Search Results - Nicole Laurent

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  1. 1
    Ketogenic metabolic therapy in the remission of chronic major depressive disorder: a retrospective case study

    Ketogenic metabolic therapy in the remission of chronic major depressive disorder: a retrospective case study by Nicole Laurent, Erin L. Bellamy, Donika Hristova, Ally Houston

    Published 2025
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  2. 2
    Fetal toxic effects and angiotensin-II-receptor antagonists

    Fetal toxic effects and angiotensin-II-receptor antagonists by Jéléna Martinovic, Alexandra Benachi, Nicole Laurent, Farida Daïkha-Dahmane, Marie‐Claire Gubler

    Published 2001
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  3. 3
    Ketogenic metabolic therapy for schizoaffective disorder: a retrospective case series of psychotic symptom remission and mood recovery

    Ketogenic metabolic therapy for schizoaffective disorder: a retrospective case series of psychotic symptom remission and mood recovery by Nicole Laurent, Erin L. Bellamy, Katherine A. Tague, Donika Hristova, Ally Houston

    Published 2025
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  4. 4
    Perspectives on the ketogenic diet as a non-pharmacological intervention for major depressive disorder

    Perspectives on the ketogenic diet as a non-pharmacological intervention for major depressive disorder by Jade Shelp, Cristiano Chaves, Alexander Roy Terpstra, Elena Koning, Fabiano A. Gomes, Jennifer Fabe, Vitor Breda, Nicole Laurent, Christopher Palmer, Elisa Brietzke

    Published 2025
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  5. 5
    The Meckel-Gruber Syndrome Gene, MKS3, Is Mutated in Joubert Syndrome

    The Meckel-Gruber Syndrome Gene, MKS3, Is Mutated in Joubert Syndrome by Lekbir Baala, Stéphane Romano, Rana Khaddour, Sophie Saunier, Ursula M. Smith, Sophie Audollent, Catherine Ozilou, Laurence Faivre, Nicole Laurent, B. Foliguet, Arnold Münnich, Stanislas Lyonnet, Rémi Salomon, Férechté Encha‐Razavi, Marie‐Claire Gubler, Nathalie Boddaert, Pascale de Lonlay, Colin A. Johnson, Michel Vekemans, Corinne Antignac, Tania Attié‐Bitach

    Published 2006
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  6. 6
    Lamin A and ZMPSTE24 (FACE-1) defects cause nuclear disorganization and identify restrictive dermopathy as a lethal neonatal laminopathy

    Lamin A and ZMPSTE24 (FACE-1) defects cause nuclear disorganization and identify restrictive dermopathy as a lethal neonatal laminopathy by Claire Navarro, Annachiara De Sandre‐Giovannoli, Rafaëlle Bernard, Irène Boccaccio, Amandine Boyer, David Geneviève, S. Hadj‐Rabia, C. Gaudy‐Marqueste, Henk Sillevis Smitt, P. Vabres, Laurence Bonhomme‐Faivre, Alain Verloès, Ton van Essen, Elisabeth Flori, Raoul C. M. Hennekam, Frits A. Beemer, Nicole Laurent, Martine Le Merrer, Pierre Cau, Nicolas Lévy

    Published 2004
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  7. 7
    Mutations in KIAA0586 Cause Lethal Ciliopathies Ranging from a Hydrolethalus Phenotype to Short-Rib Polydactyly Syndrome

    Mutations in KIAA0586 Cause Lethal Ciliopathies Ranging from a Hydrolethalus Phenotype to Short-Rib Polydactyly Syndrome by Caroline Alby, Kevin Piquand, Céline Huber, André Mégarbané, Amale Ichkou, Marine Legendre, Fanny Pelluard, Ferechté Encha-Ravazi, Georges Abi Tayeh, Bettina Bessières, Salima El Chehadeh-Djebbar, Nicole Laurent, Laurence Faivre, László Sztriha, Melinda Zombor, Hajnalka Szabó, Marion Failler, Meriem Garfa-Traoré, Christine Bole, Patrick Nitschké, Mathilde Nizon, Nadia Elkhartoufi, Françoise Clerget‐Darpoux, Arnold Münnich, Stanislas Lyonnet, Michel Vekemans, Sophie Saunier, Valérie Cormier‐Daire, Tania Attié‐Bitach, Sophie Thomas

    Published 2015
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  8. 8
    Renal Tubular Dysgenesis, a Not Uncommon Autosomal Recessive Disorder Leading to Oligohydramnios

    Renal Tubular Dysgenesis, a Not Uncommon Autosomal Recessive Disorder Leading to Oligohydramnios by Mireille Lacoste, Yi Cai, Liliane Guicharnaud, FrancCOMBINING CEDILLAoise Mounier, Yves Dumez, Raymonde Bouvier, FreCombining Acute AccentdeCombining Acute Accentrique Dijoud, Marie Gonzalès, Jane Chatten, Anne‐Lise Delezoide, Laurent Daniel, Madeleine Joubert, Nicole Laurent, Jacqueline Aziza, Tahya Sellami, H. Ben Amar, C Jarnet, Anne Marie Frances, Farida DaiCombining Diaeresiskha-Dahmane, Aurore Coulomb, Thomas J. Neuhaus, B. Foliguet, Pierre Chenal, Pascale Marcorelles, Jean Marie Gasc, Pierre Corvol, Marie‐Claire Gubler

    Published 2006
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  9. 9
    Molecular heterogeneity in fetal forms of type II lissencephaly

    Molecular heterogeneity in fetal forms of type II lissencephaly by C Bouchet, M. Gonzalés, Sandrine Vuillaumier‐Barrot, Louise Devisme, C. Lebizec, Elisabeth Alanio, Anne Bazin, B. Bessières-Grattagliano, Nicole Bigi, Patricia Blanchet, Dominique Bonneau, Maryse Bonnières, Dominique Carles, Sophie Delahaye, Catherine Fallet‐Bianco, Dominique Figarella‐Branger, Dominique Gaillard, B. Gasser, Fabien Guimiot, Madeleine Joubert, Nicole Laurent, Agnès Liprandi, Philippe Loget, Pascale Marcorelles, Jéléna Martinovic, F. Menez, Sophie Patrier, Fanny Pelluard-Nehmé, Marie-José Perez, C. Rouleau-Dubois, Stéphane Triau, A. Laquérrière, Férechté Encha‐Razavi, Nathalie Seta

    Published 2007
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  10. 10
    Cobblestone lissencephaly: neuropathological subtypes and correlations with genes of dystroglycanopathies

    Cobblestone lissencephaly: neuropathological subtypes and correlations with genes of dystroglycanopathies by Louise Devisme, C Bouchet, Marie Gonzalès, Elisabeth Alanio, Anne Bazin, Bettina Bessières, Nicole Bigi, Patricia Blanchet, Dominique Bonneau, Maryse Bonnières, Martine Bucourt, Dominique Carles, Bénédicte Clarisse, S. Delahaye, Catherine Fallet‐Bianco, Dominique Figarella‐Branger, Dominique Gaillard, Bernard Gasser, Anne‐Lise Delezoide, Fabien Guimiot, Madeleine Joubert, Nicole Laurent, Annie Laquerrière, Agnès Liprandi, Philippe Loget, Pascale Marcorelles, Jéléna Martinovic, Françoise Ménez, Sophie Patrier, Fanny Pelluard, Marie-José Perez, Caroline Rouleau, Stéphane Triau, Tania Attié‐Bitach, Sandrine Vuillaumier‐Barrot, Nathalie Seta, Férechté Encha‐Razavi

    Published 2012
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