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hemoglobinurias การใช้

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  • It is the first approved therapy for paroxysmal nocturnal hemoglobinuria.
  • Paroxysmal cold hemoglobinuria is treated by removing the underlying cause, such as infection.
  • It was initially approved to treat paroxysmal nocturnal hemoglobinuria, a rare blood disorder.
  • Red cell destruction in these acute hemolytic events is largely intravascular and therefore is associated with hemoglobinuria.
  • Hemoglobinuria is seen due to excretion of red-blood-cell lysis byproducts via the kidneys.
  • It is possible to use an ammonia sulphate precipitation test in order to distinguish between hemoglobinuria and myoglobinuria.
  • The symptoms are fever and chills, sometimes with back pain and pink or red urine ( hemoglobinuria ).
  • Most notably, deficiency of the MAC inhibitor CD59 results in an overactivity of complement and Paroxysmal nocturnal hemoglobinuria.
  • :: : : The most dramatic disease which causes the symptoms you describe, is Paroxysmal cold hemoglobinuria.
  • Sir Dacie is credited with characterizing the relationship between paroxysmal nocturnal hemoglobinuria and bone marrow failure syndromes like aplastic anemia.
  • Splenomegaly, severe headache, hepatomegaly ( enlarged liver ), hypoglycemia, and hemoglobinuria with renal failure may occur.
  • In animals, babesiosis is suspected by observation of clinical signs ( hemoglobinuria and anemia ) in animals in endemic areas.
  • Castle and his team later characterized the red blood cell defects that are responsible for paroxysmal nocturnal hemoglobinuria and hereditary spherocytosis.
  • Two colour charts are provided that correspond to the reactions that occur with hemoglobinuria, myoglobinuria and hematuria ( RBCs ).
  • Mutations affecting GPI that reduce expression of CD59 and decay-accelerating factor on red blood cells result in paroxysmal nocturnal hemoglobinuria.
  • In 1931, he described Paroxysmal nocturnal hemoglobinuria in depth, and also a rare form of this disease Str黚ing-Marchiafava-Micheli Syndrome.
  • To formally diagnose agranulocytosis, other pathologies with a similar presentation must be excluded, such as aplastic anemia, paroxysmal nocturnal hemoglobinuria, myelodysplasia and leukemias.
  • Disorders of the proteins in these membranes are associated with many disorders, such as hereditary spherocytosis, hereditary elliptocytosis, hereditary stomatocytosis, and paroxysmal nocturnal hemoglobinuria.
  • Although diamphotoxin has no neurotoxic effect, its hemolytic effect is lethal, and may reduce hemoglobin levels by as much as 75 %, leading to hemoglobinuria.
  • Hemoglobinuria can be caused by hemolytic anaemia, blood transfusions, extensive burns, the bite of the recluse spider ( Loxosceles ), infections and strenuous exercise.
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