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

5. Clinical Characteristics of Homozygous Familial Hypercholesterolemia in Japan: A Survey Using a National Database

11. Worldwide experience of homozygous familial hypercholesterolaemia: retrospective cohort study

13. Increase of serum uric acid levels associated with APOE ε2 haplotype: a clinico-genetic investigation and in vivo approach

15. Global perspective of familial hypercholesterolaemia: a cross-sectional study from the EAS Familial Hypercholesterolaemia Studies Collaboration (FHSC)

18. The Association of the Cholesterol Efflux Capacity with the Paraoxonase 1 Q192R Genotype and the Paraoxonase Activity

20. Obicetrapib as an Adjunct to Stable Statin Therapy in Japanese Subjects: Results from a Randomized Phase 2 Trial

21. Impaired Cholesterol Efflux Capacity rather than Low HDL-C Reflects Oxidative Stress under Acute Myocardial Infarction

22. Transitional Medicine of Intractable Primary Dyslipidemias in Japan

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

30. Serum Values of Cholesterol Absorption and Synthesis Biomarkers in Japanese Healthy Subjects: The CACHE Study HEALTHY Analysis

33. HOFH is a life limiting condition: The life journey of deceased HOFH patients in the HICC registry

39. Overview of the current status of familial hypercholesterolaemia care in over 60 countries - The EAS Familial Hypercholesterolaemia Studies Collaboration (FHSC)

41. Association between Familial Hypercholesterolemia and Serum Levels of Cholesterol Synthesis and Absorption Markers: The CACHE Study FH Analysis

42. Clinical Characteristics of Homozygous Familial Hypercholesterolemia in Japan

43. Clinical Genetic Testing for Familial Hypercholesterolemia: JACC Scientific Expert Panel

45. Autosomal Recessive Hypercholesterolemia: Long-Term Cardiovascular Outcomes

47. 2023 Update on European Atherosclerosis Society Consensus Statement on Homozygous Familial Hypercholesterolaemia: new treatments and clinical guidance

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