Management of congenital nephrotic syndrome of the Finnish type.
about
Structure of the gene for congenital nephrotic syndrome of the finnish type (NPHS1) and characterization of mutationsNephrin localizes at the podocyte filtration slit area and is characteristically spliced in the human kidneyFyn binds to and phosphorylates the kidney slit diaphragm component NephrinInteraction with podocin facilitates nephrin signalingTiming of renal replacement therapy does not influence survival and growth in children with congenital nephrotic syndrome caused by mutations in NPHS1: data from the ESPN/ERA-EDTA Registry.Inducible nephrin transgene expression in podocytes rescues nephrin-deficient mice from perinatal deathClinico-pathological correlations of congenital and infantile nephrotic syndrome over twenty years.Mutations in the human laminin beta2 (LAMB2) gene and the associated phenotypic spectrum.Genetic kidney diseases disclose the pathogenesis of proteinuria.Extrarenal effects on the pathogenesis and relapse of idiopathic nephrotic syndrome in Buffalo/Mna ratsRelevance of VEGF and nephrin expression in glomerular diseases.Improved prognosis for congenital nephrotic syndrome of the Finnish type in Irish families.Congenital nephrotic syndrome responsive to captopril and indometacin.Fine mapping and haplotype analysis of the locus for congenital nephrotic syndrome on chromosome 19q13.1.Cloning and expression of the rat nephrin homolog.Congenital nephrotic syndrome of the finnish type.Cardiac findings in congenital nephrotic syndrome.Educational paper: the podocytopathies.Congenital nephrotic syndrome and recurrence of proteinuria after renal transplantation.Oedema in kwashiorkor is caused by hypoalbuminaemia.An update: the role of Nephrin inside and outside the kidney.Thyroid dysfunction and kidney disease: An update.Congenital Nephrotic Syndrome - Finish Type.Ultrastructural study on nephrin expression in experimental puromycin aminonucleoside nephrosis.Parent-child and spousal relationships in families with a young child with end-stage renal disease.Domiciliary administration of intravenous albumin in congenital nephrotic syndrome.Neurodevelopmental outcome in high-risk patients after renal transplantation in early childhood.Long-term outcome of congenital nephrotic syndrome after kidney transplantation in Japan.Genetic abnormalities and prognosis in patients with congenital and infantile nephrotic syndrome.Treatment of Genetic Forms of Nephrotic Syndrome.
P2860
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P2860
Management of congenital nephrotic syndrome of the Finnish type.
description
1995 nî lūn-bûn
@nan
1995年の論文
@ja
1995年論文
@yue
1995年論文
@zh-hant
1995年論文
@zh-hk
1995年論文
@zh-mo
1995年論文
@zh-tw
1995年论文
@wuu
1995年论文
@zh
1995年论文
@zh-cn
name
Management of congenital nephrotic syndrome of the Finnish type.
@en
type
label
Management of congenital nephrotic syndrome of the Finnish type.
@en
prefLabel
Management of congenital nephrotic syndrome of the Finnish type.
@en
P2093
P356
P1433
P1476
Management of congenital nephrotic syndrome of the Finnish type.
@en
P2093
K Rönnholm
M Ala Houhala
M Antikainen
P2888
P356
10.1007/BF00858984
P577
1995-02-01T00:00:00Z
P6179
1008028111