Results 21 to 30 of about 1,820,267 (314)
Selective measurement of anti-tTG antibodies in coeliac disease and IgA deficiency : an alternative pathway [PDF]
Objective To determine the ability of selective antibody testing to screen for coeliac disease in the presence of IgA deficiency and to define the sensitivity of a pathway using this method (Figure1).
Arasaradnam, Ramesh P. +5 more
core +1 more source
Deficiencies of immersions [PDF]
zbMATH Open Web Interface contents unavailable due to conflicting licenses.
openaire +3 more sources
Granulomatous inflammation in inborn errors of immunity
Granulomas have been defined as inflammatory infiltrates formed by recruitment of macrophages and T cells. The three-dimensional spherical structure typically consists of a central core of tissue resident macrophages which may merge into multinucleated ...
Keith A. Sacco +3 more
doaj +1 more source
IntroductionThe Sars-CoV-2 pandemic caused great concern for this novel virus among patients with primary immunodeficiency (PID) or inborn errors of immunity (IEI) and their families.
Martine Pergent +7 more
doaj +1 more source
GATA2 deficiency is a germline disease that causes a wide spectrum of phenotypes including viral and bacterial infections, cytopenias, myelodysplasia, myeloid leukemias, pulmonary alveolar proteinosis and lymphedema. The age of clinical presentation ranges from early childhood to late adulthood, with most occurring in adolescence to early adulthood. We
Amy P, Hsu +2 more
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"Test me and treat me" - attitudes to vitamin D deficiency and supplementation: a qualitative study [PDF]
© 2015 BMJ Open, "Test me and treat me"-attitudes to vitamin D deficiency and supplementation: a qualitative study.
Jakeways, Niki; id_orcid +17 more
core +1 more source
Clinical and molecular characterization of patients with adenylosuccinate lyase deficiency
Background Adenylosuccinate lyase deficiency (ADSLD) is an ultrarare neurometabolic recessive disorder caused by loss-of-function mutations in the ADSL gene. The disease is characterized by wide clinical variability.
Gerarda Mastrogiorgio +11 more
doaj +1 more source
High risk of severe anaemia after chlorproguanil-dapsone+artesunate antimalarial treatment in patients with G6PD (A-) deficiency. [PDF]
BACKGROUND: Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common inherited human enzyme defect. This deficiency provides some protection from clinical malaria, but it can also cause haemolysis after administration of drugs with oxidant ...
Modiano David +36 more
core +2 more sources
Objectives: Possible immunomodulatory effect of amantadine in patients treated in intensive care unit (ICU), mostly among patients with brain injuries or vascular diseases was observed in several studies.
Daniel Chober +9 more
doaj +1 more source
This study was carried out on 40 camels in Assuite governorate, 10 of them apparently healthy, 20, suffering from moderate respiratory signs and 10 cases suffering from severe respiratory signs.
EMAN M.A. EL-NASER, G.F.A. KHAMIS
doaj +1 more source

