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

Year Number of Results
1982 1
1983 1
1984 3
1985 2
1986 1
1987 1
1988 1
1989 3
1990 1
1992 1
1997 1
2000 2
2001 1
2002 1
2003 3
2005 1
2006 3
2007 4
2009 1
2011 2
2013 2
2014 4
2015 3
2016 1
2020 1
2021 1
2024 0

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41 results

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Page 1
[Noise-induced epilepsy].
Giroud M, Couillault G, Nivelon JL. Giroud M, et al. Among authors: couillault g. Ann Pediatr (Paris). 1984 Oct;31(8):667-70. Ann Pediatr (Paris). 1984. PMID: 6497259 French. No abstract available.
Constitutional mismatch repair deficiency syndrome: clinical description in a French cohort.
Lavoine N, Colas C, Muleris M, Bodo S, Duval A, Entz-Werle N, Coulet F, Cabaret O, Andreiuolo F, Charpy C, Sebille G, Wang Q, Lejeune S, Buisine MP, Leroux D, Couillault G, Leverger G, Fricker JP, Guimbaud R, Mathieu-Dramard M, Jedraszak G, Cohen-Hagenauer O, Guerrini-Rousseau L, Bourdeaut F, Grill J, Caron O, Baert-Dusermont S, Tinat J, Bougeard G, Frébourg T, Brugières L. Lavoine N, et al. Among authors: couillault g. J Med Genet. 2015 Nov;52(11):770-8. doi: 10.1136/jmedgenet-2015-103299. Epub 2015 Aug 28. J Med Genet. 2015. PMID: 26318770 Review.
Development of primary early-onset colorectal cancers due to biallelic mutations of the FANCD1/BRCA2 gene.
Degrolard-Courcet E, Sokolowska J, Padeano MM, Guiu S, Bronner M, Chery C, Coron F, Lepage C, Chapusot C, Loustalot C, Jouve JL, Hatem C, Ferrant E, Martin L, Coutant C, Baurand A, Couillault G, Delignette A, El Chehadeh S, Lizard S, Arnould L, Fumoleau P, Callier P, Mugneret F, Philippe C, Frebourg T, Jonveaux P, Faivre L. Degrolard-Courcet E, et al. Among authors: couillault g. Eur J Hum Genet. 2014 Aug;22(8):979-87. doi: 10.1038/ejhg.2013.278. Epub 2013 Dec 4. Eur J Hum Genet. 2014. PMID: 24301060 Free PMC article. Review.
[Post-adoption consultations].
de Monléon JV, Ferrier ME, Guérin MN, Couillault G, Huet F. de Monléon JV, et al. Among authors: couillault g. Arch Pediatr. 2003 May;10 Suppl 1:240s-242s. doi: 10.1016/s0929-693x(03)90455-6. Arch Pediatr. 2003. PMID: 14509815 French. No abstract available.
Development and Testing of Reduced Versions of the Manual Muscle Test-8 in Juvenile Dermatomyositis.
Rosina S, Varnier GC, Pistorio A, Pilkington C, Maillard S, Civino A, Tsitsami E, Bracaglia C, Jelusic M, Cespedes-Cruz A, Espada G, Cimaz R, Couillault G, Joos R, Quartier P, Rao AP, Malattia C, Ruperto N, Consolaro A, Ravelli A; Pediatric Rheumatology International Trials Organization (PRINTO). Rosina S, et al. Among authors: couillault g. J Rheumatol. 2021 Jun;48(6):898-906. doi: 10.3899/jrheum.200543. Epub 2020 Nov 15. J Rheumatol. 2021. PMID: 33191283 Free article.
Human RTEL1 deficiency causes Hoyeraal-Hreidarsson syndrome with short telomeres and genome instability.
Le Guen T, Jullien L, Touzot F, Schertzer M, Gaillard L, Perderiset M, Carpentier W, Nitschke P, Picard C, Couillault G, Soulier J, Fischer A, Callebaut I, Jabado N, Londono-Vallejo A, de Villartay JP, Revy P. Le Guen T, et al. Among authors: couillault g. Hum Mol Genet. 2013 Aug 15;22(16):3239-49. doi: 10.1093/hmg/ddt178. Epub 2013 Apr 15. Hum Mol Genet. 2013. PMID: 23591994
Diversity of the clinical presentation of the MMR gene biallelic mutations.
Bougeard G, Olivier-Faivre L, Baert-Desurmont S, Tinat J, Martin C, Bouvignies E, Vasseur S, Huet F, Couillault G, Vabres P, Le Pessot F, Chapusot C, Malka D, Bressac-de Paillerets B, Tosi M, Frebourg T. Bougeard G, et al. Among authors: couillault g. Fam Cancer. 2014 Mar;13(1):131-5. doi: 10.1007/s10689-013-9676-1. Fam Cancer. 2014. PMID: 24068316
Prednisone versus prednisone plus ciclosporin versus prednisone plus methotrexate in new-onset juvenile dermatomyositis: a randomised trial.
Ruperto N, Pistorio A, Oliveira S, Zulian F, Cuttica R, Ravelli A, Fischbach M, Magnusson B, Sterba G, Avcin T, Brochard K, Corona F, Dressler F, Gerloni V, Apaz MT, Bracaglia C, Cespedes-Cruz A, Cimaz R, Couillault G, Joos R, Quartier P, Russo R, Tardieu M, Wulffraat N, Bica B, Dolezalova P, Ferriani V, Flato B, Bernard-Medina AG, Herlin T, Trachana M, Meini A, Allain-Launay E, Pilkington C, Vargova V, Wouters C, Angioloni S, Martini A; Paediatric Rheumatology International Trials Organisation (PRINTO). Ruperto N, et al. Among authors: couillault g. Lancet. 2016 Feb 13;387(10019):671-678. doi: 10.1016/S0140-6736(15)01021-1. Epub 2015 Nov 30. Lancet. 2016. PMID: 26645190 Clinical Trial.
Coffin-Lowry syndrome: a multicenter study.
Gilgenkrantz S, Mujica P, Gruet P, Tridon P, Schweitzer F, Nivelon-Chevallier A, Nivelon JL, Couillault G, David A, Verloes A, et al. Gilgenkrantz S, et al. Among authors: couillault g. Clin Genet. 1988 Oct;34(4):230-45. doi: 10.1111/j.1399-0004.1988.tb02870.x. Clin Genet. 1988. PMID: 3069251 Clinical Trial.
41 results