288 results on '"Nissen, Peter H."'
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2. Reduce energy consumption in your laboratory – switch ultra-low temperature freezers from – 80 °C to –70 °C. A pilot study on short term storage of plasma samples for coagulation testing.
3. Association of whole blood microRNA expression with platelet function and turnover in patients with coronary artery disease
4. Asymmetric amyloid deposition in preclinical Alzheimer’s disease: A PET study
5. Pazopanib-Induced Liver Toxicity in Patients With Metastatic Renal Cell Carcinoma: Effect of UGT1A1 Polymorphism on Pazopanib Dose Reduction, Safety, and Patient Outcomes
6. Protein C deficiency; PROC gene variants in a Danish population
7. SERPINC1 variants causing hereditary antithrombin deficiency in a Danish population
8. Platelet Function and Maturity and Related microRNA Expression in Whole Blood in Patients with ST-Segment Elevation Myocardial Infarction
9. Lactase persistence genotyping on whole blood by loop-mediated isothermal amplification and melting curve analysis
10. Platelet Function and Maturity and Related microRNA Expression in Whole Blood in Patients with ST-Segment Elevation Myocardial Infarction.
11. Performance on complex memory tests is associated with β-amyloid in individuals at risk of developing Alzheimer's disease
12. Short-term biological variation of plasma uracil in a Caucasian healthy population
13. Advanced Flow Cytometry Using the SYTO-13 Dye for the Assessment of Platelet Reactivity and Maturity in Whole Blood
14. Expression of microRNA Predicts Cardiovascular Events in Patients with Stable Coronary Artery Disease
15. Impact of age‐dependent red blood cell parameters on α‐globin gene genotyping in children
16. A case of platelet δ-granule defect identified by decreased CD63 expression and decreased serotonin release measured by flow cytometry and liquid chromatography tandem mass spectrometry.
17. The LMNA mutation p.Arg321Ter associated with dilated cardiomyopathy leads to reduced expression and a skewed ratio of lamin A and lamin C proteins
18. Long-term Outcome of 4 Patients With Transcobalamin Deficiency Caused by 2 Novel TCN2 Mutations
19. Identification of rare and frequent variants of the CASR gene by high-resolution melting
20. Flow Cytometric Assessment of Changes in Platelet Reactivity after Acute Coronary Syndrome: A Systematic Review
21. The Role of Plasminogen Activator Inhibitor Type 1 (PAI-1) in Placenta-Mediated Pregnancy Complications: A Systematic Review
22. Increased Trabecular Volumetric Bone Mass Density in Familial Hypocalciuric Hypercalcemia (FHH) Type 1: A Cross-Sectional Study
23. Impact of age‐dependent red blood cell parameters on α‐globin gene genotyping in children.
24. Platelet function assessed by ROTEM®plateletin patients receiving antiplatelet therapy during cardiac and vascular surgery
25. Impact of centrifugation time and pneumatic tube transport on plasma concentrations of direct oral anticoagulants
26. Genetic Variants in the Protein S (PROS1) Gene and Protein S Deficiency in a Danish Population
27. Genetic diversity of eleven European pig breeds
28. Forearm Bone Mineral Density in Familial Hypocalciuric Hypercalcemia and Primary Hyperparathyroidism: A Comparative Study
29. Transcobalamin deficiency caused by compound heterozygosity for two novel mutations in the TCN2 gene: a study of two affected siblings, their brother, and their parents
30. Congenital bovine spinal dysmyelination is caused by a missense mutation in the SPAST gene
31. Activating calcium-sensing receptor gene variants in children: a case study of infant hypocalcaemia and literature review
32. ASSESSMENT OF PLATELET FUNCTION BY A NEWLY DEVELOPED FLOW CYTOMETRY BASED ASSAY: 323
33. MicroRNA as Biomarkers for Platelet Function and Maturity in Patients with Cardiovascular Disease
34. Mutated Desmoglein-2 Proteins are Incorporated into Desmosomes and Exhibit Dominant-Negative Effects in Arrhythmogenic Right Ventricular Cardiomyopathy
35. Three family members with elevated plasma cobalamin, transcobalamin and soluble transcobalamin receptor (sCD320)
36. Sudden Cardiac Death in Young Adults: Environmental Risk Factors and Genetic Aspects of Premature Atherosclerosis*†
37. Multiplex ligation-dependent probe amplification (MLPA) screening for exon copy number variation in the calcium sensing receptor gene: no large rearrangements identified in patients with calcium metabolic disorders
38. Skeletal consequences of familial hypocalciuric hypercalcaemia vs. primary hyperparathyroidism
39. The relationship of molecular genetic to clinical diagnosis of familial hypercholesterolemia in a Danish population
40. Impact of centrifugation time and pneumatic tube transport on plasma concentrations of direct oral anticoagulants.
41. Platelet function assessed by ROTEM®platelet in patients receiving antiplatelet therapy during cardiac and vascular surgery.
42. Platelet function assessed by ROTEMVR® platelet in patients receiving antiplatelet therapy during cardiac and vascular surgery.
43. MicroRNA as Biomarkers for Platelet Function and Maturity in Patients with Cardiovascular Disease.
44. Discriminative power of three indices of renal calcium excretion for the distinction between familial hypocalciuric hypercalcaemia and primary hyperparathyroidism: a follow-up study on methods
45. Molecular Genetic Analysis of the Calcium Sensing Receptor Gene in Patients Clinically Suspected to Have Familial Hypocalciuric Hypercalcemia: Phenotypic Variation and Mutation Spectrum in a Danish Population
46. False low holotranscobalamin levels in a patient with a novel TCN2 mutation
47. Genetic mapping of spinal dysmyelination in cross-bred American Brown Swiss cattle to bovine Chromosome 11
48. The clinical outcome of LMNA missense mutations can be associated with the amount of mutated protein in the nuclear envelope
49. Expanding the spectrum of genetic variants in the calcium‐sensing receptor ( CASR ) gene in hypercalcemic individuals
50. Platelet microRNA expression and association with platelet maturity and function in patients with essential thrombocythemia
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