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Recommendations for live viral and bacterial vaccines in immunodeficient patients and their close contacts.

  • Read more about 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.

  • Read more about B-cell development and functions and therapeutic options in adenosine deaminase-deficient patients.

Survey on retransplantation criteria for patients with severe combined immunodeficiency.

  • Read more about 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.

  • Read more about 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.

  • Read more about A systematic analysis of recombination activity and genotype-phenotype correlation in human recombination-activating gene 1 deficiency.

Primary Immune Deficiency Treatment Consortium (PIDTC) report.

  • Read more about 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.

  • Read more about 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.

  • Read more about 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.

  • Read more about 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.

  • Read more about Dominant gain-of-function STAT1 mutations in FOXP3 wild-type immune dysregulation-polyendocrinopathy-enteropathy-X-linked-like syndrome.

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