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PedAM

Pediatric Disease Annotations & Medicines




Disease paroxysmal nocturnal hemoglobinuria
Phenotype C0002871|anemia
Sentences 7
PubMedID- 24369265 [autoimmune hemolytic anemia with a paroxysmal nocturnal hemoglobinuria-like defect: report of one case].
PubMedID- 22851928 In the present, replacement therapy of c1-inhibitor is also another established treatment for hereditary angioedema in addition to anti-c5 antibodies for c-dependent hemolytic anemia in patients with paroxysmal nocturnal hemoglobinuria, respectively [155,156].
PubMedID- 24267002 [the variation and clinical significance of paroxysmal nocturnal hemoglobinuria clone in patients with aplastic anemia before and after immunosuppressive therapy].
PubMedID- 21447004 Objective: to investigate the natural history of paroxysmal nocturnal hemoglobinuria (pnh) clones in patients with acquired aplastic anemia (aa).
PubMedID- 22937317 Response of paroxysmal nocturnal hemoglobinuria clone with aplastic anemia to rituximab.
PubMedID- 20509122 [anemia with aplastic anemia, paroxysmal nocturnal hemoglobinuria and myelodysplastic syndromes].
PubMedID- 25914813 paroxysmal nocturnal hemoglobinuria presents with hemolytic anemia, although it is also associated with thrombosis and pancytopenia.

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