The Case for Mandatory Newborn Screening for Severe Combined Immunodeficiency (SCID)
暂无分享,去创建一个
[1] J. Puck,et al. Newborn screening for severe combined immunodeficiency and T-cell lymphopenia in California: results of the first 2 years. , 2013, The Journal of allergy and clinical immunology.
[2] A. Thrasher,et al. Current progress on gene therapy for primary immunodeficiencies , 2013, Gene Therapy.
[3] B. Kuehn. After 50 years, newborn screening continues to yield public health gains. , 2013, JAMA.
[4] L. Hammarström,et al. Guidelines for newborn screening of primary immunodeficiency diseases , 2013, Current opinion in hematology.
[5] H. Gaspar. Gene therapy for ADA-SCID: defining the factors for successful outcome. , 2012, Blood.
[6] K. Schwarz,et al. Delayed-onset adenosine deaminase deficiency: strategies for an early diagnosis. , 2012, The Journal of allergy and clinical immunology.
[7] A. Fischer,et al. Transplantation in patients with SCID: mismatched related stem cells or unrelated cord blood? , 2012, Blood.
[8] U. Sack,et al. Neonatal screening for severe primary immunodeficiency diseases using high-throughput triplex real-time PCR. , 2012, Blood.
[9] T. Fleisher,et al. The Wisconsin Approach to Newborn Screening for Severe Combined Immunodeficiency , 2012, Pediatrics.
[10] W. Grossman,et al. Newborn Screening for Severe Combined Immunodeficiency; The Wisconsin Experience (2008–2011) , 2012, Journal of Clinical Immunology.
[11] S. Dixon,et al. Putting a value on the avoidance of false positive results when screening for inherited metabolic disease in the newborn , 2012, Journal of Inherited Metabolic Disease.
[12] J. Puck. The case for newborn screening for severe combined immunodeficiency and related disorders , 2011, Annals of the New York Academy of Sciences.
[13] L. Hammarström,et al. Newborn screening for primary immunodeficiencies: beyond SCID and XLA , 2011, Annals of the New York Academy of Sciences.
[14] J. Puck. Neonatal screening for severe combined immunodeficiency , 2011, Current opinion in pediatrics.
[15] Kee Chan,et al. A Markov model to analyze cost-effectiveness of screening for severe combined immunodeficiency (SCID). , 2011, Molecular genetics and metabolism.
[16] J. Verbsky,et al. Screening newborns for primary T-cell immunodeficiencies: consensus and controversy , 2011, Expert review of clinical immunology.
[17] Kathryn L. Parsley,et al. Long-Term Persistence of a Polyclonal T Cell Repertoire After Gene Therapy for X-Linked Severe Combined Immunodeficiency , 2011, Science Translational Medicine.
[18] Kathryn L. Parsley,et al. Hematopoietic Stem Cell Gene Therapy for Adenosine Deaminase–Deficient Severe Combined Immunodeficiency Leads to Long-Term Immunological Recovery and Metabolic Correction , 2011, Science Translational Medicine.
[19] Kathryn L. Parsley,et al. Immunodeficiency: Long-term persistence of a polyclonal t cell repertoire after gene therapy for X-linked severe combined immunodeficiency , 2011 .
[20] O. Ohara,et al. Quantification of κ-deleting recombination excision circles in Guthrie cards for the identification of early B-cell maturation defects. , 2011, The Journal of allergy and clinical immunology.
[21] M. van der Burg,et al. Educational paper , 2011, European Journal of Pediatrics.
[22] A. Gennery,et al. Neonatal diagnosis of severe combined immunodeficiency leads to significantly improved survival outcome: the case for newborn screening. , 2011, Blood.
[23] A. Fischer,et al. Immune deficiencies , infection , and systemic immune disorders Transplantation of hematopoietic stem cells and long-term survival for primary immunodeficiencies in Europe : Entering a new century , do we do better ? , 2010 .
[24] Frederic D. Bushman,et al. Efficacy of gene therapy for X-linked severe combined immunodeficiency. , 2010, The New England journal of medicine.
[25] L. Notarangelo,et al. Guidelines for implementation of population-based newborn screening for severe combined immunodeficiency , 2010, Journal of Inherited Metabolic Disease.
[26] R. Laessig,et al. Implementing Routine Testing for Severe Combined Immunodeficiency within Wisconsin's Newborn Screening Program , 2010, Public health reports.
[27] L. Prosser,et al. Systematic Evidence Review of Newborn Screening and Treatment of Severe Combined Immunodeficiency , 2010, Pediatrics.
[28] A. Fischer,et al. Gene therapy for primary immunodeficiencies. , 2010, Immunology and allergy clinics of North America.
[29] Alessandro Aiuti,et al. Gene therapy for immunodeficiency due to adenosine deaminase deficiency. , 2009, The New England journal of medicine.
[30] R. Laessig,et al. Statewide newborn screening for severe T-cell lymphopenia. , 2009, JAMA.
[31] H. Kanegane,et al. Identification of severe combined immunodeficiency by T-cell receptor excision circles quantification using neonatal guthrie cards. , 2009, The Journal of pediatrics.
[32] R. Laessig,et al. Development of a routine newborn screening protocol for severe combined immunodeficiency. , 2009, The Journal of allergy and clinical immunology.
[33] A. Fischer,et al. Long-term outcome after hematopoietic stem cell transplantation of a single-center cohort of 90 patients with severe combined immunodeficiency. , 2009, Blood.
[34] L. Notarangelo,et al. Omenn syndrome: inflammation in leaky severe combined immunodeficiency. , 2008, The Journal of allergy and clinical immunology.
[35] T. Cole,et al. Cognitive and behavioral abnormalities in children after hematopoietic stem cell transplantation for severe congenital immunodeficiencies. , 2008, Blood.
[36] A. Andermann,et al. Revisiting Wilson and Jungner in the genomic age: a review of screening criteria over the past 40 years. , 2008, Bulletin of the World Health Organization.
[37] J. Puck. Neonatal screening for severe combined immune deficiency , 2007, Current opinion in allergy and clinical immunology.
[38] L. Notarangelo,et al. Long-term immune reconstitution and clinical outcome after stem cell transplantation for severe T-cell immunodeficiency. , 2007, The Journal of allergy and clinical immunology.
[39] F. Miedema,et al. Early determinants of long-term T-cell reconstitution after hematopoietic stem cell transplantation for severe combined immunodeficiency. , 2006, Blood.
[40] A. Thrasher,et al. Gene therapy for severe combined immunodeficiencies , 2005, Expert opinion on biological therapy.
[41] J. Puck,et al. Development of population-based newborn screening for severe combined immunodeficiency. , 2005, The Journal of allergy and clinical immunology.
[42] A. Fischer,et al. Long-term survival and transplantation of haemopoietic stem cells for immunodeficiencies: report of the European experience 1968–99 , 2003, The Lancet.
[43] J. Puck,et al. Hematopoietic stem cell transplantation for severe combined immunodeficiency in the neonatal period leads to superior thymic output and improved survival. , 2002, Blood.
[44] M. Cowan,et al. Cutaneous manifestations of maternal engraftment in patients with severe combined immunodeficiency: a clinicopathologic study , 2001, Bone Marrow Transplantation.
[45] J. Roberts,et al. Hematopoietic stem-cell transplantation for the treatment of severe combined immunodeficiency. , 1999, The New England journal of medicine.
[46] A. Fischer,et al. European experience of bone-marrow transplantation for severe combined immunodeficiency , 1990, The Lancet.
[47] A. Gennery,et al. The expanding clinical and immunological spectrum of severe combined immunodeficiency , 2011 .
[48] Ja Wilson,et al. Principles and practice of screening for disease , 1968 .