A. B. Hansen

发表

Detection and characterization of a novel splice mutation in the LDL receptor intron 12 resulting in two different mutant mRNA variants.

P. Guldberg, M. Hørder, H. Nissen, 1997, Atherosclerosis.

Phenotypic presentation of the FH-Cincinnati type 5 low density lipoprotein receptor mutation.

P. Guldberg, M. L. Larsen, T. Haghfelt, 1996, Scandinavian journal of clinical and laboratory investigation.

Effect of atorvastatin on renal NO availability and tubular function in patients with stage II-III chronic kidney disease and type 2 diabetes

E. B. Pedersen, J. Bech, F. Mose, 2014, Scandinavian journal of clinical and laboratory investigation.

Effect of cholecalciferol supplementation during winter months in patients with hypertension: a randomized, placebo-controlled trial.

E. B. Pedersen, J. Bech, F. Mose, 2012, American journal of hypertension.

Stability of 35 biochemical and immunological routine tests after 10 hours storage and transport of human whole blood at 21°C

E. Nexo, A. B. Hansen, L. O. Henriksen, 2014, Scandinavian journal of clinical and laboratory investigation.

Characterization of a disease‐causing Glu119‐Lys mutation in the low‐density lipoprotein receptor gene in two Danish families with heterozygous familial hypercholesterolemia

L. Bolund, T. Jensen, B. Andresen, 1994, Human mutation.

Clinically applicable mutation screening in familial hypercholesterolemia

P. Guldberg, M. Hørder, H. Nissen, 1996, Human mutation.

Genetic diagnosis with the denaturing gradient gel electrophoresis technique improves diagnostic precision in familial hypercholesterolemia.

P. Guldberg, M. L. Larsen, T. Haghfelt, 1995, Circulation.

Detection of a single base deletion in codon 424 of the low density lipoprotein receptor gene in a Danish family with familial hypercholesterolemia.

P. Guldberg, M. L. Larsen, T. Haghfelt, 1994, Atherosclerosis.

Evaluation of a clinically applicable mutation screening technique for genetic diagnosis of familial hypercholesterolemia and familial defective apolipoprotein B

P. Guldberg, H. Nissen, A. B. Hansen, 1998, Clinical genetics.

No certain predictors for mutation status in a Danish cohort with familial hypercholesterolemia: a descriptive study.

K. Brusgaard, M. Nybo, A. B. Hansen, 2007, Clinical biochemistry.

Molecular genetic analysis of 1053 Danish individuals with clinical signs of familial hypercholesterolemia

K. Brusgaard, M. Hørder, A. B. Hansen, 2006, Clinical genetics.

Variation in risk indicators of cardiovascular disease during the menstrual cycle: an investigation of within-subject variations in glutathione peroxidase, haemostatic variables, lipids and lipoproteins in healthy young women.

H. R. Andersen, O. Andersen, A. B. Hansen, 1996, Scandinavian journal of clinical and laboratory investigation.

The influence of N-acetylcysteine on the measurement of prothrombin time and activated partial thromboplastin time in healthy subjects.

A. B. Hansen, S. Jepsen, A. Hansen, 1994, Scandinavian journal of clinical and laboratory investigation.

Effect of nebivolol on renal nitric oxide availability and tubular function in patients with essential hypertension.

J. Bech, F. Mose, A. B. Hansen, 2015, British journal of clinical pharmacology.

Effects of atorvastatin on systemic and renal NO dependency in patients with non-diabetic stage II-III chronic kidney disease.

J. Bech, F. Mose, Thomas M. Larsen, 2014, British journal of clinical pharmacology.

Two Mutations in Exon XII of the Protein Sα Gene in Four Thrombophilic Families Resulting in Premature Stop Codons and Depressed Levels of Mutated mRNA

J. Ingerslev, B. Lind, S. Thorsen, 1996, Thrombosis and Haemostasis.

Cut-offs for thyroid peroxidase and thyroglobulin antibodies in early pregnancy

P. Vestergaard, A. Handberg, N. Bruun, 2022, European thyroid journal.

Classification of thyroid dysfunction in pregnant women differs by analytical method and type of thyroid function test.

P. Vestergaard, A. Handberg, P. A. Christensen, 2020, The Journal of clinical endocrinology and metabolism.

Pathophysiology of incomplete renal tubular acidosis in recurrent renal stone formers: evidence of disturbed calcium, bone and citrate metabolism

J. Bollerslev, P. Osther, A. B. Hansen, 1993, Urological Research.

Screening renal stone formers for distal renal tubular acidosis.

P. Osther, A. B. Hansen, H. Røhl, 1989, British journal of urology.

Renal acidification defects in medullary sponge kidney.

P. Osther, A. B. Hansen, H. Røhl, 1988, British journal of urology.

Distal renal tubular acidosis in recurrent renal stone formers.

P. Osther, A. B. Hansen, H. Røhl, 1989, Danish medical bulletin.