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

Year Number of Results
1946 1
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1967 1
1968 1
1973 2
1974 2
1975 3
1976 5
1977 6
1978 5
1979 3
1980 6
1981 5
1982 5
1983 6
1984 2
1985 5
1986 1
1987 3
1988 6
1989 10
1990 3
1991 4
1992 8
1993 7
1994 8
1995 10
1996 10
1997 8
1998 7
1999 11
2000 8
2001 11
2002 10
2003 10
2004 5
2005 7
2006 9
2007 3
2008 12
2009 7
2010 2
2011 4
2012 3
2013 3
2014 10
2015 7
2016 7
2017 7
2018 2
2019 4
2020 10
2021 8
2022 5
2023 3
2024 0

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296 results

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Page 1
Nephrinuria and podocytopathies.
Kostovska I, Trajkovska KT, Topuzovska S, Cekovska S, Labudovic D, Kostovski O, Spasovski G. Kostovska I, et al. Adv Clin Chem. 2022;108:1-36. doi: 10.1016/bs.acc.2021.08.001. Epub 2021 Sep 10. Adv Clin Chem. 2022. PMID: 35659057
Many kidney diseases involve podocytopathy including congenital nephrotic syndrome of Finnish type, diffuse mesangial sclerosis, minimal change disease, focal segmental glomerulosclerosis, collapsing glomerulonephropathy, diabetic nephropathy, lupus nephropathy, hypertensi …
Many kidney diseases involve podocytopathy including congenital nephrotic syndrome of Finnish type, diffuse mesangial sclerosis, mini …
Congenital nephrotic syndrome.
Hamed RM. Hamed RM. Saudi J Kidney Dis Transpl. 2003 Jul-Sep;14(3):328-35. Saudi J Kidney Dis Transpl. 2003. PMID: 17657104
A characteristic phenotype may be seen in children with CNS. The majority of reported cases of CNS are of the Finnish type (CNF). Although the role of the glomerular basement membrane has been emphasized as the barrier for retaining plasma proteins, recent studies have cle …
A characteristic phenotype may be seen in children with CNS. The majority of reported cases of CNS are of the Finnish type (CNF). Alt …
A zebrafish model of congenital nephrotic syndrome of the Finnish type.
Lee MS, Devi S, He JC, Zhou W. Lee MS, et al. Front Cell Dev Biol. 2022 Sep 14;10:976043. doi: 10.3389/fcell.2022.976043. eCollection 2022. Front Cell Dev Biol. 2022. PMID: 36187478 Free PMC article.
Mutations of NPHS1, encoding NEPHRIN, a podocyte protein essential for normal GFB, cause congenital nephrotic syndrome (CNS) of the Finnish type (CNF), which accounts for about 50% of CNS cases. We generated zebrafish nphs1 mutants by using CRISPR/Cas9. ...
Mutations of NPHS1, encoding NEPHRIN, a podocyte protein essential for normal GFB, cause congenital nephrotic syndrome (CNS) of the Finni …
Genetics of the nephrotic syndrome.
Salomon R, Gubler MC, Niaudet P. Salomon R, et al. Curr Opin Pediatr. 2000 Apr;12(2):129-34. doi: 10.1097/00008480-200004000-00008. Curr Opin Pediatr. 2000. PMID: 10763762 Review.
Familial forms of idiopathic nephrotic syndrome with focal and segmental glomerular sclerosis/hyalinosis have been identified with an autosomal dominant or recessive mode of inheritance and linkage analysis have allowed to localize several genes on chromosomes 1, 11 and 17. The g …
Familial forms of idiopathic nephrotic syndrome with focal and segmental glomerular sclerosis/hyalinosis have been identified with an autoso …
Congenital nephrotic syndrome: is early aggressive treatment needed? Yes.
Hölttä T, Jalanko H. Hölttä T, et al. Pediatr Nephrol. 2020 Oct;35(10):1985-1990. doi: 10.1007/s00467-020-04578-4. Epub 2020 May 6. Pediatr Nephrol. 2020. PMID: 32377865 Free PMC article. Review.
In Finland, early aggressive treatment protocol was adopted from the USA and further developed for treatment of children with the Finnish type of CNS. The aim of this review is to state reasons for "early aggressive treatment" including daily albumin infusions, intensified …
In Finland, early aggressive treatment protocol was adopted from the USA and further developed for treatment of children with the Finnish …
Congenital Nephrotic Syndrome of the Finnish Type in a Dominican Newborn: An Overview and Case Report.
Anderson S. Anderson S. Neonatal Netw. 2022 Mar 1;41(2):83-88. doi: 10.1891/11-T-745. Neonatal Netw. 2022. PMID: 35260424 Review.
Congenital nephrotic syndrome of the Finnish type (CNS-FT) is a rare genetic condition that causes massive proteinuria, hypoproteinemia, hypercholesterolemia, and edema that progresses to end-stage renal disease. ...
Congenital nephrotic syndrome of the Finnish type (CNS-FT) is a rare genetic condition that causes massive proteinuria, hypoproteinem …
Pathology of Podocytopathies Causing Nephrotic Syndrome in Children.
Ranganathan S. Ranganathan S. Front Pediatr. 2016 Mar 31;4:32. doi: 10.3389/fped.2016.00032. eCollection 2016. Front Pediatr. 2016. PMID: 27066465 Free PMC article. Review.
This review will restrict itself to the pathology of congenital NS, minimal change disease (MCD), and its variants and focal segmental glomerulosclerosis (FSGS). The two major types of congenital NS are Finnish type characterized by dilated sausage shaped tubules morpholog …
This review will restrict itself to the pathology of congenital NS, minimal change disease (MCD), and its variants and focal segmental glome …
Genetic basis of nephrotic syndrome--review.
Obeidová H, Merta M, Reiterová J, Maixnerová D, Stekrová J, Rysavá R, Tesar V. Obeidová H, et al. Prague Med Rep. 2006;107(1):5-16. Prague Med Rep. 2006. PMID: 16752799 Review.
In cases of mutation in NPHS1 gene, causing congenital nephrotic syndrome of the Finnish type (CNF), resistance to steroid therapy occurs regularly and recurrence of proteinuria after renal transplantation is about 20-25%. ...
In cases of mutation in NPHS1 gene, causing congenital nephrotic syndrome of the Finnish type (CNF), resistance to steroid therapy oc …
Gastric duplication cyst in an infant with Finnish-type congenital nephrotic syndrome: concurrence or coincidence?
Güngör T, Eroğlu FK, Kargın Çakıcı E, Yazılıtaş F, Can G, Çelikkaya E, Karakaya D, Kurt Şükür ED, Özaltın F, Yağız B, Bülbül M. Güngör T, et al. Acta Clin Belg. 2021 Apr;76(2):155-157. doi: 10.1080/17843286.2019.1675333. Epub 2019 Oct 5. Acta Clin Belg. 2021. PMID: 31587616
CNS can be caused by congenital infections, allo-immune maternal disease or due to the genetic defects of podocyte proteins most commonly NPHS1. Here we present a case of Finnish-type congenital nephrotic syndrome along with feeding problems and abdominal distention which …
CNS can be caused by congenital infections, allo-immune maternal disease or due to the genetic defects of podocyte proteins most commonly NP …
Cholelithiasis in infants with congenital nephrotic syndrome of the Finnish type.
Nada T, Sato M, Yoshikawa T, Ogura M, Kamei K. Nada T, et al. Pediatr Nephrol. 2021 Nov;36(11):3795-3798. doi: 10.1007/s00467-021-05225-2. Epub 2021 Aug 12. Pediatr Nephrol. 2021. PMID: 34383124
BACKGROUND: Congenital nephrotic syndrome of the Finnish type (CNF) caused by NPHS1 mutations is a rare disease. Infants with CNF can develop many complications, but hepatobiliary complications are uncommon. ...
BACKGROUND: Congenital nephrotic syndrome of the Finnish type (CNF) caused by NPHS1 mutations is a rare disease. Infants with CNF can …
296 results