作者: Nerve-Block 時(shí)間: 2025-3-21 23:50 作者: intrigue 時(shí)間: 2025-3-22 02:43
Introduction: Nomenclature and Classificationation and diagnosis of antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV). Physicians and scientists have made remarkable advances in the classification and diagnosis of vasculitides since the seminal observations in the 1800s; however, validated and widely applied classification作者: Popcorn 時(shí)間: 2025-3-22 07:43
Genetics of ANCA-Associated Vasculitis in complex susceptibility loci and disease mechanisms. Finally, we discuss the limitations of current methods and the challenges that we still have to approach in order to translate genomic and epigenomic data into clinical practice.作者: 衰弱的心 時(shí)間: 2025-3-22 09:49
ANCA: Methods and Clinical Significanceoassays for PR3-ANCA and MPO-ANCA. New guidelines for ANCA testing have been developed based on a recent European multicenter study, and according to the revised 2017 international consensus recommendations, testing for ANCA in small-vessel vasculitis can be done by PR3-ANCA and MPO-ANCA immunoassay作者: Frisky 時(shí)間: 2025-3-22 15:49 作者: Interregnum 時(shí)間: 2025-3-22 20:30 作者: Nonflammable 時(shí)間: 2025-3-23 01:08
Granulomatosis with Polyangiitisccurring within 1?year of the first symptoms. With current treatments, which include first an induction phase, based on the combination of corticosteroids and an immunosuppressant, then a maintenance treatment phase, remission can be achieved in more than 80% of cases. However, the relapse-free surv作者: UTTER 時(shí)間: 2025-3-23 03:44
Microscopic Polyangiitiseart disease..Anti-neutrophil cytoplasmic antibodies, usually P-ANCA/MPO-ANCA, are detected in up to 80–90% of patients with active MPA..Untreated MPA has an unfavorable course and is associated with increased mortality and end-stage renal disease (ESRD). Factors independently related to death are t作者: 主講人 時(shí)間: 2025-3-23 05:50 作者: Heterodoxy 時(shí)間: 2025-3-23 12:45 作者: Orgasm 時(shí)間: 2025-3-23 17:57 作者: plasma-cells 時(shí)間: 2025-3-23 20:35
Peripheral Nervous System Involvementon of patients with suspected vasculitic neuropathy usually includes EMG, laboratory studies, and nerve/muscle biopsy. In patients lacking definite vasculitis in nerve biopsy, clinically probable vasculitic neuropathy can be diagnosed by recourse to supportive clinicopathologic findings. Vasculitic 作者: 有危險(xiǎn) 時(shí)間: 2025-3-24 00:05 作者: Compassionate 時(shí)間: 2025-3-24 04:39 作者: poliosis 時(shí)間: 2025-3-24 09:53
Miscellaneous Organ Involvement in ANCA-Associated Vasculitisand may range from mild to life-threatening complications, even requiring surgery. A small number of granulomatosis with polyangiitis (GPA) male patients develop prostatitis as the most common urogenital manifestation, while therapy based on cyclophosphamide may cause hemorrhagic cystitis and urothe作者: 變異 時(shí)間: 2025-3-24 11:47
Prognosis and Outcomes of ANCA-Associated Vasculitisham Vasculitis Activity Score (BVAS) and its subsequent modifications are routinely used for activity assessment, while the vasculitis damage index (VDI) has been developed to assess all-cause damage after the vasculitis diagnosis. Disease-specific quality-of-life tools are in development and approa作者: 前面 時(shí)間: 2025-3-24 17:32 作者: Ligneous 時(shí)間: 2025-3-24 19:21 作者: headway 時(shí)間: 2025-3-25 00:26 作者: 我沒有命令 時(shí)間: 2025-3-25 05:38
https://doi.org/10.1007/978-3-642-91970-1oassays for PR3-ANCA and MPO-ANCA. New guidelines for ANCA testing have been developed based on a recent European multicenter study, and according to the revised 2017 international consensus recommendations, testing for ANCA in small-vessel vasculitis can be done by PR3-ANCA and MPO-ANCA immunoassay作者: Budget 時(shí)間: 2025-3-25 07:29 作者: 無法治愈 時(shí)間: 2025-3-25 15:12 作者: CLAM 時(shí)間: 2025-3-25 16:41
Kraftanlagen mit innerer Verbrennung,ccurring within 1?year of the first symptoms. With current treatments, which include first an induction phase, based on the combination of corticosteroids and an immunosuppressant, then a maintenance treatment phase, remission can be achieved in more than 80% of cases. However, the relapse-free surv作者: 有角 時(shí)間: 2025-3-25 23:45
,K?lteanlagen und W?rmepumpenanlagen,eart disease..Anti-neutrophil cytoplasmic antibodies, usually P-ANCA/MPO-ANCA, are detected in up to 80–90% of patients with active MPA..Untreated MPA has an unfavorable course and is associated with increased mortality and end-stage renal disease (ESRD). Factors independently related to death are t作者: 和音 時(shí)間: 2025-3-26 01:17 作者: 小臼 時(shí)間: 2025-3-26 07:51 作者: 神刊 時(shí)間: 2025-3-26 08:44 作者: engrossed 時(shí)間: 2025-3-26 15:59
Einführung in die Maschinenelementeon of patients with suspected vasculitic neuropathy usually includes EMG, laboratory studies, and nerve/muscle biopsy. In patients lacking definite vasculitis in nerve biopsy, clinically probable vasculitic neuropathy can be diagnosed by recourse to supportive clinicopathologic findings. Vasculitic 作者: 責(zé)怪 時(shí)間: 2025-3-26 19:54
Einführung in die Maschinenelemente in half of the patients given the involvement of small-sized vessels, which are beyond the detection capacity of the procedure. Biopsy is rarely performed in clinical practice but can help diagnosis. A complete workup including infective and autoimmune serologies (especially ANCA dosage) as well as作者: gustation 時(shí)間: 2025-3-26 23:09 作者: 短程旅游 時(shí)間: 2025-3-27 04:58 作者: Aviary 時(shí)間: 2025-3-27 07:34 作者: 抑制 時(shí)間: 2025-3-27 09:26 作者: Arbitrary 時(shí)間: 2025-3-27 15:41
Springer Nature Switzerland AG 2020作者: 無動(dòng)于衷 時(shí)間: 2025-3-27 20:50
Einführung in die Markscheidekundeiple patterns of injury, diverse known etiologies and pathogenic mechanisms, absence of known etiologies and pathogenic mechanisms in some forms of vasculitis, and the myriad overlapping and nonspecific signs and symptoms caused by vasculitides. The goals of nomenclature, classification, and diagnos作者: Ataxia 時(shí)間: 2025-3-27 23:51 作者: Memorial 時(shí)間: 2025-3-28 04:28
Einführung in die Markscheidekundeher MPO or PR3 proteins play a key role. Molecular mimicry through bacterial antigens, the presentation of peptides complementary to PR3, and the presentation of MPO and PR3 proteins through NETs can induce the production of anti-MPO or anti-PR3 autoantibodies, especially in the context of TH17/Treg作者: 十字架 時(shí)間: 2025-3-28 08:27
https://doi.org/10.1007/978-3-642-91970-1culitis (AAV). Such autoantibodies may also be detected in a wide range of inflammatory and infectious diseases leading to a critical reappraisal in the diagnostic significance. ANCA-associated vasculitides are a heterogeneous group of rare syndromes characterized by necrotizing inflammation of smal作者: Goblet-Cells 時(shí)間: 2025-3-28 13:33
https://doi.org/10.1007/978-3-642-91970-1A major factor in defining optimal therapy and in measuring the success or failure of therapy is careful evaluation of each case. There are no simple measurements to define disease activity or response to treatment. A combination of a structured clinical assessment together with key laboratory measu作者: VERT 時(shí)間: 2025-3-28 17:17 作者: 信徒 時(shí)間: 2025-3-28 20:45 作者: 共同給與 時(shí)間: 2025-3-29 01:26 作者: 愚笨 時(shí)間: 2025-3-29 05:57 作者: expeditious 時(shí)間: 2025-3-29 07:36 作者: figurine 時(shí)間: 2025-3-29 15:19
https://doi.org/10.1007/978-3-663-05920-2ly characterized by a pauci-immune necrotizing and crescentic glomerulonephritis with a very rapid decline of renal function (rapidly progressive glomerulonephritis)..Even though there are no qualitative differences in glomerular lesions in patients with granulomatosis with polyangiitis (GPA) or mic作者: 熒光 時(shí)間: 2025-3-29 15:49
Einführung in die Maschinenelementeculitic neuropathy) but more frequently evolves in the setting of a systemic vasculitis. Polyarteritis nodosa, anti-neutrophil antibody-associated vasculitides (especially microscopic polyangiitis and eosinophilic granulomatosis with polyangiitis), rheumatoid vasculitis, and cryoglobulinemic vasculi作者: floodgate 時(shí)間: 2025-3-29 20:10 作者: ICLE 時(shí)間: 2025-3-30 01:15 作者: 激勵(lì) 時(shí)間: 2025-3-30 05:59
Wolfgang G?pel,Christiane Zieglerscellaneous organ manifestations including the involvement of cardiovascular and musculoskeletal system, gastrointestinal and urogenital tract, occur in only a minority of patients but may have a profound impact on morbidity and mortality. As an example, cardiac involvement, including subclinical fo作者: MAOIS 時(shí)間: 2025-3-30 11:56 作者: Prostatism 時(shí)間: 2025-3-30 12:38
https://doi.org/10.1007/3-540-35122-1g ANCA in >30–90% of the affected patients. Granulomatosis with polyangiitis (GPA, formerly Wegener’s granulomatosis), eosinophilic granulomatosis with polyangiitis (EGPA, formerly Churg–Strauss syndrome), and microscopic polyangiitis (MPA) are AAVs [1]. Renal-limited vasculitis, another AAV, is a b作者: 帶來 時(shí)間: 2025-3-30 19:14
Renato Alberto Sinico,Lo?c GuillevinWritten by well-known experts in the field.Presents updates with regard to rare disorders.Addresses to specialists in different diseases作者: 多余 時(shí)間: 2025-3-31 00:32
Rare Diseases of the Immune Systemhttp://image.papertrans.cn/a/image/158348.jpg作者: FAZE 時(shí)間: 2025-3-31 01:57 作者: Badger 時(shí)間: 2025-3-31 06:13
Introduction: Nomenclature and Classificationiple patterns of injury, diverse known etiologies and pathogenic mechanisms, absence of known etiologies and pathogenic mechanisms in some forms of vasculitis, and the myriad overlapping and nonspecific signs and symptoms caused by vasculitides. The goals of nomenclature, classification, and diagnos作者: 或者發(fā)神韻 時(shí)間: 2025-3-31 10:25 作者: MAOIS 時(shí)間: 2025-3-31 14:27
Etiopathogenesis of ANCA-Associated Vasculitisher MPO or PR3 proteins play a key role. Molecular mimicry through bacterial antigens, the presentation of peptides complementary to PR3, and the presentation of MPO and PR3 proteins through NETs can induce the production of anti-MPO or anti-PR3 autoantibodies, especially in the context of TH17/Treg作者: 良心 時(shí)間: 2025-3-31 19:56
ANCA: Methods and Clinical Significanceculitis (AAV). Such autoantibodies may also be detected in a wide range of inflammatory and infectious diseases leading to a critical reappraisal in the diagnostic significance. ANCA-associated vasculitides are a heterogeneous group of rare syndromes characterized by necrotizing inflammation of smal作者: ensemble 時(shí)間: 2025-4-1 00:52
Activity and DamageA major factor in defining optimal therapy and in measuring the success or failure of therapy is careful evaluation of each case. There are no simple measurements to define disease activity or response to treatment. A combination of a structured clinical assessment together with key laboratory measu作者: ENDOW 時(shí)間: 2025-4-1 05:38
