Renier D - Search Results

1

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

Dollfus H, Biswas P, Kumaramanickavel G, Stoetzel C, Quillet R, Biswas J, Lajeunie E, Renier D, Perrin-Schmitt F. Dollfus H, et al. Among authors: renier d. Am J Med Genet. 2002 May 1;109(3):218-25. doi: 10.1002/ajmg.10349. Am J Med Genet. 2002. PMID: 11977182

2

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

Lajeunie E, Heuertz S, El Ghouzzi V, Martinovic J, Renier D, Le Merrer M, Bonaventure J. Lajeunie E, et al. Among authors: renier d. Eur J Hum Genet. 2006 Mar;14(3):289-98. doi: 10.1038/sj.ejhg.5201558. Eur J Hum Genet. 2006. PMID: 16418739 Free article.

3

Clinical spectrum and outcomes in families with coronal synostosis and TCF12 mutations.

di Rocco F, Baujat G, Arnaud E, Rénier D, Laplanche JL, Daire VC, Collet C. di Rocco F, et al. Among authors: renier d. Eur J Hum Genet. 2014 Dec;22(12):1413-6. doi: 10.1038/ejhg.2014.57. Epub 2014 Apr 16. Eur J Hum Genet. 2014. PMID: 24736737 Free PMC article.

4

Crouzon syndrome with acanthosis nigricans: a case-based update.

Di Rocco F, Collet C, Legeai-Mallet L, Arnaud E, Le Merrer M, Hadj-Rabia S, Renier D. Di Rocco F, et al. Among authors: renier d. Childs Nerv Syst. 2011 Mar;27(3):349-54. doi: 10.1007/s00381-010-1347-z. Epub 2010 Dec 7. Childs Nerv Syst. 2011. PMID: 21136065

5

Bilambdoid and sagittal synostosis: Report of 39 cases.

Chivoret N, Arnaud E, Giraudat K, O'Brien F, Pamphile L, Meyer P, Renier D, Collet C, Di Rocco F. Chivoret N, et al. Among authors: renier d. Surg Neurol Int. 2018 Oct 11;9:206. doi: 10.4103/sni.sni_454_17. eCollection 2018. Surg Neurol Int. 2018. PMID: 30386676 Free PMC article.

6

Scaphocephaly part II: Secondary coronal synostosis after scaphocephalic surgical correction.

Arnaud E, Capon-Degardin N, Michienzi J, Di Rocco F, Renier D. Arnaud E, et al. Among authors: renier d. J Craniofac Surg. 2009 Sep;20 Suppl 2:1843-50. doi: 10.1097/SCS.0b013e3181b6c4c3. J Craniofac Surg. 2009. PMID: 19816363

7

Pediatric craniofacial osteosynthesis and distraction using an ultrasonic-assisted pinned resorbable system: a prospective report with a minimum 30 months' follow-up.

Arnaud E, Renier D. Arnaud E, et al. Among authors: renier d. J Craniofac Surg. 2009 Nov;20(6):2081-6. doi: 10.1097/SCS.0b013e3181be8854. J Craniofac Surg. 2009. PMID: 19881368 Clinical Trial.

8

The posterior coronal incision.

Pavri SN, Arnaud E, Renier D, Persing JA. Pavri SN, et al. Among authors: renier d. J Craniofac Surg. 2015 Jan;26(1):243-4. doi: 10.1097/SCS.0000000000001374. J Craniofac Surg. 2015. PMID: 25478982

9

Focus session on the changing "epidemiology" of craniosynostosis (comparing two quinquennia: 1985-1989 and 2003-2007) and its impact on the daily clinical practice: a review from Necker Enfants Malades.

Di Rocco F, Arnaud E, Meyer P, Sainte-Rose C, Renier D. Di Rocco F, et al. Among authors: renier d. Childs Nerv Syst. 2009 Jul;25(7):807-11. doi: 10.1007/s00381-009-0864-0. Epub 2009 Apr 9. Childs Nerv Syst. 2009. PMID: 19357856

10

The role of endoscopic third ventriculostomy in the treatment of hydrocephalus associated with faciocraniosynostosis.

Di Rocco F, Jucá CE, Arnaud E, Renier D, Sainte-Rose C. Di Rocco F, et al. Among authors: renier d. J Neurosurg Pediatr. 2010 Jul;6(1):17-22. doi: 10.3171/2010.3.PEDS09484. J Neurosurg Pediatr. 2010. PMID: 20593982

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