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

Year Number of Results
1990 1
1991 2
1994 1
1999 1
2002 1
2004 2
2009 1
2011 1
2012 1
2013 1
2014 2
2016 1
2017 1
2018 3
2022 2
2024 0

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18 results

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Page 1
Refining the phenotype associated with biallelic DNAJC21 mutations.
D'Amours G, Lopes F, Gauthier J, Saillour V, Nassif C, Wynn R, Alos N, Leblanc T, Capri Y, Nizard S, Lemyre E, Michaud JL, Pelletier VA, Pastore YD, Soucy JF. D'Amours G, et al. Among authors: nizard s. Clin Genet. 2018 Aug;94(2):252-258. doi: 10.1111/cge.13370. Epub 2018 Jun 7. Clin Genet. 2018. PMID: 29700810
Novel ABCC6 mutations in pseudoxanthoma elasticum.
Chassaing N, Martin L, Mazereeuw J, Barrié L, Nizard S, Bonafé JL, Calvas P, Hovnanian A. Chassaing N, et al. Among authors: nizard s. J Invest Dermatol. 2004 Mar;122(3):608-13. doi: 10.1111/j.0022-202X.2004.22312.x. J Invest Dermatol. 2004. PMID: 15086542 Free article.
[Isolated familial corpus callosum agenesis prognosis].
Nizard S, Barthez-Carpentier MA, Gelot A, Hebert C, Abimelech M, Esperandieu O. Nizard S, et al. Arch Pediatr. 2004 May;11(5):429-31. doi: 10.1016/j.arcped.2004.02.011. Arch Pediatr. 2004. PMID: 15135425 French.
Indexing Effects of Copy Number Variation on Genes Involved in Developmental Delay.
Uddin M, Pellecchia G, Thiruvahindrapuram B, D'Abate L, Merico D, Chan A, Zarrei M, Tammimies K, Walker S, Gazzellone MJ, Nalpathamkalam T, Yuen RK, Devriendt K, Mathonnet G, Lemyre E, Nizard S, Shago M, Joseph-George AM, Noor A, Carter MT, Yoon G, Kannu P, Tihy F, Thorland EC, Marshall CR, Buchanan JA, Speevak M, Stavropoulos DJ, Scherer SW. Uddin M, et al. Among authors: nizard s. Sci Rep. 2016 Jul 1;6:28663. doi: 10.1038/srep28663. Sci Rep. 2016. PMID: 27363808 Free PMC article.
Genomic study of severe fetal anomalies and discovery of GREB1L mutations in renal agenesis.
Boissel S, Fallet-Bianco C, Chitayat D, Kremer V, Nassif C, Rypens F, Delrue MA, Dal Soglio D, Oligny LL, Patey N, Flori E, Cloutier M, Dyment D, Campeau P, Karalis A, Nizard S, Fraser WD, Audibert F, Lemyre E, Rouleau GA, Hamdan FF, Kibar Z, Michaud JL. Boissel S, et al. Among authors: nizard s. Genet Med. 2018 Jul;20(7):745-753. doi: 10.1038/gim.2017.173. Epub 2017 Oct 26. Genet Med. 2018. PMID: 29261186 Free article.
Therapeutic management and outcome of patients with advanced systemic mastocytosis treated with midostaurin: A comprehensive real-life study in the French national healthcare database.
Rossignol J, Nizard S, Blanc AS, Filipovics A, Lortet-Tieulent J, Bouktit H, Poinsot G, Schmidt A, Raguideau F, Hermine O. Rossignol J, et al. Among authors: nizard s. Hematol Oncol. 2022 Dec;40(5):1030-1040. doi: 10.1002/hon.3062. Epub 2022 Aug 29. Hematol Oncol. 2022. PMID: 35949110
Renal lesions and pheochromocytoma in von Hippel-Lindau disease.
Richard S, Chauveau D, Chrétien Y, Beigelman C, Denys A, Fendler JP, Fromont G, Paraf F, Hélénon O, Nizard S, et al. Richard S, et al. Among authors: nizard s. Adv Nephrol Necker Hosp. 1994;23:1-27. Adv Nephrol Necker Hosp. 1994. PMID: 8154348 Review. No abstract available.
Measuring and Estimating the Effect Sizes of Copy Number Variants on General Intelligence in Community-Based Samples.
Huguet G, Schramm C, Douard E, Jiang L, Labbe A, Tihy F, Mathonnet G, Nizard S, Lemyre E, Mathieu A, Poline JB, Loth E, Toro R, Schumann G, Conrod P, Pausova Z, Greenwood C, Paus T, Bourgeron T, Jacquemont S; IMAGEN Consortium. Huguet G, et al. Among authors: nizard s. JAMA Psychiatry. 2018 May 1;75(5):447-457. doi: 10.1001/jamapsychiatry.2018.0039. JAMA Psychiatry. 2018. PMID: 29562078 Free PMC article.
18 results