Relevant bibliographies by topics / Steroid-resistant nephrotic syndrome

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers

Academic literature on the topic 'Steroid-resistant nephrotic syndrome'

Author: Grafiati
Published: 2 June 2025
Last updated: 31 July 2025

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Journal articles on the topic "Steroid-resistant nephrotic syndrome"

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Warejko, Jillian K., Weizhen Tan, Ankana Daga, et al. "Whole Exome Sequencing of Patients with Steroid-Resistant Nephrotic Syndrome." Clinical Journal of the American Society of Nephrology 13, no. 1 (2017): 53–62. http://dx.doi.org/10.2215/cjn.04120417.

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Background and objectivesSteroid-resistant nephrotic syndrome overwhelmingly progresses to ESRD. More than 30 monogenic genes have been identified to cause steroid-resistant nephrotic syndrome. We previously detected causative mutations using targeted panel sequencing in 30% of patients with steroid-resistant nephrotic syndrome. Panel sequencing has a number of limitations when compared with whole exome sequencing. We employed whole exome sequencing to detect monogenic causes of steroid-resistant nephrotic syndrome in an international cohort of 300 families.Design, setting, participants, &
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K., Ramya, Balasubramanian M., and Sharon S. "Urinary Interleukin 18 in Children with Nephrotic Syndrome and Its Role in Steroid Responsiveness." International Journal of Pharmaceutical and Clinical Research 16, no. 3 (2024): 909–14. https://doi.org/10.5281/zenodo.10968918.

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<strong>Introduction:&nbsp;</strong>Nephrotic syndrome includes the clinical manifestation of glomerular diseases associated with heavy proteinuria i.e., nephrotic range (40 mg/m&sup2;/hr or &gt;1000 mg/m&sup2;/day; spot Up/Uc&gt;2 mg/mg; 3-4+ by urine dipstick); hypoalbuminemia (albumin &lt;3.0 g/dL); and edema. In children, the most common cause of nephrotic syndrome is idiopathic or primary nephrotic syndrome (INS), also called nephrosis. In the kidney, the predominant source of IL-18 is the tubular epithelial cells. In the recent years, the biological and pathological roles of IL-18 have b
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Burlaka, Ie A., and I. V. Bagdasarova. "Molecular factors predicting steroid resistance in pediatric nephrotic syndrome." Ukrainian Journal of Nephrology and Dialysis, no. 2(70) (March 21, 2021): 32–37. http://dx.doi.org/10.31450/ukrjnd.2(70).2021.04.

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Objectives: the objective of this paper was to study the levels of cellular hypoxia, apoptosis controlling factors in children with steroid-sensitive and steroid-resistant nephrotic syndrome.&#x0D; Background: patients with steroid-resistant nephrotic syndrome (SRNS) represent a challenging subset of patients with nephrotic syndrome who often fail standard immunosuppression and have a higher likelihood of progressing to end-stage renal disease. The search of the biochemical markers undergoing the steroid-resistance is under urgent need.&#x0D; Methods: an examination of kidney biopsies and bloo
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Banerjee, Sushmita. "Steroid resistant nephrotic syndrome." Indian Journal of Pediatrics 69, no. 12 (2002): 1065–69. http://dx.doi.org/10.1007/bf02724390.

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Kitamura, Akiko, Hiroyasu Tsukaguchi, Kenichi Maruyama, et al. "Steroid-resistant nephrotic syndrome." Kidney International 74, no. 9 (2008): 1209–15. http://dx.doi.org/10.1038/ki.2008.297.

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Quader, Mohammed Maruf Ul. "Familial nephrotic syndrome: Does it matter?" Paediatric Nephrology Journal of Bangladesh 8, no. 2 (2023): 69–77. http://dx.doi.org/10.4103/pnjb.pnjb_15_23.

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Abstract Steroid sensitive nephrotic syndrome (SSNS) is the most common form of nephrotic syndrome in childhood. Familial SSNS seems to be clinically homogeneous but reports on genetically informative SSNS families are lacking. Familial SSNS was found to be genetically distinct from familial steroid resistant nephrotic syndrome (SRNS). Several genes have been identified for SRNS. In general, genetic forms of nephrotic syndrome are resistant to common therapeutic approaches. But different cohort of steroid sensitive familial nephrotic syndrome were published. So precise clinical and genetic inf
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Doku Diamant Shtiza, Ana. "Case Report on Steroid - Resistant Nephrotic Syndrome in Children." International Journal of Science and Research (IJSR) 12, no. 4 (2023): 595–97. http://dx.doi.org/10.21275/sr23331181047.

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Bunde, Saili Vishwanath, Mumtaz Sharif, and Amit Saxena. "Bacterial meningitis in a known case of steroid-resistant nephrotic syndrome." Indian Journal of Child Health 8, no. 9 (2021): 338–39. http://dx.doi.org/10.32677/ijch.v8i9.3039.

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Nephrotic syndrome (NS) is a kidney disorder in which, excess protein is being excreted through urine. While most cases of idiopathic nephrotic syndrome respond to steroid therapy and experience a limited number of relapses prior to complete remission, some cases suffer from frequent relapses and become steroid-dependent or are primarily steroid-resistant. Treatment options are limited to immunosuppressive drugs with significant side effect profiles. Infections in nephrotic syndrome are common and can be severe. Meningitis is one of the complications associated with nephrotic syndrome. Here, w
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Gaikwad, Dr Sarita Pradip. "Effective Ayurvedic Management of Steroid Resistant Nephrotic Syndrome - Case Study." Journal of Medical Science And clinical Research 11, no. 10 (2023): 25–32. http://dx.doi.org/10.18535/jmscr/v11i10.05.

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Nephrotic syndrome presents with heavy proteinuria (3.5 g Proteins/ 1.73 m2 body surface area/24 hour), dyslipidaemia/ hypercholesterolemia, hypoalbuminema, edema and hypertension. If left untreated or undiagnosed, there is progressive damage to glomeruli causing renal failure. Heavy proteinuria is the most characteristic feature of this syndrome. Several studies have noted that higher the 24-h urine protein excretion, more rapid is the decline in GFR. It may be primary or secondary to other systemic diseases. Case study: This 2 year old male child developed Nephrotic syndrome and was placed o
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ITAMI, NORITOMO, YASUSHI AKUTSU, HLROYUKI TOCHIMARU, YASUO TAKEKOSHI, TOSHIMORI SEKI, and MASAKI TOGASHI. "RECURRENT STEROID-RESISTANT NEPHROTIC SYNDROME." Transplantation 49, no. 1 (1990): 234–35. http://dx.doi.org/10.1097/00007890-199001000-00057.

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Dissertations / Theses on the topic "Steroid-resistant nephrotic syndrome"

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Bierzynska, Agnieszka. "Investigating the genotype-phenotype correlations in paediatric steroid resistant nephrotic syndrome patients." Thesis, University of Bristol, 2016. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.702425.

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Steroid Resistant Nephrotic Syndrome (SRNS) is characterised by either primary or late onset resistance to immunosuppression. Prognosis is poor and often results in rapid progression to end stage renal failure (ESRF). Generally, the incidence of disease-causing mutations in paediatric SRNS is 20-30%. 50 genes are currently associated with SRNS and since the advent of next generation sequencing, new genes are being linked each year. This study aimed to discover the true extent and spectrum of genetic variation in a comprehensive national NS population, selected by clinically relevant inclusion
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Iatropoulos, Paraskevas. "Next-generation sequencing for new gene identification and for diagnosis in steroid-resistant nephrotic syndrome." Thesis, Open University, 2017. http://oro.open.ac.uk/50329/.

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Nephrotic syndrome is clinically characterized by massive proteinuria, and hypoalbuminemia. It represents a heterogeneous group of glomerular disorders characterized by distinct causes and histopathologic lesions. The present thesis evaluates the contribution of genetics in conditions commonly associated with NS: the immune complex-mediated membranoproliferative glomerulonephritis (IC-MPGN), the C3 glomerulopathy (C3G) and the podocytopathies, usually characterized by steroid-resistant nephrotic syndrome (SRNS). The first part of the thesis focused on IC-MPGN and C3G. We found likely pathogeni
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Almeida, Gonçalves Sara de. "Identification of new genes involved in hereditary steroid-resistant nephrotic syndrome using next generation sequencing and in vivo functional characterization in drosophila melanogaster." Thesis, Sorbonne Paris Cité, 2017. http://www.theses.fr/2017USPCB030/document.

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Pas de résumé<br>Nephrotic syndrome (NS) is a kidney disease characterized by disruption of the glomerular filtration barrier and the massive loss of proteins into the urine. Although in the majority of cases treatment with steroids leads to remission of the disease, in 15-20% of cases the disease is not responsive to this therapy and is classified as steroid-resistant nephrotic syndrome (SRNS). SRNS is a clinical condition with high morbidity leading to progressive renal failure as well as multiple metabolic and cardiovascular complications. Extensive research over the last 20 years has ident
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Books on the topic "Steroid-resistant nephrotic syndrome"

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Miller-Hodges, Eve, and Christopher Mitchell. The patient with Wilms tumour. Edited by Giuseppe Remuzzi. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199592548.003.0173_update_001.

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Wilms tumour is the most common renal tumour in childhood. It is most commonly identified as a large abdominal mass. Treatment by surgical removal and chemotherapy, and radiotherapy in more advanced stages, is curative in most patients. Five year survival is over 90%. Survivors may be at some risk from long term complications including the effects of radiotherapy on the remaining kidney.A small minority of Wilms tumours occur in individuals with an underlying mutation in the WT1 gene. WT1 mutations may also cause developmental abnormalities of the genitourinary system, and renal disease includ
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Hastie, Nick, and Eve Miller-Hodges. WT1 and its disorders. Edited by Neil Turner. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199592548.003.0329_update_001.

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Mutations in the Wilms tumour suppressor gene, WT1, are associated with Wilms tumour in childhood. However, in addition WT1 has a key role in renal development, emerging roles in podocyte function, and a potential role in tissue regeneration. An understanding of WT1 is of increasing importance to clinical practice. WT1 is a complex gene with multiple isoforms. It is crucial for normal embryonic development, especially kidney development, where it is necessary for mesenchymal-to-epithelial transition to form the nephron. WT1 mutations lead to abnormalities in renal and genitourinary development
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Niaudet, Patrick, and Alain Meyrier. Minimal change disease. Edited by Neil Turner. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199592548.003.0056_update_001.

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Minimal change disease is characteristically responsive to high-dose corticosteroids. As this is the most common cause of nephrotic syndrome in children, and responses are usually prompt, response to 60 mg/m2/day of oral prednisolone (max. 80 mg) is often used as a diagnostic test. Adults respond more slowly and have a wider differential diagnosis, and often a high risk of side effects, so therapy is not recommended without confirmation by renal biopsy. Then first-line treatment is again prednisolone or prednisone, at 1 mg/kg/day (max. 60 mg). KDIGO and other treatment protocols recommend 6 we
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Book chapters on the topic "Steroid-resistant nephrotic syndrome"

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Gbadegesin, Rasheed, Keisha L. Gibson, and William E. Smoyer. "Steroid Resistant Nephrotic Syndrome." In Pediatric Kidney Disease. Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-662-52972-0_16.

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Gbadegesin, Rasheed, Keisha Gibson, and Kimberly Reidy. "Steroid Resistant Nephrotic Syndrome." In Pediatric Kidney Disease. Springer International Publishing, 2023. http://dx.doi.org/10.1007/978-3-031-11665-0_14.

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Froehlich, Stephan J., Carlo A. Lackerbauer, Guenter Rudolph, et al. "Nephrotic Syndrome, Steroid Resistant." In Encyclopedia of Molecular Mechanisms of Disease. Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-29676-8_1671.

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Leung, Alexander K. C., Cham Pion Kao, Andrew L. Wong, et al. "Steroid Resistant Nephrotic Syndrome." In Encyclopedia of Molecular Mechanisms of Disease. Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-29676-8_9359.

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Kemper, Markus Josef, Keisha Gibson, and Aditi Sinha. "Nongenetic Forms of Steroid-Resistant Nephrotic Syndrome." In Pediatric Nephrology. Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-030-52719-8_93.

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Kemper, Markus Josef, Keisha Gibson, and Aditi Sinha. "Nongenetic Forms of Steroid-Resistant Nephrotic Syndrome." In Pediatric Nephrology. Springer Berlin Heidelberg, 2021. http://dx.doi.org/10.1007/978-3-642-27843-3_93-1.

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Riegler, P., R. Corradini, P. Eder, A. Valli, and W. Huber. "Steroid-Resistant Nephrotic Syndrome Treated with Cyclosporin A(CyA)." In Current Therapy in Nephrology. Springer US, 1989. http://dx.doi.org/10.1007/978-1-4613-0865-2_27.

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Traum, Avram Z., and Asher D. Schachter. "Urinary Proteome Profiling to Search for Biomarkers in Steroid-Resistant Nephrotic Syndrome." In Proteomics in Nephrology - Towards Clinical Applications. KARGER, 2008. http://dx.doi.org/10.1159/000125925.

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Hoyer, Peter F., Udo Vester, and Jan Ulrich Becker. "Steroid-Resistant Nephrotic Syndrome." In Comprehensive Pediatric Nephrology. Elsevier, 2008. http://dx.doi.org/10.1016/b978-0-323-04883-5.50022-2.

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Straatmann, Caroline, and V. Matti Vehaskari. "Steroid-Resistant Nephrotic Syndrome." In Pediatric Nephrology. WORLD SCIENTIFIC, 2012. http://dx.doi.org/10.1142/9789814327565_0015.

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Conference papers on the topic "Steroid-resistant nephrotic syndrome"

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E.V, Plotnikova, Borisova M.A, Belova E.G, and Borisov V.S. "P322 Treatment optimisation of steroid-resistant paediatric nephrotic syndrome." In 8th Europaediatrics Congress jointly held with, The 13th National Congress of Romanian Pediatrics Society, 7–10 June 2017, Palace of Parliament, Romania, Paediatrics building bridges across Europe. BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health, 2017. http://dx.doi.org/10.1136/archdischild-2017-313273.410.

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Virgilio-da-Silva, João Victor, Mara Sanches Guaragna, Liliane Prates, et al. "Molecular study of genes associated with steroid-resistant nephrotic syndrome." In XXV Congresso de Iniciação Cientifica da Unicamp. Galoa, 2017. http://dx.doi.org/10.19146/pibic-2017-78102.

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Sladkov, Dmitry, Kirill Savostyanov, Alexey Nikitin, et al. "OC8 High prevalence ofwt1gene mutations in patients with steroid-resistant nephrotic syndrome." In Faculty of Paediatrics of the Royal College of Physicians of Ireland, 9th Europaediatrics Congress, 13–15 June, Dublin, Ireland 2019. BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health, 2019. http://dx.doi.org/10.1136/archdischild-2019-epa.8.

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Kirill, Savostyanov, Sladkov Dmitry, Tsygin Alexey, et al. "OC-63 Novel mutations in children with steroid-resistant nephrotic syndrome in russian population." In 8th Europaediatrics Congress jointly held with, The 13th National Congress of Romanian Pediatrics Society, 7–10 June 2017, Palace of Parliament, Romania, Paediatrics building bridges across Europe. BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health, 2017. http://dx.doi.org/10.1136/archdischild-2017-313273.63.

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Stanzelova, Anna, Anna Krepelova, Michaela Nemcikova, and Jakub Zieg. "GP61 Swollen eyes with an unpleasant surprise – a case report of a steroid resistant nephrotic syndrome." In Faculty of Paediatrics of the Royal College of Physicians of Ireland, 9th Europaediatrics Congress, 13–15 June, Dublin, Ireland 2019. BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health, 2019. http://dx.doi.org/10.1136/archdischild-2019-epa.127.

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Hilmanto, Dany, Ahmedz Widiasta, Yunia Sribudiani, Husna Nugrahapraja, Kurnia Wahyudi та Dedi Rachmadi. "The Role of miR-21 on the Expression of β2-Microglobulin in Steroid-resistant Nephrotic Syndrome Children". У BECB 2021: 2021 International Symposium on Biomedical Engineering and Computational Biology. ACM, 2021. http://dx.doi.org/10.1145/3502060.3502320.

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Webb, H., and S. McKeever. "002 Influence of a renal biopsy result on treatment and management of steroid-resistant, idiopathic nephrotic syndrome in children." In Great Ormond Street Hospital Conference 2018: Continuous Care. BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health, 2018. http://dx.doi.org/10.1136/goshabs.2.

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Susanti, Susanti, Krisni Subandiyah та Husnul Khotimah. "The role of vitamin D3 supplementation to transforming growth factor β1 and tumor necrosis factor α levels in steroid resistant nephrotic syndrome". У INTERNATIONAL CONFERENCE ON LIFE SCIENCES AND TECHNOLOGY (ICoLiST 2020). AIP Publishing, 2021. http://dx.doi.org/10.1063/5.0052610.

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