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22 ta ish

Ish: Genetic yield of next-generation sequencing for detecting monogenic familial hypercholesterolemia in uzbek patients with coronary artery disease

  1. Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology

    Sue Richards, Nazneen Aziz, Sherri J. Bale +9

    Maqola20159 iqtibos
    ABI

  2. Familial hypercholesterolaemia is underdiagnosed and undertreated in the general population: guidance for clinicians to prevent coronary heart disease: Consensus Statement of the European Atherosclerosis Society

    Børge G. Nordestgaard, M. John Chapman, Steve E. Humphries +26

    MaqolaOchiq kirish20138 iqtibos
    ABI

  3. Familial Hypercholesterolemia in the Danish General Population: Prevalence, Coronary Artery Disease, and Cholesterol-Lowering Medication

    Marianne Benn, Gerald F. Watts, Anne Tybjærg‐Hansen +1

    Maqola20125 iqtibos
    ABI

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

    Antonio J. Vallejo‐Vaz, Christophe Stevens, Alexander R.M. Lyons +97

    MaqolaOchiq kirish20215 iqtibos
    ABI

  5. Clinical Genetic Testing for Familial Hypercholesterolemia

    Amy C. Sturm, Joshua W. Knowles, Samuel S. Gidding +29

    Sharh maqolaOchiq kirish20183 iqtibos
    ABI

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

    Kanika Dharmayat, Antonio J. Vallejo‐Vaz, Christophe Stevens +97

    MaqolaOchiq kirish20233 iqtibos
    ABI

  7. Homozygous familial hypercholesterolaemia: new insights and guidance for clinicians to improve detection and clinical management. A position paper from the Consensus Panel on Familial Hypercholesterolaemia of the European Atherosclerosis Society

    M. Cuchel, Éric Bruckert, H. N. Ginsberg +41

    Maqola20143 iqtibos
    ABI

  8. The Clinical Genome Resource (ClinGen) Familial Hypercholesterolemia Variant Curation Expert Panel consensus guidelines for LDLR variant classification

    Joana Rita Chora, Michael A. Iacocca, Lukáš Tichý +25

    Maqola20213 iqtibos
    ABI

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

    Antonio J. Vallejo‐Vaz, Martina De Marco, Christophe Stevens +82

    MaqolaOchiq kirishLipoproteins and Cardiovascular HealthAtherosclerosis20182 iqtibos
    ABI

  10. Sarlavhasiz

    Boshqa2 iqtibos
    ABI

  11. Burden of familial heterozygous hypercholesterolemia in Uzbekistan: Time is muscle

    Aleksandr B. Shek, Rano Alieva, R. D. Kurbanov +4

    MaqolaLipoproteins and Cardiovascular HealthAtherosclerosis20181 iqtibos
    ABI

  12. Overweight, obesity, and cardiovascular disease in heterozygous familial hypercholesterolaemia: the EAS FH Studies Collaboration registry

    Amany Elshorbagy, Antonio J. Vallejo‐Vaz, Fotios Barkas +80

    MaqolaOchiq kirishLipoproteins and Cardiovascular HealthEuropean Heart Journal20251 iqtibos
    ABI

  13. Sarlavhasiz

    Boshqa1 iqtibos
    ABI

  14. Sarlavhasiz

    Boshqa1 iqtibos
    ABI

  15. Sarlavhasiz

    Boshqa1 iqtibos
    ABI

  16. Sarlavhasiz

    Boshqa1 iqtibos
    ABI

  17. Sarlavhasiz

    Boshqa1 iqtibos
    ABI

  18. Sarlavhasiz

    Boshqa1 iqtibos
    ABI

  19. Sarlavhasiz

    Boshqa1 iqtibos
    ABI

  20. E670G PCSK9 polymorphism in HeFH & CAD with diabetes: is the bridge to personalized therapy within reach?

    Р Алиева, Aleksandr B. Shek, А. А. Абдуллаев +7

    MaqolaOchiq kirish20231 iqtibos
    ABI

  21. Sarlavhasiz

    Boshqa1 iqtibos
    ABI

  22. Sarlavhasiz

    Boshqa1 iqtibos
    ABI