anchor instance (Q104419)

From ScienceSource
Jump to: navigation, search
No description defined
edit
Language Label Description Also known as
English
anchor instance
No description defined

    Statements

    analyzed. A heterozygous c.442G > C (pE148Q) mutation in the MEFV gene was identified.DiscussionRenal
    0 references
    is a rare cause of proteinuria in children. The prevalence of amyloidosis is higher in patients with
    0 references
    1,131
    0 references
    74
    0 references
    10,198
    0 references
    17 April 2019
    0 references
    0 references
    Clinical improvement of renal amyloidosis in a patient with systemic-onset juvenile idiopathic arthritis who received tocilizumab treatment: a case report and literature review. (5429510)
    0 references
     
    edit
      edit
        edit
          edit
            edit
              edit