Grimbacher, Bodo 1967-
Bodo Grimbacher researcher
VIAF ID: 35151872 (Personal)
Permalink: http://viaf.org/viaf/35151872
Preferred Forms
- 100 0 _ ‡a Bodo Grimbacher ‡c researcher
-
- 100 1 _ ‡a Grimbacher, Bodo ‡d 1967-
- 100 1 _ ‡a Grimbacher, Bodo ‡d 1967-
4xx's: Alternate Name Forms (1)
5xx's: Related Names (3)
- 551 _ _ ‡a Bietigheim ‡4 ortg ‡4 https://d-nb.info/standards/elementset/gnd#placeOfBirth
- 510 2 _ ‡a Centrum für Chronische Immundefizienz ‡4 affi ‡4 https://d-nb.info/standards/elementset/gnd#affiliation ‡e Affiliation
- 510 2 _ ‡a Medizinische Hochschule Hannover ‡4 affi ‡4 https://d-nb.info/standards/elementset/gnd#affiliation ‡e Affiliation
Works
Title | Sources |
---|---|
14 years after discovery : clinical follow-up on 15 patients with Inducible CO-Stimulatior deficiency | |
ABACHAI clinical trial protocol: Safety and efficacy of abatacept (s.c.) in patients with CTLA-4 insufficiency or LRBA deficiency: A non controlled phase 2 clinical trial | |
Activation-induced deaminase is critical for the establishment of DNA methylation patterns prior to the germinal center reaction | |
Activation of early growth response transcripts and cytokines in rheumatoid synovial fibroblasts | |
Allele-specific disruption of a common STAT3 autosomal dominant allele is not sufficient to restore downstream signaling in patient-derived T cells | |
Altered microbiota, impaired quality of life, malabsorption, infection, and inflammation in CVID patients with diarrhoea | |
Altered spectrum of lymphoid neoplasms in a single-center cohort of common variable immunodeficiency with immune dysregulation | |
ARPC5 deficiency leads to severe early onset systemic inflammation and mortality | |
Assessing the functional relevance of variants in the IKAROS family zinc finger protein 1 (IKZF1) in a cohort of patients with primary immunodeficiency | |
Autoantibodies against type I IFNs in humans with alternative NF-κB pathway deficiency | |
Autosomal dominant STAT6 gain of function causes severe atopy associated with lymphoma | |
BAFFR activates PI3K/AKT signaling in human naive but not in switched memory B cells through direct interactions with B cell antigen receptors | |
Beeinflussung des intestinalen Mikrobioms und Mykobioms durch Darmoperationen bzw. Ernährungsinterventionen – Ergebnisse einer prospektiven Kohortenstudie und einer randomisierten Interventionsstudie | |
Bile acids regulate intestinal antigen presentation and reduce graft-versus-host disease without impairing the graft-versus-leukemia effect | |
Bowel histology of CVID patients reveals distinct patterns of mucosal inflammation | |
BTK operates a phospho-tyrosine switch to regulate NLRP3 inflammasome activity | |
burden of common variable immunodeficiency disorders: a retrospective analysis of the European Society for Immunodeficiency (ESID) registry data | |
characteristics of viral skin infections in the immunocompromised host | |
Clinical phenotype, functional assessment, and impact prediction of NF-κB1 missense variants | |
Clinical spectrum and features of activated phosphoinositide 3-kinase δ syndrome: a large patient cohort study | |
Confirmation of hyperimmunoglobulin E syndrome in two patients with an ocular problem: Detection of two new DOCK8 mutations | |
Copy number analysis in a large cohort suggestive of inborn errors of immunity indicates a wide spectrum of relevant chromosomal losses and gains | |
Deleterious mutations in LRBA are associated with a syndrome of immune deficiency and autoimmunity | |
Detrimental NFKB1 missense variants affecting the Rel-homology domain of p105/p50 | |
Disease evolution and response to rapamycin in activated phosphoinositide 3-kinase [delta] syndrome: the european society for immunodeficiencies-activated phosphoinositide 3-kinase [delta] syndrome registry | |
A distinct CD38+CD45RA+ population of CD4+, CD8+, and double-negative T cells is controlled by FAS | |
Do common infections trigger disease-onset or -severity in CTLA-4 insufficiency? | |
DOCK8 deficiency in six Iranian patients | |
Dominant-negative mutations in human IL6ST underlie hyper-IgE syndrome | |
Dysregulated immunity in PID patients with low GARP expression on Tregs due to mutations in LRRC32 | |
Dysregulated PI3K signaling in B cells of CVID patients | |
E3-Ligase MARCH9: experimentelle Untersuchung eines Sarkoidose-Risikogens - Splicevarianten, Expressionsmuster, Stimulationsreaktionen und funktionelle Rolle | |
Efficacy of dupilumab for the treatment of severe skin disease in cytotoxic T lymphocyte antigen-4 insufficiency: a role of type 2 inflammation? | |
Enabling external inquiries to an existing patient registry by using the open source registry system for rare diseases: demonstration of the system using the European Society for Immunodeficiencies registry | |
The ESID online clinical and research database | |
Establishing the molecular diagnoses in a cohort of 291 patients with predominantly antibody deficiency by targeted next-generation sequencing: Experience from a monocentric study | |
Evaluation and management of deficiency of adenosine deaminase 2 : an international consensus statement | |
Functional relevance of CTLA4 variants: an upgraded approach to assess CTLA4-dependent transendocytosis by flow cytometry | |
Future directions in the diagnosis and treatment of APDS and IEI: a survey of German IEI centers | |
GAIN Registry - a new prospective study for patients with multi-organ autoimmunity and autoinflammation | |
Genetic analysis of a cohort of 275 patients with hyper-IgE syndromes and/or chronic mucocutaneous candidiasis | |
genetischen Ursachen der angeborenen Antikörpermangelsyndrome | |
GenIA, genetic immunology advisor database for inborn errors of immunity | |
Genomic characterization of lymphomas in patients with inborn errors of immunity | |
German national registry of primary immunodeficiencies (2012–2017) | |
Gut microbiota and lymphocyte profiling in patients with common variable immunodeficiency and inflammatory bowel disease | |
Health-related quality of life, depression and anxiety in adult patients with chronic granulomatous disease | |
Hematopoietic stem cell transplantation resolves the immune deficit associated with STAT3-Dominant-Negative Hyper-IgE syndrome | |
Identifikation des genetischen Defekts in einer iranischen Familie mit chronischer mucocutaner Candidose | |
Immune checkpoint deficiencies and autoimmune lymphoproliferative syndromes | |
“Immune TOR-opathies,” a novel disease entity in clinical immunology | |
Immunological phenotype of LRBA-deficient mice | |
Inborn errors of immunity associated with defects of self‐tolerance checkpoints: the CD28 family | |
Increased risk for malignancies in 131 affected CTLA4 mutation carriers | |
Interferon-driven immune dysregulation in common variable immunodeficiency-associated villous atrophy and norovirus infection | |
Is it safe to switch from intravenous immunoglobulin to subcutaneous immunoglobulin in patients with common variable immunodeficiency and autoimmune thrombocytopenia? | |
JAKs and STATs from a clinical perspective: loss-of-function mutations, gain-of-function mutations, and their multidimensional consequences | |
Klinische Erforschung der CTLA-4-Insuffizienz | |
Late-onset antibody deficiency due to monoallelic alterations in NFKB1 | |
Long-term outcome of LRBA deficiency in 76 patients after various treatment modalities as evaluated by the immune deficiency and dysregulation activity (IDDA) score | |
Multi-omics analysis of naïve B cells of patients harboring the C104R mutation in TACI | |
Observation and long-term follow-up of patients with isolated hypogammaglobulinaemia at the Royal Free Hospital, London | |
A pathogenic missense variant in NFKB1 causes common variable immunodeficiency due to detrimental protein damage | |
Patientenregister für Seltene Erkrankungen in Deutschland: Konzeptpapier der Strategiegruppe „Register“ des Nationalen Aktionsbündnisses für Menschen mit Seltenen Erkrankungen (NAMSE) = Patient registries for rare diseases in Germany: concept paper of the NAMSE strategy group | |
Pembrolizumab for treatment of progressive multifocal leukoencephalopathy in primary immunodeficiency and/or hematologic malignancy: a case series of five patients | |
Rapid flow cytometry-based test for the diagnosis of lipopolysaccharide responsive beige-like anchor (LRBA) deficiency | |
Sequencing the B cell receptor repertoires of antibody-deficient individuals with and without infection susceptibility | |
Simple measurement of IgA predicts immunity and mortality in Ataxia-Telangiectasia | |
STAT1-Mutationen in einer Kohorte von 62 Patienten mit chronischer mukokutaner Kandidose | |
Therapeutic targeting of endoplasmic reticulum stress in acute graft-versus-host disease | |
A toolkit for monitoring immunoglobulin G levels from dried blood spots of patients with primary immunodeficiencies | |
Treatment of infantile inflammatory bowel disease and autoimmunity by allogeneic stem cell transplantation in LPS-responsive beige-like anchor deficiency |