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2019 1
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2023 8
2024 2

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Page 1
Characterization of the clinical and immunologic phenotype and management of 157 individuals with 56 distinct heterozygous NFKB1 mutations.
Lorenzini T, Fliegauf M, Klammer N, Frede N, Proietti M, Bulashevska A, Camacho-Ordonez N, Varjosalo M, Kinnunen M, de Vries E, van der Meer JWM, Ameratunga R, Roifman CM, Schejter YD, Kobbe R, Hautala T, Atschekzei F, Schmidt RE, Schröder C, Stepensky P, Shadur B, Pedroza LA, van der Flier M, Martínez-Gallo M, Gonzalez-Granado LI, Allende LM, Shcherbina A, Kuzmenko N, Zakharova V, Neves JF, Svec P, Fischer U, Ip W, Bartsch O, Barış S, Klein C, Geha R, Chou J, Alosaimi M, Weintraub L, Boztug K, Hirschmugl T, Dos Santos Vilela MM, Holzinger D, Seidl M, Lougaris V, Plebani A, Alsina L, Piquer-Gibert M, Deyà-Martínez A, Slade CA, Aghamohammadi A, Abolhassani H, Hammarström L, Kuismin O, Helminen M, Allen HL, Thaventhiran JE, Freeman AF, Cook M, Bakhtiar S, Christiansen M, Cunningham-Rundles C, Patel NC, Rae W, Niehues T, Brauer N, Syrjänen J, Seppänen MRJ, Burns SO, Tuijnenburg P, Kuijpers TW; NIHR BioResource; Warnatz K, Grimbacher B; NIHR BioResource. Lorenzini T, et al. J Allergy Clin Immunol. 2020 Oct;146(4):901-911. doi: 10.1016/j.jaci.2019.11.051. Epub 2020 Apr 9. J Allergy Clin Immunol. 2020. PMID: 32278790 Free PMC article.
However, the high frequency of autoimmunity (57.4%), lymphoproliferation (52.4%), noninfectious enteropathy (23.1%), opportunistic infections (15.7%), autoinflammation (29.6%), and malignancy (16.8%) identified NF-kappaB1-related disease as an inborn error of imm
However, the high frequency of autoimmunity (57.4%), lymphoproliferation (52.4%), noninfectious enteropathy (23.1%), opportunistic infection …
Newborn Screening in the Diagnosis of Primary Immunodeficiency.
Kobrynski LJ. Kobrynski LJ. Clin Rev Allergy Immunol. 2022 Aug;63(1):9-21. doi: 10.1007/s12016-021-08876-z. Epub 2021 Jul 22. Clin Rev Allergy Immunol. 2022. PMID: 34292457 Review.
Newborn screening for severe combined immune deficiency (SCID) is the first inborn error of immunity (IEI) to be detected through population screening. ...Advances in the clinical care and new therapeutics for many inborn errors of imm
Newborn screening for severe combined immune deficiency (SCID) is the first inborn error of immunity (IEI) to be detect …
Newborn screening for severe combined immunodeficiency and inborn errors of immunity.
Lev A, Somech R, Somekh I. Lev A, et al. Curr Opin Pediatr. 2023 Dec 1;35(6):692-702. doi: 10.1097/MOP.0000000000001291. Epub 2023 Sep 14. Curr Opin Pediatr. 2023. PMID: 37707504 Review.
Newborn screening (NBS) programs play a crucial role in facilitating early diagnoses and timely interventions for affected infants. RECENT FINDINGS: SCID marked the pioneering inborn error of immunity (IEI) to undergo NBS, a milestone achieved 15 years ago th …
Newborn screening (NBS) programs play a crucial role in facilitating early diagnoses and timely interventions for affected infants. RECENT F …
Activated PI3Kdelta syndrome - reviewing challenges in diagnosis and treatment.
Vanselow S, Wahn V, Schuetz C. Vanselow S, et al. Front Immunol. 2023 Jul 20;14:1208567. doi: 10.3389/fimmu.2023.1208567. eCollection 2023. Front Immunol. 2023. PMID: 37600808 Free PMC article. Review.
Activated PI3Kdelta syndrome (APDS) is a rare inborn error of immunity (IEI) characterized primarily by frequent infections, lymphoproliferation and autoimmunity. ...Treatment of APDS has so far been mostly symptom-oriented with immunoglobulin replacement …
Activated PI3Kdelta syndrome (APDS) is a rare inborn error of immunity (IEI) characterized primarily by frequent infect …
Recent advances in primary immunodeficiency: from molecular diagnosis to treatment.
Bucciol G, Meyts I. Bucciol G, et al. F1000Res. 2020 Mar 19;9:F1000 Faculty Rev-194. doi: 10.12688/f1000research.21553.1. eCollection 2020. F1000Res. 2020. PMID: 32226610 Free PMC article. Review.
This review examines recent developments in the field of inborn errors of immunity, from their definition to their treatment. We will summarize the challenges posed by the growth of next-generation sequencing in the clinical setting, touch briefly on the expansion o …
This review examines recent developments in the field of inborn errors of immunity, from their definition to their treatment. …
Genomics Driving Diagnosis and Treatment of Inborn Errors of Immunity With Cancer Predisposition.
Barmettler S, Sharapova SO, Milota T, Greif PA, Magg T, Hauck F. Barmettler S, et al. J Allergy Clin Immunol Pract. 2022 Jul;10(7):1725-1736.e2. doi: 10.1016/j.jaip.2022.03.012. Epub 2022 Mar 29. J Allergy Clin Immunol Pract. 2022. PMID: 35364342 Review.
Inborn errors of immunity (IEI) are genetically and clinically heterogeneous disorders that, in addition to infection susceptibility and immune dysregulation, can have an enhanced cancer predisposition. ...However, broad application of unbiased genetics in these nei
Inborn errors of immunity (IEI) are genetically and clinically heterogeneous disorders that, in addition to infection suscepti
COPA Syndrome from Diagnosis to Treatment: A Clinician's Guide.
Simchoni N, Vogel TP, Shum AK. Simchoni N, et al. Rheum Dis Clin North Am. 2023 Nov;49(4):789-804. doi: 10.1016/j.rdc.2023.06.005. Epub 2023 Jul 21. Rheum Dis Clin North Am. 2023. PMID: 37821196 Review.
COPA syndrome is a recently described autosomal dominant inborn error of immunity characterized by high titer autoantibodies and interstitial lung disease, with many individuals also having arthritis and nephritis. ...
COPA syndrome is a recently described autosomal dominant inborn error of immunity characterized by high titer autoantib …
JAK inhibitor treatment for inborn errors of JAK/STAT signaling: An ESID/EBMT-IEWP retrospective study.
Fischer M, Olbrich P, Hadjadj J, Aumann V, Bakhtiar S, Barlogis V, von Bismarck P, Bloomfield M, Booth C, Buddingh EP, Cagdas D, Castelle M, Chan AY, Chandrakasan S, Chetty K, Cougoul P, Crickx E, Dara J, Deyà-Martínez A, Farmand S, Formankova R, Gennery AR, Gonzalez-Granado LI, Hagin D, Hanitsch LG, Hanzlikovà J, Hauck F, Ivorra-Cortés J, Kisand K, Kiykim A, Körholz J, Leahy TR, van Montfrans J, Nademi Z, Nelken B, Parikh S, Plado S, Ramakers J, Redlich A, Rieux-Laucat F, Rivière JG, Rodina Y, Júnior PR, Salou S, Schuetz C, Shcherbina A, Slatter MA, Touzot F, Unal E, Lankester AC, Burns S, Seppänen MRJ, Neth O, Albert MH, Ehl S, Neven B, Speckmann C. Fischer M, et al. J Allergy Clin Immunol. 2024 Jan;153(1):275-286.e18. doi: 10.1016/j.jaci.2023.10.018. Epub 2023 Nov 5. J Allergy Clin Immunol. 2024. PMID: 37935260
BACKGROUND: Inborn errors of immunity (IEI) with dysregulated JAK/STAT signaling present with variable manifestations of immune dysregulation and infections. ...OBJECTIVE: We evaluated the current off-label JAKi treatment experience for JAK/STAT inborn errors …
BACKGROUND: Inborn errors of immunity (IEI) with dysregulated JAK/STAT signaling present with variable manifestations of immun …
Advances in the treatment of severe combined immunodeficiency.
Slatter MA, Gennery AR. Slatter MA, et al. Clin Immunol. 2022 Sep;242:109084. doi: 10.1016/j.clim.2022.109084. Epub 2022 Aug 5. Clin Immunol. 2022. PMID: 35940359 Review.
Severe Combined Immunodeficiency (SCID) is the most profound inborn error of immunity affecting cellular and humoral immunity. ...Huge progress has been made since then in understanding the underlying genetics, improving outcomes from transplant, and i …
Severe Combined Immunodeficiency (SCID) is the most profound inborn error of immunity affecting cellular and humoral …
20 results