Detalhe da pesquisa
1.
Survival in primary hemophagocytic lymphohistiocytosis, 2016 to 2021: etoposide is better than its reputation.
Blood
; 143(10): 872-881, 2024 Mar 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-37992218
2.
Chemotherapy for a secondary malignancy nearly restores complete chimerism in an SCID-patient after HSCT.
Clin Immunol
; 259: 109891, 2024 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-38185266
3.
Prospective Newborn Screening for SCID in Germany: A First Analysis by the Pediatric Immunology Working Group (API).
J Clin Immunol
; 43(5): 965-978, 2023 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-36843153
4.
[Newborn screening for severe combined immunodeficiencies (SCID) in Germany]. / Neugeborenenscreening auf schwere kombinierte Immundefekte (SCID) in Deutschland.
Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz
; 66(11): 1222-1231, 2023 Nov.
Artigo
em Alemão
| MEDLINE | ID: mdl-37726421
5.
Human RIPK1 deficiency causes combined immunodeficiency and inflammatory bowel diseases.
Proc Natl Acad Sci U S A
; 116(3): 970-975, 2019 01 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-30591564
6.
Successful hematopoietic stem cell transplantation in a 4-1BB deficient patient with EBV-induced lymphoproliferation.
Clin Immunol
; 222: 108639, 2021 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33259966
7.
Persisting enteropathy and disturbed adaptive mucosal immunity due to MHC class II deficiency.
Clin Immunol
; 203: 125-133, 2019 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-31028919
8.
Increased proportions of γδ T lymphocytes in atypical SCID associate with disease manifestations.
Clin Immunol
; 201: 30-34, 2019 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-30776520
9.
Regulated expression of nuclear receptor RORγt confers distinct functional fates to NK cell receptor-expressing RORγt(+) innate lymphocytes.
Immunity
; 33(5): 736-51, 2010 Nov 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-21093318
10.
CD4+ T cell-derived IL-21 and deprivation of CD40 signaling favor the in vivo development of granzyme B-expressing regulatory B cells in HIV patients.
J Immunol
; 194(8): 3768-77, 2015 Apr 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-25780036
11.
Key findings to expedite the diagnosis of hyper-IgE syndromes in infants and young children.
Pediatr Allergy Immunol
; 27(2): 177-84, 2016 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-26592211
12.
DOCK8 deficiency: clinical and immunological phenotype and treatment options - a review of 136 patients.
J Clin Immunol
; 35(2): 189-98, 2015 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-25627830
13.
Mass Cytometry-A Tool for the Curious: Networking in Berlin.
Cytometry A
; 97(8): 764-767, 2020 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-32298052
14.
Late thymic deficiency after HLA-haploidentical hematopoietic stem cell transplantation for severe combined immunodeficiency.
J Allergy Clin Immunol
; 143(4): 1623-1626.e13, 2019 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-30529243
15.
Comparison of outcomes of hematopoietic stem cell transplantation without chemotherapy conditioning by using matched sibling and unrelated donors for treatment of severe combined immunodeficiency.
J Allergy Clin Immunol
; 134(4): 935-943.e15, 2014 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-25109802
16.
Outcome of hematopoietic stem cell transplantation for adenosine deaminase-deficient severe combined immunodeficiency.
Blood
; 120(17): 3615-24; quiz 3626, 2012 Oct 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-22791287
17.
Long-term outcome and lineage-specific chimerism in 194 patients with Wiskott-Aldrich syndrome treated by hematopoietic cell transplantation in the period 1980-2009: an international collaborative study.
Blood
; 118(6): 1675-84, 2011 Aug 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-21659547
18.
A multimorphic mutation in IRF4 causes human autosomal dominant combined immunodeficiency.
Sci Immunol
; 8(79): eade7953, 2023 01 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-36662884
19.
Multicenter survey on the outcome of transplantation of hematopoietic cells in patients with the complete form of DiGeorge anomaly.
Blood
; 116(13): 2229-36, 2010 Sep 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-20530285
20.
The most frequent DCLRE1C (ARTEMIS) mutations are based on homologous recombination events.
Hum Mutat
; 31(2): 197-207, 2010 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-19953608