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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 adolescents
A Hinney, A Bornscheuer, M Depenbusch, et al.
Neuroscience and Biobehavioral Reviews
|
November 6, 2004
Molecular genetic aspects of attention-deficit/hyperactivity disorder
P 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 gene
M 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 study
B 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 regulation
F 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 15
G 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 syndrome
S 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 15
M M Nöthen, G Schulte-Körne, T Grimm, et al.
Page
of 29
Search research articles
Search
Showing results (231-240 of 287) with videos related to
Sort By:
Page
of 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 adolescents
A Hinney, A Bornscheuer, M Depenbusch, et al.
Neuroscience and Biobehavioral Reviews
|
November 6, 2004
Molecular genetic aspects of attention-deficit/hyperactivity disorder
P 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 gene
M 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 study
B 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 regulation
F 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 15
G 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 syndrome
S 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 15
M M Nöthen, G Schulte-Körne, T Grimm, et al.
Page
of 29