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4. Ethnic Diversity and Distinctive Features of Familial Versus Multifactorial Chylomicronemia Syndrome: Insights From the UK FCS National Registry

6. Soluble Epoxide Hydrolase Derived Linoleic Acid Oxylipins, Small Vessel Disease Markers, and Neurodegeneration in Stroke

8. Association of BMI, lipid-lowering medication, and age with prevalence of type 2 diabetes in adults with heterozygous familial hypercholesterolaemia: a worldwide cross-sectional study

9. International Atherosclerosis Society guidance for implementing best practice in the care of familial hypercholesterolaemia

10. Prevention and Management of Cardiovascular Disease in Primary Care: A Comment on the PEER Simplified Lipid Guideline

12. Contributors

16. Expanding the phenotypic and molecular spectrum of NFS1‐related disorders that cause functional deficiencies in mitochondrial and cytosolic iron–sulfur cluster containing enzymes

26. Familial hypercholesterolaemia in children and adolescents from 48 countries: a cross-sectional study

27. Extreme LDL-C concentration is associated with increased cardiovascular disease in women with homozygous familial hypercholesterolemia

28. Implementation of a Kidney Genetic Service Into the Diagnostic Pathway for Patients With CKD in Canada

33. Improving reporting standards for polygenic scores in risk prediction studies

36. Intermittent chylomicronemia caused by intermittent GPIHBP1 autoantibodies

44. Disorders of Lipoprotein Metabolism

48. Ankyrin-B dysfunction predisposes to arrhythmogenic cardiomyopathy and is amenable to therapy

49. Guidance for the diagnosis and treatment of hypolipidemia disorders

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