about
The value of family history in diagnosing primary immunodeficiency disordersA nonsense mutation in IKBKB causes combined immunodeficiency.Broad-spectrum antibodies against self-antigens and cytokines in RAG deficiencyClinical application of whole-genome sequencing in patients with primary immunodeficiency.Why newborn screening for severe combined immunodeficiency is essential: a case report.THE IMPORTANCE OF EDUCATING PEDIATRICIANS ABOUT PRIMARY IMMUNODEFICIENCY DISORDERS: A TERTIARY HOSPITAL EXPERIENCE.Antibiotics for simple upper respiratory tract infections: a survey of academic, pediatric, and adult clinical allergists.Persistent antibody depletion after rituximab in three children with autoimmune cytopenias.
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description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Mehdi Adeli
@ast
Mehdi Adeli
@en
Mehdi Adeli
@es
Mehdi Adeli
@nl
type
label
Mehdi Adeli
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Mehdi Adeli
@en
Mehdi Adeli
@es
Mehdi Adeli
@nl
prefLabel
Mehdi Adeli
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Mehdi Adeli
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Mehdi Adeli
@es
Mehdi Adeli
@nl
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P31
P496
0000-0002-3051-3080