نتایج جستجو برای: antibody deficiency syndrome

تعداد نتایج: 889912  

Journal: :journal of research in health sciences 0
laleh ghanei amir ziaee parsa rostami sonia oveisi neda esmailzadehha amir mohammad kazemifar

background: association between the vitamin d deficiency and metabolic syndrome (mets) has previously been noted and reported to be controversial. the aim of this study was to determine the association of serum 25 (oh) d level and vitamin d dietary intake with mets among iranian population . methods: this analytical study was conducted on 122 patients with mets based on the atpiii criteria and ...

2003
Scott H. Sicherer Allen Adinoff Joseph A. Church

Gennery A, Barge D, O’Sullivan J, et al. Arch Dis Child. 2002;86:422–425 Purpose of the Study. The aim of this study was to investigate humoral immunity, particularly antibody response to pneumococcal polysaccharide, and autoimmune anomalies in a cohort of patients with 22q11 deletion. Study Population. Thirty-two patients from the Newcastle, United Kingdom (UK) Pediatric Immunology Clinic were...

Golafshan, Habibollah, Kohan Mozaffari, Sara, Nasiri, Nahid,

Antiphospholipid syndrome (APS) is a systemic autoimmune disease with the appearance of anti-phospholipid antibody (ACLA), Anti β2GPI and lupus anticoagulant (LAC) in serum. The antigen-antibody reaction on cell surface leads to thrombosis, miscarriage and inflammation. Clinical findings are diverse and include thrombosis in veins and arteries, pregnancy loss, thrombocytopenia, neurological and...

Adel M Wahadneh Mohammad A. Almutereen Mohammad E Abu-Shukair Raed M. Alzyoud Zeyad M.Habahbeh

Background: Primary antibody deficiency, the most common primary immunodeficiency disorder, represents a heterogeneous spectrum of conditions caused by a defect in any critical stage of B cell development and is characterized by impaired production of normal amounts of antigen-specific antibodies. Objective: This retrospective study aimed at description and analysis of demographic, clinical, im...

2015
Mihaela Spârchez Iulia Lupan Dan Delean Aurel Bizo Laura Damian Laura Muntean Maria Magdalena Tămaș Claudia Bolba Bianca Simionescu Cristina Slăvescu Ioana Felea Călin Lazăr Zeno Spârchez Simona Rednic

BACKGROUND Our aim was to investigate the prevalence and clinical relevance of inherited complement and antibody deficiency states in a large series of patients with various autoimmune rheumatologic diseases (ARD) with juvenile onset. METHODS A total number of 117 consecutive patients from 2 tertiary referral hospitals were included in the study. All patients underwent genetic screening for t...

2012
Jung Woo Rhim Kyung Hyo Kim Dong Soo Kim Bong Seong Kim Jung Soo Kim Chang Hwi Kim Hwang Min Kim Hee Ju Park Ki Soo Pai Byong Kwan Son Kyung Sue Shin Moo Young Oh Young Jong Woo Young Yoo Kun Soo Lee Kyung Yil Lee Chong Guk Lee Joon Sung Lee Eun Hee Chung Eun Hwa Choi Youn Soo Hahn Hyun Young Park Joong Gon Kim

This study represents the first epidemiological study based on the national registry of primary immunodeficiencies (PID) in Korea. Patient data were collected from 23 major hospitals. A total of 152 patients with PID (under 19 yr of age), who were observed from 2001 to 2005, have been entered in this registry. The period prevalence of PID in Korea in 2005 is 11.25 per million children. The foll...

Ashraf Moini, Ladan Hosseini Marzieh Ahmadzadeh Nooshin Shirzad Reihaneh Hosseini, Shahideh Jahanian Sadatmahalleh

Background Given the relationship of vitamin D deficiency with insulin resistance syndrome as the component of polycystic ovary syndrome (PCOS), the main aim of this study was to compare serum level of 25- hydroxyvitamin D [25(OH)D] between PCOS patients and normal individuals. MaterialsAndMethods A cross sectional study was conducted to compare 25(OH)D level between117 normal and 125 untreated...

Journal: :European Respiratory Journal 2005

Journal: :acta medica iranica 0
zohreh kavehmanesh department of pediatrics, faculty of medicine, baqiyatallah university of medical sciences, tehran, iran. zahra khalili matinzadeh department of pediatrics, faculty of medicine, baqiyatallah university of medical sciences, tehran, iran. susan amirsalari department of pediatrics, faculty of medicine, baqiyatallah university of medical sciences, tehran, iran. mohammad torkaman department of pediatrics, faculty of medicine, baqiyatallah university of medical sciences, tehran, iran. shahla afsharpayman department of pediatrics, faculty of medicine, baqiyatallah university of medical sciences, tehran, iran. morteza javadipour department of pediatrics, faculty of medicine, baqiyatallah university of medical sciences, tehran, iran.

leukocyte adhesion deficiency type 1 (lad 1) is an autosomal recessive hereditary disorder resulting from deficiency of cd18, characterized by recurrent bacterial infections. we report two consanguineous patients with leukocyte adhesion deficiency type 1( lad1). these two infant boy patients were referred to us, within a short period of time, with the complaints of recurrent infections at the a...

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