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Klaus Brusgaard

Showing results (1-10 of 94) with videos related to

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Clinical Biochemistry|October 27, 2007
No certain predictors for mutation status in a Danish cohort with familial hypercholesterolemia: a descriptive studyMads 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 geneTorben 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 hyperinsulinismHenrik T Christesen, Klaus Brusgaard, Khalid Hussain
Diseases of the Colon and Rectum|July 8, 2016
Juvenile Polyps in Denmark From 1995 to 2014Anne 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 hypoglycemiaAnnette 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 ricketsSigne 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 dataKirstine 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 findingsAnne Marie Jelsig, Niels Qvist, Klaus Brusgaard, et al.
Pageof 10

Showing results (1-10 of 94) with videos related to

Sort By:
Pageof 10
Clinical Biochemistry|October 27, 2007
No certain predictors for mutation status in a Danish cohort with familial hypercholesterolemia: a descriptive studyMads 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 geneTorben 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 hyperinsulinismHenrik T Christesen, Klaus Brusgaard, Khalid Hussain
Diseases of the Colon and Rectum|July 8, 2016
Juvenile Polyps in Denmark From 1995 to 2014Anne 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 hypoglycemiaAnnette 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 ricketsSigne 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 dataKirstine 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 findingsAnne Marie Jelsig, Niels Qvist, Klaus Brusgaard, et al.
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