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Number of items: 3.

Schwieger-Briel, Agnes; Fuentes, Ignacia; Castiglia, Daniele; Barbato, Antonio; Greutmann, Matthias; Leppert, Juna; Duchatelet, Sabine; Hovnanian, Alain; Burattini, Sofia; Yubero, M Joao; Ibañez-Arenas, Rodrigo; Rebolledo-Jaramillo, Boris; Gräni, Christoph; Ott, Hagen; Theiler, Martin; Weibel, Lisa; Paller, Amy S; Zambruno, Giovanna; Fischer, Judith; Palisson, Francis; Has, Cristina (2019). Epidermolysis Bullosa Simplex With KLHL24 Mutations Is Associated With Dilated Cardiomyopathy. Journal of Investigative Dermatology, 139(1):244-249.

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.

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, Céline; 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 Sat Aug 17 19:24:49 2019 CEST.