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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1975 1
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1989 1
1990 3
1993 4
1994 1
1995 1
1996 5
1997 1
1998 2
1999 1
2001 6
2002 3
2003 2
2004 4
2006 2
2007 2
2008 4
2009 2
2010 2
2012 1
2013 1
2014 1
2015 3
2016 7
2017 5
2018 3
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2020 4
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2023 3
2024 0

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79 results

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Page 1
Nephrotic syndrome in infants and children: pathophysiology and management.
Downie ML, Gallibois C, Parekh RS, Noone DG. Downie ML, et al. Paediatr Int Child Health. 2017 Nov;37(4):248-258. doi: 10.1080/20469047.2017.1374003. Epub 2017 Sep 15. Paediatr Int Child Health. 2017. PMID: 28914167 Review.
Nephrotic syndrome is defined by nephrotic-range proteinuria (40 mg/m(2)/hour or urine protein/creatinine ratio 200 mg/mL or 3+ protein on urine dipstick), hypoalbuminaemia (<25 g/L) and oedema. This review focuses on the classification, epidemiology, path …
Nephrotic syndrome is defined by nephrotic-range proteinuria (40 mg/m(2)/hour or urine protein/creatinine ratio 200 mg/ …
Renal amyloidosis: an update on diagnosis and pathogenesis.
Gupta N, Kaur H, Wajid S. Gupta N, et al. Protoplasma. 2020 Sep;257(5):1259-1276. doi: 10.1007/s00709-020-01513-0. Epub 2020 May 24. Protoplasma. 2020. PMID: 32447467 Review.
It is generally composed of serum amyloid A-related protein or an immunoglobulin light chain; other rare forms lysozyme, gelsolin, fibrinogen alpha chain, transthyretin, apolipoproteins AI/AII/AIV/CII/CIII; and the recently identified form ALECT2. This disease typically manifests …
It is generally composed of serum amyloid A-related protein or an immunoglobulin light chain; other rare forms lysozyme, gelsolin, fibrinoge …
Interventions for focal segmental glomerulosclerosis in adults.
Hodson EM, Sinha A, Cooper TE. Hodson EM, et al. Cochrane Database Syst Rev. 2022 Feb 28;2(2):CD003233. doi: 10.1002/14651858.CD003233.pub3. Cochrane Database Syst Rev. 2022. PMID: 35224732 Free PMC article. Review.
BACKGROUND: Focal segmental glomerulosclerosis (FSGS) can be separated into primary, genetic or secondary causes. Primary disease results in nephrotic syndrome while genetic and secondary forms may be associated with asymptomatic proteinuria or with nephrotic …
BACKGROUND: Focal segmental glomerulosclerosis (FSGS) can be separated into primary, genetic or secondary causes. Primary disease results in …
Membranous nephropathy: Mechanistic insights and therapeutic perspectives.
Hua MR, Zhao YL, Yang JZ, Zou L, Zhao YY, Li X. Hua MR, et al. Int Immunopharmacol. 2023 Jul;120:110317. doi: 10.1016/j.intimp.2023.110317. Epub 2023 May 17. Int Immunopharmacol. 2023. PMID: 37207447 Review.
Membranous nephropathy (MN) is one of the most common causes of non-diabetic nephrotic syndrome in adults. About 80% of cases are renal limited (primary MN) and 20% are associated with other systemic diseases or exposures (secondary MN). Autoimmune reaction is the m …
Membranous nephropathy (MN) is one of the most common causes of non-diabetic nephrotic syndrome in adults. About 80% of cases …
Childhood nephrotic syndrome in tropical Africa: then and now.
Olowu WA, Ademola A, Ajite AB, Saad YM. Olowu WA, et al. Paediatr Int Child Health. 2017 Nov;37(4):259-268. doi: 10.1080/20469047.2017.1374002. Epub 2017 Sep 26. Paediatr Int Child Health. 2017. PMID: 28949280 Review.
This descriptive and comparative review examines the changing epidemiology, treatment, renal and patient outcome of childhood nephrotic syndrome (NS) in tropical Africa (TpAfr). In the 1960s to 1980s, corticosteroid-resistant non-minimal change disease (nMCD) includ …
This descriptive and comparative review examines the changing epidemiology, treatment, renal and patient outcome of childhood nephrotic …
[Four cases of nephrotic syndrome with TRPC6 gene variations and literature review].
Sun LW, Sun L, Wang P, Kang YL, Wu Y, Zhu GH, Huang WY. Sun LW, et al. Zhonghua Er Ke Za Zhi. 2021 Mar 2;59(3):223-227. doi: 10.3760/cma.j.cn112140-20200824-00822. Zhonghua Er Ke Za Zhi. 2021. PMID: 33657698 Review. Chinese.
Objective: To investigate the clinical characteristics, treatment and prognosis of TRPC6 variation induced children with steroid-resistant nephrotic syndrome (SRNS). Methods: Clinical data of four patients with nephrotic syndrome carrying TRPC6 variati …
Objective: To investigate the clinical characteristics, treatment and prognosis of TRPC6 variation induced children with steroid-resistant …
Gonadal tumor in Frasier syndrome: a review and classification.
Ezaki J, Hashimoto K, Asano T, Kanda S, Akioka Y, Hattori M, Yamamoto T, Shibata N. Ezaki J, et al. Cancer Prev Res (Phila). 2015 Apr;8(4):271-6. doi: 10.1158/1940-6207.CAPR-14-0415. Epub 2015 Jan 26. Cancer Prev Res (Phila). 2015. PMID: 25623218 Review.
Frasier syndrome is a rare inherited disease characterized by steroid-resistant nephrotic syndrome, gonadal tumor, and male pseudohermaphroditism (female external genitalia with sex chromosomes XY), which is based on a splice site mutation of Wilms tumor-supp …
Frasier syndrome is a rare inherited disease characterized by steroid-resistant nephrotic syndrome, gonadal tumor, and …
Advances in molecular diagnosis and therapeutics in nephrotic syndrome and focal and segmental glomerulosclerosis.
Sharif B, Barua M. Sharif B, et al. Curr Opin Nephrol Hypertens. 2018 May;27(3):194-200. doi: 10.1097/MNH.0000000000000408. Curr Opin Nephrol Hypertens. 2018. PMID: 29465426 Review.
In nephrology, one of the best examples of this is seen in focal and segmental glomerulosclerosis (FSGS) and nephrotic syndrome. We review advances made in 2017 as a result of human and molecular genetic studies as it relates to FSGS and nephrotic syndrome …
In nephrology, one of the best examples of this is seen in focal and segmental glomerulosclerosis (FSGS) and nephrotic syndrome …
Sphingosine phosphate lyase insufficiency syndrome: a systematic review.
Pournasiri Z, Madani A, Nazarpack F, Sayer JA, Chavoshzadeh Z, Nili F, Tran P, Saba JD, Jamee M. Pournasiri Z, et al. World J Pediatr. 2023 May;19(5):425-437. doi: 10.1007/s12519-022-00615-4. Epub 2022 Nov 12. World J Pediatr. 2023. PMID: 36371483 Review.
BACKGROUND: Sphingosine-1-phosphate lyase insufficiency syndrome (SPLIS) or nephrotic syndrome type-14 is caused by biallelic mutations in SGPL1. ...Kidney disorders (42, 80.8%) were mainly in the form of steroid-resistant nephrotic syndrome …
BACKGROUND: Sphingosine-1-phosphate lyase insufficiency syndrome (SPLIS) or nephrotic syndrome type-14 is caused …
Chinese herbal medicine Huangqi type formulations for nephrotic syndrome.
Feng M, Yuan W, Zhang R, Fu P, Wu T. Feng M, et al. Cochrane Database Syst Rev. 2013 Jun 5;(6):CD006335. doi: 10.1002/14651858.CD006335.pub3. Cochrane Database Syst Rev. 2013. PMID: 23740567 Review.
OBJECTIVES: To assess the benefits and harms of Huangqi and Huangqi type formulations in treating nephrotic syndrome in any age group, either as sole agents or in addition to other drug therapies. ...SELECTION CRITERIA: All randomised controlled trials (RCTs) …
OBJECTIVES: To assess the benefits and harms of Huangqi and Huangqi type formulations in treating nephrotic syndrome in …
79 results