Newborn Screening for Severe Combined Immunodeficiency; The Wisconsin Experience (2008–2011)

Neonatal diagnosis of severe combined immunodeficiency leads to significantly improved survival outcome: the case for newborn screening

(2011) L. Brown et al.   BLOOD

Transplantation of hematopoietic stem cells in human severe combined immunodeficiency: longterm outcomes

(2010) Rebecca H. Buckley   IMMUNOLOGIC RESEARCH

Human phagocyte defect caused by a Rac2 mutation detected by means of neonatal screening for T-cell lymphopenia

(2010) Deborah Accetta et al.   JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY

Statewide Newborn Screening for Severe T-Cell Lymphopenia

(2009) John M. Routes   JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION

Improving cellular therapy for primary immune deficiency diseases: Recognition, diagnosis, and management

(2009) Linda M. Griffith et al.   JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY

Development of a routine newborn screening protocol for severe combined immunodeficiency

(2009) Mei W. Baker et al.   JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY

Persistent low thymic activity and non-cardiac mortality in children with chromosome 22q11·2 microdeletion and partial DiGeorge syndrome

(2008) P. Eberle et al.   CLINICAL AND EXPERIMENTAL IMMUNOLOGY