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PUBMED FOR HANDHELDS

Journal Abstract Search


629 related items for PubMed ID: 30270083

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  • 6. Clinical characterization and mutation spectrum of German patients with familial hypercholesterolemia.
    Grenkowitz T, Kassner U, Wühle-Demuth M, Salewsky B, Rosada A, Zemojtel T, Hopfenmüller W, Isermann B, Borucki K, Heigl F, Laufs U, Wagner S, Kleber ME, Binner P, März W, Steinhagen-Thiessen E, Demuth I.
    Atherosclerosis; 2016 Oct; 253():88-93. PubMed ID: 27596133
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  • 7. Next-generation-sequencing-based identification of familial hypercholesterolemia-related mutations in subjects with increased LDL-C levels in a latvian population.
    Radovica-Spalvina I, Latkovskis G, Silamikelis I, Fridmanis D, Elbere I, Ventins K, Ozola G, Erglis A, Klovins J.
    BMC Med Genet; 2015 Sep 28; 16():86. PubMed ID: 26415676
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  • 8. Next generation sequencing to identify novel genetic variants causative of autosomal dominant familial hypercholesterolemia associated with increased risk of coronary heart disease.
    Al-Allaf FA, Athar M, Abduljaleel Z, Taher MM, Khan W, Ba-Hammam FA, Abalkhail H, Alashwal A.
    Gene; 2015 Jul 01; 565(1):76-84. PubMed ID: 25839937
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  • 11. Genetic analysis of familial hypercholesterolaemia in Western Australia.
    Hooper AJ, Nguyen LT, Burnett JR, Bates TR, Bell DA, Redgrave TG, Watts GF, van Bockxmeer FM.
    Atherosclerosis; 2012 Oct 01; 224(2):430-4. PubMed ID: 22883975
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  • 13. Genetic analysis of familial hypercholesterolemia in Asian Indians: A single-center study.
    Setia N, Movva S, Balakrishnan P, Biji IK, Sawhney JPS, Puri R, Arora A, Puri RD, Saxena R, Mishra S, Apte S, Kulshrestha S, Ramprasad VL, Verma IC.
    J Clin Lipidol; 2020 Oct 01; 14(1):35-45. PubMed ID: 32044282
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  • 14. Cascade Screening for Familial Hypercholesterolemia in South Africa: The Wits FIND-FH Program.
    Raal FJ, Bahassi EM, Stevens B, Turner TA, Stein EA.
    Arterioscler Thromb Vasc Biol; 2020 Nov 01; 40(11):2747-2755. PubMed ID: 32878475
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  • 15. DIAgnosis and Management Of familial hypercholesterolemia in a Nationwide Design (DIAMOND-FH): Prevalence in Switzerland, clinical characteristics and the diagnostic value of clinical scores.
    Miserez AR, Martin FJ, Spirk D.
    Atherosclerosis; 2018 Oct 01; 277():282-288. PubMed ID: 30270060
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  • 17. The island of Gran Canaria: A genetic isolate for familial hypercholesterolemia.
    Sánchez-Hernández RM, Tugores A, Nóvoa FJ, Brito-Casillas Y, Expósito-Montesdeoca AB, Garay P, Bea AM, Riaño M, Pocovi M, Civeira F, Wägner AM, Boronat M.
    J Clin Lipidol; 2019 Oct 01; 13(4):618-626. PubMed ID: 31153816
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  • 18. Genetic Analysis in a Taiwanese Cohort of 750 Index Patients with Clinically Diagnosed Familial Hypercholesterolemia.
    Huang CC, Niu DM, Charng MJ.
    J Atheroscler Thromb; 2022 May 01; 29(5):639-653. PubMed ID: 33994402
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  • 19. The LDLR, APOB, and PCSK9 Variants of Index Patients with Familial Hypercholesterolemia in Russia.
    Meshkov A, Ershova A, Kiseleva A, Zotova E, Sotnikova E, Petukhova A, Zharikova A, Malyshev P, Rozhkova T, Blokhina A, Limonova A, Ramensky V, Divashuk M, Khasanova Z, Bukaeva A, Kurilova O, Skirko O, Pokrovskaya M, Mikova V, Snigir E, Akinshina A, Mitrofanov S, Kashtanova D, Makarov V, Kukharchuk V, Boytsov S, Yudin S, Drapkina O.
    Genes (Basel); 2021 Jan 06; 12(1):. PubMed ID: 33418990
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  • 20. Identification of New Genetic Determinants in Pediatric Patients with Familial Hypercholesterolemia Using a Custom NGS Panel.
    Rutkowska L, Sałacińska K, Salachna D, Matusik P, Pinkier I, Kępczyński Ł, Piotrowicz M, Starostecka E, Lewiński A, Gach A.
    Genes (Basel); 2022 Jun 01; 13(6):. PubMed ID: 35741760
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