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1دورية أكاديمية
المؤلفون: Futema, Marta, Ramaswami, Uma, Tichy, Lukas, Bogsrud, Martin P, Holven, Kirsten B, Roeters van Lennep, Jeanine, Wiegman, Albert, Descamps, Olivier S, De Leener, Anne, Fastre, Elodie, Vrablik, Michal, Freiberger, Tomas, Esterbauer, Harald, Dieplinger, Hans, Greber-Platzer, Susanne, Medeiros, Ana M, Bourbon, Mafalda, Mollaki, Vasiliki, Drogari, Euridiki, Humphries, Steve E
المساهمون: UCL - SSS/IREC/SLUC - Pôle St.-Luc, UCL - SSS/DDUV/SIGN - Cell signalling, UCL - (SLuc) Centre de génétique médicale UCL
المصدر: Atherosclerosis, Vol. 319, p. 108-117 (2021)
مصطلحات موضوعية: Austria, Belgium, Child, Czech Republic, DNA Mutational Analysis, Europe, Greece, Humans, Hyperlipoproteinemia Type II, Lipids, Mutation, Netherlands, Norway, Portugal, Proprotein Convertase 9, Receptors, LDL, Heterozygous familial hypercholesterolaemia, LDL-C concentrations, Mutation spectrum, Statin treatment
العلاقة: boreal:261190; http://hdl.handle.net/2078.1/261190Test; info:pmid/33508743; urn:ISSN:0021-9150; urn:EISSN:1879-1484
الإتاحة: https://doi.org/10.1016/j.atherosclerosis.2021.01.008Test
http://hdl.handle.net/2078.1/261190Test -
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المؤلفون: Martin Prøven Bogsrud, Albert Wiegman, Elodie Fastré, Tomáš Freiberger, Jeanine E. Roeters van Lennep, Anne De Leener, Olivier S. Descamps, Kirsten B. Holven, Steve E. Humphries, Vasiliki Mollaki, Michal Vrablík, Lukas Tichy, Hans Dieplinger, Harald Esterbauer, Marta Futema, Euridiki Drogari, Ana Margarida Medeiros, Susanne Greber-Platzer, Uma Ramaswami, Mafalda Bourbon
المساهمون: Paediatric Metabolic Diseases, ACS - Diabetes & metabolism, Amsterdam Gastroenterology Endocrinology Metabolism, ACS - Heart failure & arrhythmias, ACS - Atherosclerosis & ischemic syndromes, Cardiology, Internal Medicine, UCL - SSS/IREC/SLUC - Pôle St.-Luc, UCL - SSS/DDUV/SIGN - Cell signalling, UCL - (SLuc) Centre de génétique médicale UCL
المصدر: Atherosclerosis, 319, 108-117. Elsevier Ireland Ltd
Atherosclerosis, Vol. 319, p. 108-117 (2021)مصطلحات موضوعية: 0301 basic medicine, Apolipoprotein B, DNA Mutational Analysis, Heterozygous Familial Hypercholesterolaemia, 030204 cardiovascular system & hematology, Doenças Cardio e Cérebro-vasculares, LDL-C concentrations, 0302 clinical medicine, Belgium, Low density, Mutation Spectrum, Medicine, Family history, Child, Pre and post, Czech Republic, Netherlands, Greece, biology, Norway, Statin Treatment, Lipids, 3. Good health, Europe, Austria, Mutation (genetic algorithm), lipids (amino acids, peptides, and proteins), Proprotein Convertase 9, Cardiology and Cardiovascular Medicine, LDL-C Concentrations, medicine.medical_specialty, Statin treatment, Heterozygous familial hypercholesterolaemia, Hyperlipoproteinemia Type II, 03 medical and health sciences, Mutation spectrum, Internal medicine, Humans, Portugal, business.industry, PCSK9, nutritional and metabolic diseases, 030104 developmental biology, Receptors, LDL, Mutation, LDL receptor, biology.protein, business
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b9ca2e1be952f46244c5d3eebc8850aeTest
https://pure.amc.nl/en/publications/comparison-of-the-mutation-spectrum-and-association-with-pre-and-post-treatment-lipid-measures-of-children-with-heterozygous-familial-hypercholesterolaemia-fh-from-eight-european-countriesTest(ffdaf067-8c49-425c-a03d-6fa0d6ba5def).html