Torthaí cuardaigh - Helmut Remschmidt
- 1 - 20 toradh as 28 á dtaispeáint
- Téigh chuig an gcéad leathanach eile
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1
The Children of Mentally Ill Parents de réir Fritz Mattejat, Helmut Remschmidt
Foilsithe / Cruthaithe 2008Artigo -
2
Growing Up Is Hard de réir Beate Herpertz‐Dahlmann, Katharina Bühren, Helmut Remschmidt
Foilsithe / Cruthaithe 2013Revisão -
3
5-HT2A receptor gene polymorphisms, anorexia nervosa, and obesity de réir Anke Hinney, Andreas Ziegler, Markus M. Nöthen, Helmut Remschmidt, Johannes Hebebrand
Foilsithe / Cruthaithe 1997Carta -
4
Epidemic obesity: are genetic factors involved via increased rates of assortative mating? de réir Johannes Hebebrand, Heiko Wulftange, T Goerg, Andreas Ziegler, Anke Hinney, Nikolaus Barth, Hermann Mayer, Helmut Remschmidt
Foilsithe / Cruthaithe 2000Artigo -
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6
Evidence for the Late MMN as a Neurophysiological Endophenotype for Dyslexia de réir Nina Neuhoff, Jennifer Bruder, Jürgen Bartling, Andreas Warnke, Helmut Remschmidt, Bertram Müller‐Myhsok, Gerd Schulte‐Körne
Foilsithe / Cruthaithe 2012Artigo -
7
Trio study and meta-analysis support the association of genetic variation at the serotonin transporter with early-onset obsessive–compulsive disorder de réir Susanne Walitza, Zoya Marinova, Edna Grünblatt, Stanley E. Lazic, Helmut Remschmidt, Timo D. Vloet, Jens R. Wendland
Foilsithe / Cruthaithe 2014Revisão -
8
Ghrelin Gene: Identification of Missense Variants and a Frameshift Mutation in Extremely Obese Children and Adolescents and Healthy Normal Weight Students de réir Anke Hinney, Anne Z. Hoch, Frank Geller, H. Schäfer, Wolfgang Siegfried, Hanspeter Goldschmidt, Helmut Remschmidt, Johannes Hebebrand
Foilsithe / Cruthaithe 2002Artigo -
9
Phenotypes in Three Pedigrees with Autosomal Dominant Obesity Caused by Haploinsufficiency Mutations in the Melanocortin-4 Receptor Gene de réir Mani Sina, Anke Hinney, Andreas Ziegler, Tanja Neupert, Hermann Mayer, Wolfgang Siegfried, Werner Blum, Helmut Remschmidt, Johannes Hebebrand
Foilsithe / Cruthaithe 1999Artigo -
10
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11
Evidence for Linkage of Spelling Disability to Chromosome 15 de réir Gerd Schulte‐Körne, T. Grimm, Markus M. Nöthen, Bertram Müller‐Myhsok, Sven Cichon, Ina R. Vogt, Peter Propping, Helmut Remschmidt
Foilsithe / Cruthaithe 1998Carta -
12
Rates of psychiatric disorders in a clinical study group of adolescents with extreme obesity and in obese adolescents ascertained via a population based study de réir B Britz, Wolfgang Siegfried, Andreas Ziegler, Christina Maria Lamertz, B-M Herpertz-Dahlmann, Helmut Remschmidt, Hans‐Ulrich Wïttchen, Johannes Hebebrand
Foilsithe / Cruthaithe 2000Artigo -
13
Leptin levels in patients with anorexia nervosa are reduced in the acute stage and elevated upon short-term weight restoration de réir Johannes Hebebrand, Werner Blum, Nikolaus Barth, H Coners, P. Englaro, Anders Juul, Andreas Ziegler, Andreas Warnke, Wolfgang Rascher, Helmut Remschmidt
Foilsithe / Cruthaithe 1997Artigo -
14
Age-dependent changes in the neural substrates of empathy in autism spectrum disorder de réir Martin Schulte‐Rüther, Ellen Greimel, Martina Piefke, Inge Kamp‐Becker, Helmut Remschmidt, Gereon R. Fink, Beate Herpertz‐Dahlmann, Kerstin Konrad
Foilsithe / Cruthaithe 2013Artigo -
15
Systematic Mutation Screening of the Estrogen Receptor Beta Gene in Probands of Different Weight Extremes: Identification of Several Genetic Variants de réir K. A. Rosenkranz, Anke Hinney, Andreas Ziegler, H. Hermann, Manfred Fichter, Hermann Mayer, Wolfgang Siegfried, JK. Young, Helmut Remschmidt, Johannes Hebebrand
Foilsithe / Cruthaithe 1998Artigo -
16
Systematic Mutation Screening of the Pro-Opiomelanocortin Gene: Identification of Several Genetic Variants Including Three Different Insertions, One Nonsense and Two Missense Point... de réir Anke Hinney, Ingrid Becker, O. Heibült, K. Nottebom, Albrecht Schmidt, Andreas Ziegler, Hermann Mayer, Wolfgang Siegfried, W. F. Blum, Helmut Remschmidt, Johannes Hebebrand
Foilsithe / Cruthaithe 1998Artigo -
17
Melanocortin-4 Receptor Gene: Case-Control Study and Transmission Disequilibrium Test Confirm that Functionally Relevant Mutations Are Compatible with a Major Gene Effect for Extre... de réir Anke Hinney, Sarah Hohmann, Frank Geller, CONSTANZE VOGEL, Claudia Hess, Anne‐Kathrin Wermter, Britta Brokamp, Hanspeter Goldschmidt, Wolfgang Siegfried, Helmut Remschmidt, H. Schäfer, Thomas Gudermann, Johannes Hebebrand
Foilsithe / Cruthaithe 2003Artigo -
18
Several Mutations in the Melanocortin-4 Receptor Gene Including a Nonsense and a Frameshift Mutation Associated with Dominantly Inherited Obesity in Humans de réir Anke Hinney, Albrecht Schmidt, K. Nottebom, O. Heibült, Ingrid Becker, Andreas Ziegler, G Gerber, Mani Sina, T. Görg, Hermann Mayer, Wolfgang Siegfried, M. Fichter, Helmut Remschmidt, Johannes Hebebrand
Foilsithe / Cruthaithe 1999Artigo -
19
Neurophysiological correlates of relatively enhanced local visual search in autistic adolescents de réir Zina M. Manjaly, Nicole Bruning, Susanne Neufang, Klaas Ε. Stephan, Sarah Brieber, John C. Marshall, Inge Kamp‐Becker, Helmut Remschmidt, Beate Herpertz‐Dahlmann, Kerstin Konrad, Gereon R. Fink
Foilsithe / Cruthaithe 2007Artigo -
20
Elevated Physical Activity and Low Leptin Levels Co-occur in Patients with Anorexia Nervosa de réir Kristian Holtkamp, Beate Herpertz‐Dahlmann, Claudia Mika, Martina Heer, N Heussen, Manfred Fichter, Stephan Herpertz, W Senf, Werner Blum, Ulrich Schweiger, Andreas Warnke, Anne Ballauff, Helmut Remschmidt, Johannes Hebebrand
Foilsithe / Cruthaithe 2003Artigo
Uirlisí cuardaigh:
Ábhair a bhaineann le hábhar
Medicine
Biology
Genetics
Gene
Internal medicine
Endocrinology
Allele
Psychiatry
Genotype
Obesity
Single-nucleotide polymorphism
Eating disorders
Psychology
Mutation
Anorexia nervosa
Haplotype
Receptor
Body mass index
Genetic association
Linkage disequilibrium
Missense mutation
Transmission disequilibrium test
Candidate gene
Developmental psychology
Dyslexia
Leptin
Neuroscience
Reading (process)
Audiology
Autism