Niehues, Tim
Tim Niehues researcher (ORCID 0000-0002-9945-8833)
VIAF ID: 305270062 (Personal)
Permalink: http://viaf.org/viaf/305270062
Preferred Forms
- 100 1 _ ‡a Niehues, Tim
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- 100 1 _ ‡a Niehues, Tim
- 100 1 _ ‡a Niehues, Tim
- 100 0 _ ‡a Tim Niehues ‡c researcher (ORCID 0000-0002-9945-8833)
4xx's: Alternate Name Forms (1)
5xx's: Related Names (3)
Works
Title | Sources |
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Acute rheumatic fever in a patient with glycogen storage disease type Ib: causal or coincidental simultaneous occurrence? | |
Association of SARS-CoV-2 seropositivity with myalgic encephalomyelitis and/or chronic fatigue syndrome mong children and adolescents in Germany | |
ATP6AP1 deficiency causes an immunodeficiency with hepatopathy, cognitive impairment and abnormal protein glycosylation | |
Autoimmunity, autoinflammation and lymphoma in combined immunodeficiency (CID). | |
Autosomal dominant immune dysregulation syndrome in humans with CTLA4 mutations | |
Broad-spectrum antibodies against self-antigens and cytokines in RAG deficiency. | |
Characterization of the clinical and immunological phenotype and management of 157 individuals with 56 distinct heterozygous NFKB1 mutations | |
Clinical and immunological manifestations of patients with atypical severe combined immunodeficiency. | |
Comparing SARS-CoV-2 variants among children and adolescents in Germany: relative risk of COVID-19-related hospitalization, ICU admission and mortality | |
Curative treatment of POMP-related autoinflammation and immune dysregulation (PRAID) by hematopoietic stem cell transplantation | |
Diastolic heart murmur, nocturnal back pain, and lumbar rigidity in a 7-year girl: an unusual manifestation of lyme disease in childhood | |
Evans syndrome in a patient with chromosome 22q11.2 deletion syndrome: a case report | |
Evidence-based use of methotrexate in children with rheumatic diseases: a consensus statement of the Working Groups Pediatric Rheumatology Germany (AGKJR) and Pediatric Rheumatology Austria | |
Expansion of immunoglobulin-secreting cells and defects in B cell tolerance in Rag-dependent immunodeficiency | |
Experimental strategies for combined suicide and immune cancer gene therapy. An overview. | |
Extended clinical and immunological phenotype and transplant outcome in CD27 and CD70 deficiency | |
The extended clinical phenotype of 64 patients with dedicator of cytokinesis 8 deficiency | |
Familial Mediterranean fever in children and adolescents: factors for colchicine dosage and predicting parameters for dose increase | |
Favourable Outcome in Two Pregnancies in a Patient with 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency | |
The febrile child: diagnosis and treatment | |
Früher herausgegeben von D. Reinhardt u.a. | |
Girls homozygous for an IL-2-inducible T cell kinase mutation that leads to protein deficiency develop fatal EBV-associated lymphoproliferation | |
HIV Infektion im Kindesalter: T-Zell Rekonstitution nach antiretroviraler Therapie | |
Human RAD52 - a novel player in DNA repair in cancer and immunodeficiency | |
Immunisation practices in centres caring for children with perinatally acquired HIV: A call for harmonisation | |
Immunodeficiency with susceptibility to lymphoma with complex genotype affecting energy metabolism (FBP1, ACAD9) and vesicle trafficking (RAB27A) | |
Key findings to expedite the diagnosis of hyper-IgE syndromes in infants and young children. | |
Leitlinien Kinder- und Jugendmedizin | |
Lymphozytenhomöostase im IL-7 defizienten Mausmodell und Vergleich der Lymphozytensubpopulationen in Abhängigkeit vom Alter | |
More than just SCID--the phenotypic range of combined immunodeficiencies associated with mutations in the recombinase activating genes (RAG) 1 and 2. | |
Mutations in STAT3 and diagnostic guidelines for hyper-IgE syndrome | |
Mutations of the gene FNIP1 associated with a syndromic autosomal recessive immunodeficiency with cardiomyopathy and pre-excitation syndrome | |
NEMO is a key component of NF-κB- and IRF-3-dependent TLR3-mediated immunity to herpes simplex virus. | |
The NEMO mutation creating the most-upstream premature stop codon is hypomorphic because of a reinitiation of translation. | |
Novel mutations in TNFRSF7/CD27: Clinical, immunologic, and genetic characterization of human CD27 deficiency | |
Nuclear factor kappaB essential modulator-deficient child with immunodeficiency yet without anhidrotic ectodermal dysplasia | |
Optimizing treatment in paediatric rheumatology--lessons from oncology | |
Painful rash and swelling of the limbs after recurrent infections in a teenager: polyarteritis nodosa. | |
PENTA 2009 guidelines for the use of antiretroviral therapy in paediatric HIV-1 infection | |
A phase I trial to evaluate the safety and pharmacokinetics of low-dose methotrexate as an anti-malarial drug in Kenyan adult healthy volunteers | |
polyethylene glycol-conjugated adenosine deaminase (ADA) therapy provides temporary immune reconstitution to a child with delayed-onset ADA deficiency | |
Post-pandemic seroprevalence of pandemic influenza A (H1N1) 2009 infection (swine flu) among children <18 years in Germany | |
Prevalence of hepatitis E virus antibodies in children in Germany | |
Primäre Immundefekte, [2013]: | |
A prospective study on the natural history of patients with profound combined immunodeficiency: An interim analysis. | |
Recommendations for the use of methotrexate in juvenile idiopathic arthritis | |
Relationship between histiocytosis and abnormal lymphoid differentiation. Case report and review of the literature. | |
Reversible pancytopenia and immunodeficiency in a patient with hereditary folate malabsorption | |
Risk adapted transmission prophylaxis to prevent vertical HIV-1 transmission: effectiveness and safety of an abbreviated regimen of postnatal oral zidovudine | |
Rolle von Proteinen in der Säuglingsnahrung bei Entstehen und Prävention allergischer Erkrankungen | |
Topical tacrolimus is effective against eczema in Wiskott-Aldrich syndrome (WAS). | |
Translational research network and patient registry for auto-inflammatory diseases | |
Treatment and management of primary antibody deficiency: German interdisciplinary evidence‐based consensus guideline |