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Clinical and Experimental Dermatology|October 13, 2015
Novel mutation in NIPAL4 in a Romanian family with autosomal recessive congenital ichthyosisD Maier, J Mazereeuw-Hautier, M Tilinca, et al.
The British Journal of Dermatology|May 8, 2008
Alterations in the desquamation-related proteolytic cleavage of corneodesmosin and other corneodesmosomal proteins in psoriatic lesional epidermisM Simon, R Tazi-Ahnini, N Jonca, et al.
Orphanet Journal of Rare Diseases|July 15, 2022
New developments in the molecular treatment of ichthyosis: review of the literatureM D W Joosten, J M K Clabbers, N Jonca, et al.
Annales De Dermatologie Et De Venereologie|August 6, 2018
[Ichthyosis prematurity syndrome: Two new cases]M Severino-Freire, A-C Bing Lecointe, E Bourrat, et al.
The Journal of Biological Chemistry|March 30, 2001
Refined characterization of corneodesmosin proteolysis during terminal differentiation of human epidermis and its relationship to desquamationM Simon, N Jonca, M Guerrin, et al.
The British Journal of Dermatology|August 21, 2013
Identification of the first nonsense CDSN mutation with expression of a truncated protein causing peeling skin syndrome type BA Mallet, M Kypriotou, K George, et al.
Annales De Dermatologie Et De Venereologie|March 21, 2024
French national protocol for the management of congenital ichthyosisM Severino-Freire, C Granier Tournier, C Chiaverini, et al.
The British Journal of Dermatology|September 15, 2018
Management of congenital ichthyoses: European guidelines of care, part oneJ Mazereeuw-Hautier, A Vahlquist, H Traupe, et al.
The British Journal of Dermatology|June 14, 2018
Management of congenital ichthyoses: European guidelines of care, part twoJ Mazereeuw-Hautier, A Hernández-Martín, E A O'Toole, et al.
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