Hasil Pencarian - Judith Sinzig

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  1. 1
    Rare mutations of CACNB2 found in autism spectrum disease-affected families alter calcium channel function.

    Rare mutations of CACNB2 found in autism spectrum disease-affected families alter calcium channel function. oleh Alexandra F S Breitenkamp, Jan Matthes, Robert Daniel Nass, Judith Sinzig, Gerd Lehmkuhl, Peter Nürnberg, Stefan Herzig

    Diterbitkan 2014-01-01
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  2. 2
    Seasonal variation of BMI at admission in German adolescents with anorexia nervosa.

    Seasonal variation of BMI at admission in German adolescents with anorexia nervosa. oleh David R Kolar, Katharina Bühren, Beate Herpertz-Dahlmann, Katja Becker, Karin Egberts, Stefan Ehrlich, Christian Fleischhaker, Alexander von Gontard, Freia Hahn, Michael Huss, Charlotte Jaite, Michael Kaess, Tanja Legenbauer, Tobias J Renner, Veit Roessner, Ulrike Schulze, Judith Sinzig, Ida Wessing, Johannes Hebebrand, Manuel Föcker, Ekkehart Jenetzky

    Diterbitkan 2018-01-01
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  3. 3
    Clinical Characteristics of Inpatients with Childhood vs. Adolescent Anorexia Nervosa

    Clinical Characteristics of Inpatients with Childhood vs. Adolescent Anorexia Nervosa oleh Charlotte Jaite, Katharina Bühren, Brigitte Dahmen, Astrid Dempfle, Katja Becker, Christoph U. Correll, Karin M. Egberts, Stefan Ehrlich, Christian Fleischhaker, Alexander von Gontard, Freia Hahn, David Kolar, Michael Kaess, Tanja Legenbauer, Tobias J. Renner, Ulrike Schulze, Judith Sinzig, Ellen Thomae, Linda Weber, Ida Wessing, Gisela Antony, Johannes Hebebrand, Manuel Föcker, Beate Herpertz-Dahlmann

    Diterbitkan 2019-10-01
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  4. 4
    Reasons for admission and variance of body weight at referral in female inpatients with anorexia nervosa in Germany

    Reasons for admission and variance of body weight at referral in female inpatients with anorexia nervosa in Germany oleh Triinu Peters, David Kolar, Manuel Föcker, Katharina Bühren, Brigitte Dahmen, Katja Becker, Linda Weber, Christoph U. Correll, Charlotte Jaite, Karin M. Egberts, Marcel Romanos, Stefan Ehrlich, Maria Seidel, Veit Roessner, Christian Fleischhaker, Alexander von Gontard, Freia Hahn, Michael Huss, Michael Kaess, Tanja Legenbauer, Tobias J. Renner, Ulrike M. E. Schulze, Judith Sinzig, Ida Wessing, Gisela Antony, Beate Herpertz-Dahlmann, Gertraud Gradl-Dietsch, Johannes Hebebrand

    Diterbitkan 2021-12-01
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  5. 5
    DCLK1 variants are associated across schizophrenia and attention deficit/hyperactivity disorder.

    DCLK1 variants are associated across schizophrenia and attention deficit/hyperactivity disorder. oleh Bjarte Håvik, Franziska A Degenhardt, Stefan Johansson, Carla P D Fernandes, Anke Hinney, André Scherag, Helle Lybæk, Srdjan Djurovic, Andrea Christoforou, Kari M Ersland, Sudheer Giddaluru, Michael C O'Donovan, Michael J Owen, Nick Craddock, Thomas W Mühleisen, Manuel Mattheisen, Benno G Schimmelmann, Tobias Renner, Andreas Warnke, Beate Herpertz-Dahlmann, Judith Sinzig, Özgür Albayrak, Marcella Rietschel, Markus M Nöthen, Clive R Bramham, Thomas Werge, Johannes Hebebrand, Jan Haavik, Ole A Andreassen, Sven Cichon, Vidar M Steen, Stéphanie Le Hellard

    Diterbitkan 2012-01-01
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