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Omalizumab in the treatment of bullous pemphigoid resistant to first-line therapy: a French national multicentre retrospective study of 100 patients.
Chebani R, Lombart F, Chaby G, Dadban A, Debarbieux S, Viguier MA, Ingen-Housz-Oro S, Pham-Ledard A, Bedane CR, Picard-Dahan C, Berthin C, Dereure O, Konstantinou MP, Castel M, Jouen F, Joly P, Seta V, Duvert-Lehembre S, Le Roux C, Quereux G, Sassolas B, Brenaut E, Sin C, Richard MA, Bérard F, Giusti D, Belmondo T, Gille T, Caux F, Prost-Squarcioni C, Grootenboer-Mignot S, Alexandre M; French Study Group on Autoimmune Bullous Diseases. Chebani R, et al. Among authors: caux f. Br J Dermatol. 2024 Jan 23;190(2):258-265. doi: 10.1093/bjd/ljad369. Br J Dermatol. 2024. PMID: 37792727
Novel FH mutations in families with hereditary leiomyomatosis and renal cell cancer (HLRCC) and patients with isolated type 2 papillary renal cell carcinoma.
Gardie B, Remenieras A, Kattygnarath D, Bombled J, Lefèvre S, Perrier-Trudova V, Rustin P, Barrois M, Slama A, Avril MF, Bessis D, Caron O, Caux F, Collignon P, Coupier I, Cremin C, Dollfus H, Dugast C, Escudier B, Faivre L, Field M, Gilbert-Dussardier B, Janin N, Leport Y, Leroux D, Lipsker D, Malthieu F, McGilliwray B, Maugard C, Méjean A, Mortemousque I, Plessis G, Poppe B, Pruvost-Balland C, Rooker S, Roume J, Soufir N, Steinraths M, Tan MH, Théodore C, Thomas L, Vabres P, Van Glabeke E, Meric JB, Verkarre V, Lenoir G, Joulin V, Deveaux S, Cusin V, Feunteun J, Teh BT, Bressac-de Paillerets B, Richard S; French National Cancer Institute "Inherited predisposition to kidney cancer" network. Gardie B, et al. Among authors: caux f. J Med Genet. 2011 Apr;48(4):226-34. doi: 10.1136/jmg.2010.085068. Epub 2011 Mar 12. J Med Genet. 2011. PMID: 21398687 Free article.
[Linear IgA dermatoses in children].
Caux F, Prost C. Caux F, et al. Ann Dermatol Venereol. 1999 Oct;126(10):732-5. Ann Dermatol Venereol. 1999. PMID: 10604019 French. No abstract available.
[Kaposi's sarcoma: an exuberant African form during HIV infection].
Braun T, Stirnemann J, Caux F, Kettaneh A, Letellier E, Fain O, Thomas M. Braun T, et al. Among authors: caux f. Rev Med Interne. 2005 Mar;26(3):247-8. doi: 10.1016/j.revmed.2004.07.016. Rev Med Interne. 2005. PMID: 15777588 French. No abstract available.
LMNA mutations in atypical Werner's syndrome.
Vigouroux C, Caux F, Capeau J, Christin-Maitre S, Cohen A. Vigouroux C, et al. Among authors: caux f. Lancet. 2003 Nov 8;362(9395):1585; author reply 1586. doi: 10.1016/S0140-6736(03)14760-5. Lancet. 2003. PMID: 14615128 No abstract available.
177 results