Familial Hypercholesterolemia: Screening, diagnosis and management of pediatric and adult patients

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Items 101–200 of 622

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  19. Challenges in the Diagnosis and Treatment of Homozygous Familial Hypercholesterolemia
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  32. Screening for familial hypercholesterolaemia in primary care: Time for general practice to play its part
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  36. Existing and emerging therapies for the treatment of familial hypercholesterolemia
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  37. Improved cardiovascular outcomes following temporal advances in lipid-lowering therapy in a genetically-characterised cohort of familial hypercholesterolaemia homozygotes
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  38. The genetics of familial hypercholesterolemia and emerging therapies
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  39. Effectiveness of alternative strategies to define index case phenotypes to aid genetic diagnosis of familial hypercholesterolaemia
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  40. LOWER, a registry of lomitapide-treated patients with homozygous familial hypercholesterolemia: Rationale and design
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  41. Pediatric experience with mipomersen as adjunctive therapy for homozygous familial hypercholesterolemia
    Frederick Johan Raal, Marjet J.A.M. Braamskamp, Sheryl Selvey, Charlotte Sensinger, John J.P. Kastelein · 2016 · Journal of clinical lipidology
  42. The lipid-lowering effects of lomitapide are unaffected by adjunctive apheresis in patients with homozygous familial hypercholesterolaemia – A post-hoc analysis of a Phase 3, single-arm, open-label trial
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  43. High burden of recurrent cardiovascular events in heterozygous familial hypercholesterolemia: The French Familial Hypercholesterolemia Registry
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  47. Early diagnosis and treatment of familial hypercholesterolemia: improving patient outcomes
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  48. Statins decrease the risk of stroke in individuals with heterozygous familial hypercholesterolemia: A systematic review and meta-analysis
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  49. My Approach to the Patient With Familial Hypercholesterolemia
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  54. Familial hypercholesterolemia and estimation of US patients eligible for low-density lipoprotein apheresis after maximally tolerated lipid-lowering therapy
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  57. A 3-year study of atorvastatin in children and adolescents with heterozygous familial hypercholesterolemia
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  61. Barriers and Facilitators to Genetic Testing for Familial Hypercholesterolemia in the United States: A Review
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  63. Early Prevention of Atherosclerosis: Detection and Management of Hypercholesterolaemia in Children and Adolescents
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