Search Results - Laquerrière, Annie

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  1. 1
    Microangiopathy in primary familial brain calcification: Evidence from skin biopsies

    Microangiopathy in primary familial brain calcification: Evidence from skin biopsies by Nicolas, Gaël, Marguet, Florent, Laquerrière, Annie, Mendes de Oliveira, João Ricardo, Hannequin, Didier

    Published 2017
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  2. 2
    Role of cytoskeletal abnormalities in the neuropathology and pathophysiology of type I lissencephaly

    Role of cytoskeletal abnormalities in the neuropathology and pathophysiology of type I lissencephaly by Friocourt, Gaëlle, Marcorelles, Pascale, Saugier-Veber, Pascale, Quille, Marie-Lise, Marret, Stephane, Laquerrière, Annie

    Published 2010
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  3. 3
    Diagnosis and Management of Glioblastoma: A Comprehensive Perspective

    Diagnosis and Management of Glioblastoma: A Comprehensive Perspective by Gilard, Vianney, Tebani, Abdellah, Dabaj, Ivana, Laquerrière, Annie, Fontanilles, Maxime, Derrey, Stéphane, Marret, Stéphane, Bekri, Soumeya

    Published 2021
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  4. 4
    Restoration of diaphragmatic function after diaphragm reinnervation by inferior laryngeal nerve; experimental study in rabbits

    Restoration of diaphragmatic function after diaphragm reinnervation by inferior laryngeal nerve; experimental study in rabbits by Derrey, Stephane, verin, Eric, Laquerrière, Annie, de Barros, Angelique Boishardy, Lacoume, Yann, Fréger, Pierre, Marie, Jean Paul

    Published 2006
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  5. 5
    Plasma and Urinary Aluminum Concentrations in Severely Anemic Geophagous Pregnant Women in the Bas Maroni Region of French Guiana: A Case-Control Study

    Plasma and Urinary Aluminum Concentrations in Severely Anemic Geophagous Pregnant Women in the Bas Maroni Region of French Guiana: A Case-Control Study by Lambert, Veronique, Boukhari, Rachida, Nacher, Mathieu, Goullé, Jean-Pierre, Roudier, Estelle, Elguindi, Wael, Laquerrière, Annie, Carles, Gabriel

    Published 2010
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  6. 6
    An Autopsy Case of Amyotrophic Lateral Sclerosis with Waldenström Macroglobulinemia and Anti-MAG Gammopathy

    An Autopsy Case of Amyotrophic Lateral Sclerosis with Waldenström Macroglobulinemia and Anti-MAG Gammopathy by Jurici, Snejana, Laquerrière, Annie, Bedat-Millet, Anne-Laure, Jardin, Fabrice, Musset, Lucile, Vallat, Jean-Michel, Hannequin, Didier, Martinaud, Olivier

    Published 2011
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  7. 7
    Prenatal alcohol exposure is a leading cause of interneuronopathy in humans

    Prenatal alcohol exposure is a leading cause of interneuronopathy in humans by Marguet, Florent, Friocourt, Gaëlle, Brosolo, Mélanie, Sauvestre, Fanny, Marcorelles, Pascale, Lesueur, Céline, Marret, Stéphane, Gonzalez, Bruno J., Laquerrière, Annie

    Published 2020
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  8. 8
    Oligodendrocyte lineage is severely affected in human alcohol-exposed foetuses

    Oligodendrocyte lineage is severely affected in human alcohol-exposed foetuses by Marguet, Florent, Brosolo, Mélanie, Friocourt, Gaëlle, Sauvestre, Fanny, Marcorelles, Pascale, Lesueur, Céline, Marret, Stéphane, Gonzalez, Bruno J., Laquerrière, Annie

    Published 2022
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  9. 9
    PLGF, a placental marker of fetal brain defects after in utero alcohol exposure

    PLGF, a placental marker of fetal brain defects after in utero alcohol exposure by Lecuyer, Matthieu, Laquerrière, Annie, Bekri, Soumeya, Lesueur, Céline, Ramdani, Yasmina, Jégou, Sylvie, Uguen, Arnaud, Marcorelles, Pascale, Marret, Stéphane, Gonzalez, Bruno J.

    Published 2017
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  10. 10
    Clinical and Molecular Characterization of Patients with Mucopolysaccharidosis Type I in an Algerian Series

    Clinical and Molecular Characterization of Patients with Mucopolysaccharidosis Type I in an Algerian Series by Tebani, Abdellah, Zanoutene-Cheriet, Lahouaria, Adjtoutah, Zoubir, Abily-Donval, Lenaig, Brasse-Lagnel, Carole, Laquerrière, Annie, Marret, Stephane, Chalabi Benabdellah, Abla, Bekri, Soumeya

    Published 2016
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  11. 11
    Neuropathological hallmarks of fetal hydrocephalus linked to CCDC88C pathogenic variants

    Neuropathological hallmarks of fetal hydrocephalus linked to CCDC88C pathogenic variants by Marguet, Florent, Vezain, Myriam, Marcorelles, Pascale, Audebert-Bellanger, Séverine, Cassinari, Kévin, Drouot, Nathalie, Chambon, Pascal, Gonzalez, Bruno J., Horowitz, Arie, Laquerriere, Annie, Saugier-Veber, Pascale

    Published 2021
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  12. 12
    Prenatal alcohol exposure impairs autophagy in neonatal brain cortical microvessels

    Prenatal alcohol exposure impairs autophagy in neonatal brain cortical microvessels by Girault, Virginie, Gilard, Vianney, Marguet, Florent, Lesueur, Céline, Hauchecorne, Michelle, Ramdani, Yasmina, Laquerrière, Annie, Marret, Stéphane, Jégou, Sylvie, Gonzalez, Bruno Jose, Brasse-Lagnel, Carole, Bekri, Soumeya

    Published 2017
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  13. 13
    De novo mutations of SCN1A are responsible for arthrogryposis broadening the SCN1A-related phenotypes

    De novo mutations of SCN1A are responsible for arthrogryposis broadening the SCN1A-related phenotypes by Jaber, Dana, Gitiaux, Cyril, Blesson, Sophie, Marguet, Florent, Buard, David, Varela Salgado, Maritzaida, Kaminska, Anna, Saada, Julien, Fallet-Bianco, Catherine, Martinovic, Jelena, Laquerriere, Annie, Melki, Judith

    Published 2021
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  14. 14
    Lethal Neonatal Progression of Fetal Cardiomegaly Associated to ACAD9 Deficiency

    Lethal Neonatal Progression of Fetal Cardiomegaly Associated to ACAD9 Deficiency by Lagoutte-Renosi, Jennifer, Ségalas-Milazzo, Isabelle, Crahes, Marie, Renosi, Florian, Menu-Bouaouiche, Laurence, Torre, Stéphanie, Lardennois, Caroline, Rio, Marlène, Marret, Stéphane, Brasse-Lagnel, Carole, Laquerrière, Annie, Bekri, Soumeya

    Published 2015
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  15. 15
    Foetal onset of EIF2B related disorder in two siblings: cerebellar hypoplasia with absent Bergmann glia and severe hypomyelination

    Foetal onset of EIF2B related disorder in two siblings: cerebellar hypoplasia with absent Bergmann glia and severe hypomyelination by Trimouille, Aurélien, Marguet, Florent, Sauvestre, Fanny, Lasseaux, Eulalie, Pelluard, Fanny, Martin-Négrier, Marie-Laure, Plaisant, Claudio, Rooryck, Caroline, Lacombe, Didier, Arveiler, Benoît, Boespflug-Tanguy, Odile, Naudion, Sophie, Laquerrière, Annie

    Published 2020
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  16. 16
    Mosaic PTEN alteration in the neural crest during embryogenesis results in multiple nervous system hamartomas

    Mosaic PTEN alteration in the neural crest during embryogenesis results in multiple nervous system hamartomas by Goldenberg, Alice, Marguet, Florent, Gilard, Vianney, Cardine, Aude-Marie, Hassani, Adnan, Doz, François, Radi, Sophie, Vasseur, Stéphanie, Bou, Jacqueline, Branchaud, Maud, Houdayer, Claude, Baert-Desurmont, Stéphanie, Laquerriere, Annie, Frebourg, Thierry

    Published 2019
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  17. 17
    Hydrocephalus due to multiple ependymal malformations is caused by mutations in the MPDZ gene

    Hydrocephalus due to multiple ependymal malformations is caused by mutations in the MPDZ gene by Saugier-Veber, Pascale, Marguet, Florent, Lecoquierre, François, Adle-Biassette, Homa, Guimiot, Fabien, Cipriani, Sara, Patrier, Sophie, Brasseur-Daudruy, Marie, Goldenberg, Alice, Layet, Valérie, Capri, Yline, Gérard, Marion, Frébourg, Thierry, Laquerrière, Annie

    Published 2017
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  18. 18
    Deep intronic hotspot variant explaining rhabdoid tumor predisposition syndrome in two patients with atypical teratoid and rhabdoid tumor

    Deep intronic hotspot variant explaining rhabdoid tumor predisposition syndrome in two patients with atypical teratoid and rhabdoid tumor by Tauziède-Espariat, Arnault, Masliah-Planchon, Julien, Brugières, Laurence, Puget, Stéphanie, Dufour, Christelle, Schneider, Pascale, Laquerrière, Annie, Frebourg, Thierry, Bodet, Damien, Lechapt-Zalcman, Emmanuèle, Pierron, Gaëlle, Delattre, Olivier, Varlet, Pascale, Bourdeaut, Franck

    Published 2017
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  19. 19
    Cell-free DNA and circulating TERT promoter mutation for disease monitoring in newly-diagnosed glioblastoma

    Cell-free DNA and circulating TERT promoter mutation for disease monitoring in newly-diagnosed glioblastoma by Fontanilles, Maxime, Marguet, Florent, Beaussire, Ludivine, Magne, Nicolas, Pépin, Louis-Ferdinand, Alexandru, Cristina, Tennevet, Isabelle, Hanzen, Chantal, Langlois, Olivier, Jardin, Fabrice, Laquerrière, Annie, Sarafan-Vasseur, Nasrin, Di Fiore, Fréderic, Clatot, Florian

    Published 2020
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  20. 20
    Patterns and severity of vascular amyloid in Alzheimer’s disease associated with duplications and missense mutations in APP gene, Down syndrome and sporadic Alzheimer’s disease

    Patterns and severity of vascular amyloid in Alzheimer’s disease associated with duplications and missense mutations in APP gene, Down syndrome and sporadic Alzheimer’s disease by Mann, David M. A., Davidson, Yvonne S., Robinson, Andrew C., Allen, Nancy, Hashimoto, Tadafumi, Richardson, Anna, Jones, Matthew, Snowden, Julie S., Pendleton, Neil, Potier, Marie-Claude, Laquerrière, Annie, Prasher, Vee, Iwatsubo, Takeshi, Strydom, Andre

    Published 2018
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