Provaznikova, Dana <br/><br/>
Manifestation of atypical hemolytic uremic syndrome caused by novel mutations in MCP.  [electronic resource] 

 -  Pediatric nephrology (Berlin, Germany)  Jan 2012 
 - 73-81 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1432-198X 
<br/><br/><label>Standard No.: </label>10.1007/s00467-011-1943-5  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Age of Onset<br/>Atypical Hemolytic Uremic Syndrome<br/>Child<br/>Czech Republic<br/>DNA Mutational Analysis<br/>Female<br/>Genetic Predisposition to Disease<br/>Granulocytes--immunology<br/>Hemolytic-Uremic Syndrome--genetics<br/>Humans<br/>Male<br/>Membrane Cofactor Protein--genetics<br/>Mutation<br/>Pedigree<br/>Penetrance<br/>Phenotype<br/>Prognosis<br/>Recurrence<br/>Severity of Illness Index<br/>Young Adult