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26 results on '"Dueckers, Gregor"'

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1. Wiskott-Aldrich syndrome: a study of 577 patients defines the genotype as a biomarker for disease severity and survival

2. Diagnostic evaluation of paediatric autoimmune lymphoproliferative immunodeficiencies (ALPID): a prospective cohort study

4. Initial presenting manifestations in 16,486 patients with inborn errors of immunity include infections and noninfectious manifestations

5. Wiskott-Aldrich syndrome: a study of 577 patients defines the genotype as a biomarker for disease severity and survival

6. Wiskott-Aldrich Syndrome: A study on 577 patients defining the genotype as a predictive biomarker for disease severity

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

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

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

10. Update of evidence- and consensus-based guidelines for the treatment of juvenile idiopathic arthritis (JIA) by the German Society of Pediatric and Juvenile Rheumatic Diseases (GKJR): New perspectives on interdisciplinary care

11. Infection-triggered familial or recurrent cases of acute necrotizing encephalopathy caused by mutations in a component of the nuclear pore, RANBP2

12. German evidence- and consensus-based guidelines 2011 for the treatment of juvenile idiopathic arthritis (JIA)

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

15. A combined immunodeficiency with severe infections, inflammation, and allergy caused by ARPC1B deficiency

16. The German National Registry of Primary Immunodeficiencies (2012-2017)

17. Increasing Mixed Chimerism Is an Important Prognostic Factor for Unfavorable Outcome in Children With Acute Lymphoblastic Leukemia After Allogeneic Stem-Cell Transplantation: Possible Role For Pre-Emptive Immunotherapy?

18. Outcome of children with centrally reviewed low-grade gliomas treated with chemotherapy with or without radiotherapy on children's cancer group high-grade glioma study CCG-945

19. Wiskott-Aldrich Syndrome: A Retrospective Study on 575 Patients Analyzing the Impact of Splenectomy, Stem Cell Transplantation, or No Definitive Treatment on Frequency of Disease-Related Complications and Physician-Perceived Quality of Life

20. The extended clinical phenotype of 64 patients with DOCK8 deficiency

21. Wiskott-Aldrich syndrome: a retrospective study of 577 patients defines the genotype as a predictive biomarker for disease severity and survival

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

23. Autosomal dominant immune dysregulation syndrome in humans with CTLA4 mutations

24. HSCT for DOCK8 Deficiency - an International Study on 74 Patients

25. Infection-triggered familial or recurrent cases of acute necrotizing encephalopathy caused by mutations in a component of the nuclear pore, RANBP2

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

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