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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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1993 | 1 |
2015 | 2 |
2016 | 1 |
2024 | 0 |
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Page 1
Spectrum of mutations in a cohort of UK patients with ADA deficient SCID: Segregation of genotypes with specific ethnicities.
Clin Immunol. 2015 Dec;161(2):174-9. doi: 10.1016/j.clim.2015.08.001. Epub 2015 Aug 5.
Clin Immunol. 2015.
PMID: 26255240
Diagnosis, Treatment and Long-Term Follow Up of Patients with ADA Deficiency: a Single-Center Experience.
Baffelli R, Notarangelo LD, Imberti L, Hershfield MS, Serana F, Santisteban I, Bolda F, Porta F, Lanfranchi A.
Baffelli R, et al.
J Clin Immunol. 2015 Oct;35(7):624-37. doi: 10.1007/s10875-015-0191-z. Epub 2015 Sep 16.
J Clin Immunol. 2015.
PMID: 26376800
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Two new mutations at the adenosine deaminase (ADA) locus (Q254X and del nt1050-54) unusual for not being missense mutations.
Hirschhorn R, Chen AS, Israni A, Yang DR, Huie ML.
Hirschhorn R, et al.
Hum Mutat. 1993;2(4):320-3. doi: 10.1002/humu.1380020415.
Hum Mutat. 1993.
PMID: 8401541
No abstract available.
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Rapid molecular diagnostics of severe primary immunodeficiency determined by using targeted next-generation sequencing.
Yu H, Zhang VW, Stray-Pedersen A, Hanson IC, Forbes LR, de la Morena MT, Chinn IK, Gorman E, Mendelsohn NJ, Pozos T, Wiszniewski W, Nicholas SK, Yates AB, Moore LE, Berge KE, Sorte H, Bayer DK, ALZahrani D, Geha RS, Feng Y, Wang G, Orange JS, Lupski JR, Wang J, Wong LJ.
Yu H, et al.
J Allergy Clin Immunol. 2016 Oct;138(4):1142-1151.e2. doi: 10.1016/j.jaci.2016.05.035. Epub 2016 Jul 12.
J Allergy Clin Immunol. 2016.
PMID: 27484032
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