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Publications

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Publications générales

Phénotypes et thérapeutiques implanto-prothétiques précoces de la dysplasie ectodermique hypohidrotique liée à l'X (DEX)
François CLAUSS - Matthieu SCHMITTBUHL - Etienne WALTMANN - Frédéric OBRY - Marie-Cécile MANIÈRE

Publications scientifiques

The EDAR370A allele attenuates the severity of hypohidrotic ectodermal dysplasia caused by EDA gene mutation.
Cluzeau C, Hadj-Rabia S, Bal E, Clauss F, Munnich A, Bodemer C, Headon D, Smahi A.

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.

Quantification of taurodontism: interests in the early diagnosis of hypohidrotic ectodermal dysplasia.
Gros CI, Clauss F, Obry F, Manière MC, Schmittbuhl M.

X-linked and autosomal recessive Hypohidrotic Ectodermal Dysplasia: genotypic-dental phenotypic findings.
Clauss F, Chassaing N, Smahi A, Vincent MC, Calvas P, Molla M, Lesot H, Alembik Y, Hadj-Rabia S, Bodemer C, Manière MC, Schmittbuhl M.

Consequences of X-linked hypohidrotic ectodermal dysplasia for the human jaw bone.
Lesot H, Clauss F, Manière MC, Schmittbuhl M.

Dento-craniofacial phenotypes and underlying molecular mechanisms in hypohidrotic ectodermal dysplasia (HED): a review.
Clauss F, Manière MC, Obry F, Waltmann E, Hadj-Rabia S, Bodemer C, Alembik Y, Lesot H, Schmittbuhl M.

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