Titlebook: Glomerulonephritis; Howard Trachtman,Jonathan J. Hogan,Edgar V. Lerma Living reference work 20200th edition Chronic Kidney Disease.Glomer

Detrusor-Muscle

書(shū)目名稱(chēng)Glomerulonephritis影響因子(影響力)




書(shū)目名稱(chēng)Glomerulonephritis影響因子(影響力)學(xué)科排名




書(shū)目名稱(chēng)Glomerulonephritis網(wǎng)絡(luò)公開(kāi)度




書(shū)目名稱(chēng)Glomerulonephritis網(wǎng)絡(luò)公開(kāi)度學(xué)科排名




書(shū)目名稱(chēng)Glomerulonephritis被引頻次




書(shū)目名稱(chēng)Glomerulonephritis被引頻次學(xué)科排名




書(shū)目名稱(chēng)Glomerulonephritis年度引用




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書(shū)目名稱(chēng)Glomerulonephritis讀者反饋




書(shū)目名稱(chēng)Glomerulonephritis讀者反饋學(xué)科排名

膽汁

Heart-Rate

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.

分發(fā)

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.

Ingratiate

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.

periodontitis

periodontitis

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.

GOAT

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.

瑣事

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.

epidermis

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.