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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

• WBR0808  + (GIP increases gastric pH by decreasing acid secretion, decreases GI motility, and increases insulin secretion.)
• WBR0936  + (GLUT3 is primarily expressed in neurons and does not translocate to the cell membrane with exercise.)
• WBR0279  + (Galactose accumulation results from galactokinase deficiency. Galactose appears in blood and urine and may cause infantile cataracts. It is a relatively mild condition.)
• WBR0907  + (Galactose-1-phosphate uridyltransferase (GALT) catalyzes the reversible conversion of galactose-1-phosphate into UDP-galactose. This enzyme is deficient in patients with classic galactosemia.)
• WBR0498  + (Gastric cancer is not the most common fatal cancer in older patients.)
• WBR1117  + (Genetic test for primary lactose malabsorption is very expensive and hence not done routinely.)
• WBR0502  + (Given this patient's high insulin levels and low C-peptide, exogenous administration of insulin is the most likely etiology.)
• WBR0578  + (Global aphasia is a speech dysfunction characterized by impaired comprehension, impaired speech fluency, and impaired repetition. It results from damage to a larger area of the brain that involves the superior temporal and inferior frontal gyri.)
• WBR0678  + (Glucagon is the antidote for beta-blocker toxicity.)
• WBR0273  + (Glucocorticoids cause an increase in anti-inflammatory cytokines such as IL-10 and TGF-β.)
• WBR0542  + (Goodpasture's syndrome is a type II hyersensitivity.)
• WBR0529  + (Griseofulvin is a fungistatic agent that inhibits microtubule polymerization and inhibits mitosis.)
• WBR0748  + (Gross hematuria is usually unlikely to be observed in membranous nephropathy. Microscopic hematuria is more common than gross hematuria. Hematuria does not help in differentiating between primary and secondary membranous nephropathies.)
• WBR0869  + (Guillan-Barre syndrome is a type IV hypersensitivity.)
• WBR1077  + (HAART is never used alone for maintenance of CMV retinitis. It may be used later in addition to valganciclovir for the treatment of HIV.)
• WBR0163  + (HCC may be secondary to chronic viral hepatitis and/or cirrhosis. Hepatocellular carcinoma (HCC) is not treated with imatinib.)
• WBR0452  + (HCV RNA is diagnostic of hepatitis C virus (HCV). HCV screening is not recommended prior to the initiation of anti-TNF therapy.)
• WBR0555  + (HDL functions in preventing thrombus formation in the arteries through an effect on platelet activation and aggregation, which results in increased protein C&S activity, fibrinolysis, and endothelial tissue factor expression.)
• WBR0559  + (HIV patients with CD4 < 200 cells/mL ma … HIV patients with CD4 < 200 cells/mL may develop ''Pneumocystis jirovecii'' pneumonia, progressive multifocal leukoencephalopathy JC virus, or cryptosporidium-associated diarrhea. HIV patients with CD4 < 200 cells/mL require TMP-SMX prophylaxis against ''P. jirovecii'' pneumonia. prophylaxis against ''P. jirovecii'' pneumonia.)
• WBR0785  + (HUS is not associated with rouleaux formation on peripheral smear. Schistocytes are classically found in patients with HUS.)
• WBR0204  + (Hairy leukoplakia is caused by Epstein-Barr virus (EBV) and is most commonly seen in HIV-infected patients.)
• WBR1131  + (Haloperidol has no role in the treatment of convulsion.)
• WBR0440  + (Heart failure is not directly associated with TS or hypertension.)
• WBR0674  + (Heart, kidney, and spleen undergo white (pale or anemic) infarction.)
• WBR0893  + (Helical CT angiography (CTA) provides a rapid evaluation of intracranial and extracranial vessels in acute, subacute, and chronic stroke settings. It is used to determine the presence of vessel occlusions or stenoses.)

• WBR0331  + (Helicase unwinds DNA templates at the replication fork.)

• WBR0394  + (Helminth infection in the lungs is not associated with Curschmann's spirals. Eosinophils are usually abundant on BAL.)
• WBR0803  + (Hemangiosarcoma is a rare, rapidly growing … Hemangiosarcoma is a rare, rapidly growing, highly invasive variety of cancer. It is a blood-fed sarcoma; that is, blood vessels grow directly into the tumor and it is typically filled with blood. A frequent cause of death is the rupturing of this tumor, causing the victim to rapidly bleed to death.sing the victim to rapidly bleed to death.)
• WBR0176  + (Hemorrhoids may be observed among patients with portal hypertension due to back-up of blood flow in the portal circulation.)
• WBR0013  + (Hemosiderin-laden macrophages in BAL may b … Hemosiderin-laden macrophages in BAL may be helpful in the diagnosis of diffuse pulmonary hemorrhage syndromes and diffuse interstitial pulmonary diseases (DIPD). They are also known as "heart failure cells since they may be observed in patients with congestive heart failure.in patients with congestive heart failure.)
• WBR0235  + (Heparin activates antithrombin III. Heparin is indicated for thromboembolic diseases, which are less likely than Lyme disease in a young patient who has recently returned from a camping trip.)
• WBR0349  + (Heparin causes activation of antithrombin III. Rat poison works by a different mechanism.)
• WBR0671  + (Hepatic cirrhosis is characterized by the … Hepatic cirrhosis is characterized by the presence of diffuse fibrosis and nodular regeneration in the liver. In advanced cirrhosis, patients have a shrunken liver. Cirrhosis is the final result of primary biliary cirrhosis, but is not the primary disease in this patient.s not the primary disease in this patient.)
• WBR252  + (Hepatic stellate cells, also known as eith … Hepatic stellate cells, also known as either perisinusoidal cells or Ito cells (earlier lipocytes or fat-storing cells), are pericytes found in the perisinusoidal space of the liver also known as the space of Disse. Following ingestion, vitamin A, a lipid soluble vitamin, undergoes hepatic metabolism, whereby hepatic parenchymal cells absorb vitamin A in the form of retinyl esters. Parenchymal cells metabolize the retinyl esters, which is subsequently transferred to the stellate cells for either storage with other long-chain fatty acids or mobilization into the plasma (bound to RBP).bilization into the plasma (bound to RBP).)
• WBR0882  + (Hepatitis B surface antigen and hepatitic C serologies should be considered in all patients with PAN due to the association between hepatitis and the development of PAN.)
• WBR0772  + (Hereditary spherocytosis is an autosomal dominant hereditary disorder characterized by mutated cytoskeletal components that render the red blood cell membrane susceptible to osmotic fragility.)
• WBR0591  + (Hirschsprung's disease is characterized by the lack of ganglion cells of the enteric nervous plexus.)
• WBR0989  + (Homocystinuria is associated with lens subluxation that is downwards and inwards.)
• WBR0293  + (Huntington's disease, hereditary hemorrhagic telangiectasia, Marfan syndrome, neurofibromatosis types 1 and 2, tuberous sclerosis, and von-Hippel Lindau are all examples of autosomal dominant disorders.)
• WBR0327  + (Hydroxyurea inhibits ribonucleotide reductase, which is not beneficial to patients with SCD.)
• WBR0681  + (Hyper-IgE syndrome is characterized by the failure of Th1 cells to produce IFN-gamma.)
• WBR0637  + (Hyperphosphorylation of the Rb protein renders it inactive and allows the progression into neoplasia as observed in Plate A.)
• WBR0494  + (Hypersensitivity type III disorders include conditions where an antigen-antibody complex forms and activates the complement system. A PPD skin test is not a type III hypersensitivity immune reaction.)
• WBR0493  + (Hypersensitivity type III disorders include conditions where an antigen-antibody complex forms and activates the complement system. Hashimoto's disease is not a type III hypersensitivity disorder.)
• WBR0244  + (Hypophosphatemic rickets is an X-linked dominant disorder.)
• WBR0563  + (Hypoplasia is defined as the presence of primordial tissue and incomplete tissue development.)
• WBR0680  + (IL-4 induces differentiation into Th2 cells and growth of B cells. It also enhances class switching into IgE)
• WBR0773  + (IL-4 is not a main mediator of cachexia syndrome. IL-4 normally functions to induce the differentiation of naive T-helper cells in lymph nodes.)
• WBR0402  + (Identification is an immature defense mechanism in which the individual models his/her behavior after a figure of authority.)
• WBR0256  + (Idiopathic thrombocytopenic purpura (ITP) … Idiopathic thrombocytopenic purpura (ITP) is an acquired bleeding disorder caused by decreased production and increased destruction of platelets due to formation of auto-antibodies against GpIIb/IIIa. ITP is associated with several environmental exposures, including hematological malignancies, HIV infection, HCV infection, and lupus erythematosus. The long history of bleeding and normal platelet counts make ITP a less likely diagnosis in this patient.P a less likely diagnosis in this patient.)
• WBR0081  + (If the infection occurs within 13–26 weeks after conception there is a 23% chance the infant will be affected by the disease. This is not the trimester during which the patient is at highest risk.)