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Clinical Endocrinology
|
May 1, 2007
Complex ABCC8 DNA variations in congenital hyperinsulinism: lessons from functional studies
Morris Muzyamba, Tabasum Farzaneh, Phillip Behe, et al.
Endocrinology, Diabetes & Metabolism Case Reports
|
May 2, 2017
Octreotide therapy and restricted fetal growth: pregnancy in familial hyperinsulinemic hypoglycemia
Marianne Geilswijk, Lise Lotte Andersen, Morten Frost, et al.
Journal of Medical Genetics
|
August 29, 2022
Hereditary haemorrhagic telangiectasia in Danish patients with pathogenic variants in <i>SMAD4:</i> a nationwide study
Anne Marie Jelsig, Anette Kjeldsen, Lise Lotte Christensen, et al.
Journal of Biomedical Informatics
|
October 19, 2004
Correspondence analysis of microarray time-course data in case-control design
Qihua Tan, Klaus Brusgaard, Torben A Kruse, et al.
Biochemical and Biophysical Research Communications
|
August 19, 2014
Testosterone treatment increases androgen receptor and aromatase gene expression in myotubes from patients with PCOS and controls, but does not induce insulin resistance
Mette Brandt Eriksen, Dorte Glintborg, Michael Friberg Bruun Nielsen, et al.
Plos One
|
October 3, 2013
Genetic alterations within the DENND1A gene in patients with polycystic ovary syndrome (PCOS)
Mette B Eriksen, Michael F B Nielsen, Klaus Brusgaard, et al.
Diabetes Care
|
November 15, 2012
Heterogeneity in phenotype of usher-congenital hyperinsulinism syndrome: hearing loss, retinitis pigmentosa, and hyperinsulinemic hypoglycemia ranging from severe to mild with conversion to diabetes
Angham N Al Mutair, Klaus Brusgaard, Bassam Bin-Abbas, et al.
Clinical Case Reports
|
June 8, 2017
Familial cerebral abscesses caused by hereditary hemorrhagic telangiectasia
Pernille Mathiesen Tørring, Mathilde Faurholdt Lauridsen, Christine I Dali, et al.
Genetic Testing
|
July 14, 2007
Arrayed primer extension in the "array of arrays" format: a rational approach for microarray-based SNP genotyping
Niels G F Klitø, Qihua Tan, Mette Nyegaard, et al.
Biochemical and Biophysical Research Communications
|
May 2, 2006
Spotting and validation of a genome wide oligonucleotide chip with duplicate measurement of each gene
Mads Thomassen, Vibe Skov, Freyja Eiriksdottir, et al.
Page
of 10
Search research articles
Search
Showing results (41-50 of 94) with videos related to
Sort By:
Page
of 10
Clinical Endocrinology
|
May 1, 2007
Complex ABCC8 DNA variations in congenital hyperinsulinism: lessons from functional studies
Morris Muzyamba, Tabasum Farzaneh, Phillip Behe, et al.
Endocrinology, Diabetes & Metabolism Case Reports
|
May 2, 2017
Octreotide therapy and restricted fetal growth: pregnancy in familial hyperinsulinemic hypoglycemia
Marianne Geilswijk, Lise Lotte Andersen, Morten Frost, et al.
Journal of Medical Genetics
|
August 29, 2022
Hereditary haemorrhagic telangiectasia in Danish patients with pathogenic variants in <i>SMAD4:</i> a nationwide study
Anne Marie Jelsig, Anette Kjeldsen, Lise Lotte Christensen, et al.
Journal of Biomedical Informatics
|
October 19, 2004
Correspondence analysis of microarray time-course data in case-control design
Qihua Tan, Klaus Brusgaard, Torben A Kruse, et al.
Biochemical and Biophysical Research Communications
|
August 19, 2014
Testosterone treatment increases androgen receptor and aromatase gene expression in myotubes from patients with PCOS and controls, but does not induce insulin resistance
Mette Brandt Eriksen, Dorte Glintborg, Michael Friberg Bruun Nielsen, et al.
Plos One
|
October 3, 2013
Genetic alterations within the DENND1A gene in patients with polycystic ovary syndrome (PCOS)
Mette B Eriksen, Michael F B Nielsen, Klaus Brusgaard, et al.
Diabetes Care
|
November 15, 2012
Heterogeneity in phenotype of usher-congenital hyperinsulinism syndrome: hearing loss, retinitis pigmentosa, and hyperinsulinemic hypoglycemia ranging from severe to mild with conversion to diabetes
Angham N Al Mutair, Klaus Brusgaard, Bassam Bin-Abbas, et al.
Clinical Case Reports
|
June 8, 2017
Familial cerebral abscesses caused by hereditary hemorrhagic telangiectasia
Pernille Mathiesen Tørring, Mathilde Faurholdt Lauridsen, Christine I Dali, et al.
Genetic Testing
|
July 14, 2007
Arrayed primer extension in the "array of arrays" format: a rational approach for microarray-based SNP genotyping
Niels G F Klitø, Qihua Tan, Mette Nyegaard, et al.
Biochemical and Biophysical Research Communications
|
May 2, 2006
Spotting and validation of a genome wide oligonucleotide chip with duplicate measurement of each gene
Mads Thomassen, Vibe Skov, Freyja Eiriksdottir, et al.
Page
of 10