265 results on '"Hoenig, Manfred"'
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2. Survival in primary hemophagocytic lymphohistiocytosis, 2016 to 2021: etoposide is better than its reputation
3. Complement and platelets: prothrombotic cell activation requires membrane attack complex–induced release of danger signals
4. Biomarkers of DNA Damage Response Enable Flow Cytometry-Based Diagnostic to Identify Inborn DNA Repair Defects in Primary Immunodeficiencies
5. BCG Disease in SCID: Three Decades of Experience in a Pediatric Transplant Center
6. Daratumumab in life-threatening autoimmune hemolytic anemia following hematopoietic stem cell transplantation.
7. Initial presenting manifestations in 16,486 patients with inborn errors of immunity include infections and noninfectious manifestations
8. Salvage HLA-haploidentical hematopoietic stem cell transplantation with post-transplant cyclophosphamide for graft failure in non-malignant disorders
9. Treatment with rapamycin can restore regulatory T-cell function in IPEX patients
10. Human RIPK1 deficiency causes combined immunodeficiency and inflammatory bowel diseases
11. Incidence of SCID in Germany from 2014 to 2015 an ESPED* Survey on Behalf of the API*** Erhebungseinheit für Seltene Pädiatrische Erkrankungen in Deutschland (German Paediatric Surveillance Unit) ** Arbeitsgemeinschaft Pädiatrische Immunologie
12. CD56 as a marker of an ILC1-like population with NK cell properties that is functionally impaired in AML
13. Immunodeficiency and EBV-induced lymphoproliferation caused by 4-1BB deficiency
14. Persisting enteropathy and disturbed adaptive mucosal immunity due to MHC class II deficiency
15. Hematopoietic stem cell transplantation for CD40 ligand deficiency: Results from an EBMT/ESID-IEWP-SCETIDE-PIDTC study
16. Hematopoietic Stem Cell Transplantation as Treatment for Patients with DOCK8 Deficiency
17. SCID patients with ARTEMIS vs RAG deficiencies following HCT: increased risk of late toxicity in ARTEMIS-deficient SCID
18. 95 Complement-associated prothrombotic state is caused by MAC-induced lysis of cells
19. Human FCHO1 deficiency reveals role for clathrin-mediated endocytosis in development and function of T cells
20. Bone marrow failure unresponsive to bone marrow transplant is caused by mutations in thrombopoietin
21. Reticular dysgenesis: international survey on clinical presentation, transplantation, and outcome
22. Severe glucose-6-phosphate dehydrogenase deficiency leads to susceptibility to infection and absent NETosis
23. Author Correction: Human FCHO1 deficiency reveals role for clathrin-mediated endocytosis in development and function of T cells
24. Chemotherapy for a secondary malignancy nearly restores complete chimerism in an SCID-patient after HSCT
25. P17 - RECURRENCE OF UNDERLYING CONGENITAL NEUTROPENIA WITHOUT MDS AFTER ALLOGENEIC STEM CELL TRANSPLANTATION IN A PATIENT WITH ELANE-MUTATED CONGENITAL NEUTROPENIA AND SECONDARY MDS
26. Multicenter experience in hematopoietic stem cell transplantation for serious complications of common variable immunodeficiency
27. Comparison of outcomes of hematopoietic stem cell transplantation without chemotherapy conditioning by using matched sibling and unrelated donors for treatment of severe combined immunodeficiency
28. Recent advances in understanding the pathogenesis and management of reticular dysgenesis
29. Eight induced pluripotent stem cell lines (iPSCs) derived from two patients with Leukocyte adhesion deficiency Type I (LAD I) with mutations in the ITGB2 gene
30. Hematopoietic cell transplantation in severe combined immunodeficiency: The SCETIDE 2006-2014 European cohort
31. Outcome of hematopoietic stem cell transplantation for adenosine deaminase–deficient severe combined immunodeficiency
32. Hematopoietic cell transplantation in severe combined immunodeficiency: The SCETIDE 2006-2014 European cohort
33. Circulating ${\rm{CD21}}^{\operatorname{low} } $ B Cells in Common Variable Immunodeficiency Resemble Tissue Homing, Innate-Like B Cells
34. Radioimmunotherapy-based conditioning for hematopoietic cell transplantation in children with malignant and nonmalignant diseases
35. Multicenter survey on the outcome of transplantation of hematopoietic cells in patients with the complete form of DiGeorge anomaly
36. Diagnostic approach to the hyper-IgE syndromes: Immunologic and clinical key findings to differentiate hyper-IgE syndromes from atopic dermatitis
37. Transplantation of hematopoietic stem cells and long-term survival for primary immunodeficiencies in Europe: Entering a new century, do we do better?
38. X-linked thrombocytopenia (XLT) due to WAS mutations: clinical characteristics, long-term outcome, and treatment options
39. HLA-haploidentical Donor Transplantation in Severe Combined Immunodeficiency
40. Initial presenting manifestations in 16,486 patients with inborn errors of immunity include infections and noninfectious manifestations
41. Biomarkers of DNA Damage Response Enable Flow Cytometry-Based Diagnostic to Identify Inborn DNA Repair Defects in Primary Immunodeficiencies
42. BCG Disease in SCID: Three Decades of Experience in a Pediatric Transplant Center
43. Differential DNA Damage Response of Peripheral Blood Lymphocyte Populations
44. F28 Novel mutations and findings in a cohort of McLeod neuroacanthocytosis, an X-linked HD phenocopy
45. Successful hematopoietic stem cell transplantation in a 4-1BB deficient patient with EBV-induced lymphoproliferation
46. Salvage HLA-haploidentical hematopoietic stem cell transplantation with post-transplant cyclophosphamide for graft failure in non-malignant disorders
47. Circulating [CD21.sup.low] B cells in common variable immunodeficiency resemble tissue homing, innate-like B cells
48. Case Report: Convalescent Plasma Achieves SARS-CoV-2 Viral Clearance in a Patient With Persistently High Viral Replication Over 8 Weeks Due to Severe Combined Immunodeficiency (SCID) and Graft Failure
49. Successful unrelated bone marrow transplantation in a child with chronic granulomatous disease complicated by pulmonary and cerebral granuloma formation
50. Hematopoietic cell transplantation in chronic granulomatous disease: a study of 712 children and adults
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