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

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
2024 0

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28 results

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Page 1
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.
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.
[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.
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.
[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.
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.
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
28 results