderma resulting from a missense mutation in DSG1

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

The molecular genetic analysis of the expanding pachyonychia congenita case collection

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

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

av 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.
I publikationen Br J Dermatol (2019)

Distinctive clinical and histological characteristics of atrophic and hypertrophic facial photoageing

av 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.
I publikationen J Eur Acad Dermatol Venereol (2020)