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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1977 1
1978 1
1989 1
1992 3
1993 1
1995 1
1996 1
1999 2
2000 1
2003 2
2004 1
2006 1
2007 1
2008 4
2009 2
2010 3
2011 3
2012 2
2013 4
2014 4
2015 2
2016 2
2018 1
2024 0

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39 results

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Page 1
Deciphering leukemic B-cell chronic lymphoproliferative disorders.
Ugo V, Leporrier N, Salaun V, Letestu R, Radford-Weiss I, Ramond S, Nataf J, Guesnu M, Picard F, Brouzes C, Perrot JY, Valensi F, Levy V, Ajchenbaum-Cymbalista F, Troussard X. Ugo V, et al. Among authors: leporrier n. Leuk Lymphoma. 2006 Oct;47(10):2088-95. doi: 10.1080/10428190600727939. Leuk Lymphoma. 2006. PMID: 17071481
Pai syndrome: challenging prenatal diagnosis and management.
Blouet M, Belloy F, Jeanne-Pasquier C, Leporrier N, Benoist G. Blouet M, et al. Among authors: leporrier n. Pediatr Radiol. 2014 Sep;44(9):1184-7. doi: 10.1007/s00247-014-2966-4. Epub 2014 Apr 20. Pediatr Radiol. 2014. PMID: 24748063
Prenatal diagnosis of a mosaic 46,XY/47,X,i(Xq)Y.
Alliet J, Leporrier N, Lebris C, Gourdier D. Alliet J, et al. Among authors: leporrier n. Prenat Diagn. 1989 Jan;9(1):61-5. doi: 10.1002/pd.1970090109. Prenat Diagn. 1989. PMID: 2748552
Diagnostic strategy in segmentation defect of the vertebrae: a retrospective study of 73 patients.
Lefebvre M, Dieux-Coeslier A, Baujat G, Schaefer E, Judith SO, Bazin A, Pinson L, Attie-Bitach T, Baumann C, Fradin M, Pierquin G, Julia S, Quélin C, Doray B, Berg S, Vincent-Delorme C, Lambert L, Bachmann N, Lacombe D, Isidor B, Laurent N, Joelle R, Blanchet P, Odent S, Kervran D, Leporrier N, Abel C, Segers K, Guiliano F, Ginglinger-Fabre E, Selicorni A, Goldenberg A, El Chehadeh S, Francannet C, Demeer B, Duffourd Y, Thauvin-Robinet C, Verloes A, Cormier-Daire V, Riviere JB, Faivre L, Thevenon J. Lefebvre M, et al. Among authors: leporrier n. J Med Genet. 2018 Jun;55(6):422-429. doi: 10.1136/jmedgenet-2017-104939. Epub 2018 Feb 19. J Med Genet. 2018. PMID: 29459493
Prenatal phenotype of Williams-Beuren syndrome and of the reciprocal duplication syndrome.
Marcato L, Turolla L, Pompilii E, Dupont C, Gruchy N, De Toffol S, Bracalente G, Bacrot S, Troilo E, Tabet AC, Rossi S, Delezoïde AL, Baldo D, Leporrier N, Maggi F, Molin A, Pilu G, Simoni G, Vialard F, Grati FR. Marcato L, et al. Among authors: leporrier n. Clin Case Rep. 2014 Apr;2(2):25-32. doi: 10.1002/ccr3.48. Epub 2014 Feb 6. Clin Case Rep. 2014. PMID: 25356238 Free PMC article.
De novo 15q13.3 microdeletion with cryptogenic West syndrome.
Lacaze E, Gruchy N, Penniello-Valette MJ, Plessis G, Richard N, Decamp M, Mittre H, Leporrier N, Andrieux J, Kottler ML, Gerard M. Lacaze E, et al. Among authors: leporrier n. Am J Med Genet A. 2013 Oct;161A(10):2582-7. doi: 10.1002/ajmg.a.36085. Epub 2013 Aug 8. Am J Med Genet A. 2013. PMID: 23929658
Pregnancy outcomes in 188 French cases of prenatally diagnosed Klinefelter syndrome.
Gruchy N, Vialard F, Decamp M, Choiset A, Rossi A, Le Meur N, Moirot H, Yardin C, Bonnet-Dupeyron MN, Lespinasse J, Herbaut-Graux M, Till M, Layet V, Leporrier N. Gruchy N, et al. Among authors: leporrier n. Hum Reprod. 2011 Sep;26(9):2570-5. doi: 10.1093/humrep/der193. Epub 2011 Jul 5. Hum Reprod. 2011. PMID: 21733853
Severe prenatal renal anomalies associated with mutations in HNF1B or PAX2 genes.
Madariaga L, Morinière V, Jeanpierre C, Bouvier R, Loget P, Martinovic J, Dechelotte P, Leporrier N, Thauvin-Robinet C, Jensen UB, Gaillard D, Mathieu M, Turlin B, Attie-Bitach T, Salomon R, Gübler MC, Antignac C, Heidet L. Madariaga L, et al. Among authors: leporrier n. Clin J Am Soc Nephrol. 2013 Jul;8(7):1179-87. doi: 10.2215/CJN.10221012. Epub 2013 Mar 28. Clin J Am Soc Nephrol. 2013. PMID: 23539225 Free PMC article.
[Partial trisonomy 22].
Taillemite JL, Baheux-Morlier G, Van den Akker J, Portnoi MF, Leporrier N, Hazael-Massieux P, Roux C. Taillemite JL, et al. Among authors: leporrier n. Ann Genet. 1977 Dec;20(4):291-3. Ann Genet. 1977. PMID: 305760 French. No abstract available.
39 results