I. Schulze

发表

Novel cell death program leads to neutrophil extracellular traps.

V. Wahn, T. Fuchs, A. Zychlinsky, 2007, The Journal of cell biology.

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

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

Relevance of biallelic versus monoallelic TNFRSF13B mutations in distinguishing disease-causing from risk-increasing TNFRSF13B variants in antibody deficiency syndromes.

A. Schäffer, E. Gertz, A. Plebani, 2008, Blood.

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

A. Schäffer, V. Lougaris, R. Geha, 2015, The Journal of allergy and clinical immunology.

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.

Novel cell death program leads to neutrophil extracellular traps

V. Wahn, T. Fuchs, A. Zychlinsky, 2007, The Journal of Cell Biology.

Children and adults with primary antibody deficiencies gain quality of life by subcutaneous IgG self-infusions at home.

Ó. Asensio, A N N Gardulf, I. Schulze, 2004, The Journal of allergy and clinical immunology.

[Interdisciplinary AWMF guideline for the diagnostics of primary immunodeficiency].

S. Ehl, H. von Bernuth, K. Warnatz, 2011, Klinische Padiatrie.

NEMO Mutations in 2 Unrelated Boys With Severe Infections and Conical Teeth

C. Bodemer, J. Casanova, C. Picard, 2005, Pediatrics.

New mutations in the ATM gene and clinical data of 25 AT patients

T. Dörk, I. Demuth, K. Chrzanowska, 2011, neurogenetics.

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.

Rapid Subcutaneous IgG Replacement Therapy is Effective and Safe in Children and Adults with Primary Immunodeficiencies—A Prospective, Multi-National Study

Ó. Asensio, A N N Gardulf, I. Schulze, 2006, Journal of Clinical Immunology.

Btk is a positive regulator in the TREM-1/DAP12 signaling pathway.

A. Cerwenka, W. Ellmeier, K. Warnatz, 2011, Blood.

Rapid Whole Blood Flow Cytometric Test to Detect ICOS Deficiency in Patients with Common Variable Immunodeficiency

V. Wahn, H. Volk, C. Höflich, 2006, International Archives of Allergy and Immunology.

Libyan Boy with Autosomal Recessive Trait (P22-phox Defect) of Chronic Granulomatous Disease

I. Schulze, A. Al-Tubuly, A. Al-Bousafy, 2006, The Libyan journal of medicine.

Libyan Boy with Autosomal Recessive Trait (P22-phox Defect) of Chronic Granulomatous Disease.

I. Schulze, A. Al-Tubuly, A. Al-Bousafy, 2006 .

Large deletions and point mutations involving the dedicator of cytokinesis 8 (DOCK8) in the autosomal-recessive form of hyper-IgE syndrome.

Edward R B McCabe, Bodo Grimbacher, Christoph Klein, 2009, The Journal of allergy and clinical immunology.

Large deletions and point mutations involving the dedicator of cytokinesis 8 (DOCK8) in the autosomal-recessive form of hyper-IgE syndrome.

T. Chatila, S. Holland, C. Klein, 2009, The Journal of allergy and clinical immunology.

De novo terminal deletion of chromosome 15q26.1 characterised by comparative genomic hybridisation and FISH with locus specific probes

H. Hennies, I. Schulze, L. Neumann, 2001, Journal of medical genetics.

X-linked agammaglobulinaemia and Pneumocystis carinii pneumonia—an unusual coincidence?

U. Wahn, V. Wahn, I. Schulze, 2003, European Journal of Pediatrics.

ORAI1-mediated calcium influx is required for human cytotoxic lymphocyte degranulation and target cell lysis

K. Schwarz, K. Mikoshiba, H. Pircher, 2011, Proceedings of the National Academy of Sciences.

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

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

Constitutive Heterochromatin of Microtus agrestis : Molecular Organization and Genetic Activity in Mitotic and Meiotic Cells

K. Sperling, I. Schulze, H. Neitzel, 2004 .

Clinical Heterogeneity of Immunodysregulation, Polyendocrinopathy, Enteropathy, X-linked: Pulmonary Involvement as a Non-Classical Disease Manifestation

K. Schwarz, S. Ehl, I. Schulze, 2014, Journal of Clinical Immunology.

Airway inflammation and dysbiosis in antibody deficiency despite the presence of IgG.

S. Burns, I. Irincheeva, D. Lowe, 2021, The Journal of allergy and clinical immunology.

Clinical Heterogeneity of Immunodysregulation, Polyendocrinopathy, Enteropathy, X-linked: Pulmonary Involvement as a Non-Classical Disease Manifestation

K. Schwarz, S. Ehl, I. Schulze, 2014, Journal of Clinical Immunology.

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

H. von Bernuth, I. Schulze, U. Baumann, 2021, Central-European journal of immunology.

Large deletions and point mutations involving the dedicator of cytokinesis 8 (DOCK8) in the autosomal-recessive form of hyper-IgE syndrome (vol 124, pg 1289, 2009)

T. Chatila, J. Puck, S. Ehl, 2010 .