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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2006 1
2008 2
2010 2
2011 1
2012 1
2013 3
2014 3
2015 9
2016 3
2017 2
2018 1
2019 1
2020 2
2021 5
2022 4
2023 2
2024 2

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39 results

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Page 1
Worldwide experience of homozygous familial hypercholesterolaemia: retrospective cohort study.
Tromp TR, Hartgers ML, Hovingh GK, Vallejo-Vaz AJ, Ray KK, Soran H, Freiberger T, Bertolini S, Harada-Shiba M, Blom DJ, Raal FJ, Cuchel M; Homozygous Familial Hypercholesterolaemia International Clinical Collaborators. Tromp TR, et al. Lancet. 2022 Feb 19;399(10326):719-728. doi: 10.1016/S0140-6736(21)02001-8. Epub 2022 Jan 28. Lancet. 2022. PMID: 35101175 Free PMC article.
Phenotypic expansion of the BPTF-related neurodevelopmental disorder with dysmorphic facies and distal limb anomalies.
Glinton KE, Hurst ACE, Bowling KM, Cristian I, Haynes D, Adstamongkonkul D, Schnappauf O, Beck DB, Brewer C, Parikh AS, Shinde DN, Donaldson A, Brautbar A, Koene S, van Haeringen A, Piton A, Capri Y, Furlan M, Gardella E, Møller RS, van de Beek I, Zuurbier L, Lakeman P, Bayat A, Martinez J, Signer R, Torring PM, Engelund MB, Gripp KW, Amlie-Wolf L, Henderson LB, Midro AT, Tarasów E, Stasiewicz-Jarocka B, Moskal-Jasinska D, Vos P, Boschann F, Stoltenburg C, Puk O, Mero IL, Lossius K, Mignot C, Keren B, Acosta Guio JC, Briceño I, Gomez A, Yang Y, Stankiewicz P. Glinton KE, et al. Among authors: zuurbier l. Am J Med Genet A. 2021 May;185(5):1366-1378. doi: 10.1002/ajmg.a.62102. Epub 2021 Jan 31. Am J Med Genet A. 2021. PMID: 33522091 Free PMC article.
Sex Differences in Diagnosis, Treatment, and Cardiovascular Outcomes in Homozygous Familial Hypercholesterolemia.
Mulder JWCM, Tromp TR, Al-Khnifsawi M, Blom DJ, Chlebus K, Cuchel M, D'Erasmo L, Gallo A, Hovingh GK, Kim NT, Long J, Raal FJ, Schonck WAM, Soran H, Truong TH, Boersma E, Roeters van Lennep JE; Homozygous Familial Hypercholesterolemia International Clinical Collaborators. Mulder JWCM, et al. JAMA Cardiol. 2024 Apr 1;9(4):313-322. doi: 10.1001/jamacardio.2023.5597. JAMA Cardiol. 2024. PMID: 38353972
Low-Cost High-Throughput Genotyping for Diagnosing Familial Hypercholesterolemia.
Ibrahim S, van Rooij J, Verkerk AJMH, de Vries J, Zuurbier L, Defesche J, Peter J, Schonck WAM, Sedaghati-Khayat B, Kees Hovingh G, Uitterlinden AG, Stroes ESG, Reeskamp LF. Ibrahim S, et al. Among authors: zuurbier l. Circ Genom Precis Med. 2023 Oct;16(5):462-469. doi: 10.1161/CIRCGEN.123.004103. Epub 2023 Sep 7. Circ Genom Precis Med. 2023. PMID: 37675602 Free PMC article.
Three authors reply.
Zuurbier LA, Kocevska D, Tiemeier H. Zuurbier LA, et al. Am J Epidemiol. 2015 Sep 1;182(5):470-1. doi: 10.1093/aje/kwv192. Epub 2015 Aug 18. Am J Epidemiol. 2015. PMID: 26290573 No abstract available.
ABCG5 and ABCG8 genetic variants in familial hypercholesterolemia.
Reeskamp LF, Volta A, Zuurbier L, Defesche JC, Hovingh GK, Grefhorst A. Reeskamp LF, et al. Among authors: zuurbier l. J Clin Lipidol. 2020 Mar-Apr;14(2):207-217.e7. doi: 10.1016/j.jacl.2020.01.007. Epub 2020 Jan 29. J Clin Lipidol. 2020. PMID: 32088153
Next-generation sequencing to confirm clinical familial hypercholesterolemia.
Reeskamp LF, Tromp TR, Defesche JC, Grefhorst A, Stroes ES, Hovingh GK, Zuurbier L. Reeskamp LF, et al. Among authors: zuurbier l. Eur J Prev Cardiol. 2020 Jul 27:2047487320942996. doi: 10.1177/2047487320942996. Online ahead of print. Eur J Prev Cardiol. 2020. PMID: 32718233 Free article.
39 results