Last Posted: Dec 11, 2019
- Where are you in your SCID journey?
Immune Deficiency Foundation, SCID Compass, 2019 - Dilemma of Reporting Incidental Findings in Newborn Screening Programs for SCID: Parents' Perspective on Ataxia Telangiectasia.
Blom Maartje et al. Frontiers in immunology 2019 102438 - Early diagnosis of ataxia telangiectasia in the neonatal phase: a parents' perspective.
Schoenaker M H D et al. European journal of pediatrics 2019 Nov - First Universal Newborn Screening Program for Severe Combined Immunodeficiency in Europe. Two-Years' Experience in Catalonia (Spain).
Argudo-Ramírez Ana et al. Frontiers in immunology 2019 102406 - Identification of 22q11.2 deletion syndrome via newborn screening for severe combined immunodeficiency. Two years' experience in Catalonia (Spain).
Martin-Nalda Andrea et al. Molecular genetics & genomic medicine 2019 Oct e1016 - Universal Newborn Screening for Severe Combined Immunodeficiency (SCID).
van der Burg Mirjam et al. Frontiers in pediatrics 2019 7373 - Newborn screening for severe combined immunodeficiency: Evaluation of a commercial T-cell receptor excision circle-based method in Victorian dried blood spots.
Richards Stephanie et al. Journal of paediatrics and child health 2018 54(1) 14-19 - What to Do with an Abnormal Newborn Screen for Severe Combined Immune Deficiency.
Chong Hey J et al. Immunology and allergy clinics of North America 2019 Nov 39(4) 535-546 - Advances and highlights in primary immunodeficiencies in 2017.
Chinen Javier et al. The Journal of allergy and clinical immunology 2018 142(4) 1041-1051 - Nonsevere combined immunodeficiency T-cell lymphopenia identified through newborn screening.
Patrawala Meera et al. Current opinion in allergy and clinical immunology 2019 Sep
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