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Immune deficiency, autoimmune disease and intellectual disability: A pleiotropic disorder caused by biallelic variants in the TPP2 gene.
Atallah I, Quinodoz M, Campos-Xavier B, Peter VG, Fouriki A, Bonvin C, Bottani A, Kumps C, Angelini F, Bellutti Enders F, Christen-Zaech S, Rizzi M, Renella R, Beck-Popovic M, Poloni C, Frossard V, Blouin JL, Rivolta C, Riccio O, Candotti F, Hofer M, Unger S, Superti-Furga A. Atallah I, et al. Clin Genet. 2021 Jun;99(6):780-788. doi: 10.1111/cge.13942. Epub 2021 Feb 21. Clin Genet. 2021. PMID: 33586135
IL-17 receptor A and adenosine deaminase 2 deficiency in siblings with recurrent infections and chronic inflammation.
Fellmann F, Angelini F, Wassenberg J, Perreau M, Arenas Ramirez N, Simon G, Boyman O, Demaria O, Christen-Zaech S, Hohl D, Belfiore M, von Scheven-Gete A, Gilliet M, Bochud PY, Perrin Y, Beck Popovic M, Bart PA, Beckmann JS, Martinet D, Hofer M. Fellmann F, et al. J Allergy Clin Immunol. 2016 Apr;137(4):1189-1196.e2. doi: 10.1016/j.jaci.2015.07.053. Epub 2015 Nov 20. J Allergy Clin Immunol. 2016. PMID: 26607704
[Rare vascular diseases, building dedicated multidisciplinary specialized center].
Krieger C, Baud D, Bouchardy J, Christen-Zaech S, De Buys A, Deglise S, El Ezzi O, Fresa M, Hofer M, Hohl D, Kirsch M, Lazor R, Michel P, Monney P, Munier F, Qanadli SD, Raffoul W, Aubry Rozier B, Saucy F, Schoepfer A, Saliou G, Sekarski N, Superti-Furga A, Wuerzner G, Wasserfallen JB, Mazzolai L. Krieger C, et al. Rev Med Suisse. 2017 Dec 6;13(586):2109-2115. Rev Med Suisse. 2017. PMID: 29211369 French.
[Pathogenesis of atopic dermatitis].
Lang C, Kypriotou M, Christen-Zaech S. Lang C, et al. Rev Med Suisse. 2010 Apr 28;6(246):860-2, 864-5. Rev Med Suisse. 2010. PMID: 20455383 French.
43 results