Search filters

Authors whose works are in public domain in at least one jurisdiction

List of works by Tim Niehues

A phase I trial to evaluate the safety and pharmacokinetics of low-dose methotrexate as an anti-malarial drug in Kenyan adult healthy volunteers ⬇️

scientific article published on March 16, 2011

A prospective study on the natural history of patients with profound combined immunodeficiency: An interim analysis.

scientific article

ATP6AP1 deficiency causes an immunodeficiency with hepatopathy, cognitive impairment and abnormal protein glycosylation

scientific article published on 27 May 2016

Acute rheumatic fever in a patient with glycogen storage disease type Ib: causal or coincidental simultaneous occurrence?

scientific article published on March 2002

Autoimmunity, autoinflammation and lymphoma in combined immunodeficiency (CID).

scientific article published on 08 February 2010

Autosomal dominant immune dysregulation syndrome in humans with CTLA4 mutations

scientific article

Broad-spectrum antibodies against self-antigens and cytokines in RAG deficiency

scientific article

Broad-spectrum antibodies against self-antigens and cytokines in RAG deficiency.

scientific article published in November 2016

Characterization of the clinical and immunological phenotype and management of 157 individuals with 56 distinct heterozygous NFKB1 mutations

scientific article published on 09 April 2020

Clinical and immunological manifestations of patients with atypical severe combined immunodeficiency.

scientific article published on 30 May 2011

Colchicine use in children and adolescents with familial Mediterranean fever: literature review and consensus statement

scientific article published on 22 January 2007

Diastolic Heart Murmur, Nocturnal Back Pain, and Lumbar Rigidity in a 7-Year Girl: An Unusual Manifestation of Lyme Disease in Childhood ⬇️

scientific article published on September 29, 2012

Evans syndrome in a patient with chromosome 22q11.2 deletion syndrome: a case report

scientific article

Evidence and consensus based GKJR guidelines for the treatment of juvenile idiopathic arthritis ⬇️

scientific article published on October 26, 2011

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

scientific article

Expansion of immunoglobulin-secreting cells and defects in B cell tolerance in Rag-dependent immunodeficiency

scientific article

Experimental strategies for combined suicide and immune cancer gene therapy. An overview.

scientific article

Extended clinical and immunological phenotype and transplant outcome in CD27 and CD70 deficiency

scientific article published on 30 June 2020

Familial Mediterranean fever in children and adolescents: factors for colchicine dosage and predicting parameters for dose increase

scientific article published on September 2017

Favourable Outcome in Two Pregnancies in a Patient with 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency

scientific article published on 21 February 2017

Girls homozygous for an IL-2-inducible T cell kinase mutation that leads to protein deficiency develop fatal EBV-associated lymphoproliferation

scientific article published on May 2009

Human RAD52 - a novel player in DNA repair in cancer and immunodeficiency

scientific article published on 15 December 2016

Immunisation practices in centres caring for children with perinatally acquired HIV: A call for harmonisation

scientific article

Incidence of TNFRSF1A mutations in German children: epidemiological, clinical and genetic characteristics

scientific article published on 18 June 2009

Key findings to expedite the diagnosis of hyper-IgE syndromes in infants and young children.

scientific article

Large deletions and point mutations involving the dedicator of cytokinesis 8 (DOCK8) in the autosomal-recessive form of hyper-IgE syndrome

scientific article

More than just SCID--the phenotypic range of combined immunodeficiencies associated with mutations in the recombinase activating genes (RAG) 1 and 2.

scientific article published on 20 February 2010

Mutations in STAT3 and diagnostic guidelines for hyper-IgE syndrome

scientific article

Mutations of the gene FNIP1 associated with a syndromic autosomal recessive immunodeficiency with cardiomyopathy and pre-excitation syndrome

scientific article published on 17 March 2020

NEMO is a key component of NF-κB- and IRF-3-dependent TLR3-mediated immunity to herpes simplex virus.

scientific article

Novel mutations in TNFRSF7/CD27: Clinical, immunologic, and genetic characterization of human CD27 deficiency

scientific article published on 02 April 2015

Nuclear factor kappaB essential modulator-deficient child with immunodeficiency yet without anhidrotic ectodermal dysplasia

scientific article

Optimizing treatment in paediatric rheumatology--lessons from oncology

scientific article published on 21 April 2015

Outcome and Trends in Treatment of Systemic Juvenile Idiopathic Arthritis in the German National Pediatric Rheumatologic Database, 2000-2013.

scientific article published on 22 June 2016

PENTA 2009 guidelines for the use of antiretroviral therapy in paediatric HIV-1 infection

scientific article

Painful rash and swelling of the limbs after recurrent infections in a teenager: polyarteritis nodosa.

scientific article

Post-pandemic seroprevalence of pandemic influenza A (H1N1) 2009 infection (swine flu) among children <18 years in Germany

scientific article

Prevalence of hepatitis E virus antibodies in children in Germany

scientific article published on March 2014

Recommendations for the use of methotrexate in juvenile idiopathic arthritis

scientific article published on January 2006

Reversible pancytopenia and immunodeficiency in a patient with hereditary folate malabsorption

scientific article

Risk adapted transmission prophylaxis to prevent vertical HIV–1 transmission: Effectiveness and safety of an abbreviated regimen of postnatal oral Zidovudine ⬇️

scientific article published on January 24, 2013

The Extended Clinical Phenotype of 26 Patients with Chronic Mucocutaneous Candidiasis due to Gain-of-Function Mutations in STAT1

scientific article

The NEMO mutation creating the most-upstream premature stop codon is hypomorphic because of a reinitiation of translation.

scientific article

The extended clinical phenotype of 64 patients with dedicator of cytokinesis 8 deficiency

scientific article

The febrile child: diagnosis and treatment

scientific article

Topical tacrolimus is effective against eczema in Wiskott-Aldrich syndrome (WAS).

scientific article

Translational research network and patient registry for auto-inflammatory diseases ⬇️

scientific article published on January 1, 2011

Treatment and management of primary antibody deficiency: German interdisciplinary evidence-based consensus guideline

scientific article published on 26 August 2020

polyethylene glycol-conjugated adenosine deaminase (ADA) therapy provides temporary immune reconstitution to a child with delayed-onset ADA deficiency

scientific article

Paulina is supported by:

About Paulina

Help