Identificación de variantes genéticas asociadas a hipercolesterolemia familiar en niños y adolescentes de la Región del Biobío, Chile

Sánchez, Andrea; Bustos, Paulina; Honorato, Paula; Sáez, Katia; Elim-Jannes, Cinthia; Barriga, Natalia; Ibieta, Guillermo; Pérez, Luis; Alonso, Rodrigo; Radojkovic, Claudia; Asenjo, Sylvia.
Rev. méd. Chile ; 149(9): 1267-1274, sept. 2021. tab, graf, ilus
Artículo en Español | LILACS | ID: biblio-1389597

Documentos relacionados

  1. Genetic Testing for Familial Hypercholesterolemia in Clinical Practice.
  2. The Clinical Importance of Differentiating Monogenic Familial Hypercholesterolemia from Polygenic Hypercholesterolemia.
  3. Novel LDLR variants affecting low density lipoprotein metabolism identified in familial hypercholesterolemia.
  4. Diagnosis of Familial Hypercholesterolemia in Children and Young Adults.
  5. Genetic identification of familial hypercholesterolemia within whole genome sequences in 6820 newborns.
  6. Population-based screening in children for early diagnosis and treatment of familial hypercholesterolemia: design of the VRONI study.
  7. Analysis of Clinical and Biochemical Characteristics of Patients With Genetically Confirmed Familial Hypercholesterolemia in Russian North Western District Residents.
  8. Search for familial hypercholesterolemia patients in an Italian community: A real-life retrospective study.
  9. Cascade screening for familial hypercholesterolemia should be organized at a national level.
  10. Evinacumab for Pediatric Patients With Homozygous Familial Hypercholesterolemia.