標(biāo)題: Titlebook: Glomerulonephritis; Howard Trachtman,Jonathan J. Hogan,Edgar V. Lerma Living reference work 20200th edition Chronic Kidney Disease.Glomer [打印本頁(yè)] 作者: Detrusor-Muscle 時(shí)間: 2025-3-21 16:23
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: 膽汁 時(shí)間: 2025-3-21 22:57 作者: Heart-Rate 時(shí)間: 2025-3-22 03:23
Jan M. Broekman,Larry Catà Backer 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: 分發(fā) 時(shí)間: 2025-3-22 07:39
https://doi.org/10.1007/978-1-4302-4504-9ents with rheumatic diseases..Glomerular diseases are rare, with the exception of glomerular thrombosis in patients with scleroderma (scleroderma renal crisis). In most patients with rheumatic diseases and evidence of glomerular injury, a kidney biopsy is needed to establish a diagnosis and guide therapy.作者: Ingratiate 時(shí)間: 2025-3-22 11:22
https://doi.org/10.1007/978-1-349-06885-2rogressive 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: periodontitis 時(shí)間: 2025-3-22 15:31 作者: periodontitis 時(shí)間: 2025-3-22 20:44
Montrece Ransom,Emely Sanchez,Molly Berkeryr the pathologist to suspect the diagnosis and order the stain for collagen III to confirm the diagnosis. This condition in at least a subset of the patients is a progressive disease, and no specific treatment is available at the present time.作者: GOAT 時(shí)間: 2025-3-23 00:14
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: 瑣事 時(shí)間: 2025-3-23 01:32
Approach to Renal Biopsy, a variety of disease states. This chapter will outline the history of the renal 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: epidermis 時(shí)間: 2025-3-23 05:40
Collagenofibrotic Glomerulopathy,r the pathologist to suspect the diagnosis and order the stain for collagen III to confirm the diagnosis. This condition in at least a subset of the patients is a progressive disease, and no specific treatment is available at the present time.作者: 薄荷醇 時(shí)間: 2025-3-23 18:55
Basic Theory of Multivariate Maximahanistic role in the development of FGN remains unknown. A kidney biopsy and, in particular electron microscopy or DNAJB9 staining, is required for establishing the diagnosis. There is a strong propensity to end-stage renal disease. Randomized controlled clinical trials of therapies for this disease remain to be reported.作者: 美麗的寫 時(shí)間: 2025-3-23 22:37 作者: 蝕刻術(shù) 時(shí)間: 2025-3-24 06:20
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: 珊瑚 時(shí)間: 2025-3-24 09:31
Fibrillary Glomerulonephritis,hanistic role in the development of FGN remains unknown. A kidney biopsy and, in particular electron microscopy or DNAJB9 staining, is required for establishing the diagnosis. There is a strong propensity to end-stage renal disease. Randomized controlled clinical trials of therapies for this disease remain to be reported.作者: intoxicate 時(shí)間: 2025-3-24 11:19
Mediation and Lawyers: Does the Cap Fit?,merular diseases like lupus nephritis, diabetic nephropathy, and ANCA-associated vasculitis can also recur in the transplanted kidney. Several of these primary and secondary recurrent diseases can lead to significant allograft failure and loss.作者: 使迷惑 時(shí)間: 2025-3-24 17:06
Attitudes as Knowledge Structures,s glomerulonephritis (PIGN), which shares a clinical resemblance to PSGN and differs in the causing pathogen (see Table .). The second is more scarce, with a somewhat different glomerular pathology and is secondary to active bacterial or (more common) viral infection (e.g., hepatitis C virus and HIV). This chapter reviews non-strep PIGN.作者: infantile 時(shí)間: 2025-3-24 22:26
Glomerular Disease After Kidney Transplantation,merular diseases like lupus nephritis, diabetic nephropathy, and ANCA-associated vasculitis can also recur in the transplanted kidney. Several of these primary and secondary recurrent diseases can lead to significant allograft failure and loss.作者: condescend 時(shí)間: 2025-3-25 01:14
Glomerulonephritis Secondary to Non-Streptococcal Infections,s glomerulonephritis (PIGN), which shares a clinical resemblance to PSGN and differs in the causing pathogen (see Table .). The second is more scarce, with a somewhat different glomerular pathology and is secondary to active bacterial or (more common) viral infection (e.g., hepatitis C virus and HIV). This chapter reviews non-strep PIGN.作者: Lamina 時(shí)間: 2025-3-25 06:49
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: MODE 時(shí)間: 2025-3-25 09:27 作者: 出價(jià) 時(shí)間: 2025-3-25 15:20
Glomerular Disease Associated with Rheumatic Diseases Other than SLE,ents with rheumatic diseases..Glomerular diseases are rare, with the exception of glomerular thrombosis in patients with scleroderma (scleroderma renal crisis). In most patients with rheumatic diseases and evidence of glomerular injury, a kidney biopsy is needed to establish a diagnosis and guide therapy.作者: VAN 時(shí)間: 2025-3-25 17:20 作者: 愉快么 時(shí)間: 2025-3-25 23:06
Verlag von Friedr. Vieweg & Sohn 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: antidepressant 時(shí)間: 2025-3-26 02:34
Anti-Glomerular Basemement 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: FLAT 時(shí)間: 2025-3-26 06:15 作者: Acupressure 時(shí)間: 2025-3-26 08:32
Howard Trachtman,Jonathan J. Hogan,Edgar V. LermaState-of-the-art and comprehensive resource on the pathogenesis, diagnosis, and treatment of glomerular diseases.Covers the latest clinical approaches and advances in research.Authored by internationa作者: hysterectomy 時(shí)間: 2025-3-26 15:45
https://doi.org/10.1007/978-1-349-06885-2collagen genes (.) encode six unique alpha chains of type IV collagen [α1(IV)–α6(IV)]. Mutations in several of the type IV collagen genes can cause a number of progressive and nonprogressive glomerular disorders. Mutations in ., ., and . may cause Alport syndrome (AS), an inherited kidney disease th作者: 妨礙議事 時(shí)間: 2025-3-26 19:12 作者: 施魔法 時(shí)間: 2025-3-26 22:04 作者: 丑惡 時(shí)間: 2025-3-27 02:18 作者: handle 時(shí)間: 2025-3-27 09:11 作者: Melodrama 時(shí)間: 2025-3-27 11:07 作者: 猜忌 時(shí)間: 2025-3-27 15:29 作者: EXCEL 時(shí)間: 2025-3-27 19:24
Peter Mittelstaedt,Paul A. Weingartnerlly caused by underlying lymphoproliferative diseases, and nephropathy occurs in about 30% of patients of patients with type I cryoglobulinemia. The most common histology seen on light microscopy is membranoproliferative glomerulonephritis, and immunofluorescence microscopy shows deposits of a singl作者: cruise 時(shí)間: 2025-3-27 22:17 作者: 轉(zhuǎn)向 時(shí)間: 2025-3-28 02:11
Basic Theory of Multivariate Maximaarance similar to amyloid fibrils. FGN is a morphologically defined entity that is somewhat clinically heterogeneous. Until recently, the composition of the fibrillary deposits was unknown but several recent studies have shown the deposits are composed of DnaJ Heat Shock Protein Family B Member 9 (D作者: Cerebrovascular 時(shí)間: 2025-3-28 07:08 作者: overhaul 時(shí)間: 2025-3-28 14:01 作者: 結(jié)束 時(shí)間: 2025-3-28 16:36
Jan M. Broekman,Larry Catà Backeresence often heralds a relentlessly progressive loss of kidney function over time. An effective treatment is not possible in all, or even most, cases. Advances in our understanding of the causes of this pathological lesion, thought to be based on pathology of the glomerular visceral epithelial cell 作者: 細(xì)胞膜 時(shí)間: 2025-3-28 22:23
Mediation and Lawyers: Does the Cap Fit?,pients. While minimal change disease has rarely been reported to recur in the allograft, several other primary glomerular diseases like membranous nephropathy, focal segmental glomerulosclerosis, membranoproliferative glomerulonephritis, and IgA nephropathy tend to recur more commonly. Secondary glo作者: DALLY 時(shí)間: 2025-3-29 02:35 作者: 高調(diào) 時(shí)間: 2025-3-29 03:55 作者: 平 時(shí)間: 2025-3-29 07:46
Regulatory Takings in the Wetland Context,d mortality. Chronic infection with these viruses is a major cause of hepatitis, cirrhosis, and liver failure in adults throughout the world. HBV and HCV are blood-borne virus transmitted by exposure to infected blood and body fluids. Most children acquire these infections in utero or the perinatal 作者: intertwine 時(shí)間: 2025-3-29 15:18 作者: etidronate 時(shí)間: 2025-3-29 19:08 作者: 責(zé)難 時(shí)間: 2025-3-29 21:18 作者: Embolic-Stroke 時(shí)間: 2025-3-30 01:45 作者: vertebrate 時(shí)間: 2025-3-30 07:50 作者: 蛙鳴聲 時(shí)間: 2025-3-30 11:28 作者: instulate 時(shí)間: 2025-3-30 15:15
Anti-Glomerular Basemement 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: endarterectomy 時(shí)間: 2025-3-30 17:03
Approach to Renal Biopsy, tissue was available only from deceased autopsy specimens. Advances in technology, technique, and imaging have led to both an improvement in tissue yield in addition to lower morbidity from complications. The kidney biopsy is currently the diagnostic gold standard for nearly all kidney diseases. Al作者: ingrate 時(shí)間: 2025-3-30 23:44
C3 Glomerulopathy,of which is C3 dominance on immunofluorescence by at least two orders of magnitude greater than any other immuno-reactant; electron microscopy is also specific. These features should prompt a thorough evaluation of the complement system that covers four domains: 1) genetic drivers of disease; 2) acq作者: intelligible 時(shí)間: 2025-3-31 04:17 作者: 音樂會(huì) 時(shí)間: 2025-3-31 05:26 作者: Inflammation 時(shí)間: 2025-3-31 12:12
Diagnostic Testing in Glomerular Disease,ey. 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: 亞當(dāng)心理陰影 時(shí)間: 2025-3-31 17:22
Fibrillary Glomerulonephritis,arance similar to amyloid fibrils. FGN is a morphologically defined entity that is somewhat clinically heterogeneous. Until recently, the composition of the fibrillary deposits was unknown but several recent studies have shown the deposits are composed of DnaJ Heat Shock Protein Family B Member 9 (D作者: peptic-ulcer 時(shí)間: 2025-3-31 21:13
Fibronectin Glomerulopathy,amily history have been documented. Diagnosis requires a renal biopsy which typically shows a mesangiopathy with increased matrix rich in fibronectin which may impart to the glomeruli a lobular appearance. While the ultrastructural findings can suggest and in some cases can be used to make a presump作者: 延期 時(shí)間: 2025-3-31 22:13 作者: maverick 時(shí)間: 2025-4-1 03:26 作者: famine 時(shí)間: 2025-4-1 09:00 作者: Arthropathy 時(shí)間: 2025-4-1 10:18 作者: arthroplasty 時(shí)間: 2025-4-1 17:14 作者: 常到 時(shí)間: 2025-4-1 18:57
Glomerular Diseases Associated with Hepatitis B and C Infection, Pediatric,d mortality. Chronic infection with these viruses is a major cause of hepatitis, cirrhosis, and liver failure in adults throughout the world. HBV and HCV are blood-borne virus transmitted by exposure to infected blood and body fluids. Most children acquire these infections in utero or the perinatal 作者: Glower 時(shí)間: 2025-4-2 01:42
Glomerular Diseases Associated with Malignancies,rom diverse pathophysiologic links. At variance with solid tumor-associated glomerulopathies for which the pathophysiology remains poorly understood, a molecular link can usually be demonstrated in hematologic malignancy-induced glomerulopathies. This chapter provides an update on epidemiology, path作者: 思想 時(shí)間: 2025-4-2 05:45
Glomerular Diseases in Pregnancy,cern for generations of nephrologists has been and continues to be the impact that these rare renal diseases have on pregnancy outcomes. Little literature is available to guide counseling and treatment during pregnancy, and experience is often based on case reports and single-center studies. Disease作者: MUMP 時(shí)間: 2025-4-2 08:04
Glomerulonephritis Secondary to Non-Streptococcal Infections,-streptococcal glomerulonephritis (PSGN) and the less common infectious glomerulonephritis..IRGN is considered to be a cluster of glomerular diseases resulted from immunologic insult secondary to systemic nonrenal infection. Two smaller groups of IRGN have been identified. The first is postinfectiou
