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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.

Search by property

A list of all pages that have property "AnswerB" with value "Systemic corticosteroids". Since there have been only a few results, also nearby values are displayed.

Showing below up to 26 results starting with #1.

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List of results

  • WBR0843  + (Systemic corticosteroids)
  • WBR0542  + (Systemic lupus erythematosus (SLE))
  • WBR0752  + (Systolic ejection murmur)
  • WBR0035  + (T wave inversion and poor R wave progression.)
  • WBR0025  + (T wave inversion and poor R wave progression.)
  • WBR0641  + (T-cell inability to depolymerize cytoskeleton)
  • WBR1489  + (T2;N0;M0 - Stage IIA)
  • WBR1104  + (T6)
  • WBR0128  + (TSH, BUN, creatinine and LFTs)
  • WBR0462  + (Tadalafil)
  • WBR0015  + (Tall, peaked T waves)
  • WBR0424  + (Teeth clenching)
  • WBR0265  + (Temporary conductive hearing loss)
  • WBR0871  + (Tenofovir)
  • WBR1047  + (Tensilon test)
  • WBR0725  + (Teratoma)
  • WBR294  + (Tetracycline)
  • WBR0077  + (The basement membrane (Bowman's layer) and the corneal stroma)
  • WBR0096  + (The disease is associated with subcutaneous deposits)
  • WBR0533  + (The extra heart sound conveys poor prognostic outcomes)
  • WBR0276  + (The infectious agent undergoes phagocytosis by alveolar macrophages)
  • WBR0599  + (The method is precise but not accurate; it is valid but not reproducible)
  • WBR0823  + (The night before surgery)
  • WBR0134  + (The patient needs a test for IgM antibody to hepatitis A virus to rule out acute hepatitis A.)
  • WBR0102  + (The patient's condition is caused by defects in hydroxylation of proline residues)
  • WBR0103  + (The patient’s condition is caused by inactivating mutations in the ''FGFR3'' gene; and his children have a 50% chance of developing dwarfism.)