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This page provides a simple browsing interface for finding entities described by a property and a named value. Other available search interfaces include the page property search, and the ask query builder.

List of results

• WBR0171  + (GI bleeding is not a very common cause of mortality in patients with HELLP syndrome.)
• WBR0808  + (GIP decreases GI motility, increases insulin secretion, and increases gastric pH by decreasing acid secretion.)
• WBR0936  + (GLUT1 is expressed in erythrocytes and the brain. It does not translocate to the cell membrane with exercise.)
• WBR0909  + (Galactokinase catalyzes the conversion of galactose to galactose-1-phosphate. The main presentation of patients with galactokinase deficiency is early-onset cataracts.)
• WBR0910  + (Galactokinase deficiency is characterized … Galactokinase deficiency is characterized by the inability to transform galactose into galactose-1-phosphate with subsequent accumulation of galacticol. It is a relatively benign disorder, with galacticol accumulation leading to early-onset cataracts if the proper diet adjustments are not made. the proper diet adjustments are not made.)
• WBR1097  + (Ganciclovir is indicated in cytomegalovirus infection. There are no indications for adding acyclovir to ganciclovir in patient of HSV-1.)
• WBR0930  + (Gastric cancer can occur as a result of nistrosamine exposure. Nitrosamines are carcinogenic chemical compounds present in various foods, notably smoked meats.)
• WBR0656  + (Giant cell arteritis or temporal arteritis is medium to large vessel vasculitis that predominantly affects the branches of the external carotid artery. Features include jaw pain, ocular disturbances and an elevated ESR.)
• WBR0765  + (Giant cell tumor (osteoclastoma) is characterized by spindle-shaped cells with multi-nucleated giant cells.)
• WBR0749  + (Giant cell tumor presents commonly in earl … Giant cell tumor presents commonly in early adulthood at the epiphyseal end of long bones. It is a benign tumor with local aggressive features. Xray shows a "double-bubble" sign. On pathology, it is characterized by spindle-shaped cells with multinucleated giant cells, hence its name.ultinucleated giant cells, hence its name.)
• WBR0938  + (Glucagon counteracts beta-blocker toxicity by increasing intracellular cAMP.)
• WBR0273  + (Glucocorticoids cause a decrease in leukotriene production.)
• WBR0244  + (Glucose-6-Phosphate dehydrogenase (G6PD) deficiency is an X-linked recessive genetic disease.)
• WBR0935  + (Glycosylation refers to the addition of a … Glycosylation refers to the addition of a carbohydrate to a protein. The glycosylation of proteins does not target them for degradation. Glycosylation is often necessary for the proper function or folding of the modified protein. One example of a heavily glycosylated protein family is the heparin sulfate proteoglycans.mily is the heparin sulfate proteoglycans.)
• WBR0725  + (Granulosa cell tumor is an ovarian non-germ cell tumor that often secretes estradiol. It has a gray-white multilocular appearance on gross pathology and characteristic Call-Exner bodies on microscopy.)
• WBR1076  + (HAART is not indicated in the treatment of … HAART is not indicated in the treatment of CMV retinitis. It is indicated for treatment of HIV . The patient has HIV since 5 years and doesn't have any other complaints. Hence HAART is not indicated now . It may be started in combination to treatment of CMV .arted in combination to treatment of CMV .)
• WBR0555  + (HDL may have a role in the increase of blo … HDL may have a role in the increase of blood flow in patients with endothelial dysfunctions. This is carried out by its effect on vasodilation and prostacyclin synthesis. However, the anti-atherogenic properties of HDL-C are not derived from its association with prostacyclin synthesis.s association with prostacyclin synthesis.)
• WBR265  + (HHV-6 causes Roseola, a macular rash over the body that appears several days after a high-grade fever.)
• WBR0154  + (HIV infection in newborns may be transmitted from infected mothers who have significant viral load. Untreated newborns usually have a less acute presentation and develop recurrent opportunistic infections.)
• WBR0785  + (Hairy cell leukemia is not associated with rouleaux formation on peripheral smear. Typical findings include lymphocytes with irregular hair-like borders.)
• WBR0429  + (Hearing loss is not classically associated with GCA.)
• WBR0804  + (Heavy smoking is associated with several diseases, including cancers. However, history of heavy smoking is not classically associated with the development of squamous cell carcinoma of the skin.)
• WBR0772  + (Heinz bodies result from the precipitation of denatured hemoglobin due to oxidation of iron. They are frequently observed among patients with G6PD deficiency.)
• WBR0848  + (Hemagglutinin is a viral factor that promotes viral entry.)
• WBR0812  + (Hematuria and hypertension are signs of ne … Hematuria and hypertension are signs of nephritic syndrome, which are common findings among patients with glomerulonephritis such as IgA nephropathy and rapidly progressive glomerulonephritis. In children, post-infectious glomerulonephritis and Alport syndrome are common etiologies of nephritic syndrome.e common etiologies of nephritic syndrome.)

• WBR0608  + (Hepatitis A vaccine is an inactivated vaccine.)

• WBR0849  + (Hepatocytes are stable (quiescent) cells that undergo division only when stimulated.)
• WBR0745  + (Hereditary spherocytosis (HS) is an autoso … Hereditary spherocytosis (HS) is an autosomal dominant genetic disorder characterized by the hemolysis and increased bilirubin that prediposes affected patients to gallbladder stones. Since the disease is autosomal dominant, a positive family history of HS is typical and thus a positive family history of cholecystectomy should raise the suspicion of HS in young patients presenting with jaundice and anemia.ients presenting with jaundice and anemia.)
• WBR0475  + (High-output heart failure is associated with Paget's disease of the bone due to increased rate of arteriovenous shunts.)
• WBR0541  + (Histone H1 is outside the nucleosome core. It provides stability of the DNA stem and prevents the nuclease digestion of the nucleosome.)
• WBR0989  + (Homocystinuria is associated with lens subluxation that is downwards and inwards.)
• WBR0584  + (Homonymous hemianopia involves loss of vision on one side. It usually occurs due to a lesion to the optic tracts or a PCA stroke although the latter usually has associated macular sparing. This lesion is not seen with prolactinomas.)
• WBR0585  + (Homonymous hemianopia involves loss of vision on one side. It usually occurs due to a lesion to the optic tracts or a PCA stroke although the latter usually has associated macular sparing. This lesion is not seen in patients with carotid artery aneurysms.)
• WBR0373  + (Horseshoe kidney is caused by the fusion of the inferior poles of both kidneys. It is not associated with Potter’s syndrome.)
• WBR282  + (Huntington disease has an autosomal dominant mode of inheritance similar to familial hypertrophic cardiomyopathy (HCM).)
• WBR0603  + (Hyaline cartilage contains type II collagen)
• WBR0943  + (Hydrochlorathiazide is not particularly helpful in this patient, considering that large doses of thiazide diuretics increase uric acid retention.)
• WBR0327  + (Hydroxyurea is beneficial in patients with sickle cell disease (SCD) because it increases HbF levels.)
• WBR0773  + (IL-2 is not a main mediator of cachexia syndrome. IL-2 is secreted by T cells and helps to activate other T cells.)
• WBR0680  + (IL-8 is a chemotactic factor for neutrophils.)
• WBR0372  + (IV benzodiazepines are reasonable in a case of cocaine induced MI or significant anxiety. No such history of here.)
• WBR0895  + (IV thrombolytics must only be administered after ensuring a blood pressure ≤180/110 mmHg. IV thrombolytics are generally administered within 4.5 hours of onset of symptom ONLY in patients without contraindicationS (i.e., eligible patients).)
• WBR0794  + (Ibuprofen is not associated with kidney stones.)
• WBR0081  + (If infection occurs within 0–28 days before conception, there is a 43% chance the infant will be affected. This is not the period during which the patient is at highest risk.)
• WBR230  + (IgA nephropathy (Berger’s disease) is the … IgA nephropathy (Berger’s disease) is the most common primary glomerulonephritis worldwide. It is characterized by deposition of IgA in the glomerular mesangium leading to mesangial proliferation. The IgA1 is almost always the subclass involved and contains O-glycans deficient in galactose.contains O-glycans deficient in galactose.)
• WBR0872  + (IgG, C3 and C4 deposits can be seen in the renal biopsies of patients with membranoproliferative glomerulonephritis. They are not seen in skin biopsies of patients with Henoch-Schönlein purpura.)
• WBR0748  + (IgG4 subtype is most commonly observed in … IgG4 subtype is most commonly observed in idiopathic membranous nephropathy. In contrast, IgG1, 2, and 3 are more commonly observed in secondary forms of membranous nephropathy. The difference between the two may aid in the differentiation between primary (idiopathic) and secondary membranous nephropathy.hic) and secondary membranous nephropathy.)
• WBR0760  + (In life-or-death emergency situations, a minor's urgent care must not be withheld under any circumstance.)
• WBR0358  + (In this situation anticipated door to balloon time is greater than 90 minutes which typically favors thrombolytic therapy. However, transfer to the medical center for angioplasty is correct in this case becase thrombolysis is contraindicated)
• WBR0883  + (Incorrect)
• WBR0702  + (Incorrect Therapy with one nucleoside reverse transcriptase inhibitor and one protease is not recommended)