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Clinical Biochemistry
|
October 27, 2007
No certain predictors for mutation status in a Danish cohort with familial hypercholesterolemia: a descriptive study
Mads Nybo, Klaus Brusgaard, Annebirthe Bo Hansen
Thrombosis Research
|
April 20, 2010
Severe arterial thrombosis in a family with type III protein S deficiency caused by a frameshift mutation in the PROS1 gene
Torben Bjerregaard Larsen, Klaus Brusgaard, Mads Nybo
European Journal of Cancer (Oxford, England : 1990)
|
February 14, 2018
Letter to the Editor regarding the paper by N. Azzam et al. 'Germline polymorphisms on RET proto-oncogene involved in medullary thyroid carcinoma in a Druze family'
Jes Sloth Mathiesen, Christian Godballe, Klaus Brusgaard
Clinical Endocrinology
|
October 11, 2011
Recurrent spontaneous hypoglycaemia causes loss of neurogenic and neuroglycopaenic signs in infants with congenital hyperinsulinism
Henrik T Christesen, Klaus Brusgaard, Khalid Hussain
Diseases of the Colon and Rectum
|
July 8, 2016
Juvenile Polyps in Denmark From 1995 to 2014
Anne Marie Jelsig, Lilian Bomme Ousager, Klaus Brusgaard, et al.
Ugeskrift for Laeger
|
August 5, 2015
[A patient diagnosed herself with erythropoietic protoporphyria after googling photosensitivity]
Anne L Christiansen, Klaus Brusgaard, Jens Michael Hertz, et al.
Histology and Histopathology
|
February 2, 2024
Genotype-histotype-phenotype correlations in hyperinsulinemic hypoglycemia
Annette Rønholt Larsen, Klaus Brusgaard, Henrik Thybo Christesen, et al.
Journal of Human Genetics
|
June 15, 2012
Mutational analysis of PHEX, FGF23, DMP1, SLC34A3 and CLCN5 in patients with hypophosphatemic rickets
Signe S Beck-Nielsen, Kim Brixen, Jeppe Gram, et al.
Frontiers in Endocrinology
|
June 13, 2024
Well-differentiated G1 and G2 pancreatic neuroendocrine tumors: a meta-analysis of published expanded DNA sequencing data
Kirstine Øster Andersen, Sönke Detlefsen, Klaus Brusgaard, et al.
European Journal of Human Genetics : EJHG
|
January 22, 2015
Research participants in NGS studies want to know about incidental findings
Anne Marie Jelsig, Niels Qvist, Klaus Brusgaard, et al.
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Search research articles
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Showing results (1-10 of 94) with videos related to
Sort By:
Page
of 10
Clinical Biochemistry
|
October 27, 2007
No certain predictors for mutation status in a Danish cohort with familial hypercholesterolemia: a descriptive study
Mads Nybo, Klaus Brusgaard, Annebirthe Bo Hansen
Thrombosis Research
|
April 20, 2010
Severe arterial thrombosis in a family with type III protein S deficiency caused by a frameshift mutation in the PROS1 gene
Torben Bjerregaard Larsen, Klaus Brusgaard, Mads Nybo
European Journal of Cancer (Oxford, England : 1990)
|
February 14, 2018
Letter to the Editor regarding the paper by N. Azzam et al. 'Germline polymorphisms on RET proto-oncogene involved in medullary thyroid carcinoma in a Druze family'
Jes Sloth Mathiesen, Christian Godballe, Klaus Brusgaard
Clinical Endocrinology
|
October 11, 2011
Recurrent spontaneous hypoglycaemia causes loss of neurogenic and neuroglycopaenic signs in infants with congenital hyperinsulinism
Henrik T Christesen, Klaus Brusgaard, Khalid Hussain
Diseases of the Colon and Rectum
|
July 8, 2016
Juvenile Polyps in Denmark From 1995 to 2014
Anne Marie Jelsig, Lilian Bomme Ousager, Klaus Brusgaard, et al.
Ugeskrift for Laeger
|
August 5, 2015
[A patient diagnosed herself with erythropoietic protoporphyria after googling photosensitivity]
Anne L Christiansen, Klaus Brusgaard, Jens Michael Hertz, et al.
Histology and Histopathology
|
February 2, 2024
Genotype-histotype-phenotype correlations in hyperinsulinemic hypoglycemia
Annette Rønholt Larsen, Klaus Brusgaard, Henrik Thybo Christesen, et al.
Journal of Human Genetics
|
June 15, 2012
Mutational analysis of PHEX, FGF23, DMP1, SLC34A3 and CLCN5 in patients with hypophosphatemic rickets
Signe S Beck-Nielsen, Kim Brixen, Jeppe Gram, et al.
Frontiers in Endocrinology
|
June 13, 2024
Well-differentiated G1 and G2 pancreatic neuroendocrine tumors: a meta-analysis of published expanded DNA sequencing data
Kirstine Øster Andersen, Sönke Detlefsen, Klaus Brusgaard, et al.
European Journal of Human Genetics : EJHG
|
January 22, 2015
Research participants in NGS studies want to know about incidental findings
Anne Marie Jelsig, Niels Qvist, Klaus Brusgaard, et al.
Page
of 10