M. Hönig

发表

Radioimmunotherapy-based conditioning for hematopoietic cell transplantation in children with malignant and nonmalignant diseases.

G. Glatting, S. Reske, A. Schulz, 2011, Blood.

Successful Haploidentical Hematopoietic Stem Cell Transplantation in a Patient with SCID due to CD3ε Deficiency: Need for IgG-Substitution 6 Years Later

U. Pannicke, K. Schwarz, A. Schulz, 2014, Klinische Pädiatrie.

Immunological reconstitution in a patient with ZAP-70 deficiency following transfusion of blood lymphocytes from a previously transplanted sibling without conditioning

K. Schwarz, A. Schulz, W. Friedrich, 2012, Bone Marrow Transplantation.

Patients with adenosine deaminase deficiency surviving after hematopoietic stem cell transplantation are at high risk of CNS complications.

U. Pannicke, K. Schwarz, A. Schulz, 2007, Blood.

CD4+ T Cell–Derived IL-21 and Deprivation of CD40 Signaling Favor the In Vivo Development of Granzyme B–Expressing Regulatory B Cells in HIV Patients

K. Schwarz, A. Schulz, F. Kirchhoff, 2015, The Journal of Immunology.

Increased proportions of γδ T lymphocytes in atypical SCID associate with disease manifestations.

L. Notarangelo, C. Picard, P. Soler-Palacín, 2019, Clinical immunology.

Persisting enteropathy and disturbed adaptive mucosal immunity due to MHC class II deficiency.

K. Schwarz, A. Schulz, T. Barth, 2019, Clinical immunology.

Multicenter survey on the outcome of transplantation of hematopoietic cells in patients with the complete form of DiGeorge anomaly.

A. Fischer, W. Friedrich, A. Gennery, 2010, Blood.

Key findings to expedite the diagnosis of hyper‐IgE syndromes in infants and young children

K. Schwarz, V. Wahn, A. Wollenberg, 2016, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.

EBMT/ESID inborn errors working party guidelines for hematopoietic stem cell transplantation for inborn errors of immunity

A. Schulz, P. Veys, B. Neven, 2021, Bone Marrow Transplantation.

Reticular dysgenesis (aleukocytosis) is caused by mutations in the gene encoding mitochondrial adenylate kinase 2

U. Pannicke, K. Schwarz, A. Schulz, 2009, Nature Genetics.

The German National Registry of Primary Immunodeficiencies (2012–2017)

K. Schwarz, D. Foell, A. Schulz, 2019, Front. Immunol..

Stem cell transplantation in children with infantile osteopetrosis is associated with a high incidence of VOD, which could be prevented with defibrotide

A. Schulz, W. Friedrich, S. Corbacioglu, 2006, Bone Marrow Transplantation.

Long-term outcome and lineage-specific chimerism in 194 patients with Wiskott-Aldrich syndrome treated by hematopoietic cell transplantation in the period 1980-2009: an international collaborative study.

A. Fischer, A. Schulz, W. Friedrich, 2011, Blood.

Long-term follow-up of children conditioned with Treosulfan: German and Austrian experience

A. Schulz, B. Gruhn, M. Eyrich, 2013, Bone Marrow Transplantation.

Immune deficiencies, infection, and systemic immune disordersComparison of outcomes of hematopoietic stem cell transplantation without chemotherapy conditioning by using matched sibling and unrelated donors for treatment of severe combined immunodeficiency

L. Notarangelo, A. Gennery, S. Pai, 2014 .

Comparison of outcomes of hematopoietic stem cell transplant without chemotherapy conditioning using matched sibling and unrelated donors for treatment of SCID

L. Notarangelo, A. Gennery, S. Pai, 2014 .

Synovial PMN show a coordinated up‐regulation of CD66 molecules

H. Peter, P. Jantscheff, F. Grunert, 1999, Journal of leukocyte biology.

Omenn syndrome: a lack of tolerance on the background of deficient lymphocyte development and maturation

K. Schwarz, M. Hönig, 2006, Current opinion in rheumatology.

Human RIPK1 deficiency causes combined immunodeficiency and inflammatory bowel diseases

U. Pannicke, K. Schwarz, C. Klein, 2018, Proceedings of the National Academy of Sciences.

Regulated expression of nuclear receptor RORγt confers distinct functional fates to NK cell receptor-expressing RORγt(+) innate lymphocytes.

U. Pannicke, K. Schwarz, C. Ware, 2010, Immunity.

Outcome of hematopoietic stem cell transplantation for adenosine deaminase-deficient severe combined immunodeficiency.

A. Fischer, W. Friedrich, L. Notarangelo, 2012, Blood.

Patients with early relapse of primary hemophagocytic syndromes or with persistent CNS involvement may benefit from immediate hematopoietic stem cell transplantation

W. Friedrich, K. Debatin, U. Stadt, 2009, Bone Marrow Transplantation.

HLA-haploidentical donor transplantation in severe combined immunodeficiency.

W. Friedrich, M. Hönig, 2011, Hematology/oncology clinics of North America.

HLA-haploidentical donor transplantation in severe combined immunodeficiency.

W. Friedrich, M. Hönig, 2010, Immunology and allergy clinics of North America.

Lesson from hypomorphic recombination-activating gene (RAG) mutations: Why asymptomatic siblings should also be tested.

U. Pannicke, K. Schwarz, A. Schulz, 2014, The Journal of allergy and clinical immunology.

Curative treatment of autosomal-recessive hyper-IgE syndrome by hematopoietic cell transplantation

U. Pannicke, K. Schwarz, A. Schulz, 2011, Bone Marrow Transplantation.

Successful hematopoietic stem-cell transplantation in a patient with chronic granulomatous disease and McLeod phenotype sensitized to Kx and K antigens

K. Schwarz, A. Schulz, W. Friedrich, 2010, Bone Marrow Transplantation.

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

J. Orange, A. Schulz, R. Geha, 2015, Journal of Clinical Immunology.

Results and long-term outcome in 39 patients with Wiskott–Aldrich syndrome transplanted from HLA-matched and -mismatched donors

A. Schulz, W. Friedrich, U. Benninghoff, 2009, Immunologic research.

Dataset of clinical, immunohistopathological and laboratory features of patients with MHC II deficiency suffering from enteropathy

K. Schwarz, A. Schulz, T. Barth, 2019, Data in brief.

Hematopoietic Stem Cell Transplantation for Severe Combined Immunodeficiency

W. Friedrich, M. Hönig, A. Schulz, 2011, Klinische Pädiatrie.

The most frequent DCLRE1C (ARTEMIS) mutations are based on homologous recombination events

U. Pannicke, K. Schwarz, A. Schulz, 2010, Human mutation.

NK Cells from RAG- or DCLRE1C-Deficient Patients Inhibit HCMV

T. Mertens, M. Hönig, Eva Jacobsen, 2019, Microorganisms.

Long-term follow-up in patients with severe combined immunodeficiency treated by bone marrow transplantation

W. Friedrich, M. Hönig, S. Müller, 2007, Immunologic research.

Late thymic deficiency after HLA-haploidentical hematopoietic stem cell transplantation for severe combined immunodeficiency.

U. Pannicke, K. Schwarz, M. Ege, 2019, The Journal of allergy and clinical immunology.

Response of mouse tongue epithelium to single doses of bleomycin and radiation.

W. Dörr, M. Hönig, E. Hirler, 1993, Radiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology.

Response of mouse oral mucosa to repeated doses of bleomycin.

W. Dörr, M. Hönig, 1994, European journal of cancer. Part B, Oral oncology.

[Interdisciplinary AWMF guideline for the treatment of primary antibody deficiencies].

H. Sitter, T. Welte, V. Wahn, 2012, Klinische Padiatrie.

Different actions of neomychin and metronidazole on breath hydrogen (H2) exhalation.

B. Lembcke, W. Caspary, M. Hönig, 1980, Zeitschrift fur Gastroenterologie.

Regulated expression of nuclear receptor RORγt confers distinct functional fates to NK cell receptor-expressing RORγt(+) innate lymphocytes.

U. Pannicke, K. Schwarz, C. Ware, 2010, Immunity.

Mass Cytometry-A Tool for the Curious: Networking in Berlin.

M. Yaspo, A. Grützkau, D. Kunkel, 2020, Cytometry. Part A : the journal of the International Society for Analytical Cytology.

Immune reconstitution in congenital disorders after HLA-haploidentical hemopoietic stem cell transplantation.

A. Schulz, W. Friedrich, M. Hönig, 2004, Blood cells, molecules & diseases.