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The Journal of Dermatological Treatment|September 12, 2025
Dupilumab for Hailey-Hailey diseaseMarie-Eline Pauline Henriette Debeuf, Pip Vlaanderen, Michel van Geel, et al.
Nature Reviews. Urology|September 16, 2010
Neuroendocrine carcinoma in a patient with Birt-Hogg-Dubé syndromeTijs Claessens, Sherry A Weppler, Michel van Geel, et al.
Lymphatic Research and Biology|October 26, 2018
Breast Cancer-Related Lymphedema and Genetic Predisposition: A Systematic Review of the LiteratureJoël Visser, Michel van Geel, Anouk J M Cornelissen, et al.
Human Mutation|December 31, 2016
Mendelian Disorders of Cornification Caused by Defects in Intracellular Calcium Pumps: Mutation Update and Database for Variants in ATP2A2 and ATP2C1 Associated with Darier Disease and Hailey-Hailey DiseaseRuud G L Nellen, Peter M Steijlen, Maurice A M van Steensel, et al.
The Journal of Dermatology|October 31, 2019
Mutations in the CDSN gene cause peeling skin disease and hypotrichosis simplex of the scalpJaap J A J van der Velden, Michel van Geel, Jans J Engelhart, et al.
International Journal of Dermatology|January 4, 2026
Biomolecular Changes Upon Ablative Laser Therapy of the Skin: A Scoping ReviewMarie-Eline Pauline Henriette Debeuf, Maartje Hendrika Pieternel Rauwenhoff, Michel van Geel, et al.
The Journal of Investigative Dermatology|January 28, 2006
Mutation S233L in the 1B domain of keratin 1 causes epidermolytic palmoplantar keratoderma with "tonotubular" keratinAna Terron-Kwiatkowski, Maurice A M van Steensel, Michel van Geel, et al.
The Journal of Investigative Dermatology|January 8, 2004
Clouston syndrome can mimic pachyonychia congenitaMaurice A M van Steensel, Marcel F Jonkman, Michel van Geel, et al.
The Journal of Investigative Dermatology|July 13, 2004
A phenotype resembling the Clouston syndrome with deafness is associated with a novel missense GJB2 mutationMaurice A M van Steensel, Peter M Steijlen, Reno S Bladergroen, et al.
Experimental Dermatology|August 3, 2006
Diffuse and segmental variants of cutaneous leiomyomatosis: novel mutations in the fumarate hydratase gene and review of the literatureSadhanna Badeloe, Michel van Geel, Maurice A M van Steensel, et al.
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