Kirsten Bienemann

Duesseldorf, NW, Germany

Last Updated: 09/26/2026

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Found 16 publications

Specific antibody deficiency and autoinflammatory disease extend the clinical and immunological spectrum of heterozygous NFKB1 loss-of-function mutations in humans.

Specific antibody deficiency and autoinflammatory disease extend the clinical and immunological spectrum of heterozygous NFKB1 loss-of-function mutations in humans.

Journal: Haematologica
Published: July 02, 2016

A novel homozygous mutation in UNC13D presenting as Epstein-Barr-virus-associated lymphoproliferative disease at 9 years of age.

A novel homozygous mutation in UNC13D presenting as Epstein-Barr-virus-associated lymphoproliferative disease at 9 years of age.

Journal: Leukemia & lymphoma
Published: April 29, 2016

Fatal Lymphoproliferative Disease in Two Siblings Lacking Functional FAAP24.

Fatal Lymphoproliferative Disease in Two Siblings Lacking Functional FAAP24.

Journal: Journal of clinical immunology
Published: April 05, 2016

A massive intestinal vaso-occlusive crisis or "girdle syndrome" in a 6-year-old boy observed as a first manifestation of sickle cell disease.

A massive intestinal vaso-occlusive crisis or "girdle syndrome" in a 6-year-old boy observed as a first manifestation of sickle cell disease.

Journal: Klinische Padiatrie
Published: November 29, 2014

High incidence of Epstein-Barr virus (EBV)-positive Hodgkin lymphoma and Hodgkin lymphoma-like B-cell lymphoproliferations with EBV latency profile 2 in children with interleukin-2-inducible T-cell kinase deficiency.

High incidence of Epstein-Barr virus (EBV)-positive Hodgkin lymphoma and Hodgkin lymphoma-like B-cell lymphoproliferations with EBV latency profile 2 in children with interleukin-2-inducible T-cell kinase deficiency.

Journal: Histopathology
Published: November 18, 2014

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

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

Journal: The Journal of allergy and clinical immunology
Published: August 27, 2014

DOCK8 deficiency: clinical and immunological phenotype and treatment options - a review of 136 patients.

DOCK8 deficiency: clinical and immunological phenotype and treatment options - a review of 136 patients.

Journal: Journal of clinical immunology
Published: August 19, 2014

Identification of ITK deficiency as a novel genetic cause of idiopathic CD4+ T-cell lymphopenia.

Identification of ITK deficiency as a novel genetic cause of idiopathic CD4+ T-cell lymphopenia.

Journal: Blood
Published: July 26, 2014

Interleukin-2-inducible T-cell kinase (ITK) deficiency - clinical and molecular aspects.

Interleukin-2-inducible T-cell kinase (ITK) deficiency - clinical and molecular aspects.

Journal: Journal of clinical immunology
Published: July 21, 2014

Targeted expression of human folylpolyglutamate synthase for selective enhancement of methotrexate chemotherapy in osteosarcoma cells.

Targeted expression of human folylpolyglutamate synthase for selective enhancement of methotrexate chemotherapy in osteosarcoma cells.

Journal: Cancer gene therapy
Published: May 10, 2013

Clinical picture and treatment of 2212 patients with common variable immunodeficiency.

Clinical picture and treatment of 2212 patients with common variable immunodeficiency.

Journal: The Journal of allergy and clinical immunology
Published: May 06, 2013

The German national registry for primary immunodeficiencies (PID).

The German national registry for primary immunodeficiencies (PID).

Journal: Clinical and experimental immunology
Published: March 10, 2013
Showing 1-12 of 16

Last Updated: 09/26/2026