Literature DB >> 14181141

PAROXYSMAL NOCTURNAL HEMOGLOBINURIA PRESENTING AS APLASTIC ANEMIA IN A CHILD. CASE REPORT WITH EVIDENCE OF DEFICIENT LEUKOCYTE ACETYLCHOLINESTERASE ACTIVITY.

J D ROSS, E ROSENBAUM.   

Abstract

Entities:  

Keywords:  ACETYLCHOLINESTERASE; ANEMIA, APLASTIC; BIOPSY; BLOOD ALKALINE PHOSPHATASE; BLOOD TRANSFUSION; BONE MARROW EXAMINATION; BONE MARROW TRANSPLANTATION; CHILD; CHLORAMPHENICOL; DEFICIENCY DISEASES; DIAGNOSIS; ENZYME TESTS; ERYTHROCYTES; GLUCOSEPHOSPHATE DEHYDROGENASE; HEMOGLOBINURIA, PAROXYSMAL; LEUKOCYTES; PATHOLOGY; PREDNISONE; TESTOSTERONE

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Year:  1964        PMID： 14181141     DOI： 10.1016/0002-9343(64)90217-7

Source DB:  PubMed          Journal:  Am J Med        ISSN： 0002-9343            Impact factor:   4.965


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  1 in total

1.  A platelet and granulocyte membrane defect in paroxysmal nocturnal hemoglobinuria: usefulness for the detection of platelet antibodies.

Authors:  R H Aster; S E Enright
Journal:  J Clin Invest       Date:  1969-07       Impact factor: 14.808
  1 in total

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