Literature DB >> 8476708

Persistent microscopic haematuria without proteinuria.

F A Flinter1.   

Abstract

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Year:  1993        PMID： 8476708     DOI： 10.1007/bf00864382

Source DB:  PubMed          Journal:  Pediatr Nephrol        ISSN： 0931-041X            Impact factor:   3.714


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  6 in total

1.  Renal disease, inner ear deafness, and ocular changes; a new heredofamilial syndrome.

Authors:  E SOHAR
Journal:  AMA Arch Intern Med       Date:  1956-05

2.  HEREDITARY FAMILIAL CONGENITAL HAEMORRHAGIC NEPHRITIS.

Authors:  A C Alport
Journal:  Br Med J       Date:  1927-03-19

3.  Identification of mutations in the COL4A5 collagen gene in Alport syndrome.

Authors:  D F Barker; S L Hostikka; J Zhou; L T Chow; A R Oliphant; S C Gerken; M C Gregory; M H Skolnick; C L Atkin; K Tryggvason
Journal:  Science       Date:  1990-06-08       Impact factor: 47.728

Review 4.  Genetics of classic Alport's syndrome.

Authors:  F A Flinter; J S Cameron; C Chantler; I Houston; M Bobrow
Journal:  Lancet       Date:  1988-10-29       Impact factor: 79.321

5.  Major rearrangements in the alpha 5(IV) collagen gene in three patients with Alport syndrome.

Authors:  E Boye; D Vetrie; F Flinter; B Buckle; T Pihlajaniemi; E R Hamalainen; J C Myers; M Bobrow; A Harris
Journal:  Genomics       Date:  1991-12       Impact factor: 5.736

6.  Ocular manifestations of Alport's syndrome: a hereditary disorder of basement membranes?

Authors:  J A Govan
Journal:  Br J Ophthalmol       Date:  1983-08       Impact factor: 4.638
  6 in total

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