E. Lajeunie

发表

Syndromal and nonsyndromal primary trigonocephaly: analysis of a series of 237 patients.

D. Rénier, M. le Merrer, M. Merrer, 1998, American journal of medical genetics.

Mutations of the TWIST gene in the Saethre-Chotzene syndrome

P. Bénit, A. Munnich, J. Bonaventure, 1997, Nature Genetics.

Increased calvaria cell differentiation and bone matrix formation induced by fibroblast growth factor receptor 2 mutations in Apert syndrome.

A. Munnich, J. Lemonnier, P. Marie, 1998, The Journal of clinical investigation.

Mutations in the basic domain and the loop–helix II junction of TWIST abolish DNA binding in Saethre–Chotzen syndrome

A. Munnich, J. Bonaventure, V. El Ghouzzi, 2001, FEBS letters.

Monozygotic twins with Crouzon syndrome: concordance for craniosynostosis and discordance for thumb duplication.

J. Bonaventure, V. El Ghouzzi, D. Rénier, 2000, American journal of medical genetics.

No evidence of genetic heterogeneity in Crouzon craniofacial dysostosis

J. Weissenbach, A. Munnich, D. Rénier, 1995, Human Genetics.

Possible genetic heterogeneity in the Saethre-Chotzen syndrome

A. Munnich, D. Rénier, M. Merrer, 1996, Human Genetics.

Mutations within or upstream of the basic helix–loop–helix domain of the TWIST gene are specific to Saethre-Chotzen syndrome

A. Munnich, J. Bonaventure, D. Rénier, 1999, European Journal of Human Genetics.

Functional Outcome after Surgery for Trigonocephaly

D. Rénier, D. Marchac, E. Lajeunie, 1998, Plastic and reconstructive surgery.

Induced mild hypothermia reduces mortality during acute inflammation in rats

D. Benhamou, E. Vicaut, O. Huet, 2007, Acta anaesthesiologica Scandinavica.

Saethre-Chotzen syndrome: notable intrafamilial phenotypic variability in a large family with Q28X TWIST mutation.

H. Dollfus, D. Rénier, J. Biswas, 2002, American journal of medical genetics.

Craniosynostosis: from a clinical description to an understanding of bone formation of the skull

D. Rénier, M. Catala, E. Lajeunie, 1999, Child's Nervous System.

Sex related expressivity of the phenotype in coronal craniosynostosis caused by the recurrent P250R FGFR3 mutation

A. Munnich, J. Bonaventure, V. El Ghouzzi, 1999, Journal of medical genetics.

FGFR2 mutations in Pfeiffer syndrome

A. Munnich, J. Bonaventure, D. Rénier, 1995, Nature Genetics.

[Antley-Bixler syndrome. Description of two new cases and review of the literature. Prognostic and therapeutic aspects].

D. Rénier, G. Cinalli, P. Labrune, 1997, Annales de chirurgie plastique et esthetique.

Jackson-Weiss syndrome: identification of two novel FGFR2 missense mutations shared with Crouzon and Pfeiffer craniosynostotic disorders

M. Tartaglia, C. Rocco, C. Di Rocco, 1997, Human Genetics.

Mutation screening in patients with syndromic craniosynostoses indicates that a limited number of recurrent FGFR2 mutations accounts for severe forms of Pfeiffer syndrome

J. Bonaventure, D. Rénier, J. Martinovic, 2006, European Journal of Human Genetics.

[Trigonocephaly: isolated, associated and syndromic forms. Genetic study in a series of 278 patients].

É. Arnaud, D. Rénier, M. le Merrer, 1998, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

Genetic study of nonsyndromic coronal craniosynostosis.

C. Bonaïti‐pellié, D. Rénier, M. le Merrer, 1995, American journal of medical genetics.

Genetic considerations in nonsyndromic midline craniosynostoses: a study of twins and their families.

É. Arnaud, D. Rénier, D. Crimmins, 2005, Journal of neurosurgery.

Genetic study of scaphocephaly.

C. Bonaïti‐pellié, D. Rénier, M. le Merrer, 1996, American journal of medical genetics.

Management of craniosynostoses

Eric Arnaud, Daniel Marchac, É. Arnaud, 2000, Child's Nervous System.

Fetal exposure to sodium valproate associated with Baller–Gerold syndrome: case report and review of the literature

É. Arnaud, D. Rénier, E. Lajeunie, 2004, Child's Nervous System.

Postoperative Mental and Morphological Outcome for Nonsyndromic Brachycephaly

É. Arnaud, D. Rénier, J. Thorne, 2002, Plastic and reconstructive surgery.

Fibroblast growth factor receptor 3 mutation in nonsyndromic coronal synostosis: clinical spectrum, prevalence, and surgical outcome.

J. Bonaventure, D. Rénier, M. le Merrer, 2000, Journal of neurosurgery.

Craniosynostosis and fetal exposure to sodium valproate.

M. Bourgeois, V. El Ghouzzi, D. Rénier, 2001, Journal of neurosurgery.

[Oxycephaly, a severe craniosynostosis. Apropos of a series of 129 cases].

É. Arnaud, D. Rénier, G. Cinalli, 1997, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

Postoperative cognitive outcome for synostotic frontal plagiocephaly.

É. Arnaud, D. Rénier, I. Mathijssen, 2006, Journal of neurosurgery.

Clinical variability in patients with Apert's syndrome.

M. Gonzalès, J. Bonaventure, V. El Ghouzzi, 1999, Journal of neurosurgery.

Inflammatory cytokines, C reactive protein, and procalcitonin as early predictors of necrosis infection in acute necrotizing pancreatitis.

E. Vicaut, B. Cholley, F. Riché, 2003, Surgery.

Antley-Bixler syndrome Description of two new cases and a review of the literature

D. Rénier, G. Cinalli, P. Labrune, 1997, Child's Nervous System.

Pfeiffer syndrome type 2: further delineation and review of the literature.

J. Fryns, A. Verloes, A. Plomp, 1998, American journal of medical genetics.

Syndactyly in Apert syndrome. Utility of a prognostic classification.

D. Rénier, P. Journeau, J. Pouliquen, 1999, Annales de chirurgie de la main et du membre superieur : organe officiel des societes de chirurgie de la main = Annals of hand and upper limb surgery.