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Journal Abstract Search

538 related items for PubMed ID: 30270076

  • 1. Homozygous familial hypercholesterolaemia in Vietnam: Case series, genetics and cascade testing of families.
    Truong TH, Kim NT, Nguyen MNT, Pang J, Hooper AJ, Watts GF, Do DL.
    Atherosclerosis; 2018 Oct; 277():392-398. PubMed ID: 30270076
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  • 2. Clinical experience of scoring criteria for Familial Hypercholesterolaemia (FH) genetic testing in Wales.
    Haralambos K, Whatley SD, Edwards R, Gingell R, Townsend D, Ashfield-Watt P, Lansberg P, Datta DB, McDowell IF.
    Atherosclerosis; 2015 May; 240(1):190-6. PubMed ID: 25797312
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  • 3. Identification of a novel LDLR disease-causing variant using capture-based next-generation sequencing screening of familial hypercholesterolemia patients in Taiwan.
    Hsiung YC, Lin PC, Chen CS, Tung YC, Yang WS, Chen PL, Su TC.
    Atherosclerosis; 2018 Oct; 277():440-447. PubMed ID: 30270083
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  • 4. Novel combined variants of LDLR and LDLRAP1 genes causing severe familial hypercholesterolemia.
    Alnouri F, Athar M, Al-Allaf FA, Abduljaleel Z, Taher MM, Bouazzaoui A, Al Ammari D, Karrar H, Albabtain M.
    Atherosclerosis; 2018 Oct; 277():425-433. PubMed ID: 30270081
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  • 5. Long-term outcome in 53 patients with homozygous familial hypercholesterolaemia in a single centre in France.
    Bruckert E, Kalmykova O, Bittar R, Carreau V, Béliard S, Saheb S, Rosenbaum D, Bonnefont-Rousselot D, Thomas D, Emery C, Khoshnood B, Carrié A.
    Atherosclerosis; 2017 Feb; 257():130-137. PubMed ID: 28131047
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  • 6. Health related quality of life in individuals at high risk for familial hypercholesterolemia undergoing genetic cascade screening in Brazil.
    Souto AC, Miname MH, Fukushima J, Jannes CE, Krieger JE, Hagger M, Pereira AC, Santos RD.
    Atherosclerosis; 2018 Oct; 277():464-469. PubMed ID: 30270086
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  • 7. Probabilistic cost-effectiveness analysis of cascade screening for familial hypercholesterolaemia using alternative diagnostic and identification strategies.
    Nherera L, Marks D, Minhas R, Thorogood M, Humphries SE.
    Heart; 2011 Jul; 97(14):1175-81. PubMed ID: 21685482
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  • 10. Reverse cascade screening for familial hypercholesterolemia in high-risk Chinese families.
    Wu X, Pang J, Wang X, Peng J, Chen Y, Wang S, Watts GF, Lin J.
    Clin Cardiol; 2017 Nov; 40(11):1169-1173. PubMed ID: 29168983
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  • 12. Spectrum of mutations in homozygous familial hypercholesterolemia in India, with four novel mutations.
    Setia N, Saxena R, Arora A, Verma IC.
    Atherosclerosis; 2016 Dec; 255():31-36. PubMed ID: 27816806
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  • 13. Molecular genetics of familial hypercholesterolemia in Israel-revisited.
    Durst R, Ibe UK, Shpitzen S, Schurr D, Eliav O, Futema M, Whittall R, Szalat A, Meiner V, Knobler H, Gavish D, Henkin Y, Ellis A, Rubinstein A, Harats D, Bitzur R, Hershkovitz B, Humphries SE, Leitersdorf E.
    Atherosclerosis; 2017 Feb; 257():55-63. PubMed ID: 28104544
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  • 14. Long-Term Cardiovascular Risk in Heterozygous Familial Hypercholesterolemia Relatives Identified by Cascade Screening.
    Kjærgaard KA, Christiansen MK, Schmidt M, Olsen MS, Jensen HK.
    J Am Heart Assoc; 2017 Jun 26; 6(6):. PubMed ID: 28652386
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  • 15. Integrated guidance on the care of familial hypercholesterolaemia from the International FH Foundation.
    Watts GF, Gidding S, Wierzbicki AS, Toth PP, Alonso R, Brown WV, Bruckert E, Defesche J, Lin KK, Livingston M, Mata P, Parhofer KG, Raal FJ, Santos RD, Sijbrands EJ, Simpson WG, Sullivan DR, Susekov AV, Tomlinson B, Wiegman A, Yamashita S, Kastelein JJ, International Familial Hypercholesterolemia Foundation.
    Eur J Prev Cardiol; 2015 Jul 26; 22(7):849-54. PubMed ID: 24776375
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