標(biāo)題: Titlebook: Glomerulonephritis; Howard Trachtman,Leal C. Herlitz,Jonathan J. Hogan Reference work 2019 Springer Nature Switzerland AG 2019 Chronic Kid [打印本頁(yè)] 作者: TIBIA 時(shí)間: 2025-3-21 17:09
書目名稱Glomerulonephritis影響因子(影響力)
書目名稱Glomerulonephritis影響因子(影響力)學(xué)科排名
書目名稱Glomerulonephritis網(wǎng)絡(luò)公開度
書目名稱Glomerulonephritis網(wǎng)絡(luò)公開度學(xué)科排名
書目名稱Glomerulonephritis被引頻次
書目名稱Glomerulonephritis被引頻次學(xué)科排名
書目名稱Glomerulonephritis年度引用
書目名稱Glomerulonephritis年度引用學(xué)科排名
書目名稱Glomerulonephritis讀者反饋
書目名稱Glomerulonephritis讀者反饋學(xué)科排名
作者: 強(qiáng)制令 時(shí)間: 2025-3-21 20:52
Minimal Change Disease in Adults, adults is corticosteroids. In those patients with frequently relapsing or steroid-dependent MCD, use of alkalyting agents or calcineurin inhibitors are considered standard of care. In those patients that are unable to tolerate these therapies, use of mycophenolate mofetil or rituximab may be of uti作者: 不足的東西 時(shí)間: 2025-3-22 03:02 作者: 除草劑 時(shí)間: 2025-3-22 05:16 作者: Confidential 時(shí)間: 2025-3-22 08:53
Lupus Nephritis (Including Antiphospholipid Antibody Syndrome), Pediatric,phritis, and patient and renal survival has improved over the years. However, relapses during the transition from adolescence to adulthood are common and cardiovascular and infectious complications are frequent in long-term survivors.作者: Endometrium 時(shí)間: 2025-3-22 14:49
PLA2R- and THSD7A-Associated Primary Membranous Nephropathy,HSD7A). There is evidence of antibodies to PLA.R in up to 80% of all cases of primary MN. The identification of these antigens and their corresponding autoantibodies has allowed better precision in the diagnosis and monitoring of disease activity in primary MN. Although one-third of cases of primary作者: Endometrium 時(shí)間: 2025-3-22 17:28
ANCA-Associated Vasculitis, Adult,culitis is organ- and life-threatening in many cases, but with early and appropriate therapy, patients can remit. Therapies including corticosteroids, cyclophosphamide, rituximab, and plasmapheresis are effective in inducing a remission in the vast majority of patients. However, relapse is unfortuna作者: 說(shuō)不出 時(shí)間: 2025-3-23 00:38
Conclusion: The Trials of Lucy Snowe,hogenic mechanisms influence disease initiation or progression. We have divided the disease mechanisms into the general domains of genetics and innate and adaptive immunity and highlight how genetic background modifies the immune response to cause glomerular diseases in susceptible individuals.作者: 關(guān)節(jié)炎 時(shí)間: 2025-3-23 04:58
https://doi.org/10.1007/978-3-030-63501-5 adults is corticosteroids. In those patients with frequently relapsing or steroid-dependent MCD, use of alkalyting agents or calcineurin inhibitors are considered standard of care. In those patients that are unable to tolerate these therapies, use of mycophenolate mofetil or rituximab may be of uti作者: Breach 時(shí)間: 2025-3-23 07:06
Law for the Construction Industrymary FSGS, often presenting with nephrotic syndrome, is primarily a podocytopathy. Circulating permeability factors are thought to play a central role in podocyte foot process effacement in primary FSSG. Secondary FSGS is a result of irreversible podocyte injury from a diverse group of insults such 作者: Gentry 時(shí)間: 2025-3-23 10:32
Remedies of the Beneficiaries and Creditorsers meet the criteria but the pathologic findings are not included in the International Society of Nephrology/Renal Pathology classification of LN. In this chapter we will describe all pathologic types of LN including the atypical types..Treating patients with LN is very complex and should include a作者: MUT 時(shí)間: 2025-3-23 15:55 作者: FLIP 時(shí)間: 2025-3-23 19:29
https://doi.org/10.1007/978-90-481-9322-6HSD7A). There is evidence of antibodies to PLA.R in up to 80% of all cases of primary MN. The identification of these antigens and their corresponding autoantibodies has allowed better precision in the diagnosis and monitoring of disease activity in primary MN. Although one-third of cases of primary作者: notice 時(shí)間: 2025-3-23 22:32
https://doi.org/10.1007/978-3-319-75705-6culitis is organ- and life-threatening in many cases, but with early and appropriate therapy, patients can remit. Therapies including corticosteroids, cyclophosphamide, rituximab, and plasmapheresis are effective in inducing a remission in the vast majority of patients. However, relapse is unfortuna作者: 最低點(diǎn) 時(shí)間: 2025-3-24 06:01
owledge gap for general nephrologists, providers involved with the care of patients with glomerular diseases, and researchers.? It should also be of value to medical students, interns, residents and fellows, as978-3-319-49379-4作者: Medicaid 時(shí)間: 2025-3-24 07:19
Reference work 2019cal pediatric and internal medicine practices...Glomerulonephritis fills a considerable knowledge gap for general nephrologists, providers involved with the care of patients with glomerular diseases, and researchers.? It should also be of value to medical students, interns, residents and fellows, as作者: drusen 時(shí)間: 2025-3-24 11:25
Springer Nature Switzerland AG 2019作者: bacteria 時(shí)間: 2025-3-24 18:46
https://doi.org/10.1007/978-3-319-49379-4Chronic Kidney Disease; Glomerulonephritis; Glomerulopathy; Parenchymal Kidney Disease; Renal Pathology作者: 哺乳動(dòng)物 時(shí)間: 2025-3-24 21:10
Adequacy of Social Facilities and Services, the glomerular and alveolar basement membranes. It is extremely uncommon in children, and typically presents with acute renal failure caused by a rapidly progressive glomerulonephritis that is commonly associated with crescentic changes.作者: confide 時(shí)間: 2025-3-25 01:21
Anti-glomerular Basement Membrane Disease, the glomerular and alveolar basement membranes. It is extremely uncommon in children, and typically presents with acute renal failure caused by a rapidly progressive glomerulonephritis that is commonly associated with crescentic changes.作者: Encapsulate 時(shí)間: 2025-3-25 07:25 作者: Diverticulitis 時(shí)間: 2025-3-25 09:54 作者: STENT 時(shí)間: 2025-3-25 13:44 作者: Mobile 時(shí)間: 2025-3-25 16:30 作者: HEPA-filter 時(shí)間: 2025-3-25 23:19 作者: 空中 時(shí)間: 2025-3-26 02:37
Central Law and Peripheral Law,rogressive kidney disorder presenting with isolated microscopic hematuria. Finally, mutations in . cause hereditary angiopathy with nephropathy, aneurysms, and muscle cramps (HANAC) syndrome. This chapter will review the genetics, clinical manifestations, pathology, diagnosis, and treatment of each of these type IV collagen disorders.作者: breadth 時(shí)間: 2025-3-26 05:25
Approach to Renal Biopsy, a variety of disease states. This chapter will outline the history of the kidney biopsy, review tissue adequacy and staining, provide an overview of techniques for native and transplant kidneys along with the associated complications, and discuss future directions and possibilities with this procedure.作者: Mosaic 時(shí)間: 2025-3-26 10:10
Integration with Kidney Disease Improving Global Outcomes (KDIGO),ine development, such as formation of a global consortia for collecting data and conducting trials in glomerular disease to fill the gap to address variation in race/ethnicity, system, and healthcare providers, to include orphan glomerulonephritis, and to encourage the practice of personalized and precision medicine.作者: Aphorism 時(shí)間: 2025-3-26 14:34
Minimal Change Disease, Pediatric,ren, especially those with frequently relapsing or steroid-dependent nephrotic syndrome, may encounter major challenges related to corticosteroid and other medication-related side effects and impaired quality of life.作者: Noisome 時(shí)間: 2025-3-26 18:00
Alport Syndrome and Other Collagen Disorders,rogressive kidney disorder presenting with isolated microscopic hematuria. Finally, mutations in . cause hereditary angiopathy with nephropathy, aneurysms, and muscle cramps (HANAC) syndrome. This chapter will review the genetics, clinical manifestations, pathology, diagnosis, and treatment of each of these type IV collagen disorders.作者: abracadabra 時(shí)間: 2025-3-27 00:01
Transfer of the Family Farm by Willhrotic syndrome, and thrombotic microangiopathies are defined. An overview of how glomerulonephritis is classified based on a combination of pattern of injury, pathogenies mechanism, and etiology is provided.作者: Silent-Ischemia 時(shí)間: 2025-3-27 05:08
Law, politics, and the Security Councilsing clinical and histopathologic features defined by a uniform pathology scoring system. Although much has recently been discovered about the pathogenesis of IgAN treatment studies have given conflicting results.作者: N斯巴達(dá)人 時(shí)間: 2025-3-27 07:20
Histopathology of Glomerular Diseases,hrotic syndrome, and thrombotic microangiopathies are defined. An overview of how glomerulonephritis is classified based on a combination of pattern of injury, pathogenies mechanism, and etiology is provided.作者: 空氣傳播 時(shí)間: 2025-3-27 09:37 作者: 后退 時(shí)間: 2025-3-27 16:08
ances in research.Authored by internationally renowned glome.This Handbook serves as a convenient, state-of-the-art and comprehensive resource on the pathogenesis, diagnosis, and treatment of glomerular diseases.? Clinical approaches, modalities and challenges are provided, along with new developmen作者: dysphagia 時(shí)間: 2025-3-27 20:36 作者: Magisterial 時(shí)間: 2025-3-27 22:28
https://doi.org/10.1007/978-1-4684-7893-8 affected family members. This chapter will review the type III collagen glomerulopathies (nail-patella syndrome and collagenofibrotic glomerulopathy), fibronectin glomerulopathy, lecithin/cholesterol acyltransferase (LCAT) deficiency, .related disorders, and Pierson syndrome.作者: 細(xì)微的差異 時(shí)間: 2025-3-28 03:48 作者: 大溝 時(shí)間: 2025-3-28 09:59
Focal Segmental Glomerulosclerosis, Pediatric, Advances in our understanding of the causes of this pathological lesion, thought to be based on pathology of the glomerular visceral epithelial cell (the podocyte), may eventually lead to more specific and less toxic treatment for patients having this form of renal pathology.作者: Esophagus 時(shí)間: 2025-3-28 12:06 作者: 密碼 時(shí)間: 2025-3-28 16:22
ANCA-Associated Vasculitis, Pediatric,ronic kidney disease. Distinct clinical phenotypes of this form of vasculitis exist, and the classification and definitions of these phenotypes have evolved over the decades. As new insights into the pathophysiology of ANCA-associated vasculitis grow, new potential therapies are slowly emerging.作者: dominant 時(shí)間: 2025-3-28 19:56 作者: Melodrama 時(shí)間: 2025-3-28 23:44
Regulation of the Farming Business has emerged and is now most commonly used method to characterize the different glomerular lesions identified and classify the different glomerular diseases. In this chapter, we will review the current classification systems used in clinical practice to characterize and differentiate glomerular diseases.作者: promote 時(shí)間: 2025-3-29 06:38
Diagnostic Testing in Glomerular Disease, glomerular syndromes, nephritic and nephrotic, are discussed individually. In a patient with nephritic or nephrotic syndrome, clinical judgment based on the presentation will always be needed to determine if other diagnostic tests should be sent off in place of a kidney biopsy or along with a kidney biopsy.作者: 斜 時(shí)間: 2025-3-29 08:57 作者: 過(guò)分自信 時(shí)間: 2025-3-29 15:06 作者: 賞錢 時(shí)間: 2025-3-29 16:53
Conclusion: The Trials of Lucy Snowe, by an individual’s genome, unique environmental exposures, and, importantly, through their interaction?mediated by innate and adaptive immune responses. The astonishing complexity of each of these aspects is emerging through the lens of new technologies that provide the ability to interrogate human作者: 冰雹 時(shí)間: 2025-3-29 21:49
https://doi.org/10.1007/978-1-349-14295-8ey. While specific diseases may have a “classic” presentation, the overlap among presentations is considerable, and often the only way to diagnose a glomerular disease is by a kidney biopsy. There are many diagnostic tests that can help diagnose a glomerular disease, and more are being identified. T作者: organic-matrix 時(shí)間: 2025-3-30 02:53 作者: 真實(shí)的人 時(shí)間: 2025-3-30 05:33
Regulation of the Farming Businesso prognosis. Glomerulonephritis is a term used to broadly characterize kidney diseases that occur as a result of immunologic and inflammatory injury to the glomeruli. There are several types of glomerular diseases and these diseases can be classified based on their clinical presentation, etiology, h作者: 我不重要 時(shí)間: 2025-3-30 11:31
Juveniles: Prevention and Voluntary Action,se of a robust methodology, quality and generalizability of guidelines is limited by absence of high-quality randomized trials, lack of pathological details to guide therapy, limitations related to the use of histological pattern rather than pathophysiology-based classification system, inability to 作者: 反叛者 時(shí)間: 2025-3-30 16:15
https://doi.org/10.1007/978-3-030-63501-5h heavy proteinuria and preserved GFR with normal light microscopic architecture on pathology are hallmarks of this disease. Pathogenesis appears to be due to abnormalities in podocyte function, with newer data suggesting a two “hit” hypothesis whereby there is an initiating event that affects podoc作者: investigate 時(shí)間: 2025-3-30 20:32
,Advocacy: Speaking on Someone’s Behalf, this age group. The disease commonly presents with the classic tetrad that characterizes nephrotic syndrome (NS): generalized edema, high-grade proteinuria, hypoalbuminemia, and dyslipidemia. Increased risk of thrombosis and infection are uncommon, but potentially life-threatening associated featur作者: Organization 時(shí)間: 2025-3-30 21:23
Law for the Construction Industryfinding is the presence of segmental glomerular scars in some but not all the glomeruli. Clinically, it presents with varying degrees of proteinuria and progression to end-stage renal disease if untreated. FSGS is the leading cause of primary glomerular disease in adults who present with nephrotic s作者: 狗窩 時(shí)間: 2025-3-31 03:50 作者: Antioxidant 時(shí)間: 2025-3-31 06:50
