Zobrazeno 1 - 10
of 78
pro vyhledávání: '"Lipoprotein disorder"'
Publikováno v:
TNOA Journal of Ophthalmic Science and Research, Vol 59, Iss 2, Pp 178-180 (2021)
A 44-year-old female patient presented to our department with bilateral corneal opacity since childhood. History of similar complaints was elicited among her family members. Best-corrected visual acuity in both eyes was 6/9 with bilateral stromal cor
Externí odkaz:
https://doaj.org/article/900e7c8d8eec4a77aa11fd30e78ff89a
Akademický článek
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Publikováno v:
Berkala Penelitian Hayati. 24:84-89
Olive (Olea europaea) have been cultivated and grown well in tropical climates such as Indonesia. Indonesia local community have used olive as herbal medicines due to its active compounds known as oleuropein that has many biological activities includ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2e7652ec5e987dafe0f52d92e267cd95
https://doi.org/10.23869/bphjbr.24.1.20194
https://doi.org/10.23869/bphjbr.24.1.20194
Autor:
Nicole Soranzo, Eleftheria Zeggini, Emanuele Di Angelantonio, Interval Study, Kousik Kundu, Adam S. Butterworth, Fernando Riveros-Mckay, Willem H. Ouwehand, Clare Oliver-Williams, Klaudia Walter, Inês Barroso, Eleanor Wheeler, John Danesh, Savita Karthikeyan, David J. Roberts
Publikováno v:
PLoS Genetics, Vol 16, Iss 3, p e1008605 (2020)
PLoS Genetics
PLoS Genet. 16:e1008605 (2020)
PLoS Genetics
PLoS Genet. 16:e1008605 (2020)
Circulating metabolite levels are biomarkers for cardiovascular disease (CVD). Here we studied, association of rare variants and 226 serum lipoproteins, lipids and amino acids in 7,142 (discovery plus follow-up) healthy participants. We leveraged the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::117d076a05c4ba1621ec1e6d1e5d92b9
https://doaj.org/article/f81347d66d174b55a9280f39db55ed9f
https://doaj.org/article/f81347d66d174b55a9280f39db55ed9f
Publikováno v:
TNOA Journal of Ophthalmic Science and Research, Vol 59, Iss 2, Pp 178-180 (2021)
A 44-year-old female patient presented to our department with bilateral corneal opacity since childhood. History of similar complaints was elicited among her family members. Best-corrected visual acuity in both eyes was 6/9 with bilateral stromal cor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f5f280fd8ca8cba4dcc8850f1c07460c
https://doi.org/10.4103/tjosr.tjosr_184_20
https://doi.org/10.4103/tjosr.tjosr_184_20
Autor:
Ann Verhaegen, Olivier Van Caenegem, Raymond Kacenelenbogen, Michel Guillaume, Fabian Demeure, Caroline Wallemacq, Olivier Vanakker, Anna A.H. Mertens, Michel Hermans, Antoine Bondue, Anne De Leener, Stephane Carlier, Walter Desmet, Pieter Vermeersch, Ernst Rietzschel, Ivan Elegeert, Fabien Chenot, Jean-Louis Vanoverschelde, Emilie Castermans, Christophe Beauloye, Olivier S. Descamps, Antoine De Meester, E. Hoffer, Christophe De Block, Marc J. Claeys, Jean-Luc Balligand, Nicolas Paquot, Attilio Leone, Michel Langlois, Herbert De Raedt, Patrizio Lancellotti
Publikováno v:
Atherosclerosis
Atherosclerosis, 277
Atherosclerosis, Vol. 277, p. 369-376 (2018)
Atherosclerosis, 277
Atherosclerosis, Vol. 277, p. 369-376 (2018)
Background and aims: Familial hypercholesterolaemia (FH) is an autosomal dominant lipoprotein disorder characterized by significant elevation of low-density lipoprotein cholesterol (LDL-C) and markedly increased risk of premature cardiovascular disea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5fa7fe6a13da8ba1575f688d75a2eeb4
https://lirias.kuleuven.be/handle/123456789/629864
https://lirias.kuleuven.be/handle/123456789/629864
Autor:
Jae-Hong Lee, Seong-Nyum Jeong
Publikováno v:
Medicina, Vol 56, Iss 575, p 575 (2020)
Medicina; Volume 56; Issue 11; Pages: 575
Medicina
Volume 56
Issue 11
Medicina; Volume 56; Issue 11; Pages: 575
Medicina
Volume 56
Issue 11
This study determined the association between periodontal disease (PD) and major lifestyle-related comorbidities (LCs) using the database of the nationwide population-based National Health Insurance Service&ndash
Elderly Cohort 2002&ndash
2
Elderly Cohort 2002&ndash
2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fcdf1ba72e0960cd9fe3f21de505be1a
https://doi.org/10.3390/medicina56110575
https://doi.org/10.3390/medicina56110575
Autor:
A. Zamora Cervantes, José Luis Díaz-Díaz, L. Pérez García, N. Plana Gil, L. Reinares García, Elisenda Climent, Rosa M. Sánchez-Hernández, D. Zambón Rados, E. Ortega Martínez de la Victoria, C. Guerrero Buitrago, R. Mateo Gallego, José Rioja, F. Almagro Múgica, María José Ariza Corbo, S. Zabala López, L. Masana Martín, J. Amor, F. Civeira Murillo, Ovidio Muñiz-Grijalvo, I. Lamiquiz-Moneo, M.J. Romero Jiménez, M.A. Sánchez-Chaparro, Pedro Saenz, E. Martorell Mateu, V. Marco Benedí, María José Ariza, M.P. González García, O. Muñiz Grijalvo, F.J. Novoa Mogollón, A. Blanco Echevarría, A. Brea Hernando, Alipio Mangas, M. Suárez Tembra, L. Vila, C. Rodríguez Borjabad, V. Perea Castillo, E. Llargués Rocabruna, Gonzalo Pías Iglesias, P. Sáenz Aranzubía, Xavier Pintó, Carlos Lahoz, J. Ferrando Vela, Daiana Ibarretxe, M. Mauri Pont, M. Bueno Díez, J. Pedro-Botet, C. Morales Coca, Ana Camacho, J.M. Ramiro Lozano, J. Mostaza Prieto, D. Ibarretxe Gerediaga, J. Rioja Villodres, Daniel Mosquera, I. Soler, F.J. Fuentes Jiménez, F. Blanco Vaca, Pablo Ruiz-Ocaña, C. Ferrer, J.F. Ascaso Gimilio, S. Pérez-Calahorra, A.B. Expósito Montesdeoca, J.A. Carbayo Herencia, A. Hernández Mijares, A. Vila Belmonte, Sofía Pérez-Calahorra, Pedro Valdivielso, J. Millán Núñez-Cortés, Itziar Lamiquiz-Moneo, Julio A. Carbayo-Herencia, Luis Masana, S. Jansen Chaparro
Publikováno v:
Journal of clinical lipidology. 12(6)
Background Familial chylomicronemia syndrome (FCS) is an extremely rare lipoprotein disorder caused by mutations in at least 5 genes of the lipoprotein lipase (LPL) complex. Objective This work shows the molecular analysis of patients diagnosed with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b3befe82cd0721ad2ef61059cead7677
https://pubmed.ncbi.nlm.nih.gov/30150141
https://pubmed.ncbi.nlm.nih.gov/30150141
Autor:
Gerald F. Watts, Jean Bergeron, G.B. John Mancini, Paolo Raggi, Jack V. Tu, Robert A. Hegele, Milan Gupta, Sumayah Aljenedil, Jing Pang, Robert Dufour, Alexandre M. Bélanger, Jiri Frohlich, Patrick Couture, David Bewick, Brian W. McCrindle, Claude Gagné, Alexis Baass, Jacques Genest, James M. Brophy, Gordon A. Francis, Liam R. Brunham, Isabelle Ruel, Diane Brisson, Jean Grégoire, Zuhier Awan, Daniel Gaudet
Publikováno v:
The Canadian journal of cardiology. 34(9)
Familial hypercholesterolemia (FH) is an autosomal codominant lipoprotein disorder characterized by elevated low-density lipoprotein cholesterol (LDL-C) and high risk of premature atherosclerotic cardiovascular disease. Definitions for FH rely on com
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::81eb9765d21a82d22bae1afb11707b95
https://pubmed.ncbi.nlm.nih.gov/30093301
https://pubmed.ncbi.nlm.nih.gov/30093301
Publikováno v:
Journal of clinical lipidology. 12(4)
Background Familial hypercholesterolemia is a genetic lipoprotein disorder characterized by elevated plasma low-density lipoprotein cholesterol level, (tendinous xanthomas, xanthelasmas, and premature arcus corneus) and early onset atherosclerotic ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7215864190c9b33b7d468327e2cc29e3
https://pubmed.ncbi.nlm.nih.gov/29778561
https://pubmed.ncbi.nlm.nih.gov/29778561