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Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|November 22, 2005
[Genetic causes of obesity]Teresia Wangensteen, Dag Undlien, Serena Tonstad, et al.
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|December 24, 2003
[A watershed in Norwegian obstetrics]Teresia Wangensteen, Gry Nordal, Erlend Hem, et al.
Obesity (Silver Spring, Md.)|October 2, 2010
A common haplotype in NAPEPLD is associated with severe obesity in a Norwegian population-based cohort (the HUNT study)Teresia Wangensteen, Hanne Akselsen, Jostein Holmen, et al.
Hereditary Cancer in Clinical Practice|May 31, 2019
Diagnostic mRNA splicing assay for variants in BRCA1 and BRCA2 identified two novel pathogenic splicing aberrationsTeresia Wangensteen, Caroline Nangota Felde, Deeqa Ahmed, et al.
American Journal of Medical Genetics. Part A|May 3, 2013
De novo 19p13.2 microdeletion encompassing the insulin receptor and resistin genes in a patient with obesity and learning disabilityTeresia Wangensteen, Lars Retterstøl, Olaug K Rødningen, et al.
Acta Paediatrica (Oslo, Norway : 1992)|July 29, 2008
Ethnic differences in metabolic syndrome among overweight and obese children and adolescents: the Oslo Adiposity Intervention StudyMagnhild L Pollestad Kolsgaard, Lene Frost Andersen, Serena Tonstad, et al.
Endocrinology|August 16, 2008
Functional characterization of naturally occurring pathogenic mutations in the human leptin receptorWendy Kimber, Frank Peelman, Xavier Prieur, et al.
Hereditary Cancer in Clinical Practice|January 18, 2018
BRCA1 and BRCA2 mutation spectrum - an update on mutation distribution in a large cancer genetics clinic in NorwayCecilie Heramb, Teresia Wangensteen, Eli Marie Grindedal, et al.
Scandinavian Journal of Clinical and Laboratory Investigation|November 26, 2009
Elevated visfatin levels in overweight and obese children and adolescents with metabolic syndromeMagnhild L Kolsgaard, Teresia Wangensteen, Cathrine Brunborg, et al.
Molecular Genetics & Genomic Medicine|July 27, 2019
Neuropsychiatric phenotype in relation to gene variants in the hemizygous allele in 3q29 deletion carriers: A case seriesEva Albertsen Malt, Katalin Juhasz, Anna Frengen, et al.
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