Focal segmental glomerulosclerosis: towards a better understanding for the practicing nephrologist. - Wikidata - thesis-toulmin - TriplyDB

Focal segmental glomerulosclerosis: towards a better understanding for the practicing nephrologist.

Focal segmental glomerulosclerosis: towards a better understanding for the practicing nephrologist.

http://www.wikidata.org/entity/Q38192853

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FSGS: Diagnosis and Diagnostic Work-Up Nephrotic syndrome: what's new, what's hot?Focal and segmental glomerulosclerosis: clinical and kidney biopsy correlations.Insights into the renal pathogenesis in Schimke immuno-osseous dysplasia: A renal histological characterization and expression analysis Focal Segmental Glomerulosclerosis in a Patient with Ambiguous Genitalia: A Diagnostic Dilemma.Focal segmental glomerular sclerosis: do not overlook the role of immune response.Focal Segmental Glomerulosclerosis.What are we missing in the clinical trials of focal segmental glomerulosclerosis?Pregnancy, Proteinuria, Plant-Based Supplemented Diets and Focal Segmental Glomerulosclerosis: A Report on Three Cases and Critical Appraisal of the Literature.Differentiating Primary, Genetic, and Secondary FSGS in Adults: A Clinicopathologic Approach.Obesity-related glomerulopathy: pathogenesis, pathologic, clinical characteristics and treatment.The Incidence of Primary vs Secondary Focal Segmental Glomerulosclerosis: A Clinicopathologic Study.Application of next-generation sequencing technology to diagnosis and treatment of focal segmental glomerulosclerosis.Con: Biomarkers in glomerular diseases: putting the cart before the wheel?Clinical and pathological phenotype of genetic causes of focal segmental glomerulosclerosis in adults.

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Focal segmental glomerulosclerosis: towards a better understanding for the practicing nephrologist.

http://www.wikidata.org/entity/Q38192853

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Nephrology Dialysis Transplantation

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Fernando C Fervenza

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Richard J Glassock

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Sanjeev Sethi

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COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness.

Association of trypanolytic ApoL1 variants with kidney disease in African Americans

Apolipoprotein L1 gene variants associate with hypertension-attributed nephropathy and the rate of kidney function decline in African Americans

APOL1 genetic variants in focal segmental glomerulosclerosis and HIV-associated nephropathy

APOL1 localization in normal kidney and nondiabetic kidney disease

APOL1 and nephropathy progression in populations of African ancestry

NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome

Mutations in ACTN4, encoding alpha-actinin-4, cause familial focal segmental glomerulosclerosis

Expression of podocyte-associated molecules in acquired human kidney diseases

Podocyte foot process effacement is not correlated with the level of proteinuria in human glomerulopathies.

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375-384

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10.1093/NDT/GFU035

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3

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30

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2014-03-02T00:00:00Z

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260484894

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24589721

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