Gundula Notheis
Dr. Von Haunersches Kinderspital
Munich, BY 80337, Germany
Munich, BY 80337, Germany
Last Updated: 09/26/2026
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Found 15 publications
Molecular Assessment of Staphylococcus Aureus Strains in STAT3 Hyper-IgE Syndrome Patients.
Journal: Journal of clinical immunology
Published: January 07, 2022
A structured patient empowerment programme for primary immunodeficiency significantly improves general and health-related quality of life.
Journal: Central-European journal of immunology
Published: June 19, 2020
Class Switch Recombination Defects: impact on B cell maturation and antibody responses.
Journal: Clinical immunology (Orlando, Fla.)
Published: June 16, 2020
Allogeneic stem cell transplantation in adolescents and young adults with primary immunodeficiencies.
Journal: The journal of allergy and clinical immunology. In practice
Published: February 07, 2017
Basic diagnostics for pediatric outpatients with susceptibility to infections and immundysregulation
Basic diagnostics for pediatric outpatients with susceptibility to infections and immundysregulation
Journal: MMW Fortschritte der Medizin
Published: May 26, 2016
High seroprevalence of antibodies against Kaposi's sarcoma-associated herpesvirus (KSHV) among HIV-1-infected children and adolescents in a non-endemic population.
Journal: Medical microbiology and immunology
Published: January 19, 2016
DOCK8 deficiency: clinical and immunological phenotype and treatment options - a review of 136 patients.
Journal: Journal of clinical immunology
Published: August 19, 2014
Outcome and management of pregnancies in severe chronic neutropenia patients by the European Branch of the Severe Chronic Neutropenia International Registry.
Journal: Haematologica
Published: July 06, 2014
HIV-1 seroreversion in HIV-1-infected children: do genetic determinants play a role?
Journal: AIDS (London, England)
Published: September 24, 2013
The German national registry for primary immunodeficiencies (PID).
Journal: Clinical and experimental immunology
Published: March 10, 2013
A novel gain-of-function IKBA mutation underlies ectodermal dysplasia with immunodeficiency and polyendocrinopathy.
Journal: Journal of clinical immunology
Published: November 06, 2012
Last Updated: 09/26/2026