Literature DB >> 5763827

Familial nephritis associated with the nephrotic syndrome. In a family with severe involvement in females.

M S Albert, J M Leeming, H J Wigger.   

Abstract

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Mesh：

Year:  1969        PMID： 5763827     DOI： 10.1001/archpedi.1969.02100030155006

Source DB:  PubMed          Journal:  Am J Dis Child        ISSN： 0002-922X


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  6 in total

1.  A locus for an autosomal dominant form of progressive renal failure and hypertension at chromosome 1q21.

Authors:  D H Cohn; T Shohat; M Yahav; T Ilan; G Rechavi; L King; M Shohat
Journal:  Am J Hum Genet       Date:  2000-08-04       Impact factor: 11.025

2.  Hereditary nephritis.

Authors: 
Journal:  Br Med J       Date:  1972-08-12

3.  A family showing hereditary nephropathy.

Authors:  H Pashayan; F C Fraser; R B Goldbloom
Journal:  Am J Hum Genet       Date:  1971-11       Impact factor: 11.025

4.  Alport's syndrome as a cause of renal failure in Europe.

Authors:  N Gretz; M Broyer; F P Brunner; H Brynger; R A Donckerwolcke; C Jacobs; P Kramer; N H Selwood; A J Wing
Journal:  Pediatr Nephrol       Date:  1987-07       Impact factor: 3.714

Review 5.  Women and Alport syndrome.

Authors:  Michelle N Rheault
Journal:  Pediatr Nephrol       Date:  2011-03-05       Impact factor: 3.714

6.  The variable course of women with X-linked Alport Syndrome.

Authors:  Priya Raju; David Cimbaluk; Stephen M Korbet
Journal:  Clin Kidney J       Date:  2013-08-26
  6 in total

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