The epidemiology and clinical manifestations of autoimmunity in selective IgA deficiency
DD Odineal, ME Gershwin - Clinical reviews in allergy & immunology, 2020 - Springer
Selective immunoglobulin A deficiency (SIgAD) is the most common primary
immunodeficiency, defined as an isolated deficiency of IgA (less than 0.07 g/L). Although the …
immunodeficiency, defined as an isolated deficiency of IgA (less than 0.07 g/L). Although the …
Diagnostic approach to the patients with suspected primary immunodeficiency
Background and Objective: Primary immunodeficiency diseases (PIDs) are a group of more
than 350 disorders affecting distinct components of the innate and adaptive immune …
than 350 disorders affecting distinct components of the innate and adaptive immune …
Humoral and Complement Systems in Children With Acute Immune Thrombocytopenic Purpura
H Karami, J Ghaffari, S Moradi, L Vahedi… - Journal of Pediatrics …, 2020 - jpr.mazums.ac.ir
Background: Immune thrombocytopenia (ITP) is an autoimmune disorder associated with
decreased platelet production and accelerated platelet destruction. An impaired immune …
decreased platelet production and accelerated platelet destruction. An impaired immune …
Первичный селективный иммунодефицит IgA, выявленный у ребенка 2 лет 10 месяцев
ТН Бучкова, НИ Зрячкин, ГИ Чеботарева… - Вестник Дагестанской …, 2020 - elibrary.ru
Актуальность темы обусловлена недостаточной осведомлённостью клиницистов в
вопросах патогенеза и симптоматики первичных иммунодефицитов, что затрудняет …
вопросах патогенеза и симптоматики первичных иммунодефицитов, что затрудняет …
[PDF][PDF] Избирательный дефицит иммуноглобулина А в практике врача-педиатра
АП Продеус, ИА Корсунский, ЛА Федорова - Практика педиатра, 2020 - medi.ru
Избирательный дефицит иммуноглобулина А является самым частым первичным
иммунодефицитом. Он ассоциируется с рядом значимых с клинической точки зрения …
иммунодефицитом. Он ассоциируется с рядом значимых с клинической точки зрения …
[HTML][HTML] Hematologic problems in Hyper-IgM patients
M Sohani, S Pashangzadeh - Immunology and Genetics Journal, 2020 - igj.tums.ac.ir
Background/objectives: Hyper IgM (HIGM) syndrome is a rare kind of primary
Immunodeficiency disease (PID) characterized by normal to the increased serum IgM and …
Immunodeficiency disease (PID) characterized by normal to the increased serum IgM and …
[PDF][PDF] The physical health and quality of life of patients with X-linked agammaglobulinaemia in England and Wales Volume 1 of
BMJ Shillitoe - 2020 - core.ac.uk
Background Patients with X-linked agammaglobulinaemia (XLA) have absent peripheral
circulating B-lymphocytes and agammaglobulinaemia caused by defects in BTK. Treatment …
circulating B-lymphocytes and agammaglobulinaemia caused by defects in BTK. Treatment …
The physical health and quality of life of patients with X-linked agammaglobulinaemia in England and Wales
BMJ Shillitoe - 2020 - theses.ncl.ac.uk
Background Patients with X-linked agammaglobulinaemia (XLA) have absent peripheral
circulating Blymphocytes and agammaglobulinaemia caused by defects in BTK. Treatment …
circulating Blymphocytes and agammaglobulinaemia caused by defects in BTK. Treatment …