نتایج جستجو برای: steroid resistant nephrotic syndrome

تعداد نتایج: 842591  

Background Nephrotic syndrome (NS) characterized by a large amounts of protein into urine and a set of indications that include: protein in urine, low blood protein levels, high cholesterol levels, high triglyceride levels, and swelling. Therefore, aim of this study was to investigate the relationship between prognosis of nephrotic syndrome and blood biomarkers level in children of Arak city, I...

Journal: :Clinical journal of the American Society of Nephrology : CJASN 2013
Jonathan Hogan Andrew S Bomback Kshama Mehta Pietro A Canetta Maya K Rao Gerald B Appel Jai Radhakrishnan Richard A Lafayette

BACKGROUND AND OBJECTIVES Adrenocorticotropic hormone (ACTH) has shown efficacy as primary and secondary therapy for nephrotic syndrome due to membranous nephropathy. The data on using ACTH to treat idiopathic FSGS are limited. This report describes our experience using ACTH for nephrotic syndrome due to idiopathic FSGS in the United States. DESIGN, SETTING, PARTICIPANTS, & MEASUREMENTS Twent...

Journal: :Archives of disease in childhood 1986
R S Trompeter

The term 'minimal change nephrotic syndrome' has become synonymous with the expression 'steroid responsive nephrotic syndrome', the latter term having the merit of focusing on the most important objective characteristic of the condition. Nevertheless, it is somewhat illogical to define this condition by a negative histological feature, which in the majority of cases remains a presumption inferr...

2006

The term 'minimal change nephrotic syndrome' has become synonymous with the expression 'steroid responsive nephrotic syndrome', the latter term having the merit of focusing on the most important objective characteristic of the condition. Nevertheless, it is somewhat illogical to define this condition by a negative histological feature, which in the majority of cases remains a presumption inferr...

2016
Cengiz Zeybek Gokalp Basbozkurt Salih Hamcan Ayhan Ozcan Davut Gul Faysal Gok

Galloway-Mowat syndrome (GMS) is an autosomal recessive disorder with a poor prognosis that was first defined as a triad of central nervous system involvement, hiatal hernia, and nephrotic syndrome. However, this syndrome is now known to have a heterogeneous clinical presentation. The nephrotic syndrome is steroid resistant and is responsible for the outcome. The combination of collapsing glome...

2015
Agnes Trautmann Monica Bodria Fatih Ozaltin Alaleh Gheisari Anette Melk Marta Azocar Ali Anarat Salim Caliskan Francesco Emma Jutta Gellermann Jun Oh Esra Baskin Joanna Ksiazek Giuseppe Remuzzi Ozlem Erdogan Sema Akman Jiri Dusek Tinatin Davitaia Fotios Papachristou Agnieszka Firszt-Adamczyk Tomasz Urasinski Sara Testa Rafael T. Krmar Lidia Hyla-Klekot Andrea Pasini Peter Sallay Nilgun Cakar Monica Galanti Joelle Terzic Bilal Aoun Alberto Caldas Afonso Hanna Szymanik-Grzelak Beata S. Lipska

Background and objectives Steroid-resistant nephrotic syndrome is a rare kidney disease involving either immune-mediated or genetic alterations of podocyte structure and function. The rare nature, heterogeneity, and slow evolution of the disorder are major obstacles to systematic genotype-phenotype, intervention, and outcome studies, hampering the development of evidence-based diagnostic and th...

Journal: :Clinical journal of the American Society of Nephrology : CJASN 2016
Pietro Ravani Alice Bonanni Roberta Rossi Gianluca Caridi Gian Marco Ghiggeri

Rituximab, a chimeric anti-CD20 monoclonal antibody originally licensed for lymphoma, is emerging as a novel steroid-sparing agent for idiopathic nephrotic syndrome in children. The potential use of anti-CD20 monoclonal antibodies in idiopathic nephrotic syndrome has contributed to shifting the view of podocytopathies from T cell-mediated to more complex immunomediated disorders that can benefi...

2014
Zsuzsanna Gáll Éva Kiss Kálmán Tory Attila Fintha Carmen Duicu

Approximately 10-20% of children and 40% of adults with idiopathic nephrotic syndrome are steroid resistant and progress to end-stage renal disease requiring dialysis or renal transplantation. In these cases, renal histology typically shows focal segmental glomerulosclerosis. Mutations in NPHS1, NPHS2, WT1, CD2AP and ACTN4 genes located on different chromosomes, expressed by glomerular podocyte...

Journal: :Iranian journal of kidney diseases 2011
Doaa Mohammed Youssef Rabab Mohammed Elbehidy Hosam Salah Abdelhalim Ghada Elsyde Amr

INTRODUCTION Upregulation of interleukin-2 may be involved, not only in the pathophysiology of nephrotic syndrome, but also in steroid resistance treatment, by increasing expression of multidrug resistant gene-1 (MDR1) gene on lymphocytes and its product P-glycoprotein effluxing corticosteroid. Our aim was to assess the relation of serum soluble interleukin-2 receptor (sIL2R) levels and MDR1 ge...

Journal: :international journal of pediatrics 0
parsa yousefichaijan associate professor of pediatric nephrology, department of pediatric nephrology, amir kabir hospital, arak, iran masoud rezagholizamenjany medical student, school of medicine, arak university of medical sciences, arak, iran. fatemeh rafiei biostatistician, departman of biostatistics, arak university of medical sciences, arak, iran. hassan taherahmadi associate professor of pediatric nephrology, department of pediatric nephrology, amir kabir hospital, arak, iran mohammad rafiei biostatistician, departman of biostatistics, arak university of medical sciences, arak, iran.

background nephrotic syndrome (ns) characterized by a large amounts of protein into urine and a set of indications that include: protein in urine, low blood protein levels, high cholesterol levels, high triglyceride levels, and swelling. therefore, aim of this study was to investigate the relationship between prognosis of nephrotic syndrome and blood biomarkers level in children of arak city, i...

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