Malassezia folliculitis in an infant

Por Anane, S., Chtourou, O., Bodemer, C., Kharfi, M.
Publicado em 2013

Probable DRESS syndrome induced by IL-1 inhibitors

Por Polivka, L., Diana, J. S., Soria, A., Bodemer, C., Quartier, P., Fraitag, S., Bader-Meunier, B.
Publicado no Orphanet J Rare Dis (2017)

Respiratory involvement in juvenile dermatomyositis

Por Fabi, M, Le Bourgeois, M, Bodemer, C, Beguin, V, Prieur, AM, Quartier, P, de Blic, J
Publicado em 2008

Cytophagic histiocytic panniculitis: is it a macrophage activation syndrome in situ?

Por Bader-Meunier, B, Fraitag, S, Janssen, CEI, de Saint Basile, G, Brochard, K, Brousse, N, Bodemer, C, Wouters, C
Publicado em 2011

Deletions within COL7A1 exons distant from consensus splice sites alter splicing and produce shortened polypeptides in dominant dystrophic epidermolysis bullosa.

Por Sakuntabhai, A, Hammami-Hauasli, N, Bodemer, C, Rochat, A, Prost, C, Barrandon, Y, de Prost, Y, Lathrop, M, Wojnarowska, F, Bruckner-Tuderman, L, Hovnanian, A
Publicado em 1998

A novel form of syndromic cutis laxa with facial dysmorphism, cleft palate, and mental retardation

Por Genevieve, D, Baumann, C, Huber, C, Faivre, L, Sanlaville, D, Bodemer, C, Hadj-Rabia, S, Assoumou, A, Verloes, A, Raqbi, F, Munnich, A, Cormier-Daire, V
Publicado em 2004

Characterization of 18 new mutations in COL7A1 in recessive dystrophic epidermolysis bullosa provides evidence for distinct molecular mechanisms underlying defective anchoring fibr...

Por Hovnanian, A, Rochat, A, Bodemer, C, Petit, E, Rivers, C A, Prost, C, Fraitag, S, Christiano, A M, Uitto, J, Lathrop, M, Barrandon, Y, de Prost, Y
Publicado em 1997

Granulomatous inflammation in cartilage-hair hypoplasia: risks and benefits of anti-TNF alpha monoclonal antibodies

Por Moshous, D, Meyts, I, Fraitag, S, Janssen, C, Debré, M, Suarez, F, Toelen, J, De Boeck, K, Roskams, T, Deschildre, A, Picard, C, Bodemer, C, Wouters, C, Fischer, A
Publicado em 2011

Unusual cutaneous features associated with a heterozygous gain-of-function mutation in IFIH1: overlap between Aicardi–Goutières and Singleton–Merten syndromes

Por Bursztejn, A.-C., Briggs, T.A., del Toro Duany, Y., Anderson, B.H., O’Sullivan, J., Williams, S.G., Bodemer, C., Fraitag, S., Gebhard, F., Leheup, B., Lemelle, I., Oojageer, A., Raffo, E., Schmitt, E., Rice, G.I., Hur, S., Crow, Y.J.
Publicado no Br J Dermatol (2015)