نتایج جستجو برای: antibody deficiency syndrome

تعداد نتایج: 889912  

Jamshid Ruzbeh Malihe Kamali Mohammad Hassan Rastegar Vahide Yarmohammadi Zahra Habibagahi,

Angioedema secondary to C1 inhibitor deficiency has been rarely reported to be associated with systemic lupus erythematosus. A genetic defect of C1 inhibitor produces hereditary angioedema, which is usually presented with cutaneous painless edema, but edema of the genital area, gastrointestinal and laryngeal tracts have also been reported.In lupus patients, angioedema may be the result of an ac...

Journal: :middle east journal of digestive diseases 0
mohammad javad zahedi sodaif darvish moghadam seyed mahdi seyed mirzaei masood dehghani sara shafiei pour atefe rasti

blue rubber bleb nevus syndrome is a rare disorder that is characterized by multiple recurrent vascular malformations of skin and gastrointestinal tract . the affected patients may present with diverse manifestations including iron deficiency anemia. we report this syndrome in a 22-year-old man that was referred to our hospital for iron deficiency anemia with unknown cause and vascular malforma...

Journal: :Journal of clinical microbiology 1989
M Advani D T Imagawa M H Lee K Sano F Morales R T Mitsuyasu R Detels

A cross-sectional study of 128 individuals infected with human immunodeficiency virus type 1 (HIV-1) was conducted to determine the correlation of reverse transcriptase-inhibiting (RTI) antibody to clinical disease. Thirty-two individuals were studied in each of four clinical groups: asymptomatic individuals, those with persistent generalized lymphadenopathy, those with acquired immune deficien...

Journal: :Science Translational Medicine 2021

Clinical and basic studies shed light on the mechanism, diagnosis, treatment of cardiac ryanodine receptor Ca 2+ release deficiency syndrome.

2014
Catarina M. Quinzii Valentina Emmanuele Michio Hirano

Coenzyme Q 10 (CoQ 10 ) deficiency is a clinically and genetically heterogeneous syndrome which has been associated with 5 major clinical phenotypes: (1) encephalomyopathy, (2) severe infantile multisystemic disease, (3) nephropathy, (4) cerebellar ataxia, and (5) isolated myopathy. Of these phenotypes, cerebellar ataxia and syndromic or isolated nephrotic syndrome are the most common. CoQ 10 d...

2017
Deborah L Burnett Ian A Parish Etienne Masle-Farquhar Robert Brink Christopher C Goodnow

Inherited mutations in lipopolysaccharide-responsive beige-like anchor (LRBA) cause a recessive human immune dysregulation syndrome with memory B-cell and antibody deficiency (common variable immunodeficiency), inflammatory bowel disease, enlarged spleen and lymph nodes, accumulation of activated T cells and multiple autoimmune diseases. To understand the pathogenesis of the syndrome, C57BL/6 m...

2013
Yubo Li Yuxiu Sun Xueling Ma Xiaoxing Xue Xinlou Chai Weiming Wang Huihui Zhao Kun Chen Shuzhen Guo Jianxin Chen Wei Wang Huan Dong Lu

The objective of the present study was to make comparison between rat models of depression achieved by chronic unpredictable mild stress (CUMS) and reserpine injection from the angle of traditional Chinese medicine syndrome, depict the regularity of syndrome variation of the two models, and preliminarily explain its molecular mechanism. Rat depression models were achieved respectively by CUMS a...

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