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Publication : bmc medical genetics Publisher : biomed central Subject : emergency medical services Subject : questionnaires Subject : stroke Subject : student attitudes Filter by : Subject
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Academic Journal

Risk prediction for coronary heart disease by a genetic risk score - results from the Heinz Nixdorf Recall study.

  • Authors : Pechlivanis S; Institute for Medical Informatics, Biometry and Epidemiology, University Hospital of Essen, University Duisburg-Essen, Essen, Germany. .; Lehmann N

Subjects: Coronary Artery Disease/Coronary Artery Disease/Coronary Artery Disease/*genetics ; Myocardial Infarction/Myocardial Infarction/Myocardial Infarction/*genetics ; Risk Assessment/Risk Assessment/Risk Assessment/*statistics & numerical data

  • Source: BMC medical genetics [BMC Med Genet] 2020 Sep 10; Vol. 21 (1), pp. 178. Date of Electronic Publication: 2020 Sep 10.Publisher: BioMed Central Country of Publication: England NLM ID: 100968552 Publication Model: Electronic Cited Medium:

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Academic Journal

Genetic variants in CYP4F2 were significantly correlated with susceptibility to ischemic stroke.

  • Authors : Wu Y; Department of Critical Care Medicine, the Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an, 710004, Shaanxi, China.; Zhao J

Subjects: Genetic Variation*; Brain Ischemia/Brain Ischemia/Brain Ischemia/*genetics ; Cytochrome P450 Family 4/Cytochrome P450 Family 4/Cytochrome P450 Family 4/*genetics

  • Source: BMC medical genetics [BMC Med Genet] 2019 Sep 11; Vol. 20 (1), pp. 155. Date of Electronic Publication: 2019 Sep 11.Publisher: BioMed Central Country of Publication: England NLM ID: 100968552 Publication Model: Electronic Cited Medium:

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Academic Journal

Involvement of polymorphisms of the nerve growth factor and its receptor encoding genes in the etiopathogenesis of ischemic stroke.

  • Authors : Stepanyan A; Institute of Molecular Biology NAS RA, 7 Hasratyan Str, 0014, Yerevan, Armenia. .; Zakharyan R

Subjects: Polymorphism, Single Nucleotide*; Brain Ischemia/Brain Ischemia/Brain Ischemia/*genetics ; Nerve Growth Factor/Nerve Growth Factor/Nerve Growth Factor/*genetics

  • Source: BMC medical genetics [BMC Med Genet] 2018 Mar 02; Vol. 19 (1), pp. 33. Date of Electronic Publication: 2018 Mar 02.Publisher: BioMed Central Country of Publication: England NLM ID: 100968552 Publication Model: Electronic Cited Medium:

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Academic Journal

Association study of C-reactive protein associated gene HNF1A with ischemic stroke in Chinese population.

  • Authors : Shi H; Fujian University of Traditional Chinese Medicine, No.1 Qiuyang Road, Shangjie, Minhou, Fuzhou, 350122, China.; Fujian University of Traditional Chinese Medicine Subsidiary Rehabilitation Hospital, Fuzhou, China.

Subjects: Asian People/Asian People/Asian People/*genetics ; C-Reactive Protein/C-Reactive Protein/C-Reactive Protein/*analysis ; Hepatocyte Nuclear Factor 1-alpha/Hepatocyte Nuclear Factor 1-alpha/Hepatocyte Nuclear Factor 1-alpha/*genetics

  • Source: BMC medical genetics [BMC Med Genet] 2016 Jul 26; Vol. 17 (1), pp. 51. Date of Electronic Publication: 2016 Jul 26.Publisher: BioMed Central Country of Publication: England NLM ID: 100968552 Publication Model: Electronic Cited Medium:

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Academic Journal

Sequence variation in telomerase reverse transcriptase (TERT) as a determinant of risk of cardiovascular disease: the Atherosclerosis Risk in Communities (ARIC) study.

  • Authors : Bressler J; Human Genetics Center, School of Public Health, University of Texas Health Science Center at Houston, 1200 Pressler Street, Houston, TX, 77030, USA. .; Franceschini N

Subjects: Atherosclerosis/Atherosclerosis/Atherosclerosis/*genetics ; Coronary Disease/Coronary Disease/Coronary Disease/*genetics ; Stroke/Stroke/Stroke/*genetics

  • Source: BMC medical genetics [BMC Med Genet] 2015 Jul 23; Vol. 16, pp. 52. Date of Electronic Publication: 2015 Jul 23.Publisher: BioMed Central Country of Publication: England NLM ID: 100968552 Publication Model: Electronic Cited Medium:

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Academic Journal

Association between genetic polymorphisms of cytochrome P450 2C19 and the risk of cerebral ischemic stroke in Chinese.

Subjects: Polymorphism, Single Nucleotide*; Aryl Hydrocarbon Hydroxylases/Aryl Hydrocarbon Hydroxylases/Aryl Hydrocarbon Hydroxylases/*genetics ; Brain Ischemia/Brain Ischemia/Brain Ischemia/*genetics

  • Source: BMC medical genetics [BMC Med Genet] 2014 Jul 17; Vol. 15, pp. 83. Date of Electronic Publication: 2014 Jul 17.Publisher: BioMed Central Country of Publication: England NLM ID: 100968552 Publication Model: Electronic Cited Medium:

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Academic Journal

Association of interleukin-33 gene single nucleotide polymorphisms with ischemic stroke in north Chinese population.

  • Authors : Guo L; Department of Cardiology, the First Hospital of China Medical University, Shenyang 110001, China. .; Zhou X

Subjects: Polymorphism, Single Nucleotide*; Asian People/Asian People/Asian People/*genetics ; Interleukins/Interleukins/Interleukins/*genetics

  • Source: BMC medical genetics [BMC Med Genet] 2013 Oct 09; Vol. 14, pp. 109. Date of Electronic Publication: 2013 Oct 09.Publisher: BioMed Central Country of Publication: England NLM ID: 100968552 Publication Model: Electronic Cited Medium:

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Academic Journal

Lack of association between a functional variant of the BRCA-1 related associated protein (BRAP) gene and ischemic stroke.

  • Authors : Liao YC; Section of Neurology, Taichung Veterans General Hospital, No. 160, Sec 3, Chung-Kang Rd, Taichung 40705, Taiwan.; Lin HF

Subjects: Polymorphism, Single Nucleotide*; Stroke/Stroke/Stroke/*genetics ; Ubiquitin-Protein Ligases/Ubiquitin-Protein Ligases/Ubiquitin-Protein Ligases/*genetics

  • Source: BMC medical genetics [BMC Med Genet] 2013 Jan 28; Vol. 14, pp. 17. Date of Electronic Publication: 2013 Jan 28.Publisher: BioMed Central Country of Publication: England NLM ID: 100968552 Publication Model: Electronic Cited Medium:

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Academic Journal

Association between paraoxonase gene and stroke in the Han Chinese population.

  • Authors : Zhang G; Laboratory Diagnosis Center, Beijing Tiantan Hospital Affiliated to Capital Medical University, Beijing 100050, China.; Li W

Subjects: Polymorphism, Single Nucleotide*; Aryldialkylphosphatase/Aryldialkylphosphatase/Aryldialkylphosphatase/*genetics ; Stroke/Stroke/Stroke/*genetics

  • Source: BMC medical genetics [BMC Med Genet] 2013 Jan 28; Vol. 14, pp. 16. Date of Electronic Publication: 2013 Jan 28.Publisher: BioMed Central Country of Publication: England NLM ID: 100968552 Publication Model: Electronic Cited Medium:

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Academic Journal

An autosomal recessive leucoencephalopathy with ischemic stroke, dysmorphic syndrome and retinitis pigmentosa maps to chromosome 17q24.2-25.3.

  • Authors : Bouhouche A; Service de Neurologie et de Neurogénétique, Hôpital des Spécialités, Rabat, Morocco. ; Benomar A

Subjects: Body Dysmorphic Disorders/Body Dysmorphic Disorders/Body Dysmorphic Disorders/*genetics ; Chromosomes, Human, Pair 17/Chromosomes, Human, Pair 17/Chromosomes, Human, Pair 17/*genetics ; Retinitis Pigmentosa/Retinitis Pigmentosa/Retinitis Pigmentosa/*genetics

  • Source: BMC medical genetics [BMC Med Genet] 2012 Mar 21; Vol. 13, pp. 18. Date of Electronic Publication: 2012 Mar 21.Publisher: BioMed Central Country of Publication: England NLM ID: 100968552 Publication Model: Electronic Cited Medium:

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  • 1-10 of  18 results for ""Female""