Search Results - "Aston, C. E."
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1
A randomized controlled trial adding fluvastatin to peginterferon and ribavirin for naïve genotype 1 hepatitis C patients
Published in Journal of viral hepatitis (01-09-2013)“…Summary Fluvastatin or simvastatin has demonstrable antiviral activity against hepatitis C virus (HCV) as monotherapy. The safety and efficacy of adding…”
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2
Mutations in the cationic trypsinogen gene are associated with recurrent acute and chronic pancreatitis
Published in Gastroenterology (New York, N.Y. 1943) (01-10-1997)“…BACKGROUND & AIMS: We recently identified a single R117H mutation in the cationic trypsinogen gene in several kindreds with an inherited form of acute and…”
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3
Reduced soluble receptor for advanced glycation end-products (sRAGE) scavenger capacity precedes pre-eclampsia in Type 1 diabetes
Published in BJOG : an international journal of obstetrics and gynaecology (01-11-2012)“…Please cite this paper as: Yu Y, Hanssen K, Kalyanaraman V, Chirindel A, Jenkins A, Nankervis A, Torjesen P, Scholz H, Henriksen T, Lorentzen B, Garg S, Menard…”
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4
Anti-angiogenic factors and pre-eclampsia in type 1 diabetic women
Published in Diabetologia (2009)“…Aims/hypothesis Elevated anti-angiogenic factors such as soluble fms-like tyrosine kinase 1 (sFlt1), a soluble form of vascular endothelial growth factor…”
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5
Advanced glycation end-products and methionine sulphoxide in skin collagen of patients with type 1 diabetes
Published in Diabetologia (01-10-2006)“…Aims/hypothesis We determined whether oxidative damage in collagen is increased in (1) patients with diabetes; (2) patients with diabetic complications; and…”
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6
A gene for hereditary pancreatitis maps to chromosome 7q35
Published in Gastroenterology (New York, N.Y. 1943) (01-06-1996)“…BACKGROUND & AIMS: Hereditary pancreatitis (HP) is an autosomal- dominant disorder with incomplete penetrance characterized by recurrent bouts of severe…”
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DNA Polymorphisms in Two Paraoxonase Genes (PON1 and PON2) Are Associated with the Risk of Coronary Heart Disease
Published in American journal of human genetics (01-01-1998)“…A common polymorphism at codon 192 in the human paraoxonase (PON) 1 gene has been shown to be associated with increased risk for coronary heart disease (CHD)…”
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8
Expression and penetrance of the hereditary pancreatitis phenotype in monozygotic twins
Published in Gut (01-04-2001)“…BACKGROUND Hereditary pancreatitis (HP) is a rare autosomal dominant disorder with variable expression and an overall lifetime penetrance of 80%. We…”
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9
Genetic screening of the lipoprotein lipase gene for mutations associated with high triglyceride/low HDL-cholesterol levels
Published in Human genetics (01-09-2000)“…The lipoprotein lipase (LPL) enzyme plays a major role in lipid metabolism, primarily by regulating the catabolism of triglyceride (TG)-rich lipoprotein…”
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10
Mortality benefit of statin use in traumatic spinal cord injury: a retrospective analysis
Published in Spinal cord (01-04-2016)“…Study design: An observational study based on retrospective review of the medical charts and death records of 163 individuals with traumatic spinal cord…”
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11
Genetic Polymorphism of Paraoxonase and the Risk of Coronary Heart Disease
Published in Arteriosclerosis, thrombosis, and vascular biology (01-06-1997)“…Recent studies have implicated paraoxonase, an HDL-associated enzyme, in providing protection against LDL oxidation, thus affecting the risk of coronary heart…”
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12
Relationship of American Indian blood quantum with osteoporosis risk: a cross-sectional study of American Indian women in Oklahoma
Published in Osteoporosis international (01-10-2018)“…Summary Information regarding the prevalence and risk of osteoporosis among American Indian (AI) women is limited. This study showed that with increasing AI…”
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13
A randomized trial of dalteparin compared with ibuprofen for the treatment of superficial thrombophlebitis
Published in Journal of thrombosis and haemostasis (01-05-2012)“…Background: Superficial thrombophlebitis can produce pain and result in a deep vein thrombosis (DVT) if not treated. Conservative therapies including…”
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14
The effect of Covid-19 on pediatric surgical case volume
Published in Pediatric Anesthesia and Critical Care Journal (01-02-2024)“…Introduction The COVID-19 pandemic has had an unprecedented ef- fect on hospital systems. Policy changes lead to de- creased hospital visits as well as…”
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15
Lung cancer risk in families of nonsmoking probands: Heterogeneity by age at diagnosis
Published in Genetic epidemiology (01-11-1999)“…In an earlier investigation, we did not detect a major genetic component to lung cancer in families of nonsmoking lung cancer probands. However, heterogeneity…”
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16
Linkage and Association between Inflammatory Bowel Disease and a Locus on Chromosome 12
Published in American journal of human genetics (01-07-1998)“…Genetic epidemiological studies have shown that genetic factors are important in the pathogenesis of the idiopathic inflammatory bowel diseases (IBD), Crohn…”
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Motivations and concerns of patients with access to genetic testing for hereditary pancreatitis
Published in The American journal of gastroenterology (01-05-2001)“…Direct DNA testing is now available for hereditary pancreatitis (HP). This study aimed to identify the factors that motivated individuals to participate in…”
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18
A simplified six item checklist for screening for fragile X syndrome in the pediatric population
Published in The Journal of pediatrics (01-10-1996)“…OBJECTIVE: In our general experience, about 2% of samples referred for fragile X testing showed positive results on Southern blot analysis. The aim of this…”
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19
Plasma Apolipoprotein A-I, Apolipoprotein B, and Lipoprotein(a) Concentrations in Normoglycemic Hispanics and Non-Hispanic Whites from the San Luis Valley, Colorado
Published in American journal of epidemiology (15-12-1997)“…Lower levels of plasma apolipoprotein (apo) A-I and higher levels of apoB, lipoprotein(a) (Lp(a)), and the ratio of apoB to apoA-I are considered to be…”
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The role of heterozygosity for CYP21 in the polycystic ovary syndrome
Published in Journal of pediatric endocrinology & metabolism : JPEM (2000)“…The phenotypic heterogeneity recognized in congenital adrenal hyperplasia secondary to 21-hydroxylase deficiency appears to extend to 21hydroxylase (CYP21)…”
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