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[Pediatric myasthenia with ocular involvement].
Prud'homme L, Gitiaux C, Barnerias C, Orssaud C, Bremond-Gignac D, Robert MP. Prud'homme L, et al. Among authors: gitiaux c. J Fr Ophtalmol. 2024 Sep;47(7):104202. doi: 10.1016/j.jfo.2024.104202. Epub 2024 May 8. J Fr Ophtalmol. 2024. PMID: 38723375 French.
Skeletal Muscle Microvasculature: A Highly Dynamic Lifeline.
Latroche C, Gitiaux C, Chrétien F, Desguerre I, Mounier R, Chazaud B. Latroche C, et al. Among authors: gitiaux c. Physiology (Bethesda). 2015 Nov;30(6):417-27. doi: 10.1152/physiol.00026.2015. Physiology (Bethesda). 2015. PMID: 26525341 Free article. Review.
Epileptic and nonepileptic features in patients with early onset epileptic encephalopathy and STXBP1 mutations.
Milh M, Villeneuve N, Chouchane M, Kaminska A, Laroche C, Barthez MA, Gitiaux C, Bartoli C, Borges-Correia A, Cacciagli P, Mignon-Ravix C, Cuberos H, Chabrol B, Villard L. Milh M, et al. Among authors: gitiaux c. Epilepsia. 2011 Oct;52(10):1828-34. doi: 10.1111/j.1528-1167.2011.03181.x. Epub 2011 Jul 19. Epilepsia. 2011. PMID: 21770924 Free article.
Clinical profile of patients with ATP1A3 mutations in Alternating Hemiplegia of Childhood-a study of 155 patients.
Panagiotakaki E, De Grandis E, Stagnaro M, Heinzen EL, Fons C, Sisodiya S, de Vries B, Goubau C, Weckhuysen S, Kemlink D, Scheffer I, Lesca G, Rabilloud M, Klich A, Ramirez-Camacho A, Ulate-Campos A, Campistol J, Giannotta M, Moutard ML, Doummar D, Hubsch-Bonneaud C, Jaffer F, Cross H, Gurrieri F, Tiziano D, Nevsimalova S, Nicole S, Neville B, van den Maagdenberg AM, Mikati M, Goldstein DB, Vavassori R, Arzimanoglou A; Italian IBAHC Consortium; French AHC Consortium; International AHC Consortium. Panagiotakaki E, et al. Orphanet J Rare Dis. 2015 Sep 26;10:123. doi: 10.1186/s13023-015-0335-5. Orphanet J Rare Dis. 2015. PMID: 26410222 Free PMC article.
106 results