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2 Result(s)
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Article
Open AccessDelayed diagnosis of X-linked agammaglobulinaemia in a boy with recurrent meningitis
X-linked agammaglobulinaemia (XLA) is a rare inherited primary immunodeficiency disease characterized by the B cell developmental defect, caused by mutations in the gene coding for Bruton’s tyrosine kinase (BT...
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Open AccessClinical manifestations of severe enterovirus 71 infection and early assessment in a Southern China population
Enterovirus 71 (EV-A71) shows a potential of rapid death, but the natural history of the infection is poorly known. This study aimed to examine the natural history of EV-A71 infection.
