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Recommendations for live viral and bacterial vaccines in immunodeficient patients and their close contacts.
B-cell development and functions and therapeutic options in adenosine deaminase-deficient patients.
Survey on retransplantation criteria for patients with severe combined immunodeficiency.
Establishing diagnostic criteria for severe combined immunodeficiency disease (SCID), leaky SCID, and Omenn syndrome: the Primary Immune Deficiency Treatment Consortium experience.
A systematic analysis of recombination activity and genotype-phenotype correlation in human recombination-activating gene 1 deficiency.
Primary Immune Deficiency Treatment Consortium (PIDTC) report.
Newborn screening for severe combined immunodeficiency and T-cell lymphopenia in California: results of the first 2 years.
Unresolved issues in hematopoietic stem cell transplantation for severe combined immunodeficiency: need for safer conditioning and reduced late effects.
Intermediate phenotypes in patients with autosomal dominant hyper-IgE syndrome caused by somatic mosaicism.
Dominant gain-of-function STAT1 mutations in FOXP3 wild-type immune dysregulation-polyendocrinopathy-enteropathy-X-linked-like syndrome.