检索结果 - Catalina Betancur

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  1. 1
    Etiological heterogeneity in autism spectrum disorders: More than 100 genetic and genomic disorders and still counting

    Etiological heterogeneity in autism spectrum disorders: More than 100 genetic and genomic disorders and still counting 由 Catalina Betancur

    出版 2010
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  2. 2
    SHANK3 haploinsufficiency: a “common” but underdiagnosed highly penetrant monogenic cause of autism spectrum disorders

    SHANK3 haploinsufficiency: a “common” but underdiagnosed highly penetrant monogenic cause of autism spectrum disorders 由 Catalina Betancur, Joseph D. Buxbaum

    出版 2013
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  3. 3
    The emerging role of synaptic cell-adhesion pathways in the pathogenesis of autism spectrum disorders

    The emerging role of synaptic cell-adhesion pathways in the pathogenesis of autism spectrum disorders 由 Catalina Betancur, Takeshi Sakurai, Joseph D. Buxbaum

    出版 2009
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  4. 4
    Altered expression of vesicular glutamate transporters VGLUT1 and VGLUT2 in Parkinson disease

    Altered expression of vesicular glutamate transporters VGLUT1 and VGLUT2 in Parkinson disease 由 Alireza Kashani, Catalina Betancur, Bruno Giros, Étienne C. Hirsch, Salah El Mestikawy

    出版 2006
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  5. 5
    Hypolocomotor effects of acute and daily d-amphetamine in mice lacking the dopamine transporter

    Hypolocomotor effects of acute and daily d-amphetamine in mice lacking the dopamine transporter 由 Cécile Spielewoy, Grażyna Biała, Christine Roubert, Michel Hamon, Catalina Betancur, Bruno Giros

    出版 2001
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  6. 6
    Behavioural disturbances associated with hyperdopaminergia in dopamine-transporter knockout mice

    Behavioural disturbances associated with hyperdopaminergia in dopamine-transporter knockout mice 由 Cécile Spielewoy, Christine Roubert, M. Hamon, Marika Nosten, Catalina Betancur, Bruno Giros

    出版 2000
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  7. 7
    Neuropsychiatric decompensation in adolescents and adults with Phelan-McDermid syndrome: a systematic review of the literature

    Neuropsychiatric decompensation in adolescents and adults with Phelan-McDermid syndrome: a systematic review of the literature 由 Alexander Kolevzon, Elsa Delaby, Elizabeth Berry‐Kravis, Joseph D. Buxbaum, Catalina Betancur

    出版 2019
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  8. 8
    Absence of association between a polymorphic GGC repeat in the 5′ untranslated region of the reelin gene and autism

    Absence of association between a polymorphic GGC repeat in the 5′ untranslated region of the reelin gene and autism 由 Marie‐Odile Krebs, Catalina Betancur, Sophie Leroy, M.-C. Bourdel, Christopher Gillberg, Marion Leboyer

    出版 2002
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  9. 9
    Exploratory analysis of obsessive compulsive symptom dimensions in children and adolescents: a Prospective follow-up study

    Exploratory analysis of obsessive compulsive symptom dimensions in children and adolescents: a Prospective follow-up study 由 Richard Delorme, Arnaud Bille, Catalina Betancur, Flavie Mathieu, Nadia Chabane, Marie Christine Mouren-Siméoni, Marion Leboyer

    出版 2006
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  10. 10
    Constitutional Downregulation of <i>SEMA5A</i> Expression in Autism

    Constitutional Downregulation of <i>SEMA5A</i> Expression in Autism 由 Malin Melin, Birgit Carlsson, Henrik Anckarsäter, Maria Råstam, Catalina Betancur, Anders Isaksson, Christopher Gillberg, Niklas Dahl

    出版 2006
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  11. 11
    Optimizing the phenotyping of rodent ASD models: enrichment analysis of mouse and human neurobiological phenotypes associated with high-risk autism genes identifies morphological, electrophysiological, neurological, and behavioral features

    Optimizing the phenotyping of rodent ASD models: enrichment analysis of mouse and human neurobiological phenotypes associated with high-risk autism genes identifies morphological,... 由 Joseph D. Buxbaum, Catalina Betancur, Ozlem Bozdagi, Nate P. Dorr, Gregory A. Elder, Patrick R. Hof

    出版 2012
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  12. 12
    Psychiatric illness and regression in individuals with Phelan-McDermid syndrome

    Psychiatric illness and regression in individuals with Phelan-McDermid syndrome 由 Teresa M. Kohlenberg, M. Pilar Trelles, Brittany McLarney, Catalina Betancur, Audrey Thurm, Alexander Kolevzon

    出版 2020
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  13. 13
    Linkage and association of the glutamate receptor 6 gene with autism

    Linkage and association of the glutamate receptor 6 gene with autism 由 Stéphane Jamain, Catalina Betancur, Hélène Quach, Anne Philippe, Marc Fellous, Bruno Giros, Christopher Gillberg, Marion Leboyer, Thomas Bourgeron

    出版 2002
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  14. 14
    Shared executive dysfunctions in unaffected relatives of patients with autism and obsessive-compulsive disorder

    Shared executive dysfunctions in unaffected relatives of patients with autism and obsessive-compulsive disorder 由 Richard Delorme, Véronique Goussé, Isabelle Roy, Anca Trandafir, Flavie Mathieu, Marie‐Christine Mouren‐Siméoni, Catalina Betancur, Marion Leboyer

    出版 2006
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  15. 15
    Parallel Loss of Hippocampal LTD and Cognitive Flexibility in a Genetic Model of Hyperdopaminergia

    Parallel Loss of Hippocampal LTD and Cognitive Flexibility in a Genetic Model of Hyperdopaminergia 由 Élise Morice, Jean‐Marie Billard, Cécile V. Denis, Flavie Mathieu, Catalina Betancur, Jacques Epelbaum, Bruno Giros, Marika Nosten‐Bertrand

    出版 2007
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  16. 16
    Autism multiplex family with 16p11.2p12.2 microduplication syndrome in monozygotic twins and distal 16p11.2 deletion in their brother

    Autism multiplex family with 16p11.2p12.2 microduplication syndrome in monozygotic twins and distal 16p11.2 deletion in their brother 由 Anne‐Claude Tabet, Marion Pilorge, Richard Delorme, Frédérique Amsellem, Jean-Marc Pinard, Marion Leboyer, Alain Verloès, Brigitte Benzacken, Catalina Betancur

    出版 2012
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  17. 17
    Autism, language delay and mental retardation in a patient with 7q11 duplication

    Autism, language delay and mental retardation in a patient with 7q11 duplication 由 Christel Depienne, Delphine Héron, Catalina Betancur, B Benyahia, Oriane Trouillard, Delphine Bouteiller, Alain Verloès, Eric LeGuern, Marion Leboyer, Alexis Brice

    出版 2007
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  18. 18
    Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism

    Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism 由 Stéphane Jamain, Hélène Quach, Catalina Betancur, Maria Råstam, Catherine Colineaux, I. Carina Gillberg, Henrik Söderström, Bruno Giros, Marion Leboyer, Christopher Gillberg, Thomas Bourgeron

    出版 2003
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  19. 19
    Increased rewarding properties of morphine in dopamine‐transporter knockout mice

    Increased rewarding properties of morphine in dopamine‐transporter knockout mice 由 Cécile Spielewoy, François Gonon, Christine Roubert, Valérie Fauchey, Mohamed Jaber, Marc G. Caron, Bernárd P. Roques, M. Hamon, Catalina Betancur, Rafaël Maldonado, Bruno Giros

    出版 2000
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  20. 20
    Serotonin transporter gene polymorphisms and hyperserotonemia in autistic disorder

    Serotonin transporter gene polymorphisms and hyperserotonemia in autistic disorder 由 Catalina Betancur, Marilys Corbex, Cécile Spielewoy, Anne Philippe, Jean Laplanche, J.M. Launay, Christopher Gillberg, MC Mouren-Siméoni, M. Hamon, Bruno Giros, Marika Nosten‐Bertrand, Marion Leboyer

    出版 2002
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