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10.1681/ASN.2015040399 http://scihub22266oqcxt.onion/10.1681/ASN.2015040399 C4849830!4849830!26546258     free     free     free Deprecated: Implicit conversion from float 217.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 217.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 217.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 217.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       J+Am+Soc+Nephrol 2016 ; 27 (5): 1300-4 Nephropedia Template TP {{tp|p=26546258|t=2016. Medullary Microvascular Thrombosis and Injury in Sickle Hemoglobin C Disease |pdf=|usr=}}{{26546258}} gab.com Text Medullary Microvascular Thrombosis and Injury in Sickle Hemoglobin C Disease JO: J Am Soc Nephrol http://www.kidney.de/pget.php?&tw=1&pmid=26546258 #FOAvip Sickle cell nephropathy is a common complication in patients with sickle cell hemoglobinopathies. In these disorders, polymerization of mutated hemoglobin S results in deformation of red blood cells, which can cause endothelial cell injury in the kidney that may lead to thrombus formation when severe or manifest by multilayering of the basement membranes (glomerular and/or peritubular capillaries) in milder forms of injury. As the injury progresses, the subsequent ischemia, tubular dysfunction, and glomerular scarring can result in CKD or ESRD. Sickle cell nephropathy can occur in patients with homozygous hemoglobin SS or heterozygous hemoglobin S (hemoglobin SC, hemoglobin S/?0-thalassemia, and hemoglobin S/?+-thalassemia). Clinical manifestations resulting from hemoglobin S polymerization are often milder in patients with heterozygous hemoglobin S. These patients may not present with clinically apparent acute sickle cell crises, but these milder forms can provide a unique view of the kidney injury in sickle cell disease. Here, we report a patient with hemoglobin SC disease who showed peritubular capillary and vasa recta thrombi and capillary basement membrane alterations primarily involving the renal medulla. This patient highlights the vascular occlusion and endothelial cell injury in the medulla that contribute to sickle cell nephropathy. Twit Text FOAVip Medullary Microvascular Thrombosis and Injury in Sickle Hemoglobin C Disease ????J Am Soc Nephrol http://www.kidney.de/pget.php?&tw=1&pmid=26546258 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=26546258 #FOAvip English Wikipedia <ref>{{Cite pmid|26546258}}</ref> Medullary Microvascular Thrombosis and Injury in Sickle Hemoglobin C Disease #MMPMID26546258 Bissonnette MLZ; Henriksen KJ; Delaney K; Stankus N; Chang A J Am Soc Nephrol 2016[May]; 27 (5): 1300-4 PMID26546258show ga Sickle cell nephropathy is a common complication in patients with sickle cell hemoglobinopathies. In these disorders, polymerization of mutated hemoglobin S results in deformation of red blood cells, which can cause endothelial cell injury in the kidney that may lead to thrombus formation when severe or manifest by multilayering of the basement membranes (glomerular and/or peritubular capillaries) in milder forms of injury. As the injury progresses, the subsequent ischemia, tubular dysfunction, and glomerular scarring can result in CKD or ESRD. Sickle cell nephropathy can occur in patients with homozygous hemoglobin SS or heterozygous hemoglobin S (hemoglobin SC, hemoglobin S/?0-thalassemia, and hemoglobin S/?+-thalassemia). Clinical manifestations resulting from hemoglobin S polymerization are often milder in patients with heterozygous hemoglobin S. These patients may not present with clinically apparent acute sickle cell crises, but these milder forms can provide a unique view of the kidney injury in sickle cell disease. Here, we report a patient with hemoglobin SC disease who showed peritubular capillary and vasa recta thrombi and capillary basement membrane alterations primarily involving the renal medulla. This patient highlights the vascular occlusion and endothelial cell injury in the medulla that contribute to sickle cell nephropathy. äMedullary Microvascular Thrombosis and Injury in Sickle Hemoglobin C D(epmc).pdf DeepDyve Pubget Overpricing