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| Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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| 1 |
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Associations between smoking, components of metabolic syndrome and lipoprotein particle sizeBMC medicine, 2013-09, Vol.11 (1), p.195-195, Article 195 [Peer Reviewed Journal]COPYRIGHT 2013 BioMed Central Ltd. ;COPYRIGHT 2013 South African Sports Medicine Association ;COPYRIGHT 2013 BioMed Central Ltd. ;2013 Slagter et al.; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. ;Copyright © 2013 Slagter et al.; licensee BioMed Central Ltd. 2013 Slagter et al.; licensee BioMed Central Ltd. ;Wageningen University & Research ;ISSN: 1741-7015 ;ISSN: 1016-6742 ;EISSN: 1741-7015 ;EISSN: 2078-5143 ;DOI: 10.1186/1741-7015-11-195 ;PMID: 24228807Full text available |
| 2 |
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Vitamin D levels and vitamin D receptor genetic variants in Egyptian cardiovascular disease patients with and without diabetesEgyptian Journal of Medical Human Genetics, 2021-06, Vol.22 (1), p.1-12 [Peer Reviewed Journal]The Author(s) 2021 ;COPYRIGHT 2021 Springer ;The Author(s) 2021. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 1110-8630 ;EISSN: 2090-2441 ;DOI: 10.1186/s43042-021-00174-9Full text available |
| 3 |
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SIRT1 gene is associated with cardiovascular disease in the Iranian populationThe Egyptian journal of medical human genetics, 2015-04, Vol.16 (2), p.117-122 [Peer Reviewed Journal]2014 ;Copyright Egyptian Society of Medical Human Genetics 2015 ;ISSN: 1110-8630 ;EISSN: 2090-2441 ;DOI: 10.1016/j.ejmhg.2014.11.005Full text available |
| 4 |
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Clinical implications of PON1 (rs662) and TNF-α (rs1799964) genes polymorphism in patients with coronary artery diseaseEgyptian Journal of Medical Human Genetics, 2022-07, Vol.23 (1), p.1-7 [Peer Reviewed Journal]The Author(s) 2022 ;The Author(s) 2022. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 1110-8630 ;EISSN: 2090-2441 ;DOI: 10.1186/s43042-022-00318-5Full text available |
| 5 |
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Common variant of 5,10-methylenetetrahydrofolate reductase may increase risk of coronary artery disease in the Iranian populationThe Egyptian journal of medical human genetics, 2018-01, Vol.19 (1), p.1-5 [Peer Reviewed Journal]2017 Ain Shams University ;Copyright Egyptian Society of Medical Human Genetics Jan 2018 ;ISSN: 1110-8630 ;EISSN: 2090-2441 ;DOI: 10.1016/j.ejmhg.2017.11.004Full text available |
| 6 |
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The association of apolipoprotein-E (APOE) gene polymorphisms with coronary artery disease: a systematic review and meta-analysisEgyptian Journal of Medical Human Genetics, 2021-03, Vol.22 (1), p.1-8 [Peer Reviewed Journal]The Author(s) 2021 ;COPYRIGHT 2021 Springer ;The Author(s) 2021. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 1110-8630 ;EISSN: 2090-2441 ;DOI: 10.1186/s43042-021-00135-2Full text available |
| 7 |
Material Type: Article
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Hematological indices in pediatric patients with acyanotic congenital heart disease: a cross-sectional study of 248 patientsEgyptian Journal of Medical Human Genetics, 2022-03, Vol.23 (1), p.1-8 [Peer Reviewed Journal]The Author(s) 2022 ;COPYRIGHT 2022 Springer ;The Author(s) 2022. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 1110-8630 ;EISSN: 2090-2441 ;DOI: 10.1186/s43042-022-00262-4Full text available |
| 8 |
Material Type: Article
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Association between PON1 rs662 gene polymorphism and serum paraoxonase1 level in coronary artery disease patients in Northern IndiaEgyptian Journal of Medical Human Genetics, 2021-09, Vol.22 (1), p.1-8 [Peer Reviewed Journal]The Author(s) 2021 ;COPYRIGHT 2021 Springer ;The Author(s) 2021. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 1110-8630 ;EISSN: 2090-2441 ;DOI: 10.1186/s43042-021-00196-3Full text available |
| 9 |
Material Type: Article
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Prenatal presentation of Walker–Warburg syndrome with a POMT2 mutation: an extended fetal phenotypeEgyptian Journal of Medical Human Genetics, 2020-11, Vol.21 (1) [Peer Reviewed Journal]The Author(s) 2020 ;COPYRIGHT 2020 Springer ;The Author(s) 2020. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 1110-8630 ;EISSN: 2090-2441 ;DOI: 10.1186/s43042-020-00093-1Full text available |
| 10 |
Material Type: Article
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Cantu syndrome in an Egyptian childThe Egyptian journal of medical human genetics, 2018-10, Vol.19 (4), p.429-432 [Peer Reviewed Journal]2018 Ain Shams University ;2018. This work is published under https://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 1110-8630 ;EISSN: 2090-2441 ;DOI: 10.1016/j.ejmhg.2018.01.005Full text available |
| 11 |
Material Type: Article
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Angiotensin-converting enzyme (ACE) I/D and bradykinin B2 receptor T/C genes polymorphism in patients with ACE inhibitors-related coughThe Egyptian journal of medical human genetics, 2018-10, Vol.19 (4), p.307-313 [Peer Reviewed Journal]2018 Ain Shams University ;2018. This work is published under https://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 1110-8630 ;EISSN: 2090-2441 ;DOI: 10.1016/j.ejmhg.2018.05.006Full text available |
| 12 |
Material Type: Article
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The β fibrinogen gene G-455A polymorphism in Asian subjects with coronary heart disease: A meta analysisThe Egyptian journal of medical human genetics, 2017-01, Vol.18 (1), p.19-28 [Peer Reviewed Journal]2016 Ain Shams University ;Copyright Egyptian Society of Medical Human Genetics Jan 1, 2017 ;ISSN: 1110-8630 ;EISSN: 2090-2441 ;DOI: 10.1016/j.ejmhg.2016.06.002Full text available |
| 13 |
Material Type: Article
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Association assessment of Interleukine-10 gene polymorphism and its expression status with susceptibility to coronary artery disease in IranThe Egyptian journal of medical human genetics, 2018-01, Vol.19 (1), p.31-35 [Peer Reviewed Journal]2017 Ain Shams University ;Copyright Egyptian Society of Medical Human Genetics Jan 2018 ;ISSN: 1110-8630 ;EISSN: 2090-2441 ;DOI: 10.1016/j.ejmhg.2017.06.005Full text available |
| 14 |
Material Type: Article
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Association assessment of platelet derived growth factor B gene polymorphism and its expression status with susceptibility to coronary artery diseaseThe Egyptian journal of medical human genetics, 2017-10, Vol.18 (4), p.359-363 [Peer Reviewed Journal]2017 Ain Shams University ;Copyright Egyptian Society of Medical Human Genetics Oct 1, 2017 ;ISSN: 1110-8630 ;EISSN: 2090-2441 ;DOI: 10.1016/j.ejmhg.2017.03.004Full text available |
| 15 |
Material Type: Article
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Risk factors for congenital anomalies in high risk pregnant women: A large study from South IndiaThe Egyptian journal of medical human genetics, 2017-01, Vol.18 (1), p.79-85 [Peer Reviewed Journal]2016 Ain Shams University ;Copyright Egyptian Society of Medical Human Genetics Jan 1, 2017 ;ISSN: 1110-8630 ;EISSN: 2090-2441 ;DOI: 10.1016/j.ejmhg.2016.04.001Full text available |
| 16 |
Material Type: Article
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Evaluation of dysmorphic children according to echocardiographic findings: A single center experienceThe Egyptian journal of medical human genetics, 2018-07, Vol.19 (3), p.267-270 [Peer Reviewed Journal]2018 Ain Shams University ;Copyright Egyptian Society of Medical Human Genetics Jul 2018 ;ISSN: 1110-8630 ;EISSN: 2090-2441 ;DOI: 10.1016/j.ejmhg.2018.01.002Full text available |
| 17 |
Material Type: Article
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Association between Interleukin-18 promoter polymorphisms and risk of ischemic stroke: A case-control studyThe Egyptian journal of medical human genetics, 2018-01, Vol.19 (1), p.13-18 [Peer Reviewed Journal]2017 Ain Shams University ;Copyright Egyptian Society of Medical Human Genetics Jan 2018 ;ISSN: 1110-8630 ;EISSN: 2090-2441 ;DOI: 10.1016/j.ejmhg.2017.08.014Full text available |
| 18 |
Material Type: Article
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Alu insertion/deletion of ACE gene polymorphism might not affect significantly the serum bradykinin level in hypertensive patients taking ACE inhibitorsThe Egyptian journal of medical human genetics, 2017-04, Vol.18 (2), p.187-191 [Peer Reviewed Journal]2016 Ain Shams University ;Copyright Egyptian Society of Medical Human Genetics Apr 1, 2017 ;ISSN: 1110-8630 ;EISSN: 2090-2441 ;DOI: 10.1016/j.ejmhg.2016.08.001Full text available |
| 19 |
Material Type: Article
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Progress in genetics of coronary artery diseaseThe Egyptian journal of medical human genetics, 2018-01, Vol.19 (1), p.51-52 [Peer Reviewed Journal]2017 Ain Shams University ;Copyright Egyptian Society of Medical Human Genetics Jan 2018 ;ISSN: 1110-8630 ;EISSN: 2090-2441 ;DOI: 10.1016/j.ejmhg.2017.11.001Full text available |
| 20 |
Material Type: Article
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Open-array analysis of genetic variants in Egyptian patients with type 2 diabetes and obesityThe Egyptian journal of medical human genetics, 2017-10, Vol.18 (4), p.341-348 [Peer Reviewed Journal]2017 Ain Shams University ;Copyright Egyptian Society of Medical Human Genetics Oct 1, 2017 ;ISSN: 1110-8630 ;EISSN: 2090-2441 ;DOI: 10.1016/j.ejmhg.2017.03.002Full text available |
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