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Search for ReCQL4 mutations in 39 patients genotyped for suspected Rothmund-Thomson/Baller-Gerold syndromes.
Piard J, Aral B, Vabres P, Holder-Espinasse M, Mégarbané A, Gauthier S, Capra V, Pierquin G, Callier P, Baumann C, Pasquier L, Baujat G, Martorell L, Rodriguez A, Brady AF, Boralevi F, González-Enseñat MA, Rio M, Bodemer C, Philip N, Cordier MP, Goldenberg A, Demeer B, Wright M, Blair E, Puzenat E, Parent P, Sznajer Y, Francannet C, DiDonato N, Boute O, Barlogis V, Moldovan O, Bessis D, Coubes C, Tardieu M, Cormier-Daire V, Sousa AB, Franques J, Toutain A, Tajir M, Elalaoui SC, Geneviève D, Thevenon J, Courcet JB, Rivière JB, Collet C, Gigot N, Faivre L, Thauvin-Robinet C. Piard J, et al. Among authors: bodemer c. Clin Genet. 2015 Mar;87(3):244-51. doi: 10.1111/cge.12361. Epub 2014 Mar 26. Clin Genet. 2015. PMID: 24635570
Psoriasis and obesity in French children: a case-control, multicentre study.
Mahé E, Beauchet A, Bodemer C, Phan A, Bursztejn AC, Boralevi F, Souillet AL, Chiaverini C, Bourrat E, Miquel J, Vabres P, Barbarot S, Bessis D, Eschard C, Hadj-Rabia S; Groupe de Recherche de la Société Française de Dermatologie Pédiatrique. Mahé E, et al. Among authors: bodemer c. Br J Dermatol. 2015 Jun;172(6):1593-1600. doi: 10.1111/bjd.13507. Epub 2015 Mar 22. Br J Dermatol. 2015. PMID: 25363889
Mutation in MMP2 gene may result in scleroderma-like skin thickening.
Bader-Meunier B, Bonafé L, Fraitag S, Breton S, Bodemer C, Baujat G. Bader-Meunier B, et al. Among authors: bodemer c. Ann Rheum Dis. 2016 Jan;75(1):e1. doi: 10.1136/annrheumdis-2015-208182. Epub 2015 Sep 29. Ann Rheum Dis. 2016. PMID: 26420579 No abstract available.
[Impact of sex and age on the clinical and epidemiological aspects of childhood psoriasis: Data from a French cross-sectional multicentre study].
Bonigen J, Phan A, Hadj-Rabia S, Boralévi F, Bursztejn AC, Bodemer C, Ferneiny M, Souillet AL, Chiavérini C, Bourrat E, Miquel J, Vabres P, Barbarot S, Bessis D, Eschard C, Mazereeuw-Hautier J, Piram M, Plantin P, Abasq C, Lasek-Duriez A, Maruani A, Beauchet A, Mahé E; Groupe de recherche de la Société française de dermatologie pédiatrique. Bonigen J, et al. Among authors: bodemer c. Ann Dermatol Venereol. 2016 May;143(5):354-63. doi: 10.1016/j.annder.2016.02.006. Epub 2016 Mar 8. Ann Dermatol Venereol. 2016. PMID: 26969479 French.
Only four genes (EDA1, EDAR, EDARADD, and WNT10A) account for 90% of hypohidrotic/anhidrotic ectodermal dysplasia cases.
Cluzeau C, Hadj-Rabia S, Jambou M, Mansour S, Guigue P, Masmoudi S, Bal E, Chassaing N, Vincent MC, Viot G, Clauss F, Manière MC, Toupenay S, Le Merrer M, Lyonnet S, Cormier-Daire V, Amiel J, Faivre L, de Prost Y, Munnich A, Bonnefont JP, Bodemer C, Smahi A. Cluzeau C, et al. Among authors: bodemer c. Hum Mutat. 2011 Jan;32(1):70-2. doi: 10.1002/humu.21384. Hum Mutat. 2011. PMID: 20979233
484 results