The European internet‐based patient and research database for primary immunodeficiencies: results 2006–2008
B Gathmann, B Grimbacher, J Beauté… - Clinical & …, 2009 - Wiley Online Library
Primary immunodeficiencies (PID) are rare diseases; therefore transnational studies are
essential to maximize the scientific outcome and to improve diagnosis and therapy. In order …
essential to maximize the scientific outcome and to improve diagnosis and therapy. In order …
[HTML][HTML] The German national registry of primary immunodeficiencies (2012–2017)
Introduction: The German PID-NET registry was founded in 2009, serving as the first national
registry of patients with primary immunodeficiencies (PID) in Germany. It is part of the …
registry of patients with primary immunodeficiencies (PID) in Germany. It is part of the …
Primary immunodeficiency in Iran: first report of the National Registry of PID in Children and Adults
A Aghamohammadi, M Moein, A Farhoudi… - Journal of clinical …, 2002 - Springer
Epidemiological studies have shown wide geographical and racial variation in the
prevalence and patterns of immunodeficiency disorders. To determine the frequency of …
prevalence and patterns of immunodeficiency disorders. To determine the frequency of …
Primary immunodeficiencies in India: a perspective
S Gupta, M Madkaikar, S Singh… - Annals of the New York …, 2012 - Wiley Online Library
Although primary immunodeficiency diseases (PIDs) were first reported in India in the
1970s, those diagnoses were based predominantly on clinical presentations—very limited …
1970s, those diagnoses were based predominantly on clinical presentations—very limited …
First report on the Moroccan registry of primary immunodeficiencies: 15 years of experience (1998–2012)
AA Bousfiha, L Jeddane, N El Hafidi… - Journal of Clinical …, 2014 - Springer
Abstract Purpose Primary immunodeficiencies (PIDs) are a large group of diseases
characterized by susceptibility to infections. We provide the first comprehensive report on …
characterized by susceptibility to infections. We provide the first comprehensive report on …
Diagnostic approach to primary immunodeficiency disorders
Primary immunodeficiency disorders (PIDs) are a heterogeneous group of inherited
disorders that affect different components of the immune system. There are more than 150 …
disorders that affect different components of the immune system. There are more than 150 …
Report of the Tunisian registry of primary immunodeficiencies: 25-years of experience (1988–2012)
F Mellouli, IB Mustapha, MB Khaled, H Besbes… - Journal of clinical …, 2015 - Springer
Abstract Purpose Primary immunodeficiencies (PIDs) are a large group of diseases
characterized by susceptibility to not only recurrent infections but also autoimmune diseases …
characterized by susceptibility to not only recurrent infections but also autoimmune diseases …
Primary immunodeficiency in Africa–a review
A Erjaee, M Bagherpour, C Van Rooyen… - South African Medical …, 2019 - journals.co.za
Background. Efforts have been made worldwide to improve awareness and treatment of
primary immunodeficiency (PID). This has also gained momentum on the African continent …
primary immunodeficiency (PID). This has also gained momentum on the African continent …
The Swiss National Registry for Primary Immunodeficiencies: report on the first 6 years' activity from 2008 to 2014
K Marschall, M Hoernes… - Clinical & …, 2015 - academic.oup.com
Summary The Swiss National Registry for Primary Immunodeficiency Disorders (PID) was
established in 2008, constituting a nationwide network of paediatric and adult departments …
established in 2008, constituting a nationwide network of paediatric and adult departments …
[HTML][HTML] Primary immune deficiencies–principles of care
H Chapel, J Prevot, HB Gaspar, T Español… - Frontiers in …, 2014 - frontiersin.org
Primary immune deficiencies (PIDs) are a growing group of over 230 different disorders
caused by ineffective, absent or an increasing number of gain of function mutations in …
caused by ineffective, absent or an increasing number of gain of function mutations in …