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Hadj-Rabia, Smail; Brideau, Gaelle; Olinger, Eric; Vargas-Poussou, Rosa; Bodemer, Christine; Devuyst, Olivier; et al (2018). Multiplex epithelium dysfunction due to CLDN10 mutation: the HELIX syndrome. Genetics in Medicine, 20(2):190-201.

Leclerc-Mercier, Stephanie; Bodemer, Christine; Furio, Laetitia; Hadj-Rabia, Smail; de Peufeilhoux, Laetitia; Weibel, Lisa; Bursztejn, Anne-Claire; Bourrat, Emmanuelle; Ortonne, Nicolas; Molina, Thierry Jo; Hovnanian, Alain; Fraitag, Sylvie (2016). Skin biopsy in netherton syndrome: a histological review of a large series and new findings. American Journal of Dermatopathology, 38(2):83-91.

Hadj-Rabia, Smail; Callewaert, Bert L; Bourrat, Emmanuelle; Kempers, Marlies; Plomp, Astrid S; Layet, Valerie; Bartholdi, Deborah; Renard, Marjolijn; De Backer, Julie; Malfait, Fransiska; Vanakker, Olivier M; Coucke, Paul J; De Paepe, Anne M; Bodemer, Christine (2013). Twenty patients including 7 probands with autosomal dominant cutis laxa confirm clinical and molecular homogeneity. Orphanet Journal of Rare Diseases, 8:36.

Lacroix, Matthieu; Lacaze-Buzy, Laetitia; Furio, Laetitia; Tron, Elodie; Valari, Manthoula; Van der Wier, Gerda; Bodemer, Christine; Bygum, Anette; Bursztejn, Anne-Claire; Gaitanis, George; Paradisi, Mauro; Stratigos, Alexander; Weibel, Lisa; Deraison, CĂ©line; Hovnanian, Alain (2012). Clinical expression and new SPINK5 splicing defects in Netherton syndrome: unmasking a frequent founder synonymous mutation and unconventional intronic mutations. Journal of Investigative Dermatology, 132(3 Pt 1):575-582.

This list was generated on Wed Mar 20 06:09:18 2019 CET.