[HTML][HTML] Natural history of mevalonate kinase deficiency: a literature review
S Zhang - Pediatric Rheumatology, 2016 - Springer
Mevalonate kinase deficiency (MKD), a very rare autosomal recessive autoinflammatory
disease with multiple organ involvement, presents clinically as hyperimmunoglobulinemia D …
disease with multiple organ involvement, presents clinically as hyperimmunoglobulinemia D …
Natural history of mevalonate kinase deficiency: a literature review
S Zhang - Pediatric rheumatology online journal, 2016 - pubmed.ncbi.nlm.nih.gov
Mevalonate kinase deficiency (MKD), a very rare autosomal recessive autoinflammatory
disease with multiple organ involvement, presents clinically as hyperimmunoglobulinemia D …
disease with multiple organ involvement, presents clinically as hyperimmunoglobulinemia D …
Natural history of mevalonate kinase deficiency: a literature review
S Zhang - Pediatric Rheumatology, 2016 - infona.pl
Mevalonate kinase deficiency (MKD), a very rare autosomal recessive autoinflammatory
disease with multiple organ involvement, presents clinically as hyperimmunoglobulinemia D …
disease with multiple organ involvement, presents clinically as hyperimmunoglobulinemia D …
Natural history of mevalonate kinase deficiency: a literature review
S Zhang - Pediatric Rheumatology, 2016 - go.gale.com
Mevalonate kinase deficiency (MKD), a very rare autosomal recessive autoinflammatory
disease with multiple organ involvement, presents clinically as hyperimmunoglobulinemia D …
disease with multiple organ involvement, presents clinically as hyperimmunoglobulinemia D …
Natural history of mevalonate kinase deficiency: a literature review.
S Zhang - Pediatric Rheumatology, 2016 - search.ebscohost.com
Mevalonate kinase deficiency (MKD), a very rare autosomal recessive autoinflammatory
disease with multiple organ involvement, presents clinically as hyperimmunoglobulinemia D …
disease with multiple organ involvement, presents clinically as hyperimmunoglobulinemia D …
[HTML][HTML] Natural history of mevalonate kinase deficiency: a literature review
S Zhang - Pediatric Rheumatology Online Journal, 2016 - ncbi.nlm.nih.gov
Mevalonate kinase deficiency (MKD), a very rare autosomal recessive autoinflammatory
disease with multiple organ involvement, presents clinically as hyperimmunoglobulinemia D …
disease with multiple organ involvement, presents clinically as hyperimmunoglobulinemia D …
Natural history of mevalonate kinase deficiency: a literature review
S Zhang - Pediatric Rheumatology, 2016 - search.proquest.com
Mevalonate kinase deficiency (MKD), a very rare autosomal recessive autoinflammatory
disease with multiple organ involvement, presents clinically as hyperimmunoglobulinemia D …
disease with multiple organ involvement, presents clinically as hyperimmunoglobulinemia D …
[HTML][HTML] Natural history of mevalonate kinase deficiency: a literature review
S Zhang - Pediatric Rheumatology, 2016 - ped-rheum.biomedcentral.com
Mevalonate kinase deficiency (MKD), a very rare autosomal recessive autoinflammatory
disease with multiple organ involvement, presents clinically as hyperimmunoglobulinemia D …
disease with multiple organ involvement, presents clinically as hyperimmunoglobulinemia D …
[PDF][PDF] Natural history of mevalonate kinase deficiency: a literature review
S Zhang - 2016 - cyberleninka.org
Mevalonate kinase deficiency (MKD), a very rare autosomal recessive autoinflammatory
disease with multiple organ involvement, presents clinically as hyperimmunoglobulinemia D …
disease with multiple organ involvement, presents clinically as hyperimmunoglobulinemia D …
Natural history of mevalonate kinase deficiency: a literature review.
S Zhang - Pediatric Rheumatology Online Journal, 2016 - europepmc.org
Mevalonate kinase deficiency (MKD), a very rare autosomal recessive autoinflammatory
disease with multiple organ involvement, presents clinically as hyperimmunoglobulinemia D …
disease with multiple organ involvement, presents clinically as hyperimmunoglobulinemia D …