Bilen O, Pokharel Y, Ballantyne CM. Genetic testing in hyperlipidemia. Endocrinol Metab Clin North Am. Mar 2016;45(1):129- 140. PMID 26893002Bilen O, Pokharel Y, Ballantyne CM. Genetic Testing in Hyperlipidemia. Endocrinol Metab Clin North Am 2016; 45(1): 129-40....
Recurrent (2 or more separate, documented episodes with hyper-amylasemia) attacks of acute pancreatitis for which there is no explanation (anatomical anomalies, ampullary or main pancreatic strictures, trauma, viral infection, gallstones, alcohol, drugs, hyperlipidemia, etc.); or Unexplained (idiopathi...
Genetic Testing in Hyperlipidemia Patients with most lipodystrophy syndromes should be screened for diabetes, dyslipidemia, and liver, kidney, and heart disease annually. Diet is essential ... O Bilen,Y Pokharel,CM Ballantyne - 《Endocrinology & Metabolism Clinics of North America》 被引量: 10发表...
Gaffney D et al. (1995) Independent mutations at codon 3500 of the apolipoprotein B gene are associated with hyperlipidemia. Arterioscler Thromb Vasc Biol 15: 1025–1029 CAS PubMed Google Scholar Tai DY et al. (1998) Identification and haplotype analysis of apolipoprotein B-100 Arg3500→Trp ...
Age is the principal risk factor for neurodegeneration in both the retina and brain. The retina and brain share many biological properties; thus, insights into retinal aging and degeneration may shed light onto similar processes in the brain. Genetic mak
Familial combined hyperlipidemia in childrenClinical expression, metabolic defects, and management J Pediatr (1993) D.C. Wertz et al. Genetic testing for children and adolescents JAMA (1994) B.S. Wilfond et al. Points to considerEthical, legal, and psychological implications of genetic testing in...
For example, FDA-approved Niacin [R1; target gene:NNMT; Anatomical Therapeutic Chemical (ATC) code: C10AD02] is a B vitamin used to treat various deficiencies and diseases in the cardiovascular system, including myocardial infarctions [62], hyperlipidemia [63], and coronary artery disease [64]...
Campbell:That's really the first step in the workup. You try to see if you can find which bucket that patient belongs to. Primary FSGS classically presents with the nephrotic syndrome. This would be > 3.5 g of protein in the urine, a low serum albumin, edema, and hyperlipidemia. Those...
analysis between plasma sST2 level and AD and its related endophenotypes, adjusting for age, sex, status of cardiovascular diseases (CVDs; that is, heart disease, hypertension, diabetes mellitus and hyperlipidemia), body mass index (BMI) and education level, followed by multiple testing correction....
They usually appear in patients with homozygous FH but can also occur in patients with familial dysbetalipoproteinemia, sitosterolemia, or cerebrotendinous xanthomatosis and rarely in secondary hyperlipidemias, such as nephrotic syndrome. Download: Download high-res image (167KB) Download: Download ...