Inherited IgA glycosylation pattern in IgA nephropathy and HSP nephritis: where do we go next? Kidney International, 2011, 80: 8-10.Boyd Joanna K,Barratt Jonathan.Inherited IgA glycosylation pattern in IgA nephropathy and HSP nephritis: where do we go next?. Kidney International . 2011...
Although IgA nephropathy is a limited nonsystemic kidney disease, many systemic illnesses are sporadically associated with mesangial IgA deposition. Henoch-Schönlein purpura (HSP), a systemic illness, has been closely linked to IgA nephropathy. Other systemic diseases in which mesangial deposits of...
Randomised, double‑blind, placebo‑controlled trial to determine whether steroids reduce the incidence and severity of nephropathy in Henoch‑Schonlein purpura (HSP) [J]. Arch Dis Child, 2013, 98(10): 756‑763. DOI: 10.1136/archdischild‑2013‑303642. [54] 张莹, 夏正坤, 高远赋,...
这些模型描述在Emancipator,S.N.et al.,(1987)Animal models of IgA Nephropathy In IgANephropathy.A.R.Clarkson,editor.Martinus Nijhoff publishing,Boston.188-203中,其整体内容通过引用并入本文。一个示例性的模型描述在Gesualdo L.et al,(1990)J.Clin.Invest.86715-722中,其整体内容也通过引用并入本文。简言...
IgA nephropathy and IgA vasculitis with nephritis have a shared feature involving galactose-deficient IgA1-oriented pathogenesis. Kidney Int. 2018;93(3):700–5. https://doi.org/10.1016/j.kint.2017.10.019. Article CAS PubMed Google Scholar Al Harash A, Saeli S, Lucke M, Arora S. IgA ...
然而大部分膜性肾病的病因并不明确,属于特发性膜性肾病 (idopathic membranuous nephropathy, IMN).特发性膜性肾病在我国约占原发性肾小球疾病的 10%, 其进展缓慢,临床表现轻重不一,经过各异,预后差别也较大,40-60%的患者 5 到 20 年或更长时间 后可能进入终末期肾脏病.该病迄今没有满意的治疗方法.目前...
The term “IgAN phenotype” as used herein refers to an observable characteristic or trait, or the absence thereof, relating to IgA Nephropathy (IgAN). In some cases, an IgAN phenotype may be used to determine that a subject has IgAN. For example, an IgAN phenotype may include increased lev...
IgA Nephropathy is the most common form of glomerulonephritis worldwide and is often idiopathic but its association with Ulcerative colitis is reported in various case reports. Henoch-Schonlein purpura (HSP) is a systemic disorder with renal, gastrointestinal, articular and cutaneous manifestations in ...
Henoch–Schnlein purpura (HSP) is a small vessel systemic vasculitis characterized by small blood vessel deposition of IgA that predominantly affects the skin, joints, gut, and kidney, with nephritis that may be histologically indistinguishable from IgA nephropathy. Management—there is no treatment ...
T-cell epitopes recognized within the 65, 000 MW hsp in patients with IgA nephropathy. Immunology. 1997; 91:399±405.Warr K, Fortune F, Namie S, et al: T-cell epitopes recognized within the 65,000 MW hsp in patients with IgA nephropathy. Immu- nology 91:399-405, 1997...