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Page 1
Prenatal alcohol exposure is a leading cause of interneuronopathy in humans.
Marguet F, Friocourt G, Brosolo M, Sauvestre F, Marcorelles P, Lesueur C, Marret S, Gonzalez BJ, Laquerrière A. Marguet F, et al. Among authors: laquerriere a. Acta Neuropathol Commun. 2020 Nov 30;8(1):208. doi: 10.1186/s40478-020-01089-z. Acta Neuropathol Commun. 2020. PMID: 33256853 Free PMC article.
Oligodendrocyte lineage is severely affected in human alcohol-exposed foetuses.
Marguet F, Brosolo M, Friocourt G, Sauvestre F, Marcorelles P, Lesueur C, Marret S, Gonzalez BJ, Laquerrière A. Marguet F, et al. Among authors: laquerriere a. Acta Neuropathol Commun. 2022 May 14;10(1):74. doi: 10.1186/s40478-022-01378-9. Acta Neuropathol Commun. 2022. PMID: 35568959 Free PMC article.
Neuropathology of holoprosencephaly.
Marcorelles P, Laquerriere A. Marcorelles P, et al. Among authors: laquerriere a. Am J Med Genet C Semin Med Genet. 2010 Feb 15;154C(1):109-19. doi: 10.1002/ajmg.c.30249. Am J Med Genet C Semin Med Genet. 2010. PMID: 20104606 Review.
Mutations in tubulin genes are frequent causes of various foetal malformations of cortical development including microlissencephaly.
Fallet-Bianco C, Laquerrière A, Poirier K, Razavi F, Guimiot F, Dias P, Loeuillet L, Lascelles K, Beldjord C, Carion N, Toussaint A, Revencu N, Addor MC, Lhermitte B, Gonzales M, Martinovich J, Bessieres B, Marcy-Bonnière M, Jossic F, Marcorelles P, Loget P, Chelly J, Bahi-Buisson N. Fallet-Bianco C, et al. Among authors: laquerriere a. Acta Neuropathol Commun. 2014 Jul 25;2:69. doi: 10.1186/2051-5960-2-69. Acta Neuropathol Commun. 2014. PMID: 25059107 Free PMC article.
PLGF, a placental marker of fetal brain defects after in utero alcohol exposure.
Lecuyer M, Laquerrière A, Bekri S, Lesueur C, Ramdani Y, Jégou S, Uguen A, Marcorelles P, Marret S, Gonzalez BJ. Lecuyer M, et al. Among authors: laquerriere a. Acta Neuropathol Commun. 2017 Jun 6;5(1):44. doi: 10.1186/s40478-017-0444-6. Acta Neuropathol Commun. 2017. PMID: 28587682 Free PMC article.
Basal ganglia involvement in ARX patients: The reason for ARX patients very specific grasping?
Curie A, Friocourt G, des Portes V, Roy A, Nazir T, Brun A, Cheylus A, Marcorelles P, Retzepi K, Maleki N, Bussy G, Paulignan Y, Reboul A, Ibarrola D, Kong J, Hadjikhani N, Laquerrière A, Gollub RL. Curie A, et al. Among authors: laquerriere a. Neuroimage Clin. 2018 Apr 5;19:454-465. doi: 10.1016/j.nicl.2018.04.001. eCollection 2018. Neuroimage Clin. 2018. PMID: 29984154 Free PMC article.
Neuropathological hallmarks of fetal hydrocephalus linked to CCDC88C pathogenic variants.
Marguet F, Vezain M, Marcorelles P, Audebert-Bellanger S, Cassinari K, Drouot N, Chambon P, Gonzalez BJ, Horowitz A, Laquerriere A, Saugier-Veber P. Marguet F, et al. Among authors: laquerriere a. Acta Neuropathol Commun. 2021 Jun 6;9(1):104. doi: 10.1186/s40478-021-01207-5. Acta Neuropathol Commun. 2021. PMID: 34092257 Free PMC article.
260 results