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2. Infektiologie

3. HIV-Infektion im Kindesalter – Update

5. Disorders of Phagocytic Cells

7. DOCK8 Deficiency: Clinical and Immunological Phenotype and Treatment Options - a Review of 136 Patients

8. X-linked lymphoproliferative disease due to SAP/SH2D1A deficiency: a multicenter study on the manifestations, management and outcome of the disease

10. A Novel Gain-of-Function IKBA Mutation Underlies Ectodermal Dysplasia with Immunodeficiency and Polyendocrinopathy

13. A structured patient empowerment programme for primary immunodeficiency significantly improves general and health-related quality of life

16. Novel Missense Mutation P.M37K in IKBA Results in Impaired NF-κB Activation Causing Ectodermal Dysplasia with Immunodeficiency and Autoimmune Polyendocrinopathy

31. Outcome of HSCT in Adolescents and Young Adults with Non-SCID Primary Immunodeficiencies

32. Successful Combination of Sequential Gene Therapy and Rescue Allo-HSCT in Two Children with X-CGD - Importance of Timing

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

34. Phylodynamic and Phylogeographic Patterns of the HIV Type 1 Subtype F1 Parenteral Epidemic in Romania

38. A structured patient empowerment programme for primary immunodeficiency significantly improves general and health-related quality of life.

39. [Basic diagnostics for pediatric outpatients with susceptibility to infections and immundysregulation].

40. Outcome and management of pregnancies in severe chronic neutropenia patients by the European Branch of the Severe Chronic Neutropenia International Registry.

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