In Acute IgA Nephropathy, Proteinuria and Creatinine Are in the Spot, but Podocyturia Operates in Silence: Any Place for Amiloride? [PDF]
Case Reports in Nephrology, 2017 IgA nephropathy is the most frequent cause of primary glomerulonephritis, portends erratic patterns of clinical presentation, and lacks specific treatment. In general, it slowly progresses to end-stage renal disease.
Hernán Trimarchi +2 more
exaly +5 more sources
Podocyturia: A Clue for the Rational Use of Amiloride in Alport Renal Disease [PDF]
Case Reports in Nephrology, 2016 No specific or efficient treatment exists for Alport syndrome, an X-linked hereditary disease caused by mutations in collagen type IV, a crucial component of the glomerular basement membrane. Kidney failure is usually a major complication of the disease,
H. Trimarchi +12 more
doaj +5 more sources
Podocyturia: why it may have added value in rare diseases [PDF]
CKJ: Clinical Kidney Journal, 2019 Altres ajuts: The work was supported by Comunidad de Madrid CIFRA2 B2017/BMD-3686.Fabry disease is an inherited lysosomal disease in which defects in the GLA gene lead to α-galactosidase-A deficiency, and accumulation of glycosphingolipids, including ...
Maria Dolores Sanchez-Niño +2 more
exaly +9 more sources
A comparison of podocyturia, albuminuria and nephrinuria in predicting the development of preeclampsia: a prospective study. [PDF]
PLoS ONE, 2014 Preeclampsia, a hypertensive multisystem disease that complicates 5-8% of all pregnancy, is a major cause for maternal and fetal mortality and morbidity.
Belinda Jim +7 more
doaj +6 more sources
Podocyturia as a Diagnostic Marker for Preeclampsia amongst High-Risk Pregnant Patients [PDF]
Journal of Pregnancy, 2012 Urinary podocyte (podocyturia) has been studied as a diagnostic marker for preeclampsia. We sought to validate its use in preeclampsia and in differentiating it from other high risk pregnancy states.
Belinda Jim +7 more
doaj +5 more sources
Copious Podocyturia without Proteinuria and with Normal Renal Function in a Young Adult with Fabry Disease [PDF]
Case Reports in Nephrology, 2015 The time for starting a patient with Fabry disease on enzyme replacement therapy is still a matter of debate, particularly when no overt classical clinical signs or symptoms are present.
H. Trimarchi +11 more
doaj +3 more sources
Podocyturia in Fabry disease: a 10-year follow-up [PDF]
CKJ: Clinical Kidney Journal, 2022 AbstractBackgroundFabry disease (FD) is a rare X-linked disorder of sphingolipid metabolism that results in chronic proteinuric nephropathy. Podocytes are one of the most affected renal cells and play an important role in the development and progression of kidney disease.
Bojan Vujkovac +2 more
exaly +5 more sources
Podocyturia in Fabry disease [PDF]
Jornal Brasileiro de Nefrologia, 2016 Introduction: Fabry disease is a lysosomal storage disorder due to abnormalities in the GLA gene (Xq22). Such changes result in the reduction/absence of activity of the lysosome enzyme α-GAL, whose function is to metabolize globotriaosylceramide (Gb3 ...
José Tiburcio do Monte Neto (12730376) +4 more
core +4 more sources
Detection of podocyturia in patients with lupus nephritis [PDF]
Jornal Brasileiro de Nefrologia, 2013 INTRODUCTION: The podocyturia has been detected in glomerular diseases, such as lupus nephritis (LN), in which proteinuria is an important manifestation, and its occurrence seems to be limited to the active phase of the disease.
Mastroianni Kirsztajn, Gianna [UNIFESP] +11 more
core +3 more sources
Effects of childbirth on podocyturia in women with normotensive, uncomplicated pregnancies [PDF]
American Journal of Physiology-Renal Physiology, 2017 Changes in hemodynamics and blood pressure occur shortly before and after childbirth regardless of the mode of delivery. This study aimed to test the hypothesis that parturition induces a temporal increase in podocyturia monitored by podocyte-specific ...
Minakami, Hisanori +17 more
core +5 more sources