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P50 | author | Avi Rosenberg | Q37366935 |
Jeffrey B. Kopp | Q38359650 | ||
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Pirfenidone Slows Renal Function Decline in Patients with Focal Segmental Glomerulosclerosis | Q57691283 | ||
Sirolimus Therapy of Focal Segmental Glomerulosclerosis Is Associated With Nephrotoxicity | Q57691291 | ||
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A hitherto undescribed vulnerability of the juxtamedullary glomeruli in lipoid nephrosis | Q74487217 | ||
Progression of glomerular diseases: is the podocyte the culprit? | Q77291496 | ||
Renin-angiotensin axis blockade reduces proteinuria in presymptomatic patients with familial FSGS | Q80387822 | ||
High sirolimus levels may induce focal segmental glomerulosclerosis de novo | Q80797353 | ||
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Saquinavir in steroid-dependent and -resistant nephrotic syndrome: a pilot study | Q83699263 | ||
Proliferating cells in HIV and pamidronate-associated collapsing focal segmental glomerulosclerosis are parietal epithelial cells | Q83948540 | ||
Resolution of recurrent focal segmental glomerulosclerosis after retransplantation | Q83991578 | ||
Serum-soluble urokinase receptor concentration in primary FSGS | Q84033601 | ||
New players in the pathogenesis of focal segmental glomerulosclerosis | Q84531641 | ||
Collagen (COL4A) mutations are the most frequent mutations underlying adult focal segmental glomerulosclerosis | Q86084087 | ||
Plasma soluble urokinase receptor levels are increased but do not distinguish primary from secondary focal segmental glomerulosclerosis | Q86215247 | ||
Novel unbiased assay for circulating podocyte-toxic factors associated with recurrent focal segmental glomerulosclerosis | Q86998557 | ||
Genetic and in vivo determinants of glucocorticoid sensitivity in relation to clinical outcome of childhood nephrotic syndrome | Q87105700 | ||
Serum suPAR levels help differentiate steroid resistance from steroid-sensitive nephrotic syndrome in children | Q87407965 | ||
An update on the treatment options for focal segmental glomerulosclerosis | Q94857026 | ||
The incidence of biopsy-proven glomerulonephritis in Australia. | Q34294024 | ||
Combination therapy an ACE inhibitor and an angiotensin receptor blocker for IgA nephropathy: a meta-analysis | Q34418531 | ||
A single-gene cause in 29.5% of cases of steroid-resistant nephrotic syndrome | Q34445136 | ||
A form of apolipoprotein a-I is found specifically in relapses of focal segmental glomerulosclerosis following transplantation | Q34498293 | ||
Clinical and pathologic characteristics of focal segmental glomerulosclerosis pathologic variants | Q34499836 | ||
Dystroglycan in the diagnosis of FSGS. | Q34659224 | ||
Innate immunity pathways regulate the nephropathy gene Apolipoprotein L1 | Q35033687 | ||
A reassessment of soluble urokinase-type plasminogen activator receptor in glomerular disease | Q35132279 | ||
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Glomerular hyperfiltration and albuminuria in children with sickle cell anemia | Q35278672 | ||
A circulating antibody panel for pretransplant prediction of FSGS recurrence after kidney transplantation | Q35379384 | ||
Clinical Features and Histology of Apolipoprotein L1-Associated Nephropathy in the FSGS Clinical Trial | Q35658566 | ||
A phase 1, single-dose study of fresolimumab, an anti-TGF-β antibody, in treatment-resistant primary focal segmental glomerulosclerosis | Q35669295 | ||
Focal segmental glomerulosclerosis: molecular genetics and targeted therapies | Q35686453 | ||
Efficacy of galactose and adalimumab in patients with resistant focal segmental glomerulosclerosis: report of the font clinical trial group | Q35704498 | ||
Trends in the histopathology of childhood nephrotic syndrome in Ibadan Nigeria: preponderance of idiopathic focal segmental glomerulosclerosis | Q35869275 | ||
Acthar gel in the treatment of nephrotic syndrome: a multicenter retrospective case series | Q35976834 | ||
Role of Myeloid-Derived Suppressor Cells in Glucocorticoid-Mediated Amelioration of FSGS. | Q36003095 | ||
Growth-dependent podocyte failure causes glomerulosclerosis | Q36109205 | ||
APOL1 Risk Variants Are Strongly Associated with HIV-Associated Nephropathy in Black South Africans | Q36223249 | ||
Rapid Response to Cyclosporin A and Favorable Renal Outcome in Nongenetic Versus Genetic Steroid-Resistant Nephrotic Syndrome | Q36543103 | ||
IgM contributes to glomerular injury in FSGS | Q36638347 | ||
Treatment with Glucocorticoids or Calcineurin Inhibitors in Primary FSGS | Q36686985 | ||
Changing the Paradigm for the Treatment and Development of New Therapies for FSGS. | Q36717656 | ||
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The podocyte as a direct target for treatment of glomerular disease? | Q37139449 | ||
Focal segmental glomerulosclerosis is associated with a PDSS2 haplotype and, independently, with a decreased content of coenzyme Q10. | Q37234710 | ||
Treatment of idiopathic FSGS with adrenocorticotropic hormone gel. | Q37359035 | ||
MYH9 and APOL1 are both associated with sickle cell disease nephropathy | Q37451162 | ||
Abatacept in B7-1-positive proteinuric kidney disease | Q37633142 | ||
Collapsing focal segmental glomerulosclerosis following treatment with high-dose pamidronate. | Q43617519 | ||
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Lithium-induced nephrotic syndrome in a young pediatric patient | Q43961785 | ||
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Adrenocorticotropic hormone therapy for the treatment of idiopathic nephrotic syndrome in children and young adults: a systematic review of early clinical studies with contemporary relevance | Q37651364 | ||
Pathogenesis and therapy of focal segmental glomerulosclerosis: an update | Q37812564 | ||
Adriamycin nephropathy: a model of focal segmental glomerulosclerosis. | Q37822895 | ||
Raised serum creatinine at presentation does not adversely affect steroid response in primary focal segmental glomerulosclerosis in adults | Q37908883 | ||
Focal and segmental glomerulosclerosis: multiple pathways are involved | Q37916842 | ||
Focal segmental glomerulosclerosis and chronic kidney disease in pediatric patients | Q37928188 | ||
Focal segmental glomerulosclerosis | Q37970393 | ||
Aldosterone blockade and the mineralocorticoid receptor in the management of chronic kidney disease: current concepts and emerging treatment paradigms | Q37984206 | ||
Pathobiology of focal segmental glomerulosclerosis: new developments | Q37987334 | ||
Obesity and kidney disease: potential mechanisms | Q38078543 | ||
Current and emerging treatments for idiopathic focal and segmental glomerulosclerosis in adults | Q38085054 | ||
Serum suPAR in patients with FSGS: trash or treasure? | Q38091638 | ||
Different targets for treating focal segmental glomerular sclerosis | Q38108170 | ||
Focal segmental glomerulosclerosis: towards a better understanding for the practicing nephrologist | Q38192853 | ||
Treatment of FSGS in Children | Q38193933 | ||
The sclerosing glomerulus in mice and man: novel insights | Q38202839 | ||
A potential role for mechanical forces in the detachment of podocytes and the progression of CKD. | Q38233673 | ||
Morphologic variants of focal segmental glomerulosclerosis and their significance. | Q38244351 | ||
The treatment of idiopathic focal segmental glomerulosclerosis in adults | Q38244355 | ||
Sleep apnea and the kidney: is sleep apnea a risk factor for chronic kidney disease? | Q38257377 | ||
Causes and pathogenesis of focal segmental glomerulosclerosis | Q38275115 | ||
Apolipoprotein L1 risk variants associate with systemic lupus erythematosus-associated collapsing glomerulopathy | Q38397636 | ||
Collapsing Focal Segmental Glomerulosclerosis in a Patient with Acute Malaria | Q38559522 | ||
Mechanical challenges to the glomerular filtration barrier: adaptations and pathway to sclerosis | Q38786437 | ||
Defining Glomerular Disease in Mechanistic Terms: Implementing an Integrative Biology Approach in Nephrology | Q38821066 | ||
Computational simulation of renal biopsy accuracy in focal segmental glomerulosclerosis | Q39120807 | ||
Active proteases in nephrotic plasma lead to a podocin-dependent phosphorylation of VASP in podocytes via protease activated receptor-1. | Q39189360 | ||
Effect of galactose on glomerular permeability and proteinuria in steroid-resistant nephrotic syndrome | Q39398182 | ||
Distribution of Biopsy-Proven Presumed Primary Glomerulonephropathies in 2000-2011 Among a Racially and Ethnically Diverse US Population | Q39801045 | ||
A study of interobserver reproducibility of morphologic lesions of focal segmental glomerulosclerosis. | Q40082066 | ||
Direct effects of dexamethasone on human podocytes | Q40256235 | ||
The evolution of morphological variants of focal segmental glomerulosclerosis: a repeat biopsy-based observation. | Q40752049 | ||
Primary focal segmental glomerulosclerosis: pathology, histological variants, and pathogenesis | Q40784815 | ||
Nephron mass as a risk factor for progression of renal disease | Q41667489 | ||
Renal and Hematological Effects of CLCF-1, a B-Cell-Stimulating Cytokine of the IL-6 Family. | Q42254379 | ||
Intensive and prolonged treatment of focal and segmental glomerulosclerosis recurrence in adult kidney transplant recipients: a pilot study. | Q42616843 | ||
A role for genetic susceptibility in sporadic focal segmental glomerulosclerosis | Q42930267 | ||
Viruses and collapsing glomerulopathy: a brief critical review | Q43101728 | ||
P433 | issue | 3 | |
P921 | main subject | focal segmental glomerulosclerosis | Q1435223 |
P304 | page(s) | 502-517 | |
P577 | publication date | 2017-02-27 | |
P1433 | published in | Clinical Journal of the American Society of Nephrology | Q15757929 |
P1476 | title | Focal Segmental Glomerulosclerosis. | |
P478 | volume | 12 |
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