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Page 1
Antenatal spectrum of CHARGE syndrome in 40 fetuses with CHD7 mutations.
Legendre M, Gonzales M, Goudefroye G, Bilan F, Parisot P, Perez MJ, Bonnière M, Bessières B, Martinovic J, Delezoide AL, Jossic F, Fallet-Bianco C, Bucourt M, Tantau J, Loget P, Loeuillet L, Laurent N, Leroy B, Salhi H, Bigi N, Rouleau C, Guimiot F, Quélin C, Bazin A, Alby C, Ichkou A, Gesny R, Kitzis A, Ville Y, Lyonnet S, Razavi F, Gilbert-Dussardier B, Vekemans M, Attié-Bitach T. Legendre M, et al. Among authors: rouleau c. J Med Genet. 2012 Nov;49(11):698-707. doi: 10.1136/jmedgenet-2012-100926. Epub 2012 Sep 28. J Med Genet. 2012. PMID: 23024289
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: rouleau c. Brain. 2012 Feb;135(Pt 2):469-82. doi: 10.1093/brain/awr357. Epub 2012 Feb 9. Brain. 2012. PMID: 22323514
Epiphyseal punctate calcifications (stippling) in complete trisomy 9.
Perez MJ, Schneider A, Chaze AM, Bigi N, Lefort G, Rouleau C, Faure JM, Rahil H, Wadih N, Couture A, Boulot P, Blanchet P, Sarda P, Geneviève D. Perez MJ, et al. Among authors: rouleau c. Prenat Diagn. 2009 Nov;29(11):1085-8. doi: 10.1002/pd.2350. Prenat Diagn. 2009. PMID: 19777540 No abstract available.
Prevalence and timing of pregnancy termination for brain malformations.
Rouleau C, Gasner A, Bigi N, Couture A, Perez MJ, Blanchet P, Faure JM, Rivier F, Boulot P, Laquerrière A, Encha-Razavi F. Rouleau C, et al. Arch Dis Child Fetal Neonatal Ed. 2011 Sep;96(5):F360-4. doi: 10.1136/adc.2010.201483. Epub 2011 Jan 19. Arch Dis Child Fetal Neonatal Ed. 2011. PMID: 21252198
Array-CGH analysis indicates a high prevalence of genomic rearrangements in holoprosencephaly: an updated map of candidate loci.
Bendavid C, Rochard L, Dubourg C, Seguin J, Gicquel I, Pasquier L, Vigneron J, Laquerrière A, Marcorelles P, Jeanne-Pasquier C, Rouleau C, Jaillard S, Mosser J, Odent S, David V. Bendavid C, et al. Among authors: rouleau c. Hum Mutat. 2009 Aug;30(8):1175-82. doi: 10.1002/humu.21016. Hum Mutat. 2009. PMID: 19431187 Free article.
Radioguided occult lesion localization plus sentinel node biopsy (SNOLL) versus wire-guided localization plus sentinel node detection: a case control study of 129 unifocal pure invasive non-palpable breast cancers.
Giacalone PL, Bourdon A, Trinh PD, Taourel P, Rathat G, Sainmont M, Perocchia H, Rossi M, Rouleau C. Giacalone PL, et al. Among authors: rouleau c. Eur J Surg Oncol. 2012 Mar;38(3):222-9. doi: 10.1016/j.ejso.2011.12.003. Epub 2012 Jan 9. Eur J Surg Oncol. 2012. PMID: 22231127
212 results