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H Remschmidt

Showing results (231-240 of 287) with videos related to

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International Journal of Obesity and Related Metabolic Disorders : Journal of the International Association for the Study of Obesity|January 14, 1998
Absence of leptin deficiency mutation in extremely obese German children and adolescentsA Hinney, A Bornscheuer, M Depenbusch, et al.
Neuroscience and Biobehavioral Reviews|November 6, 2004
Molecular genetic aspects of attention-deficit/hyperactivity disorderP Heiser, S Friedel, A Dempfle, et al.
American Journal of Human Genetics|December 1, 1999
Phenotypes in three pedigrees with autosomal dominant obesity caused by haploinsufficiency mutations in the melanocortin-4 receptor geneM Sina, A Hinney, A Ziegler, et al.
Der Nervenarzt|March 24, 1999
[Body weight regulation in anorexia nervosa with special attention to leptin secretion]J Hebebrand, A Ballauff, A Hinney, et al.
International Journal of Obesity and Related Metabolic Disorders : Journal of the International Association for the Study of Obesity|December 29, 2000
Rates of psychiatric disorders in a clinical study group of adolescents with extreme obesity and in obese adolescents ascertained via a population based studyB Britz, W Siegfried, A Ziegler, et al.
Zeitschrift Fur Kinder- Und Jugendpsychiatrie Und Psychotherapie|October 3, 1998
[An inventory for assessing the quality of life of children and adolescents--a pilot study]F Mattejat, J Jungmann, M Meusers, et al.
The Pharmacogenomics Journal|September 20, 2006
No evidence for binding of clozapine, olanzapine and/or haloperidol to selected receptors involved in body weight regulationF M Theisen, M Haberhausen, M A Firnges, et al.
American Journal of Human Genetics|June 23, 1998
Evidence for linkage of spelling disability to chromosome 15G Schulte-Körne, T Grimm, M M Nöthen, et al.
Genetic Epidemiology|December 22, 1999
Complex segregation analysis of families ascertained through Gilles de la Tourette syndromeS A Seuchter, J Hebebrand, B Klug, et al.
European Child & Adolescent Psychiatry|January 19, 2000
Genetic linkage analysis with dyslexia: evidence for linkage of spelling disability to chromosome 15M M Nöthen, G Schulte-Körne, T Grimm, et al.
Pageof 29

Showing results (231-240 of 287) with videos related to

Sort By:
Pageof 29
International Journal of Obesity and Related Metabolic Disorders : Journal of the International Association for the Study of Obesity|January 14, 1998
Absence of leptin deficiency mutation in extremely obese German children and adolescentsA Hinney, A Bornscheuer, M Depenbusch, et al.
Neuroscience and Biobehavioral Reviews|November 6, 2004
Molecular genetic aspects of attention-deficit/hyperactivity disorderP Heiser, S Friedel, A Dempfle, et al.
American Journal of Human Genetics|December 1, 1999
Phenotypes in three pedigrees with autosomal dominant obesity caused by haploinsufficiency mutations in the melanocortin-4 receptor geneM Sina, A Hinney, A Ziegler, et al.
Der Nervenarzt|March 24, 1999
[Body weight regulation in anorexia nervosa with special attention to leptin secretion]J Hebebrand, A Ballauff, A Hinney, et al.
International Journal of Obesity and Related Metabolic Disorders : Journal of the International Association for the Study of Obesity|December 29, 2000
Rates of psychiatric disorders in a clinical study group of adolescents with extreme obesity and in obese adolescents ascertained via a population based studyB Britz, W Siegfried, A Ziegler, et al.
Zeitschrift Fur Kinder- Und Jugendpsychiatrie Und Psychotherapie|October 3, 1998
[An inventory for assessing the quality of life of children and adolescents--a pilot study]F Mattejat, J Jungmann, M Meusers, et al.
The Pharmacogenomics Journal|September 20, 2006
No evidence for binding of clozapine, olanzapine and/or haloperidol to selected receptors involved in body weight regulationF M Theisen, M Haberhausen, M A Firnges, et al.
American Journal of Human Genetics|June 23, 1998
Evidence for linkage of spelling disability to chromosome 15G Schulte-Körne, T Grimm, M M Nöthen, et al.
Genetic Epidemiology|December 22, 1999
Complex segregation analysis of families ascertained through Gilles de la Tourette syndromeS A Seuchter, J Hebebrand, B Klug, et al.
European Child & Adolescent Psychiatry|January 19, 2000
Genetic linkage analysis with dyslexia: evidence for linkage of spelling disability to chromosome 15M M Nöthen, G Schulte-Körne, T Grimm, et al.
Pageof 29