نتایج جستجو برای: ige syndrome

تعداد نتایج: 635857  

Journal: :European annals of allergy and clinical immunology 2017
S Miceli Sopo S Monaco G Cerchiara G Bersani

Food protein induced enterocolitis syndrome (FPIES) is a food-related gastrointestinal hypersensitivity disorder, probably non-IgE-mediated. Over the years, various diagnostic criteria have been proposed to identify FPIES. In the last few years, there was an increased interest from researchers about FPIES's syndrome, that frequently brought to discover new aspects of this disease. We describe a...

Journal: :Acta dermato-venereologica 2004
Erzsébet Szakos Gabriella Lakos Magdolna Aleksza János Hunyadi Mária Farkas Enikö Sólyom Sándor Sipka

In this study we investigated skin bacterial colonization, allergen-specific IgE and antiphospholipid/antinuclear antibodies in 72 children with atopic eczema/dermatitis syndrome (age 2-17 years). Bacteria were found on the skin in 41 cases and serological allergen-specific IgE positivity in 37. The different forms of antibodies appeared in the ratio 21/72 (33 antibodies in 21 children). The oc...

2004
ERZSÉBET SZAKOS GABRIELLA LAKOS MAGDOLNA ALEKSZA JÁNOS HUNYADI MÁRIA FARKAS ENIKÖ SÓLYOM

In this study we investigated skin bacterial colonization, allergen-specific IgE and antiphospholipid/antinuclear antibodies in 72 children with atopic eczema/dermatitis syndrome (age 2 – 17 years). Bacteria were found on the skin in 41 cases and serological allergen-specific IgE positivity in 37. The different forms of antibodies appeared in the ratio 21/72 (33 antibodies in 21 children). The ...

Journal: :Ceylon Medical Journal 2009

Journal: :International Journal of Molecular Sciences 2020

Journal: :The Netherlands journal of medicine 2002
M G Netea P M Schneeberger E de Vries B J Kullberg J W M van der Meer M I Koolen

BACKGROUND Hyperimmunoglobulin E (hyper-IgE) syndrome is a rare immunodeficiency characterised by recurrent skin and respiratory tract infections, skeletal and dental abnormalities, chronic eczema, and elevated serum IgE. We describe a family with four hyper-IgE syndrome patients (38, 37, 30 and 7 years old), in which we investigated the cytokine response to both specific and non-specific stimu...

Journal: :Clinical and experimental immunology 1984
J H Passwell B Geiger M Levanon J Davidsohn B E Cohen B Ramot

IgE was isolated from a patient with the hyper IgE, recurrent infection syndrome by immunoadsorption on sepharose bound goat anti-human IgE. Addition of this IgE to a monolayer culture of human monocytes resulted in a dose-dependent increase in PGE2 secretion. The addition of F(ab')2 fraction of goat anti-human IgE in the presence of sub-stimulating doses of IgE markedly increased PGE2 secretio...

2012

Hyper-IgE syndrome (HIES) is a complex primary immunodeficiency disorder characterized by a spectrum of abnormalities related to the immune system, bones, connective tissue and teeth. The cause of HIES is not known. The disease is also known as Job Syndrome because skin boils, a hallmark of the syndrome, are reminiscent of the biblical character Job, who was smitten by Satan “with sore boils fr...

Journal: :Indian pediatrics 1997
H Paramesh D A Satish S A Khatib M Jain

syndrome: Recurrent "Cold" staphylococ-cal abscesses. Pseudolymphoma syndrome, as a hypersensitive reaction to anticonvulsant drugs especially phenytoin, carbamaze-pine, tridone and phenobarbitone is well known(l-4). Its pathogenesis is uncertain. It consists of a triad of fever, generalized rash and lymphadenopathy. Varying degrees of VOLUME 34-SEFTEMBER 1997 7. Hill HR, Quie PG. Raised IgE le...

2013
H. BUCKLEY SUSANA. Fiscus

seen in hypogammaglobulinemic patients. Group mean IgD concentrations were also depressed in patients with Wiskott-Aldrich syndrome and in those with selective IgA deficiency; IgE concentrations were depressed in patients with X-linked immunodeficiency with hyperIgM and in those with ataxia telangiectasia. IgD and IgE were both significantly elevated in patients with extreme hyperimmunoglobulin...

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