B. Gathmann

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The European internet‐based patient and research database for primary immunodeficiencies: results 2004–06

B. Grimbacher, A. Eades-Perner, B. Gathmann, 2007, Clinical and experimental immunology.

The European internet‐based patient and research database for primary immunodeficiencies: results 2006–2008

A. Fischer, N. Mahlaoui, B. Grimbacher, 2009, Clinical and experimental immunology.

The burden of common variable immunodeficiency disorders: a retrospective analysis of the European Society for Immunodeficiency (ESID) registry data

S. Ehl, K. Bogaerts, N. Mahlaoui, 2018, Orphanet Journal of Rare Diseases.

Mannose‐binding lectin gene polymorphic variants predispose to the development of bronchopulmonary complications but have no influence on other clinical and laboratory symptoms or signs of common variable immunodeficiency

J. Litzman, T. Pavlík, B. Grimbacher, 2008, Clinical and experimental immunology.

Chapter 61 – Registries

B. Grimbacher, B. Gathmann, 2014 .

The European internet‐based patient and research database for primary immunodeficiencies: update 2011

S. Ehl, N. Binder, B. Gathmann, 2012, Clinical and experimental immunology.

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.

Immunodeficiencies

L. Notarangelo, J. Franco, C. Cunningham-Rundles, 2009, Clinical and experimental immunology.

Nijmegen Breakage Syndrome: Clinical and Immunological Features, Long-Term Outcome and Treatment Options – a Retrospective Analysis

A. Gennery, K. Chrzanowska, M. Syczewska, 2015, Journal of Clinical Immunology.

Modeling Primary Immunodeficiency Disease Epidemiology and Its Treatment to Estimate Latent Therapeutic Demand for Immunoglobulin

Jeffrey S. Stonebraker, J. Orange, J. Stonebraker, 2014, Journal of Clinical Immunology.

X-linked thrombocytopenia (XLT) due to WAS mutations: clinical characteristics, long-term outcome, and treatment options.

A. Fischer, T. Morio, H. Ochs, 2010, Blood.

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.

The European Society for Immunodeficiencies (ESID) Registry Working Definitions for the Clinical Diagnosis of Inborn Errors of Immunity.

S. Ehl, N. Mahlaoui, J. V. van Montfrans, 2019, The journal of allergy and clinical immunology. In practice.

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.

Sequential decisions on FAS sequencing guided by biomarkers in patients with lymphoproliferation and autoimmune cytopenia

K. Schwarz, W. Vach, E. Mejstrikova, 2013, Haematologica.

The use of databases in primary immunodeficiencies

B. Grimbacher, B. Gathmann, G. Kindle, 2014, Current opinion in allergy and clinical immunology.

The PedPAD study: boys predominate in the hypogammaglobulinaemia registry of the ESID online database

B. Gathmann, E. Vries, E. Schatorjé, 2014, Clinical and experimental immunology.

The German national registry for primary immunodeficiencies (PID)

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

characteristics, long-term outcome, and treatment options mutations: clinical WAS X-linked thrombocytopenia (XLT) due to

A. Fischer, T. Morio, H. Ochs, 2011 .

Therapeutic Management of Primary Immunodeficiency in Older Patients

N. Verma, B. Grimbacher, B. Gathmann, 2013, Drugs & Aging.

Clinical Phenotype and Long Term Outcome in a Large Cohort of X-Linked Thrombocytopenia (XLT)/Mild Wiskott-Aldrich-Syndrome Patients

A. Fischer, T. Morio, H. Ochs, 2008 .

Comparison of American and European practices in the management of patients with primary immunodeficiencies

J. Orange, L. Notarangelo, B. Grimbacher, 2012, Clinical and experimental immunology.

The ESID Online Database network

D. Guzman, D. Veit, V. Knerr, 2007, Bioinform..

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

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

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

P. Kralickova, J. Litzman, N. Kutukculer, 2015, Journal of Clinical Immunology.

[The ESID Online Database for primary immunodeficiencies. First analyses with regard to Germany and Europe].

B. Grimbacher, A. Eades-Perner, B. Gathmann, 2008, Medizinische Klinik.

Imaging of Bronchial Pathology in Antibody Deficiency: Data from the European Chest CT Group

V. Lougaris, A. Plebani, G. Driessen, 2018, Journal of Clinical Immunology.

The burden of common variable immunodeficiency disorders Plasma Protein Therapeutics Association (PPTA) Taskforce; Odnoletkova,

S. Ehl, K. Bogaerts, N. Mahlaoui, 2018 .

The burden of common variable immunodeficiency disorders Plasma Protein Therapeutics Association (PPTA) Taskforce