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diseases of the genitourinary system. urology (4) 4
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NEFROLOGÍA, ISSN 0211-6995, 03/2019, Volume 39, Issue 2, pp. 177 - 183
La enfermedad de Fabry (EF) es un trastorno hereditario causado por una deficiencia de la actividad de la enzima α-galactosidasa A, cuya transmisión está... 
Daño renal | Podocyturia | Podocituria | α-galactosidase | Fabry disease | α-galactosidasa | Renal damage | Albuminuria | Enfermedad de Fabry
Journal Article
NEFROLOGIA (English Edition), ISSN 2013-2514, 03/2019, Volume 39, Issue 2, pp. 177 - 183
Fabry disease (FD) is a hereditary disorder caused by a deficiency of α-galactosidase A enzyme activity. The transmission of the disorder is linked to the X... 
Daño renal | Podocyturia | α-Galactosidase | Podocituria | Fabry disease | α-galactosidasa | Renal damage | Albuminuria | Enfermedad de Fabry
Journal Article
International Journal of Nephrology, ISSN 2090-214X, 2017, Volume 2017, pp. 1287289 - 7
. Despite enzyme replacement therapy, Fabry nephropathy still progresses. Podocyturia is an irreversible event that antedates proteinuria and leads to chronic... 
Medicine, Experimental | Medical research | Enzymes | Lipids | Chronic kidney failure | Urine | Mutation | Kidney diseases | Laboratories | Patients
Journal Article
Nefrologia : publicacion oficial de la Sociedad Espanola Nefrologia, 03/2019, Volume 39, Issue 2, p. 177
Fabry disease (FD) is a hereditary disorder caused by a deficiency of α-galactosidase A enzyme activity. The transmission of the disorder is linked to the X... 
Glomerular Filtration Rate | Age Factors | Albuminuria - etiology | Humans | Risk Factors | Child, Preschool | Microfilament Proteins - analysis | Male | Fabry Disease - urine | Case-Control Studies | Fabry Disease - pathology | Time Factors | Adolescent | Sex Factors | Female | Child | Fabry Disease - diagnosis | Podocytes - chemistry
Journal Article
Clinical kidney journal, ISSN 2048-8505, 02/2019, Volume 12, Issue 1, pp. 53 - 60
In Fabry nephropathy, podocyturia is an early event that may lead to glomerulosclerosis and chronic kidney disease. The glycocalyx is a potential podocyte... 
Journal Article
Nephron Extra, ISSN 1664-5529, 05/2017, Volume 7, Issue 2, pp. 52 - 61
Podocyturia may determine the evolution to podocytopenia, glomerulosclerosis, and renal failure. According to the Oxford classification of IgA nephropathy... 
Glomerulonephritis | Glomerulosclerosis | IgA nephropathy | Podocyturia | CD80 | Urokinase-type plasminogen activator receptor | Integrins | Proteinuria
Journal Article
Nephron Extra, ISSN 1661-7649, 05/2017, Volume 7, Issue 2, pp. 52 - 61
Background: Podocyturia may determine the evolution to podocytopenia, glomerulosclerosis, and renal failure. According to the Oxford classification of IgA... 
Urine | Microscopy | Pathogenesis | Biopsy | Rodents | Classification | Kidney diseases | Patients
Journal Article
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