- ►annals.org [PDF] M Lazo, E Selvin, JM Clark - Annals of Internal Medicine, 2008 - Am Coll Physicians Background: Clinicians sometimes order liver tests as part of a screening
examination or general work-up. Current guidelines do not recommend routine
retesting of abnormal results in asymptom- atic patients. Cited by 16 - Related articles - BL Direct - All 5 versions
A Table - Ann Intern Med, 2008 - depts.washington.edu Background: Clinicians sometimes order liver tests as part of a screening
examination or general work-up. Current guidelines do not recommend routine
retesting of abnormal results in asymptom- atic patients. Related articles - View as HTML - All 3 versions
S Stepec, J Makuc, S Markovic, I Medica, B … - Annals of Hematology, 2008 - Springer Dear Editor, Hereditary hemochromatosis (HH; HFE-related or type 1 genetic
hemochromatosis) is a common autosomal reces- sive disorder of iron metabolism,
its prevalence being two to five per 1,000 in Caucasians, characterized by ... Cited by 2 - Related articles - All 3 versions
G Forlani, P Di Bonito, E Mannucci, B Capaldo … - Journal of endocrinological investigation, 2008 - ncbi.nlm.nih.gov The occurrence of liver disease and raised liver enzymes is common in Type 2
diabetes, and may be multifactorial in origin. Very few studies are available on
the exact prevalence of the phenomenon, however. We carried out an ... Cited by 3 - Related articles - BL Direct - All 2 versions
A Shankar, J Li, BEK Klein, F Javier Nieto, R … - Atherosclerosis, 2008 - Elsevier Overall, serum GGT levels were positively associated with PAD among men but not
women (p-interaction = 0.0421). Among men, the multivariable odds ratio (OR)
[95% confidence intervals (CI)] comparing the highest quartile of serum GGT ... Cited by 4 - Related articles - All 15 versions
- ►endojournals.org N Chalasani, R Vuppalanchi, NS Raikwar, … - Journal of Clinical Endocrinology & Metabolism, 2006 - Endocrine Soc Context: Recent studies demonstrated that de novo lipogenesis is increased in
patients with nonalcoholic fatty liver disease (NAFLD). Patients with NAFLD also
have plasma lipid abnormalities. These lipid abnormalities may in part be ... Cited by 5 - Related articles - BL Direct - All 4 versions
- ►nih.gov [PDF] JB Whitfield, NG Martin - American Journal of Human Genetics, 1983 - pubmedcentral.nih.gov SUMMARY Plasma alkaline phosphatase activity has been measured in 204 pairs of
twins aged 18-34. Estimated genetic variance was the same in men and women,
after exclusion of the youngest men, but environmental variance was greater ... Cited by 6 - Related articles - All 7 versions
- ►physiology.org JE Foreman, DA Blizard, G Gerhard, HA Mack, … - Physiological genomics, 2005 - Am Physiological Soc Quantitative trait locus (QTL) analyses were conducted to identify chromosomal
regions that contribute to variability in serum alkaline phosphatase (AP) enzyme
activity in mice derived from the C57BL/6J (B6) and DBA/2J (D2) inbred ... Cited by 6 - Related articles - All 4 versions
- ►eje-online.org M Moldes, G Beauregard, M Faraj, N Peretti, … - European Journal of Endocrinology, 2006 - EFES Objective: Adiponutrin is a new transmembrane protein specifically expressed in
adipose tissue. In obese subjects, short- or long-term calorie restriction diets
were associated with a reduction in adiponutrin gene expression. ... Cited by 6 - Related articles - BL Direct - All 7 versions
I Brun-Heath, AS Lia-Baldini, S Maillard, A … - European journal of medical genetics, 2007 - Elsevier Hypophosphatasia is a rare genetic disease characterized by diminished bone and
tooth mineralization due to deficient activity of tissue-nonspecific alkaline
phosphatase (TNSALP). The disease is clinically heterogeneous due to ... Cited by 8 - Related articles - All 3 versions
