Corre P - Search Results

1

Autosomal recessive Treacher Collins syndrome due to POLR1C mutations: Report of a new family and review of the literature.

Ghesh L, Vincent M, Delemazure AS, Boyer J, Corre P, Perez F, Geneviève D, Laplanche JL, Collet C, Isidor B. Ghesh L, et al. Among authors: corre p. Am J Med Genet A. 2019 Jul;179(7):1390-1394. doi: 10.1002/ajmg.a.61147. Epub 2019 Apr 8. Am J Med Genet A. 2019. PMID: 30957429 Review.

2

Can a Predetermined Grid and Multidisciplinary Consultation Improve the Description of Cleft lip with or Without Cleft Palate?

Vaillant CL, Bruand M, Corre P. Vaillant CL, et al. Among authors: corre p. Cleft Palate Craniofac J. 2023 Feb 20:10556656231156708. doi: 10.1177/10556656231156708. Online ahead of print. Cleft Palate Craniofac J. 2023. PMID: 36802821

3

Effectiveness of treatment by coronoidectomy and active rehabilitation in Langenbeck or Jacob diseases. A retrospective study of 20 cases.

Domart M, Nicot R, Mattei L, Cloître A, Lesclous P, Bertin H, Corre P. Domart M, et al. Among authors: corre p. J Stomatol Oral Maxillofac Surg. 2023 Feb;124(1S):101351. doi: 10.1016/j.jormas.2022.101351. Epub 2022 Dec 7. J Stomatol Oral Maxillofac Surg. 2023. PMID: 36496122

4

A brain abscess following dental extractions in a patient with hereditary hemorrhagic telangiectasia.

Corre P, Perret C, Isidor B, Khonsari RH. Corre P, et al. Br J Oral Maxillofac Surg. 2011 Jul;49(5):e9-11. doi: 10.1016/j.bjoms.2010.07.014. Epub 2010 Aug 16. Br J Oral Maxillofac Surg. 2011. PMID: 20719417

5

[Parotid involvement in Churg-Strauss syndrome].

Bonnet R, Bertin H, Delemazure AS, Clairand R, Mercier J, Corre P. Bonnet R, et al. Among authors: corre p. Rev Stomatol Chir Maxillofac Chir Orale. 2014 Jun;115(3):188-91. doi: 10.1016/j.revsto.2014.03.006. Epub 2014 May 3. Rev Stomatol Chir Maxillofac Chir Orale. 2014. PMID: 24797730 French.

6

Germline De Novo Mutations in GNB1 Cause Severe Neurodevelopmental Disability, Hypotonia, and Seizures.

Petrovski S, Küry S, Myers CT, Anyane-Yeboa K, Cogné B, Bialer M, Xia F, Hemati P, Riviello J, Mehaffey M, Besnard T, Becraft E, Wadley A, Politi AR, Colombo S, Zhu X, Ren Z, Andrews I, Dudding-Byth T, Schneider AL, Wallace G; University of Washington Center for Mendelian Genomics; Rosen ABI, Schelley S, Enns GM, Corre P, Dalton J, Mercier S, Latypova X, Schmitt S, Guzman E, Moore C, Bier L, Heinzen EL, Karachunski P, Shur N, Grebe T, Basinger A, Nguyen JM, Bézieau S, Wierenga K, Bernstein JA, Scheffer IE, Rosenfeld JA, Mefford HC, Isidor B, Goldstein DB. Petrovski S, et al. Among authors: corre p. Am J Hum Genet. 2016 May 5;98(5):1001-1010. doi: 10.1016/j.ajhg.2016.03.011. Epub 2016 Apr 21. Am J Hum Genet. 2016. PMID: 27108799 Free PMC article.

7

De novo MEIS2 mutation causes syndromic developmental delay with persistent gastro-esophageal reflux.

Fujita A, Isidor B, Piloquet H, Corre P, Okamoto N, Nakashima M, Tsurusaki Y, Saitsu H, Miyake N, Matsumoto N. Fujita A, et al. Among authors: corre p. J Hum Genet. 2016 Sep;61(9):835-8. doi: 10.1038/jhg.2016.54. Epub 2016 May 26. J Hum Genet. 2016. PMID: 27225850 Review.

8

Three-dimensional cone-beam CT sialography in non tumour salivary pathologies: procedure and results.

Bertin H, Bonnet R, Delemazure AS, Mourrain-Langlois E, Mercier J, Corre P. Bertin H, et al. Among authors: corre p. Dentomaxillofac Radiol. 2017 Jan;46(1):20150431. doi: 10.1259/dmfr.20150431. Epub 2016 Sep 23. Dentomaxillofac Radiol. 2017. PMID: 27588734 Free PMC article.

9

Orbital volume and shape in Treacher Collins syndrome.

Levasseur J, Nysjö J, Sandy R, Britto JA, Garcelon N, Haber S, Picard A, Corre P, Odri GA, Khonsari RH. Levasseur J, et al. Among authors: corre p. J Craniomaxillofac Surg. 2018 Feb;46(2):305-311. doi: 10.1016/j.jcms.2017.11.028. Epub 2017 Dec 8. J Craniomaxillofac Surg. 2018. PMID: 29275073

10

Familial autosomal dominant severe ankyloglossia with tooth abnormalities.

Lenormand A, Khonsari R, Corre P, Perrin JP, Boscher C, Nizon M, Pichon O, David A, Le Caignec C, Bertin H, Isidor B. Lenormand A, et al. Among authors: corre p. Am J Med Genet A. 2018 Jul;176(7):1614-1617. doi: 10.1002/ajmg.a.38690. Epub 2018 Apr 28. Am J Med Genet A. 2018. PMID: 29704302

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