J. Roesler

发表

A splice-supporting intronic mutation in the last bp position of a cryptic exon within intron 6 of the CYBB gene induces its incorporation into the mRNA causing chronic granulomatous disease (CGD).

A. Rump, M. Gahr, J. Seidenberg, 2006, Gene.

B cell–intrinsic signaling through IL-21 receptor and STAT3 is required for establishing long-lived antibody responses in humans

Sami Al-Hajjar, J. Casanova, S. Choo, 2010, The Journal of experimental medicine.

International multi-centre study of pregnancy outcomes with interleukin-1 inhibitors

P. Hawkins, J. Roesler, T. Youngstein, 2017, Rheumatology.

X-linked chronic granulomatous disease (CGD) caused by an intra-exonic splice mutation (CYBB exon 3, c.262G->A) is mimicking juvenile sarcoidosis.

A. Rösen‐Wolff, J. Roesler, J. Brunner, 2007, Clinical and experimental rheumatology.

Myeloperoxidase is required for neutrophil extracellular trap formation: implications for innate immunity.

V. Wahn, T. Fuchs, A. Zychlinsky, 2011, Blood.

COUP-TFII is regulated by high glucose in endothelial cells.

S. Bornstein, J. Roesler, W. Goettsch, 2010, Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme.

PHAGOCYTES , GRANULOCYTES , AND MYELOPOIESIS Neutrophil oxidative burst activates ATM to regulate cytokine production and apoptosis

H. von Bernuth, C. Harbort, A. Zychlinsky, 2015 .

Heterogeneity in the mobilization of cytoplasmic calcium by human polymorphonuclear leukocytes in response to fMLP, C5a and IL‐8/NAP‐1

T. Breidenbach, M. Lohmann‐Matthes, J. Roesler, 1992, Journal of leukocyte biology.

Naturally Occurring Genetic Variants of Human Caspase‐1 Differ Considerably in Structure and the Ability to Activate Interleukin‐1β

M. Gahr, E. Remmers, A. Rösen‐Wolff, 2013, Human mutation.

Somatic loss of heterozygosity, but not haploinsufficiency alone, leads to full-blown autoimmune lymphoproliferative syndrome in 1 of 12 family members with FAS start codon mutation.

F. Rieux-Laucat, F. Hauck, J. Roesler, 2013, Clinical immunology.

Canakinumab (ACZ885, a fully human IgG1 anti-IL-1β mAb) induces sustained remission in pediatric patients with cryopyrin-associated periodic syndrome (CAPS)

A. Chakraborty, J. Roesler, C. Rordorf, 2011, Arthritis Research & Therapy.

Periodic fever, mild arthralgias, and reversible moderate and severe organ inflammation associated with the V198M mutation in the CIAS1 gene in three German patients – expanding phenotype of CIAS1 related autoinflammatory syndrome

M. Gahr, A. Rösen‐Wolff, G. Heubner, 2004, European journal of haematology.

Naive and memory human B cells have distinct requirements for STAT3 activation to differentiate into antibody-secreting plasma cells

J. Casanova, S. Choo, Joanne M. Smart, 2013, The Journal of experimental medicine.

Application of purified polysaccharides from cell cultures of the plant Echinacea purpurea to test subjects mediates activation of the phagocyte system.

M. Lohmann‐Matthes, J. Roesler, A. Emmendörffer, 1991, International journal of immunopharmacology.

Application of purified polysaccharides from cell cultures of the plant Echinacea purpurea to mice mediates protection against systemic infections with Listeria monocytogenes and Candida albicans.

A. Kiderlen, M. Lohmann‐Matthes, J. Roesler, 1991, International journal of immunopharmacology.

Polysaccharides isolated from plant cell cultures of Echinacea purpurea enhance the resistance of immunosuppressed mice against systemic infections with Candida albicans and Listeria monocytogenes.

M. Lohmann‐Matthes, J. Roesler, G. Franke, 1993, International journal of immunopharmacology.

Increased susceptibility of a carrier of X-linked chronic granulomatous disease (CGD) to Aspergillus fumigatus infection associated with age-related skewing of lyonization

M. Gahr, A. Rösen‐Wolff, J. Roesler, 2001, Annals of Hematology.

Unusual late onset of X-linked chronic granulomatous disease in an adult woman after unsuspicious childhood.

H. Renz, J. Roesler, A. Lun, 2002, Clinical chemistry.

Chronic granulomatous disease (CGD) and complete myeloperoxidase deficiency both yield strongly reduced dihydrorhodamine 123 test signals but can be easily discerned in routine testing for CGD.

A. Zychlinsky, A. Rösen‐Wolff, M. O'gorman, 2007, Clinical chemistry.

Carriers of X-linked chronic granulomatous disease at risk.

J. Roesler, 2009, Clinical immunology.

Recombination events between the p47-phox gene and its highly homologous pseudogenes are the main cause of autosomal recessive chronic granulomatous disease.

S. Chanock, P. Patiño, J. Roesler, 2000, Blood.

Genetic Diagnostic Elucidation of a Patient With Multiorgan Granulomas, Facial Peculiarities, and Psychomotor Retardation

Dániel T. Soukup, J. Roesler, A. Kuechler, 2018, Front. Genet..

P67-phox (NCF2) Lacking Exons 11 and 12 Is Functionally Active and Leads to an Extremely Late Diagnosis of Chronic Granulomatous Disease (CGD)

A. Rösen‐Wolff, J. Liese, H. Morbach, 2012, PloS one.

Alu repeat-induced deletions in chronic granulomatous disease: a cause not only for p67-phox, but also for p47-phox deficiency

A. Rösen‐Wolff, D. Roos, J. Roesler, 2013, Annals of Hematology.

Hematologically important mutations: the autosomal recessive forms of chronic granulomatous disease (second update).

S. Holland, D. Kuhns, H. Malech, 2000, Blood cells, molecules & diseases.

Therapeutic strategy in p47-phox deficient chronic granulomatous disease presenting as inflammatory bowel disease.

S. Ehl, S. Koletzko, A. Ventura, 2010, The Journal of allergy and clinical immunology.

UvA-DARE ( Digital Academic Repository ) Chronic granulomatous disease : the European experience

Richard, A. Fischer, T. Kuijpers, 2009 .

Polyclonal long-term MFGS-gp91phox marking in rhesus macaques after nonmyeloablative transplantation with transduced autologous peripheral blood progenitor cells.

A. Farese, T. MacVittie, U. Choi, 2006, Molecular therapy : the journal of the American Society of Gene Therapy.

Benefit assessment of preventive medical check-ups in patients suffering from chronic granulomatous disease (CGD).

M. Gahr, H. von Bernuth, A. Rösen‐Wolff, 2005, Journal of evaluation in clinical practice.

Severe phenotype of chronic granulomatous disease presenting in a female with a de novo mutation in gp91-phox and a non familial, extremely skewed X chromosome inactivation.

S. Holland, T. Fleisher, D. Kuhns, 2003, Clinical immunology.

Disorders of Phagocytic Cells

C. Klein, T. Nicolai, S. Rosenzweig, 2012 .

Abnormal regulation in the signal transduction in neutrophils from patients with severe congenital neutropenia: relation of impaired mobilization of cytosolic free calcium to altered chemotaxis, superoxide anion generation and F-actin content.

K. Welte, M. Lohmann‐Matthes, J. Roesler, 1993, Experimental hematology.

A p47-phox pseudogene carries the most common mutation causing p47-phox- deficient chronic granulomatous disease.

E. Green, S. Chanock, P. Hopkins, 1997, The Journal of clinical investigation.

Hematologically important mutations: The autosomal forms of chronic granulomatous disease (third update).

J. L. Shephard, M. Vihinen, H. Kanegane, 2021, Blood cells, molecules & diseases.

Defects in Intrinsic and Innate Immunity: Receptors and Signaling Components

J. Casanova, C. Picard, J. Roesler, 2017 .

Hematologically important mutations: X-linked chronic granulomatous disease (third update).

S. Holland, T. Ariga, D. Kuhns, 1997, Blood cells, molecules & diseases.

Hyper-IgE and Carcinoma in CADINS Disease

D. Aust, A. Snow, R. Berner, 2022, Frontiers in Immunology.

Clinical features of dominant and recessive interferon γ receptor 1 deficiencies

M. Newport, S. Dorman, J. Casanova, 2004, The Lancet.

Viral infections in interferon-γ receptor deficiency☆☆☆

S. Dorman, S. Holland, G. Uzel, 1999, The Journal of Pediatrics.

Listeria monocytogenes and recurrent mycobacterial infections in a child with complete interferon-gamma-receptor (IFNgammaR1) deficiency: mutational analysis and evaluation of therapeutic options.

J. Casanova, M. Gahr, W. Friedrich, 1999, Experimental hematology.

561del4 defines a novel small deletion hotspot in the interferon-γ receptor 1 chain

S. Dorman, S. Rosenzweig, J. Roesler, 2002 .

Flow cytometric measurement of the respiratory burst activity of phagocytes using dihydrorhodamine 123.

G. Rothe, G. Valet, J. Roesler, 1991, Journal of immunological methods.

CARD15 Genotype and Phenotype Analysis in 55 Pediatric Patients With Crohn Disease From Saxony, Germany

A. Rösen‐Wolff, Liping Sun, J. Roesler, 2003, Journal of pediatric gastroenterology and nutrition.

Macrophage Function in Murine Allogeneic Bone Marrow Radiation Chimeras in the Early Phase After Transplantation

M. Baccarini, M. Lohmann‐Matthes, J. Roesler, 1989, Journal of leukocyte biology.

NADPH oxidase is not required for spontaneous and Staphylococcus aureus-induced apoptosis of monocytes

M. Gahr, A. Rösen‐Wolff, J. Roesler, 2004, Annals of Hematology.

Clinical picture and treatment of 2212 patients with common variable immunodeficiency.

É. Oksenhendler, P. Soler-Palacín, A. Šedivá, 2014, The Journal of allergy and clinical immunology.

Influence of CARD15 Mutations on Disease Activity and Response to Therapy in 65 Pediatric Crohn Patients from Saxony, Germany

M. Gahr, A. Rösen‐Wolff, Liping Sun, 2005, Journal of pediatric gastroenterology and nutrition.

Haploinsufficiency, rather than the effect of an excessive production of soluble CD95 (CD95{Delta}TM), is the basis for ALPS Ia in a family with duplicated 3' splice site AG in CD95 intron 5 on one allele.

J. Valcárcel, M. Gahr, M. Lenardo, 2005, Blood.

STAT3 mutations underlying autosomal dominant hyper-IgE syndrome impair human CD8 + T cell memory formation and function

S. Choo, Joanne M. Smart, C. Picard, 2013 .

Clinical features of dominant and recessive interferon gamma receptor 1 deficiencies.

M. Newport, S. Dorman, J. Casanova, 2004, Lancet.

Gene therapy for chronic granulomatous disease

J. Roesler, M. Gentsch, M. Ryser, 2007, Expert opinion on biological therapy.

Altered function and surface marker expression of neutrophils induced by rhG‐CSF treatment in severe congenital neutropenia

K. Welte, M. Lohmann‐Matthes, J. Roesler, 1992, European journal of haematology.

“Periodic fever” without fever: two cases of non-febrile TRAPS with mutations in the TNFRSF1A gene presenting with episodes of inflammation or monosymptomatic amyloidosis

B. Rudolph, D. Haffner, G. Burmester, 2005, Annals of the Rheumatic Diseases.

Autophagy proteins stabilize pathogen-containing phagosomes for prolonged MHC II antigen processing

J. Dengjel, A. C. Becker, C. Münz, 2013, The Journal of cell biology.

Granulocyte and granulocyte-macrophage colony-stimulating factors for treatment of neutropenia in glycogen storage disease type Ib.

V. Wahn, T. Breidenbach, K. Welte, 1991, The Journal of pediatrics.

NADPH oxidase is required for neutrophil‐dependent autoantibody‐induced tissue damage MT Chiriac, J Roesler, A Sindrilaru, K Scharffetter‐Kochanek, D Zillikens, C Sitaru. J Pathol 2007; 212:56–65

D. Zillikens, K. Scharffetter-Kochanek, J. Roesler, 2007 .

Caspofungin therapy for Aspergillus lung infection in a boy with chronic granulomatous disease

M. Gahr, A. Rösen‐Wolff, J. Roesler, 2003 .

Functional features of neutrophils induced by G-CSF and GM-CSF treatment: differential effects and clinical implications

K. Spiekermann, K. Welte, J. Roesler, 1997, Leukemia.

Flow cytometry reveals different lag times in rapid cytoplasmic calcium elevations in human neutrophils in response to N‐formyl peptide

J. Norgauer, J. Roesler, E. Schöpf, 1993, Journal of cellular physiology.

The cytochrome b-558 molecules involved in the fibroblast and polymorphonuclear leucocyte superoxide-generating NADPH oxidase systems are structurally and genetically distinct.

A. Jesaitis, J. Roesler, B. Meier, 1993, The Biochemical journal.

Changes in light‐scatter profile, membrane depolarization and calcium mobilization of neutrophils induced by G‐CSF in vivo

K. Spiekermann, K. Welte, M. Lohmann‐Matthes, 1994, British journal of haematology.

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

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

561del4 defines a novel small deletion hotspot in the interferon-gamma receptor 1 chain.

S. Dorman, S. Holland, S. Rosenzweig, 2002, Clinical immunology.

Hematopoietic Stem Cell Transplantation Cures Therapy-refractory Aspergillosis in Chronic Granulomatous Disease.

S. Lau, H. von Bernuth, S. Voigt, 2021, The Pediatric infectious disease journal.

Redundant ability of phagocytes to kill Aspergillus species.

A. Rösen‐Wolff, J. Roesler, 2011, The Journal of allergy and clinical immunology.

Matched Family Donor Lymphocyte Infusions as First Cellular Therapy for Patients with Severe Primary T-cell Deficiencies.

A. Schulz, B. Maecker-Kolhoff, B. Eiz-Vesper, 2020, Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.

Defects in Innate Immunity: Receptors and Signaling Components

S. Rosenzweig, N. Rezaei, J. Roesler, 2021, Reference Module in Biomedical Sciences.

A fast and easy method to determine the production of reactive oxygen intermediates by human and murine phagocytes using dihydrorhodamine 123.

M. Lohmann‐Matthes, M. Hecht, J. Roesler, 1990, Journal of immunological methods.

Staphylococci surviving intracellularly in phagocytes from patients suffering from chronic granulomatous disease are killed in vitro by antibiotics encapsulated in liposomes.

M. Lohmann‐Matthes, J. Roesler, S. Hockertz, 1991, The Journal of clinical investigation.

Chronic Granulomatous Disease: The European Experience

Dirk Roos, Theoni Petropoulou, A. Fischer, 2009, PloS one.

[Chronic recurrent aphthous stomatitis in a 15-year-old carrier of x-chromosome inherited cytochrome b558-negative septic granulomatosis].

S. Rohde, M. Melter, J. Roesler, 1990, Monatsschrift Kinderheilkunde : Organ der Deutschen Gesellschaft fur Kinderheilkunde.

Chronic Granulomatous Disease (CGD) Mimicking Neoplasms: A Suspected Mediastinal Teratoma Unmasking as Thymic Granulomas Due to X-linked CGD, and 2 Related Cases

M. Gahr, A. Rösen‐Wolff, F. Hauck, 2008, Journal of pediatric hematology/oncology.

Gain-of-function human STAT1 mutations impair IL-17 immunity and underlie chronic mucocutaneous candidiasis

A. Fischer, C. Bodemer, J. Casanova, 2011, The Journal of experimental medicine.

Successful elimination of an invasive Aspergillus nidulans lung infection by voriconazole after failure of a combination of caspofungin and liposomal amphotericin B in a boy with chronic granulomatous disease.

M. Gahr, W. Friedrich, A. Rösen‐Wolff, 2004, The Pediatric infectious disease journal.

A. Schulz, W. Friedrich, J. Roesler, 2007, European Journal of Pediatrics.

Initial presenting manifestations in 16,486 patients with Inborn Errors of Immunity include infections and non-infectious manifestations.

Nurit Assia Batzir, K. Schwarz, D. Foell, 2021, The Journal of allergy and clinical immunology.

Hematopoietic stem cell transplantation for complete IFN-gamma receptor 1 deficiency: a multi-institutional survey.

A. Fischer, J. Casanova, A. Schulz, 2004, The Journal of pediatrics.

Correction of complete interferon-gamma receptor 1 deficiency by bone marrow transplantation.

A. Schulz, W. Friedrich, K. Debatin, 2002, Blood.

Microstructural study of boron-doped Co–Re–Cr alloys by means of transmission electron microscopy and electron energy-loss spectroscopy

D. Mukherji, U. Glatzel, R. Völkl, 2012 .

Impaired IFNγ-Signaling and Mycobacterial Clearance in IFNγR1-Deficient Human iPSC-Derived Macrophages

A. Schambach, D. Jonigk, A. Mucci, 2017, Stem cell reports.

Hematologically important mutations: X-linked chronic granulomatous disease (fourth update).

J. L. Shephard, H. Kanegane, S. Holland, 2021, Blood cells, molecules & diseases.

Uncommon missense and splice mutations and resulting biochemical phenotypes in German patients with X-linked chronic granulomatous disease.

M. Gahr, A. Rösen‐Wolff, M. Burdelski, 1999, Experimental hematology.

Alu‐repeat–induced deletions within the NCF2 gene causing p67‐phox–deficient chronic granulomatous disease (CGD)

J. Casanova, M. Gahr, G. Dbaibo, 2010, Human mutation.

Evaluation of flow cytometric methods for diagnosis of chronic granulomatous disease variants under routine laboratory conditions.

K. Spiekermann, G. Rothe, M. Lohmann‐Matthes, 1994, Cytometry.

A case of recurrent herpes simplex 2 encephalitis, VZV reactivations, and dominant partial interferon-gamma-receptor-1 deficiency supports relevance of IFNgamma for antiviral defense in humans

J. Roesler, C. Schuetz, J. Schäfer, 2020, Molecular and Cellular Pediatrics.

Colony-stimulating factors for neutropenia in glycogen storage disease lb

T. Breidenbach, K. Welte, S. Burdach, 1991, The Lancet.

Defective apoptosis due to a point mutation in the death domain of CD95 associated with autoimmune lymphoproliferative syndrome, T-cell lymphoma, and Hodgkin's disease.

M. Gahr, H. Martin, B. Wörmann, 1999, Experimental hematology.

Functional Restoration of gp91phox-Oxidase Activity by BAC Transgenesis and Gene Targeting in X-linked Chronic Granulomatous Disease iPSCs

E. Schröck, B. Klink, M. Laugsch, 2015, Molecular therapy : the journal of the American Society of Gene Therapy.

Granulomatous Disease Mobilized CD34+ Cells from Patients with X-linked Chronic Oxidase Defect in NOD/SCID Mouse Repopulating Peripheral Blood 3rd Generation Self-Inactivating gp91phox Lentivector Corrects the

T. Dull, C. Civin, H. Malech, 2013 .

Third-generation, self-inactivating gp91(phox) lentivector corrects the oxidase defect in NOD/SCID mouse-repopulating peripheral blood-mobilized CD34+ cells from patients with X-linked chronic granulomatous disease.

T. Dull, C. Civin, H. Malech, 2002, Blood.

Granulomatous Disease Cells from Patients with X-linked Chronic + Mobilized CD 34 Oxidase Defect in NOD / SCID Mouse Repopulating Peripheral Blood Lentivector Corrects thephox Generation Self-Inactivating gp 91 rd

T. Dull, C. Civin, H. Malech, 2002 .

Phase analysis and lattice mismatches in superalloys DT706 and Inconel 706

R. Gilles, D. Mukherji, M. Hoelzel, 2006 .

Disturbed B-lymphocyte selection in autoimmune lymphoproliferative syndrome.

K. Schwarz, W. Vach, M. van der Burg, 2016, Blood.

In vitro functions of neutrophils induced by treatment with rhG‐CSF in severe congenital neutropenia

K. Welte, M. Lohmann‐Matthes, J. Roesler, 1991, European journal of haematology.

Kinetics of transfused neutrophils in peripheral blood and BAL fluid of a patient with variant X‐linked chronic granulomatous disease

M. Lohmann‐Matthes, J. Roesler, A. Emmendorffer, 1991, European journal of haematology.

Production of oxygen radicals by fibroblasts and neutrophils from a patient with x‐linked chronic granulomatous disease

M. Lohmann‐Matthes, J. Roesler, B. Meier, 1993, European journal of haematology.

Meningoencephalitis caused by varicella-zoster virus reactivation in a child with dominant partial interferon-gamma receptor-1 deficiency.

A. Rösen‐Wolff, J. Roesler, C. Hedrich, 2011, The Pediatric infectious disease journal.

Novel STAT1 Alleles in Otherwise Healthy Patients with Mycobacterial Disease

J. Casanova, R. Schreiber, C. Picard, 2006, PLoS genetics.

Severe infectious complications in a girl suffering from atopic dermatitis were found to be due to chronic granulomatous disease.

M. Lohmann‐Matthes, J. Roesler, A. Emmendörffer, 1993, Acta dermato-venereologica.

Diagnosis of chronic granulomatous disease and of its mode of inheritance by dihydrorhodamine 123 and flow microcytofluorometry

M. Lohmann‐Matthes, J. Roesler, J. Freihorst, 2005, European Journal of Pediatrics.

Altered surface marker expression and function of G‐CSF‐induced neutrophils from test subjects and patients under chemotherapy

K. Spiekermann, K. Welte, M. Lohmann‐Matthes, 1994, British journal of haematology.

In Vitro Functions of Granulocyte Colony-Stimulating Factor Induced Neutrophils

T. Breidenbach, K. Welte, M. Lohmann‐Matthes, 1992 .

Impaired Calcium Mobilization and Abnormalities in Microfilamentous Cytoskeletal Organization in Granulocyte Colony-Stimulating Factor Induced Neutrophils from Patients with Severe Congenital Neutropenia

T. Breidenbach, K. Welte, M. Lohmann‐Matthes, 1992 .

Outcome of chronic granulomatous disease ‐ Conventional treatment vs stem cell transplantation

A. Fischer, N. Mahlaoui, J. Schulte, 2020, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.

Human FCHO1 deficiency reveals role for clathrin-mediated endocytosis in development and function of T cells

U. Pannicke, K. Schwarz, J. Puchalka, 2020, Nature Communications.

Genomic structure of the human p47-phox (NCF1) gene.

S. Chanock, P. Hopkins, J. Roesler, 2000, Blood cells, molecules & diseases.

Diagnostic approach to the hyper-IgE syndromes: immunologic and clinical key findings to differentiate hyper-IgE syndromes from atopic dermatitis.

H. Ochs, T. Torgerson, V. Wahn, 2010, The Journal of allergy and clinical immunology.

Ar Ticle B Cell–intrinsic Signaling through Il-21 Receptor and Stat3 Is Required for Establishing Long-lived Antibody Responses in Humans Engagement of Cytokine Receptors by Specific Ligands Activate Janus Kinase–signal Transducer and Activator of Transcription (stat) Signaling Pathways. the Exact R

Sami Al-Hajjar, J. Casanova, S. Choo, 2022 .

X-linked Chronic Granulomatous Disease.

J. Roesler, 2006, The Journal of small animal practice.

The German national registry for primary immunodeficiencies (PID)

C. Klein, S. Ehl, R. Krüger, 2013, Clinical and experimental immunology.

Human Procaspase-1 Variants with Decreased Enzymatic Activity Are Associated with Febrile Episodes and May Contribute to Inflammation via RIP2 and NF-κB Signaling

C. Klein, S. Özen, A. Rösen‐Wolff, 2014, The Journal of Immunology.

Non-canonical Caspase-1 Signaling Drives RIP2-Dependent and TNF-α-Mediated Inflammation In Vivo.

M. Sarov, A. Rösen‐Wolff, M. Cooper, 2020, Cell reports.

Inflammation via RIP 2 and NF-with Febrile Episodes and May Contribute to AssociatedDecreased Enzymatic Activity Are Human Procaspase-1 Variants with Roesler

C. Klein, S. Ozen, D. Lindemann, 2014 .

Current Knowledge on Procaspase-1 Variants with Reduced or Abrogated Enzymatic Activity in Autoinflammatory Disease

A. Rösen‐Wolff, S. Hofmann, J. Roesler, 2015, Current Rheumatology Reports.

Diagnosis of chronic granulomatous disease.

J. Roesler, A. Emmendörffer, 1991, Blood.

Diagnosis of chronic granulomatous disease [letter; comment]

J. Roesler, A. Emmendorffer, 1991 .

A 58-year-old man with respiratory insufficiency after a 50-year history of hypersensitivity pneumonitis and pulmonary Aspergillus infections.

J. Liese, H. Morbach, H. Tony, 2013, The journal of allergy and clinical immunology. In practice.

Important role of corticosteroids in chronic granulomatous disease.

J. Roesler, 2007, Journal of Medical Microbiology.

A protective role for inflammasome activation following injury--Shock 2012;37(1): 47-55.

A. Rösen‐Wolff, Marcus Franke, J. Roesler, 2012, Shock.

Spectrum and Management of Complement Immunodeficiencies (Excluding Hereditary Angioedema) Across Europe

P. Kralickova, J. Litzman, A. Turley, 2015, Journal of Clinical Immunology.

A p 47-phox Pseudogene Carries the Most Common Mutation Causing p 47-phox – deficient Chronic Granulomatous Disease

E. Green, S. Chanock, P. Hopkins, 2013 .

Two German CINCA (NOMID) patients with different clinical severity and response to anti‐inflammatory treatment

M. Gahr, A. Rösen‐Wolff, J. Roesler, 2003, European journal of haematology.

Signal transducer and activator of transcription 3 (STAT3) mutations underlying autosomal dominant hyper-IgE syndrome impair human CD8(+) T-cell memory formation and function.

J. Casanova, S. Choo, Joanne M. Smart, 2013, The Journal of allergy and clinical immunology.

Rapid and Sustained Long‐Term Efficacy and Safety of Canakinumab in Patients With Cryopyrin‐Associated Periodic Syndrome Ages Five Years and Younger

L. Goffin, R. Laxer, B. Lauwerys, 2019, Arthritis & rheumatology.

Interferon-gamma receptor deficiency: relationship between genotype, environment, and phenotype (Review).

J. Casanova, E. Jouanguy, F. Altare, 1998, International journal of molecular medicine.

Twenty Year Follow up of a Patient with a New De-Novo NLRP3 Mutation (S595G) and CINCA Syndrome

A. Rösen‐Wolff, V. Schuster, J. Roesler, 2009, Klinische Padiatrie.

Good response to IL‐1β blockade by anakinra in a 23‐year‐old CINCA/NOMID patient without mutations in the CIAS1 gene. Cytokine profiles and functional studies

M. Gahr, G. Heubner, J. Roesler, 2008, Scandinavian journal of rheumatology.

NADPH oxidase is required for neutrophil‐dependent autoantibody‐induced tissue damage

D. Zillikens, K. Scharffetter-Kochanek, J. Roesler, 2007, The Journal of pathology.

Complement C2 deficiency disarranging innate and adaptive humoral immune responses in a pediatric patient: Treatment with rituximab

D. Aust, F. Hauck, F. Pessler, 2011, Arthritis care & research.

Canakinumab provides rapid and sustained long-term efficacy and safety in patients with cryopyrin-associated periodic syndrome aged ≤5 years.

L. Goffin, R. Laxer, B. Lauwerys, 2019, Arthritis & rheumatology.

More severe than CVID: Combined immunodeficiency due to a novel NFKB2 mutation

A. Rösen‐Wolff, A. Huebner, J. Roesler, 2020, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.

Colony-stimulating factors for neutropenia in glycogen storage disease Ib.

T. Breidenbach, K. Welte, S. Burdach, 1991, Lancet.

Variant PIK3R1 Hypermorphic Mutation and Clinical Phenotypes in a Family with Short Statures, Mild Immunodeficiency and Lymphoma

A. Rösen‐Wolff, F. Hauck, I. Bilic, 2017, Klinische Pädiatrie.

Human FCHO1 deficiency reveals role for clathrin-mediated endocytosis in development and function of T cells

U. Pannicke, K. Schwarz, J. Puchalka, 2020, Nature Communications.

Two familial cases with tumor necrosis factor receptor-associated periodic syndrome caused by a non-cysteine mutation (T50M) in the TNFRSF1A gene associated with severe multiorganic amyloidosis.

B. Rudolph, D. Haffner, U. Querfeld, 2004, The Journal of rheumatology.

Remarks on the article Genetics and immunopathology of chronic granulomatous disease by Marie José Stasia and Xing Jun Li

J. Roesler, 2008, Seminars in Immunopathology.

Disturbed B-lymphocyte selection in autoimmune lymphoproliferative syndrome.

K. Schwarz, W. Vach, M. van der Burg, 2016, Blood.