Schrezenmeier, H <br/><br/>
A pathogenetic link between aplastic anemia and paroxysmal nocturnal hemoglobinuria is suggested by a high frequency of aplastic anemia patients with a deficiency of phosphatidylinositol glycan anchored proteins.  [electronic resource] 

 -  Experimental hematology  Jan 1995 
 - 81-7 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0301-472X 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Aged<br/>Anemia, Aplastic--blood<br/>Antibodies, Monoclonal<br/>Erythrocytes--chemistry<br/>Female<br/>Flow Cytometry<br/>Glycosylphosphatidylinositols--blood<br/>Granulocytes--chemistry<br/>Hemoglobinuria, Paroxysmal--blood<br/>Humans<br/>Immunosuppression Therapy<br/>Lymphocytes--chemistry<br/>Male<br/>Middle Aged<br/>Monocytes--chemistry