Literature DB >> 6047603

Main features of the congenital nephrotic syndrome.

N Hallman, R Norio, K Kouvalainen.   

Abstract

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Year:  1967        PMID: 6047603     DOI: 10.1111/j.1651-2227.1967.tb15279.x

Source DB:  PubMed          Journal:  Acta Paediatr Scand        ISSN: 0001-656X


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  9 in total

1.  Congenital nephrotic syndrome of Finnish type. Study of 75 patients.

Authors:  N P Huttunen
Journal:  Arch Dis Child       Date:  1976-05       Impact factor: 3.791

2.  Enzyme changes in experimental renal microcystic disease.

Authors:  J E McGeoch; E M Darmady
Journal:  Br J Exp Pathol       Date:  1973-10

3.  Congenital nephrotic syndrome and renal vein thrombosis in infancy.

Authors:  F Alexander; W A Campbell
Journal:  J Clin Pathol       Date:  1971-02       Impact factor: 3.411

4.  Congenital nephrotic syndrome of the Finnish type maps to the long arm of chromosome 19.

Authors:  M Kestilä; M Männikkö; C Holmberg; G Gyapay; J Weissenbach; E R Savolainen; L Peltonen; K Tryggvason
Journal:  Am J Hum Genet       Date:  1994-05       Impact factor: 11.025

5.  Morphologic considerations on the placenta in congenital nephrotic syndrome of Finnish type.

Authors:  C Inferrera; G Barresi; S Chimicata; F De Luca; G Baviera; V Gulli; M Gemelli
Journal:  Virchows Arch A Pathol Anat Histol       Date:  1980

6.  Nephrin localizes at the podocyte filtration slit area and is characteristically spliced in the human kidney.

Authors:  H Holthöfer; H Ahola; M L Solin; S Wang; T Palmen; P Luimula; A Miettinen; D Kerjaschki
Journal:  Am J Pathol       Date:  1999-11       Impact factor: 4.307

7.  No evidence for genotype/phenotype correlation in NPHS1 and NPHS2 mutations.

Authors:  Michael Schultheiss; Rainer G Ruf; Bettina E Mucha; Roger Wiggins; Arno Fuchshuber; Anne Lichtenberger; Friedhelm Hildebrandt
Journal:  Pediatr Nephrol       Date:  2004-12       Impact factor: 3.714

8.  Protein and lipid metabolism in nephrotic infants on peritoneal dialysis after nephrectomy.

Authors:  M Antikainen
Journal:  Pediatr Nephrol       Date:  1993-08       Impact factor: 3.714

9.  A comprehensive analysis of NPHS1 gene mutations in patients with sporadic focal segmental glomerulosclerosis.

Authors:  Ling Zhuo; Lulin Huang; Zhenglin Yang; Guisen Li; Li Wang
Journal:  BMC Med Genet       Date:  2019-06-19       Impact factor: 2.103

  9 in total

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