Striate palmoplantar keratoderma resulting from a missense mutation in DSG1

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

The molecular genetic analysis of the expanding pachyonychia congenita case collection

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

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

von 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.
Veröffentlicht in Br J Dermatol (2019)

Distinctive clinical and histological characteristics of atrophic and hypertrophic facial photoageing

von 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.
Veröffentlicht in J Eur Acad Dermatol Venereol (2020)