145 related articles for article (PubMed ID: 38159157)
1. BCL10 Deficiency Presenting as Severe Combined Immunodeficiency Escaping Newborn Screening.
Salou S; Voelkl S; Keller B; Ehl S; Naumann-Bartsch N
J Clin Immunol; 2023 Dec; 44(1):37. PubMed ID: 38159157
[No Abstract] [Full Text] [Related]
2. BCL10 loss-of-function novel mutation leading to atypical severe combined immunodeficiency.
Al-Tamemi S; Alhinai Z; Al-Rahbi N; Al-Abdawani R; Al-Yazidi L; Al-Shekaili J; Al-Kindi M; Al-Maawali A
Clin Immunol; 2022 Aug; 241():109067. PubMed ID: 35750252
[TBL] [Abstract][Full Text] [Related]
3. Limitation of TREC-based newborn screening for ZAP70 Severe Combined Immunodeficiency.
Grazioli S; Bennett M; Hildebrand KJ; Vallance H; Turvey SE; Junker AK
Clin Immunol; 2014 Jul; 153(1):209-10. PubMed ID: 24797280
[No Abstract] [Full Text] [Related]
4. Evaluation of the T-cell receptor excision circle assay performances for severe combined immunodeficiency neonatal screening on Guthrie cards in a French single centre study.
Audrain M; Thomas C; Mirallie S; Bourgeois N; Sebille V; Rabetrano H; Durand-Zaleski I; Boisson R; Persyn M; Pierres C; Mahlaoui N; Fischer A
Clin Immunol; 2014 Feb; 150(2):137-9. PubMed ID: 24412905
[No Abstract] [Full Text] [Related]
5. More states screen for severe combined immunodeficiency: screening finds other genetic syndromes marked by immunodeficiency.
Am J Med Genet A; 2012 Aug; 158A(8):viii-ix. PubMed ID: 22821837
[No Abstract] [Full Text] [Related]
6. Newborn Screening for IKBKB Deficiency in Manitoba, Using Genetic Mutation Analysis.
Rubin TS; Rockman-Greenberg C; Van Caeseele P; Cuvelier GDE; Kwan L; Schroeder ML
J Clin Immunol; 2018 Oct; 38(7):742-744. PubMed ID: 30288645
[No Abstract] [Full Text] [Related]
7. Newborn Screening for Severe Combined Immunodeficiency.
Routes J; Verbsky J
Curr Allergy Asthma Rep; 2018 May; 18(6):34. PubMed ID: 29749587
[TBL] [Abstract][Full Text] [Related]
8. Lessons for Sequencing from the Addition of Severe Combined Immunodeficiency to Newborn Screening Panels.
Puck JM
Hastings Cent Rep; 2018 Jul; 48 Suppl 2(Suppl 2):S7-S9. PubMed ID: 30133735
[TBL] [Abstract][Full Text] [Related]
9. TRECs/KRECs: Beyond the Diagnosis of Severe Combined Immunodeficiency.
Ramos BC; Aranda CS; Sobrinho AO; Sole D; Condino-Neto A
J Clin Immunol; 2023 Jan; 43(1):80-81. PubMed ID: 36109419
[No Abstract] [Full Text] [Related]
10. Primary immunodeficiency update and newborn screening.
Amado MC
Mo Med; 2011; 108(5):350-3. PubMed ID: 22073493
[TBL] [Abstract][Full Text] [Related]
11. The effect of delayed and early diagnosis in siblings, and importance of newborn screening for SCID.
Krantz MS; Stone CA; Connelly JA; Norton AE; Khan YW
Ann Allergy Asthma Immunol; 2019 Feb; 122(2):211-213. PubMed ID: 30439467
[No Abstract] [Full Text] [Related]
12. Swiss newborn screening for severe T and B cell deficiency with a combined TREC/KREC assay - management recommendations.
Trück J; Prader S; Natalucci G; Hagmann C; Brotschi B; Kelly J; Bassler D; Steindl K; Rauch A; Baumgartner M; Fingerhut R; Hauri-Hohl M; Güngör T; Pachlopnik Schmid J; Berger C; Reichenbach J
Swiss Med Wkly; 2020 Jun; 150():w20254. PubMed ID: 32579701
[TBL] [Abstract][Full Text] [Related]
13. State, federal efforts under way to identify children with "bubble boy syndrome".
Kuehn BM
JAMA; 2010 Oct; 304(16):1771-3. PubMed ID: 20978250
[No Abstract] [Full Text] [Related]
14. Omenn Syndrome Identified by Newborn Screening.
Tallar M; Routes J
Clin Perinatol; 2020 Mar; 47(1):77-86. PubMed ID: 32000930
[TBL] [Abstract][Full Text] [Related]
15. [Neonatal screening of severe combined immunodeficiencies].
Erdős M
Orv Hetil; 2018 Jun; 159(23):948-956. PubMed ID: 29860883
[TBL] [Abstract][Full Text] [Related]
16. Expert commentary: practical issues in newborn screening for severe combined immune deficiency (SCID).
Puck JM; Routes J; Filipovich AH; Sullivan K
J Clin Immunol; 2012 Feb; 32(1):36-8. PubMed ID: 22012274
[No Abstract] [Full Text] [Related]
17. The scary world of variants of uncertain significance (VUS): A hitchhiker's guide to interpretation.
Sullivan KE
J Allergy Clin Immunol; 2021 Feb; 147(2):492-494. PubMed ID: 32598897
[No Abstract] [Full Text] [Related]
18. Neonatal screening for severe primary immunodeficiency diseases using high-throughput triplex real-time PCR.
Borte S; von Döbeln U; Fasth A; Wang N; Janzi M; Winiarski J; Sack U; Pan-Hammarström Q; Borte M; Hammarström L
Blood; 2012 Mar; 119(11):2552-5. PubMed ID: 22130802
[TBL] [Abstract][Full Text] [Related]
19. Newborn screening for severe combined immunodeficiency does not identify bare lymphocyte syndrome.
Kuo CY; Chase J; Garcia Lloret M; Stiehm ER; Moore T; Aguilera MJ; Lopez Siles J; Church JA
J Allergy Clin Immunol; 2013 Jun; 131(6):1693-5. PubMed ID: 23453137
[No Abstract] [Full Text] [Related]
20. Neonatal screening for severe combined immune deficiency.
Puck JM
Curr Opin Allergy Clin Immunol; 2007 Dec; 7(6):522-7. PubMed ID: 17989529
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]