Mori, M <br/><br/>
Mutation analysis and therapeutic response to granulocyte colony-stimulating factor in a case of hyperimmunoglobulin M syndrome with chronic neutropenia.  [electronic resource] 

 -  Journal of pediatric hematology/oncology   
 - 288-9 p.  digital 
<br/><br/> Publication Type: Case Reports; Letter 
<br/><br/><label>ISSN: </label>1077-4114 
<br/><br/><label>Standard No.: </label>10.1097/00043426-200005000-00020  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Agammaglobulinemia--complications<br/>B-Lymphocytes--pathology<br/>CD40 Ligand<br/>Common Variable Immunodeficiency--diagnosis<br/>DNA Mutational Analysis<br/>Diagnostic Errors<br/>Granulocyte Colony-Stimulating Factor--deficiency<br/>Humans<br/>Hypergammaglobulinemia--complications<br/>IgA Deficiency--complications<br/>IgG Deficiency--complications<br/>Immunoglobulin D--deficiency<br/>Immunoglobulin E--deficiency<br/>Immunoglobulin M--genetics<br/>Immunoglobulins, Intravenous--therapeutic use<br/>Male<br/>Membrane Glycoproteins--deficiency<br/>Neutropenia--etiology<br/>Sequence Deletion<br/>Syndrome