P. Spek

A novel nicastrin mutation in a three‐generation Dutch family with hidradenitis suppurativa: a search for functional significance

A. Vossen, K. R. van Straalen, S. Swagemakers, 2020, Journal of the European Academy of Dermatology and Venereology : JEADV.

A 10‐year follow‐up of a child with mild case of xeroderma pigmentosum complementation group D diagnosed by whole‐genome sequencing

W. Sakai, K. Sugasawa, P. Spek, 2016, Photodermatology, photoimmunology & photomedicine.

The monocyte transcriptome during pregnancy in multiple sclerosis: prominent expression of the Fc-receptor CD64

E. Steegers, R. Hintzen, J. Laman, 2011, Multiple sclerosis.

Vitreous proteomics, a gateway to improved understanding and stratification of diverse uveitis aetiologies

P. J. van der Spek, A. Langerak, T. Missotten, 2021, Acta ophthalmologica.