186 related articles for article (PubMed ID: 30391351)
21. Combined immunodeficiency with marginal zone lymphoma due to a novel homozygous mutation in
Edeer Karaca N; Özek G; Ataseven E; Tökmeci N; Şenol HD; Kıran E; Aykut A; Durmaz A; Aksu G; Aksoylar S; Aydoğdu S; Çetingül N; Kütükçüler N
Pediatr Hematol Oncol; 2021 Nov; 38(8):745-752. PubMed ID: 33966600
[TBL] [Abstract][Full Text] [Related]
22. Inherited human c-Rel deficiency disrupts myeloid and lymphoid immunity to multiple infectious agents.
Lévy R; Langlais D; Béziat V; Rapaport F; Rao G; Lazarov T; Bourgey M; Zhou YJ; Briand C; Moriya K; Ailal F; Avery DT; Markle J; Lim AI; Ogishi M; Yang R; Pelham S; Emam M; Migaud M; Deswarte C; Habib T; Saraiva LR; Moussa EA; Guennoun A; Boisson B; Belkaya S; Martinez-Barricarte R; Rosain J; Belkadi A; Breton S; Payne K; Benhsaien I; Plebani A; Lougaris V; Di Santo JP; Neven B; Abel L; Ma CS; Bousfiha AA; Marr N; Bustamante J; Liu K; Gros P; Geissmann F; Tangye SG; Casanova JL; Puel A
J Clin Invest; 2021 Sep; 131(17):. PubMed ID: 34623332
[TBL] [Abstract][Full Text] [Related]
23. The impact of early viral infections and graft-versus-host disease on immune reconstitution following paediatric stem cell transplantation.
Olkinuora H; von Willebrand E; Kantele JM; Vainio O; Talvensaari K; Saarinen-Pihkala U; Siitonen S; Vettenranta K
Scand J Immunol; 2011 Jun; 73(6):586-93. PubMed ID: 21323694
[TBL] [Abstract][Full Text] [Related]
24. Multisystem Anomalies in Severe Combined Immunodeficiency with Mutant BCL11B.
Punwani D; Zhang Y; Yu J; Cowan MJ; Rana S; Kwan A; Adhikari AN; Lizama CO; Mendelsohn BA; Fahl SP; Chellappan A; Srinivasan R; Brenner SE; Wiest DL; Puck JM
N Engl J Med; 2016 Dec; 375(22):2165-2176. PubMed ID: 27959755
[TBL] [Abstract][Full Text] [Related]
25. Impaired control of multiple viral infections in a family with complete IRF9 deficiency.
Bravo García-Morato M; Calvo Apalategi A; Bravo-Gallego LY; Blázquez Moreno A; Simón-Fuentes M; Garmendia JV; Méndez Echevarría A; Del Rosal Rabes T; Domínguez-Soto Á; López-Granados E; Reyburn HT; Rodríguez Pena R
J Allergy Clin Immunol; 2019 Jul; 144(1):309-312.e10. PubMed ID: 30826365
[No Abstract] [Full Text] [Related]
26. A novel monoallelic gain of function mutation in p110δ causing atypical activated phosphoinositide 3-kinase δ syndrome (APDS-1).
Lougaris V; Baronio M; Moratto D; Tampella G; Gazzurelli L; Facchetti M; Martire B; Cardinale F; Lanzarotto F; Bondioni MP; Villanacci V; Grimbacher B; Plebani A
Clin Immunol; 2019 Mar; 200():31-34. PubMed ID: 30639166
[TBL] [Abstract][Full Text] [Related]
27. The Phenotype and Treatment of WIP Deficiency: Literature Synopsis and Review of a Patient With Pre-transplant Serial Donor Lymphocyte Infusions to Eliminate CMV.
Schwinger W; Urban C; Ulreich R; Sperl D; Karastaneva A; Strenger V; Lackner H; Boztug K; Albert MH; Benesch M; Seidel MG
Front Immunol; 2018; 9():2554. PubMed ID: 30450104
[TBL] [Abstract][Full Text] [Related]
28. Case Report: A Novel Synonymous ARPC1B Gene Mutation Causes a Syndrome of Combined Immunodeficiency, Asthma, and Allergy With Significant Intrafamilial Clinical Heterogeneity.
Papadatou I; Marinakis N; Botsa E; Tzanoudaki M; Kanariou M; Orfanou I; Kanaka-Gantenbein C; Traeger-Synodinos J; Spoulou V
Front Immunol; 2021; 12():634313. PubMed ID: 33679784
[TBL] [Abstract][Full Text] [Related]
29. [The immune response in pediatric infections].
Martín Mateos MA
An Esp Pediatr; 1989 Sep; 31 Suppl 38():20-4. PubMed ID: 2490620
[No Abstract] [Full Text] [Related]
30. [Prevention of infections in immune deficiency].
Lange B; Neumann S; Hirsch HH; Kern WV
Dtsch Med Wochenschr; 2014 Oct; 139(40):1999-2002. PubMed ID: 25254394
[No Abstract] [Full Text] [Related]
31. Human IκBα Gain of Function: a Severe and Syndromic Immunodeficiency.
Boisson B; Puel A; Picard C; Casanova JL
J Clin Immunol; 2017 Jul; 37(5):397-412. PubMed ID: 28597146
[TBL] [Abstract][Full Text] [Related]
32. Long-term neurocognitive function of pediatric patients with severe combined immune deficiency (SCID): pre- and post-hematopoietic stem cell transplant (HSCT).
Lin M; Epport K; Azen C; Parkman R; Kohn DB; Shah AJ
J Clin Immunol; 2009 Mar; 29(2):231-7. PubMed ID: 18807155
[TBL] [Abstract][Full Text] [Related]
33. Successful Allogeneic Hematopoietic Stem Cell Transplant for CARMIL2 Deficiency.
Rastogi N; Thakkar D; Yadav SP
J Pediatr Hematol Oncol; 2021 Nov; 43(8):e1270-e1271. PubMed ID: 34486557
[No Abstract] [Full Text] [Related]
34. Next generation sequencing analysis of consecutive Russian patients with clinical suspicion of inborn errors of immunity.
Suspitsin EN; Guseva MN; Kostik MM; Sokolenko AP; Skripchenko NV; Levina AS; Goleva OV; Dubko MF; Tumakova AV; Makhova MA; Lyazina LV; Bizin IV; Sokolova NE; Gabrusskaya TV; Ditkovskaya LV; Kozlova OP; Vahliarskaya SS; Kondratenko IV; Imyanitov EN
Clin Genet; 2020 Sep; 98(3):231-239. PubMed ID: 32441320
[TBL] [Abstract][Full Text] [Related]
35. Virus-Specific T Cells: Current and Future Use in Primary Immunodeficiency Disorders.
Harris KM; Davila BJ; Bollard CM; Keller MD
J Allergy Clin Immunol Pract; 2019 Mar; 7(3):809-818. PubMed ID: 30581131
[TBL] [Abstract][Full Text] [Related]
36. Approach to primary immunodeficiency.
Devonshire AL; Makhija M
Allergy Asthma Proc; 2019 Nov; 40(6):465-469. PubMed ID: 31690396
[TBL] [Abstract][Full Text] [Related]
37. Chronic Cholangiopathy Associated with Primary Immune Deficiencies Can Be Resolved by Effective Hematopoietic Stem Cell Transplantation.
Hadžić N; Nademi Z; Deheragoda M; Zen Y; Elfeky R; Worth A; Veys P; Mieli-Vergani G; Davies EG
J Pediatr; 2019 Jun; 209():97-106.e2. PubMed ID: 30850087
[TBL] [Abstract][Full Text] [Related]
38. Overview of 15-year severe combined immunodeficiency in the Netherlands: towards newborn blood spot screening.
de Pagter AP; Bredius RG; Kuijpers TW; Tramper J; van der Burg M; van Montfrans J; Driessen GJ;
Eur J Pediatr; 2015 Sep; 174(9):1183-8. PubMed ID: 25875249
[TBL] [Abstract][Full Text] [Related]
39. A prospective study on the natural history of patients with profound combined immunodeficiency: An interim analysis.
Speckmann C; Doerken S; Aiuti A; Albert MH; Al-Herz W; Allende LM; Scarselli A; Avcin T; Perez-Becker R; Cancrini C; Cant A; Di Cesare S; Finocchi A; Fischer A; Gaspar HB; Ghosh S; Gennery A; Gilmour K; González-Granado LI; Martinez-Gallo M; Hambleton S; Hauck F; Hoenig M; Moshous D; Neven B; Niehues T; Notarangelo L; Picard C; Rieber N; Schulz A; Schwarz K; Seidel MG; Soler-Palacin P; Stepensky P; Strahm B; Vraetz T; Warnatz K; Winterhalter C; Worth A; Fuchs S; Uhlmann A; Ehl S;
J Allergy Clin Immunol; 2017 Apr; 139(4):1302-1310.e4. PubMed ID: 27658761
[TBL] [Abstract][Full Text] [Related]
40. A dominant activating RAC2 variant associated with immunodeficiency and pulmonary disease.
Smits BM; Lelieveld PHC; Ververs FA; Turkenburg M; de Koning C; van Dijk M; Leavis HL; Boelens JJ; Lindemans CA; Bloem AC; van de Corput L; van Montfrans J; Nierkens S; van Gijn ME; Geerke DP; Waterham HR; Koenderman L; Boes M
Clin Immunol; 2020 Mar; 212():108248. PubMed ID: 31382036
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]