Bonneau D - Search Results

1

Binder phenotype in mothers affected with autoimmune disorders.

Colin E, Touraine R, Levaillant JM, Pasquier L, Boussion F, Ferry M, Guichet A, Barth M, Mercier A, Gérard-Blanluet M, Odent S, Bonneau D. Colin E, et al. Among authors: bonneau d. J Matern Fetal Neonatal Med. 2012 Aug;25(8):1413-8. doi: 10.3109/14767058.2011.636105. Epub 2011 Dec 7. J Matern Fetal Neonatal Med. 2012. PMID: 22082304

2

Heterotaxy-neural tube defect and holoprosencephaly occuring independently in two sib fetuses.

Bonneau D, Maréchaud M, Odent S, Piegay I, Godard A, Amati P. Bonneau D, et al. Am J Med Genet. 1999 Jun 4;84(4):373-6. doi: 10.1002/(sici)1096-8628(19990604)84:4<373::aid-ajmg13>3.0.co;2-8. Am J Med Genet. 1999. PMID: 10340655

3

The association of autosomal dominant optic atrophy and moderate deafness may be due to the R445H mutation in the OPA1 gene.

Amati-Bonneau P, Odent S, Derrien C, Pasquier L, Malthiéry Y, Reynier P, Bonneau D. Amati-Bonneau P, et al. Among authors: bonneau d. Am J Ophthalmol. 2003 Dec;136(6):1170-1. doi: 10.1016/s0002-9394(03)00665-2. Am J Ophthalmol. 2003. PMID: 14644237

4

Prenatal diagnosis of primary anophthalmia with a 3q27 interstitial deletion involving SOX2.

Guichet A, Triau S, Lépinard C, Esculapavit C, Biquard F, Descamps P, Encha-Razavi F, Bonneau D. Guichet A, et al. Among authors: bonneau d. Prenat Diagn. 2004 Oct;24(10):828-32. doi: 10.1002/pd.997. Prenat Diagn. 2004. PMID: 15503273

5

Prenatal diagnosis of absence of the septum pellucidum associated with septo-optic dysplasia.

Lepinard C, Coutant R, Boussion F, Loisel D, Delorme B, Biquard F, Bonneau D, Guichet A, Descamps P. Lepinard C, et al. Among authors: bonneau d. Ultrasound Obstet Gynecol. 2005 Jan;25(1):73-5. doi: 10.1002/uog.1807. Ultrasound Obstet Gynecol. 2005. PMID: 15593257 Free article.

6

OPA1 R445H mutation in optic atrophy associated with sensorineural deafness.

Amati-Bonneau P, Guichet A, Olichon A, Chevrollier A, Viala F, Miot S, Ayuso C, Odent S, Arrouet C, Verny C, Calmels MN, Simard G, Belenguer P, Wang J, Puel JL, Hamel C, Malthièry Y, Bonneau D, Lenaers G, Reynier P. Amati-Bonneau P, et al. Among authors: bonneau d. Ann Neurol. 2005 Dec;58(6):958-63. doi: 10.1002/ana.20681. Ann Neurol. 2005. PMID: 16240368

7

Mitochondrial coupling defect in Charcot-Marie-Tooth type 2A disease.

Loiseau D, Chevrollier A, Verny C, Guillet V, Gueguen N, Pou de Crescenzo MA, Ferré M, Malinge MC, Guichet A, Nicolas G, Amati-Bonneau P, Malthièry Y, Bonneau D, Reynier P. Loiseau D, et al. Among authors: bonneau d. Ann Neurol. 2007 Apr;61(4):315-23. doi: 10.1002/ana.21086. Ann Neurol. 2007. PMID: 17444508

8

Endocrine function in a 48,XXYY adult with type 2 diabetes: case report with a review of the literature.

Dubois S, Illouz F, Pinson L, Bonneau D, Rohmer V, Guichet A. Dubois S, et al. Among authors: bonneau d. Ann Endocrinol (Paris). 2007 Oct;68(5):384-8. doi: 10.1016/j.ando.2007.07.002. Epub 2007 Sep 11. Ann Endocrinol (Paris). 2007. PMID: 17850758

9

Molecular cytogenetic characterization of terminal 14q32 deletions in two children with an abnormal phenotype and corpus callosum hypoplasia.

Schneider A, Benzacken B, Guichet A, Verloes A, Bonneau D, Collot N, Dastot-Le-Moal F, Goossens M, Taine L, Landais E, Gaillard D, Doco-Fenzy M. Schneider A, et al. Among authors: bonneau d. Eur J Hum Genet. 2008 Jun;16(6):680-7. doi: 10.1038/sj.ejhg.5201977. Epub 2008 Jan 16. Eur J Hum Genet. 2008. PMID: 18197200

10

Carotid artery dissection in an adult with the Simpson-Golabi-Behmel syndrome.

Pénisson-Besnier I, Lebouvier T, Moizard MP, Ferré M, Barth M, Marc G, Raynaud M, Bonneau D. Pénisson-Besnier I, et al. Among authors: bonneau d. Am J Med Genet A. 2008 Feb 15;146A(4):464-7. doi: 10.1002/ajmg.a.32154. Am J Med Genet A. 2008. PMID: 18203194

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