Höchsmann, Britta <br/><br/>
Complement and inflammasome overactivation mediates paroxysmal nocturnal hemoglobinuria with autoinflammation.  [electronic resource] 

 -  The Journal of clinical investigation  12 2019 
 - 5123-5136 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1558-8238 
<br/><br/><label>Standard No.: </label>10.1172/JCI123501  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Aged<br/>Alleles<br/>Antibodies, Monoclonal, Humanized--therapeutic use<br/>Complement System Proteins--immunology<br/>Female<br/>Gene Deletion<br/>Genes, X-Linked<br/>Germany<br/>Glycosylphosphatidylinositols--metabolism<br/>Hemoglobinuria, Paroxysmal--immunology<br/>Hemolysis--drug effects<br/>Humans<br/>Inflammasomes--immunology<br/>Inflammation--immunology<br/>Japan<br/>Leukocytes--immunology<br/>Male<br/>Membrane Proteins--genetics<br/>Middle Aged<br/>Mutation<br/>Point Mutation<br/>THP-1 Cells