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.

مصطلحات موضوعية: Heterozygous Familial Hypercholesterolaemia, Mutation Spectrum, LDL-C Concentrations, Statin Treatment, Europe, Portugal, Doenças Cardio e Cérebro-vasculares

العلاقة: SFRH/BD/113017/2015; https://www.atherosclerosis-journal.com/article/S0021-9150Test(21)00008-3/fulltext; Atherosclerosis. 2021 Feb;319:108-117. doi:10.1016/j.atherosclerosis.2021.01.008. Epub 2021 Jan 13.; http://hdl.handle.net/10400.18/7993Test

الإتاحة: https://doi.org/10.1016/j.atherosclerosis.2021.01.008Test
http://hdl.handle.net/10400.18/7993Test

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

المؤلفون: Futema, M, Ramaswami, U, Tichy, L, Bogsrud, MP, Holven, KB, van Lennep, JR, Wiegman, A, Descamps, OS, De Leener, A, Fastre, E, Vrablik, M, Freiberger, T, Esterbauer, H, Dieplinger, H, Greber-Platzer, S, Medeiros, AM, Bourbon, M, Mollaki, V, Drogari, E, Humphries, SE

المصدر: Atherosclerosis , 319 pp. 108-117. (2021)

مصطلحات موضوعية: Heterozygous familial hypercholesterolaemia, Mutation spectrum, LDL-C concentrations, Statin treatment

وصف الملف: text

العلاقة: https://discovery.ucl.ac.uk/id/eprint/10124727/1/Futema_adjusted_ATH-D-20-00178_R2.pdfTest; https://discovery.ucl.ac.uk/id/eprint/10124727Test/

الإتاحة: https://discovery.ucl.ac.uk/id/eprint/10124727/1/Futema_adjusted_ATH-D-20-00178_R2.pdfTest
https://discovery.ucl.ac.uk/id/eprint/10124727Test/

المؤلفون: Ramaswami, U. (Uma), Futema, M. (Marta), Bogsrud, M.P. (Martin P.), Holven, K.B. (Kirsten B.), Roeters van Lennep, J.E. (Jeanine), Wiegman, A. (Albert), Descamps, O.S. (Olivier S.), Vrablik, M. (Michal), Freiberger, T. (Tomáš), Dieplinger, H. (Hans), Greber-Platzer, S. (Susanne), Hanauer-Mader, G. (Gabriele), Bourbon, M. (Mafalda), Drogari, E. (Euridiki), Humphries, S.E. (Steve)

المصدر: Atherosclerosis vol. 292, pp. 178-187

مصطلحات موضوعية: Heterozygous familial hypercholesterolaemia, LDL-C concentrations, Paediatric FH, Statin treatment

وصف الملف: application/pdf

العلاقة: http://repub.eur.nl/pub/122151Test; urn:hdl:1765/122151

الإتاحة: https://doi.org/10.1016/j.atherosclerosis.2019.11.012Test
http://repub.eur.nl/pub/122151Test

المؤلفون: Ramaswami, U, Futema, M, Bogsrud, MP, Holven, KB, Roeters van Lennep, J, Wiegman, A, Descamps, OS, Vrablik, M, Freiberger, T, Dieplinger, H, Greber-Platzer, S, Hanauer-Mader, G, Bourbon, M, Drogari, E, Humphries, SE

المصدر: Atherosclerosis , 292 pp. 178-187. (2020)

مصطلحات موضوعية: Heterozygous familial hypercholesterolaemia, Paediatric FH, LDL-C concentrations, Statin treatment

وصف الملف: text

العلاقة: https://discovery.ucl.ac.uk/id/eprint/10086523/1/Humphries_Comparison%20of%20the%20characteristics%20at%20diagnosis%20and%20treatment%20of%20children%20with%20heterozygous%20familial%20hypercholesterolaemia%20%28FH%29%20from%20eight%20European%20countries_VoR.pdfTest; https://discovery.ucl.ac.uk/id/eprint/10086523Test/

الإتاحة: https://discovery.ucl.ac.uk/id/eprint/10086523/1/Humphries_Comparison%20of%20the%20characteristics%20at%20diagnosis%20and%20treatment%20of%20children%20with%20heterozygous%20familial%20hypercholesterolaemia%20%28FH%29%20from%20eight%20European%20countries_VoR.pdfTest
https://discovery.ucl.ac.uk/id/eprint/10086523Test/

المؤلفون: Humphries, Steve E., Ramaswami, Uma, Futema, Marta, Bogsrud, Martin P., Holven, Kirsten B., Roeters van Lennep, Jeanine, Wiegman, Albert, Descamps, Olivier S., Vrablik, Michal, Freiberger, Tomas, Dieplinger, Hans, Greber-Platzer, Susanne, Hanauer-Mader, Gabriele, Bourbon, Mafalda, Drogari, Euridiki

مصطلحات موضوعية: Heterozygous familial hypercholesterolaemia, Paediatric FH, LDL-C concentrations, Statin treatment

جغرافية الموضوع: UMW:14638

وصف الملف: text/html

العلاقة: vignette : https://repositorium.meduniwien.ac.at/titlepage/urn/urn:nbn:at:at-ubmuw:3-63181/128Test; urn:nbn:at:at-ubmuw:3-63181; https://resolver.obvsg.at/urn:nbn:at:at-ubmuw:3-63181Test; local:99147059240503331; system:AC16701448

الإتاحة: https://doi.org/10.1016/j.atherosclerosis.2019.11.012Test
https://resolver.obvsg.at/urn:nbn:at:at-ubmuw:3-63181Test

المؤلفون: Kirsten B. Holven, Mafalda Bourbon, Tomáš Freiberger, Olivier S. Descamps, Susanne Greber-Platzer, Albert Wiegman, Jeanine E. Roeters van Lennep, Michal Vrablík, Gabriele Hanauer-Mader, Marta Futema, Euridiki Drogari, Uma Ramaswami, Hans Dieplinger, Martin Prøven Bogsrud, Steve E. Humphries

المساهمون: Cardiology, Internal Medicine, Paediatric Metabolic Diseases, AGEM - Amsterdam Gastroenterology Endocrinology Metabolism, ACS - Heart failure & arrhythmias, ACS - Diabetes & metabolism, ACS - Atherosclerosis & ischemic syndromes

المصدر: Atherosclerosis, 292, 178-187. Elsevier Ireland Ltd
Atherosclerosis

مصطلحات موضوعية: Male, 0301 basic medicine, Heterozygote, Pediatrics, medicine.medical_specialty, Statin, Statin treatment, medicine.drug_class, Heterozygous familial hypercholesterolaemia, Paediatric FH, Age at diagnosis, Low density lipoprotein cholesterol, Heterozygous Familial Hypercholesterolaemia, 030204 cardiovascular system & hematology, Article, Doenças Cardio e Cérebro-vasculares, Hyperlipoproteinemia Type II, LDL-C concentrations, 03 medical and health sciences, 0302 clinical medicine, Ezetimibe, Humans, Medicine, Child, Retrospective Studies, business.industry, Cholesterol, LDL, Statin Treatment, Treatment characteristics, 3. Good health, Europe, 030104 developmental biology, Lifestyle advice, Child, Preschool, Female, lipids (amino acids, peptides, and proteins), Statin therapy, Hydroxymethylglutaryl-CoA Reductase Inhibitors, Cardiology and Cardiovascular Medicine, business, LDL-C Concentrations, medicine.drug

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::61124bbc44f5e8d6ec46d690f10c2cb7Test
https://doi.org/10.1016/j.atherosclerosis.2019.11.012Test

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

المؤلفون: Ramaswami, Uma, Futema, Marta, Bogsrud, Martin P., Holven, Kirsten B., Roeters van Lennep, Jeanine, Wiegman, Albert, Descamps, Olivier S., Vrablik, Michal, Freiberger, Tomas, Dieplinger, Hans, Greber-Platzer, Susanne, Hanauer-Mader, Gabriele, Bourbon, Mafalda, Drogari, Euridiki, Humphries, Steve E.

المساهمون: Repositório Científico do Instituto Nacional de Saúde

مصطلحات موضوعية: Heterozygous Familial Hypercholesterolaemia, LDL-C Concentrations, Paediatric FH, Statin Treatment, Doenças Cardio e Cérebro-vasculares

وصف الملف: application/pdf

العلاقة: Atherosclerosis. 2020 Jan;292:178-187. doi: 10.1016/j.atherosclerosis.2019.11.012. Epub 2019 Nov 15; 0021-9150

الإتاحة: http://hdl.handle.net/10400.18/6610Test

المصدر: Atherosclerosis, Vol. 319, no.319, p. 108-117 (2021)

مصطلحات الفهرس: 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, info:eu-repo/semantics/article

URL: http://hdl.handle.net/2078.1/261190Test