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- 2009
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Mark
Gastroparesis is associated with oxytocin deficiency, oesophageal dysmotility with hyperCCKemia, and autonomic neuropathy with hypergastrinemia
(
- Contribution to journal › Article
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Mark
Relation between human vasopressin 1a gene variance, fat intake, and diabetes.
(
- Contribution to journal › Article
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Mark
Associations Between Human Leukocyte Antigen (HLA) Genotype And Acute Myocardial Infarction
2009) 15th International Symposium on Atherosclerosis In Atherosclerosis Supplements 10(2). p.953-953(
- Contribution to journal › Published meeting abstract
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Mark
Chromosome 2q12, the ADRA2B I/D polymorphism and metabolic syndrome.
(
- Contribution to journal › Article
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Mark
Gender differences in the association between NT proBNP and glucometabolic disturbances in a population-based cohort
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- Contribution to journal › Published meeting abstract
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Mark
The myocardial infarction associated CDKN2A/CDKN2B locus on chromosome 9p21 is associated with stroke independently of coronary events in patients with hypertension.
(
- Contribution to journal › Article
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Mark
Common Genetic Variants on Chromosome 9p21 Confers Risk of Ischemic Stroke A Large-Scale Genetic Association Study
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- Contribution to journal › Article
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Mark
Distribution and Correlates of Midregional Proadrenomedullin in the General Population.
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- Contribution to journal › Article
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Mark
ION Mobility Analysis Of Lipoprotein Subfractions Suggests Three Independent Mechanisms Of Cardiovascular Risk
(
- Contribution to journal › Published meeting abstract
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Mark
Genetic variation in serum and glucocortocoid regulated kinase 1 (SGK-1), a regulator of the epithelial sodium channel, is associated with ischemic stroke
(
- Contribution to journal › Published meeting abstract