Osthoff, Michael <br/><br/>
Role of lectin pathway complement proteins and genetic variants in organ damage and disease severity of systemic sclerosis: a cross-sectional study.  [electronic resource] 

 -  Arthritis research & therapy  03 2019 
 - 76 p.  digital 
<br/><br/> Publication Type: Journal Article; Multicenter Study; Observational Study; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1478-6362 
<br/><br/><label>Standard No.: </label>10.1186/s13075-019-1859-1  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Aged<br/>Biomarkers--blood<br/>Complement Pathway, Mannose-Binding Lectin--genetics<br/>Complement System Proteins--genetics<br/>Connective Tissue Diseases--complications<br/>Cross-Sectional Studies<br/>Humans<br/>Lectins--blood<br/>Male<br/>Middle Aged<br/>Polymorphism, Single Nucleotide<br/>Prospective Studies<br/>Raynaud Disease--complications<br/>Scleroderma, Systemic--complications<br/>Severity of Illness Index<br/>Ficolins