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Year Number of Results
2003 2
2007 1
2009 2
2010 1
2012 1
2014 4
2015 2
2016 1
2017 2
2018 3
2019 3
2020 4
2021 2
2022 2
2023 2
2025 2

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30 results

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Page 1
IL-22BP production is heterogeneously distributed in Crohn's disease.
Fantou A, Lagrue E, Laurent T, Delbos L, Blandin S, Jarry A, Beriou G, Braudeau C, Salabert N, Marin E, Moreau A, Podevin J, Bourreille A, Josien R, Martin JC. Fantou A, et al. Among authors: lagrue e. Front Immunol. 2022 Oct 13;13:1034570. doi: 10.3389/fimmu.2022.1034570. eCollection 2022. Front Immunol. 2022. PMID: 36311796 Free PMC article.
Health-related quality of life in children with von Willebrand disease: results of the French real-life Willebrand Study Health-related Quality of Life study.
Goudemand J, Susen S, Berger C, Bayart S, Chambost H, Genre-Volot F, Desprez D, Claeyssens S, Pan-Petesch B, Harroche A, Ardillon L, Veyradier A, Barthez-Toullec M, Marin G, Lagrue E, André-Bonnet MH, Repessé Y, Borel-Derlon A, von Mackensen S. Goudemand J, et al. Among authors: lagrue e. J Thromb Haemost. 2025 Sep;23(9):2736-2750. doi: 10.1016/j.jtha.2025.05.017. Epub 2025 May 27. J Thromb Haemost. 2025. PMID: 40436273 Free article.
[Congenital myasthenic syndromes in childhood: Drug therapeutic strategies].
de la Vaissière S, Toutain A, Chêne MA, Lagrue E, Cantagrel S, Provost S, Eymard B, Castelnau P. de la Vaissière S, et al. Among authors: lagrue e. Arch Pediatr. 2015 Jul;22(7):724-8. doi: 10.1016/j.arcped.2015.04.009. Epub 2015 May 28. Arch Pediatr. 2015. PMID: 26028221 Review. French.
Prospective Multicenter Validation of a Simple Blood Test for the Diagnosis of Glut1 Deficiency Syndrome.
Mochel F, Gras D, Luton MP, Nizou M, Giovannini D, Delattre C, Aubart M, Barth M, De Saint-Martin A, Doummar D, Essid N, Garros A, Le Camus CH, Hoebeke C, The Tich SN, Perivier M, Rivera S, Rolland A, Roubertie A, Sarret C, Sevin C, Ville D, Sitbon M, Costa JM, Pons R, Garcia-Cazorla A, Vuillaumier S, Petit V, Boespflug-Tanguy O, De Vivo DC; MetaGlut1 Study Group. Mochel F, et al. Neurology. 2023 Jun 6;100(23):e2360-e2373. doi: 10.1212/WNL.0000000000207296. Epub 2023 Apr 19. Neurology. 2023. PMID: 37076312 Free PMC article.
Heterozygous CLCN1 mutations can modulate phenotype in sodium channel myotonia.
Furby A, Vicart S, Camdessanché JP, Fournier E, Chabrier S, Lagrue E, Paricio C, Blondy P, Touraine R, Sternberg D, Fontaine B. Furby A, et al. Among authors: lagrue e. Neuromuscul Disord. 2014 Nov;24(11):953-9. doi: 10.1016/j.nmd.2014.06.439. Epub 2014 Jul 2. Neuromuscul Disord. 2014. PMID: 25088311
International retrospective natural history study of LMNA-related congenital muscular dystrophy.
Ben Yaou R, Yun P, Dabaj I, Norato G, Donkervoort S, Xiong H, Nascimento A, Maggi L, Sarkozy A, Monges S, Bertoli M, Komaki H, Mayer M, Mercuri E, Zanoteli E, Castiglioni C, Marini-Bettolo C, D'Amico A, Deconinck N, Desguerre I, Erazo-Torricelli R, Gurgel-Giannetti J, Ishiyama A, Kleinsteuber KS, Lagrue E, Laugel V, Mercier S, Messina S, Politano L, Ryan MM, Sabouraud P, Schara U, Siciliano G, Vercelli L, Voit T, Yoon G, Alvarez R, Muntoni F, Pierson TM, Gómez-Andrés D, Reghan Foley A, Quijano-Roy S, Bönnemann CG, Bonne G. Ben Yaou R, et al. Among authors: lagrue e. Brain Commun. 2021 Apr 11;3(3):fcab075. doi: 10.1093/braincomms/fcab075. eCollection 2021 Jul. Brain Commun. 2021. PMID: 34240052 Free PMC article.
[Radiology clinical case].
Lagrue E, Martinerie L, Adamsbaum C. Lagrue E, et al. Arch Pediatr. 2003 Nov;10(11):1027-8. doi: 10.1016/j.arcped.2003.08.004. Arch Pediatr. 2003. PMID: 14613704 French. No abstract available.
The clinical, histologic, and genotypic spectrum of SEPN1-related myopathy: A case series.
Villar-Quiles RN, von der Hagen M, Métay C, Gonzalez V, Donkervoort S, Bertini E, Castiglioni C, Chaigne D, Colomer J, Cuadrado ML, de Visser M, Desguerre I, Eymard B, Goemans N, Kaindl A, Lagrue E, Lütschg J, Malfatti E, Mayer M, Merlini L, Orlikowski D, Reuner U, Salih MA, Schlotter-Weigel B, Stoetter M, Straub V, Topaloglu H, Urtizberea JA, van der Kooi A, Wilichowski E, Romero NB, Fardeau M, Bönnemann CG, Estournet B, Richard P, Quijano-Roy S, Schara U, Ferreiro A. Villar-Quiles RN, et al. Among authors: lagrue e. Neurology. 2020 Sep 15;95(11):e1512-e1527. doi: 10.1212/WNL.0000000000010327. Epub 2020 Aug 13. Neurology. 2020. PMID: 32796131 Free PMC article.
Absent CNKSR2 causes seizures and intellectual, attention, and language deficits.
Vaags AK, Bowdin S, Smith ML, Gilbert-Dussardier B, Brocke-Holmefjord KS, Sinopoli K, Gilles C, Haaland TB, Vincent-Delorme C, Lagrue E, Harbuz R, Walker S, Marshall CR, Houge G, Kalscheuer VM, Scherer SW, Minassian BA. Vaags AK, et al. Among authors: lagrue e. Ann Neurol. 2014 Nov;76(5):758-64. doi: 10.1002/ana.24274. Epub 2014 Oct 4. Ann Neurol. 2014. PMID: 25223753
30 results