IL2RG reversion event in a common lymphoid progenitor leads to delayed diagnosis and milder phenotype. Read more about IL2RG reversion event in a common lymphoid progenitor leads to delayed diagnosis and milder phenotype.
Nijmegen breakage syndrome detected by newborn screening for T cell receptor excision circles (TRECs). Read more about Nijmegen breakage syndrome detected by newborn screening for T cell receptor excision circles (TRECs).
Coronin-1A: immune deficiency in humans and mice. Read more about Coronin-1A: immune deficiency in humans and mice.
Combined immunodeficiency due to MALT1 mutations, treated by hematopoietic cell transplantation. Read more about Combined immunodeficiency due to MALT1 mutations, treated by hematopoietic cell transplantation.
USIDNET: a strategy to build a community of clinical immunologists. Read more about USIDNET: a strategy to build a community of clinical immunologists.
Bone density and fractures in autosomal dominant hyper IgE syndrome. Read more about Bone density and fractures in autosomal dominant hyper IgE syndrome.
The natural history of children with severe combined immunodeficiency: baseline features of the first fifty patients of the primary immune deficiency treatment consortium prospective study 6901. Read more about The natural history of children with severe combined immunodeficiency: baseline features of the first fifty patients of the primary immune deficiency treatment consortium prospective study 6901.
A phenotypic approach for IUIS PID classification and diagnosis: guidelines for clinicians at the bedside. Read more about A phenotypic approach for IUIS PID classification and diagnosis: guidelines for clinicians at the bedside.
Newborn screening for SCID identifies patients with ataxia telangiectasia. Read more about Newborn screening for SCID identifies patients with ataxia telangiectasia.
Type17 T-cells in central nervous system autoimmunity and tumors. Read more about Type17 T-cells in central nervous system autoimmunity and tumors.
