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310 results

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Page 1
Cobblestone lissencephaly: neuropathological subtypes and correlations with genes of dystroglycanopathies.
Devisme L, Bouchet C, Gonzalès M, Alanio E, Bazin A, Bessières B, Bigi N, Blanchet P, Bonneau D, Bonnières M, Bucourt M, Carles D, Clarisse B, Delahaye S, Fallet-Bianco C, Figarella-Branger D, Gaillard D, Gasser B, Delezoide AL, Guimiot F, Joubert M, Laurent N, Laquerrière A, Liprandi A, Loget P, Marcorelles P, Martinovic J, Menez F, Patrier S, Pelluard F, Perez MJ, Rouleau C, Triau S, Attié-Bitach T, Vuillaumier-Barrot S, Seta N, Encha-Razavi F. Devisme L, et al. Among authors: gasser b. Brain. 2012 Feb;135(Pt 2):469-82. doi: 10.1093/brain/awr357. Epub 2012 Feb 9. Brain. 2012. PMID: 22323514
Molecular heterogeneity in fetal forms of type II lissencephaly.
Bouchet C, Gonzales M, Vuillaumier-Barrot S, Devisme L, Lebizec C, Alanio E, Bazin A, Bessières-Grattagliano B, Bigi N, Blanchet P, Bonneau D, Bonnières M, Carles D, Delahaye S, Fallet-Bianco C, Figarella-Branger D, Gaillard D, Gasser B, Guimiot F, Joubert M, Laurent N, Liprandi A, Loget P, Marcorelles P, Martinovic J, Menez F, Patrier S, Pelluard-Nehmé F, Perez MJ, Rouleau-Dubois C, Triau S, Laquerrière A, Encha-Razavi F, Seta N. Bouchet C, et al. Among authors: gasser b. Hum Mutat. 2007 Oct;28(10):1020-7. doi: 10.1002/humu.20561. Hum Mutat. 2007. PMID: 17559086
Bardet-Biedl syndrome: Antenatal presentation of forty-five fetuses with biallelic pathogenic variants in known Bardet-Biedl syndrome genes.
Mary L, Chennen K, Stoetzel C, Antin M, Leuvrey A, Nourisson E, Alanio-Detton E, Antal MC, Attié-Bitach T, Bouvagnet P, Bouvier R, Buenerd A, Clémenson A, Devisme L, Gasser B, Gilbert-Dussardier B, Guimiot F, Khau Van Kien P, Leroy B, Loget P, Martinovic J, Pelluard F, Perez MJ, Petit F, Pinson L, Rooryck-Thambo C, Poch O, Dollfus H, Schaefer E, Muller J. Mary L, et al. Among authors: gasser b. Clin Genet. 2019 Mar;95(3):384-397. doi: 10.1111/cge.13500. Clin Genet. 2019. PMID: 30614526
p57-discordant villi in hydropic products of conception: a clinicopathological study of 70 cases.
Gaillot-Durand L, Patrier S, Aziza J, Devisme L, Riera AC, Marcorelles P, Pelluard F, Gasser B, Mauduit C, Hajri T, Massardier J, Bolze PA, Golfier F, Devouassoux-Shisheboran M, Allias F. Gaillot-Durand L, et al. Among authors: gasser b. Hum Pathol. 2020 Jul;101:18-30. doi: 10.1016/j.humpath.2020.04.011. Epub 2020 May 6. Hum Pathol. 2020. PMID: 32387104
Contribution of referent pathologists to the quality of trophoblastic diseases diagnosis.
Golfier F, Clerc J, Hajri T, Massardier J, Frappart L, Duvillard P, Rabreau M, Patrier S, Devisme L, Carles D, Pelluard F, Gasser B, Tarranger-Charpin C, Schott AM, Raudrant D. Golfier F, et al. Among authors: gasser b. Hum Reprod. 2011 Oct;26(10):2651-7. doi: 10.1093/humrep/der265. Epub 2011 Aug 12. Hum Reprod. 2011. PMID: 21840909
Prenatal diagnosis of Walker-Warburg syndrome in three sibs.
Gasser B, Lindner V, Dreyfus M, Feidt X, Leissner P, Treisser A, Stoll C. Gasser B, et al. Am J Med Genet. 1998 Mar 5;76(2):107-10. doi: 10.1002/(sici)1096-8628(19980305)76:2<107::aid-ajmg1>3.3.co;2-b. Am J Med Genet. 1998. PMID: 9511971
Neural tube defects: the experience of the registry of congenital malformations of Alsace, France, 1995-2009.
Timbolschi D, Schaefer E, Monga B, Fattori D, Dott B, Favre R, Kohler M, Nisand I, Viville B, Astruc D, Kehrli P, Gasser B, Lindner V, Marcellin L, Flori E, Girard-Lemaire F, Dollfus H, Doray B. Timbolschi D, et al. Among authors: gasser b. Fetal Diagn Ther. 2015;37(1):6-17. doi: 10.1159/000362663. Epub 2014 Nov 11. Fetal Diagn Ther. 2015. PMID: 25402326
[Epidemiology of orofacial clefts (1995-2006) in France (Congenital Malformations of Alsace Registry)].
Doray B, Badila-Timbolschi D, Schaefer E, Fattori D, Monga B, Dott B, Favre R, Kohler M, Nisand I, Viville B, Kauffmann I, Bruant-Rodier C, Grollemund B, Rinkenbach R, Astruc D, Gasser B, Lindner V, Marcellin L, Flori E, Girard-Lemaire F, Dollfus H. Doray B, et al. Among authors: gasser b. Arch Pediatr. 2012 Oct;19(10):1021-9. doi: 10.1016/j.arcped.2012.07.002. Epub 2012 Aug 24. Arch Pediatr. 2012. PMID: 22925539 French.
310 results