Literature DB >> 14165881

HEREDITARY NEPHROPATHY (ALPORT'S SYNDROME). A CAUSE OF HEMATURIA IN CHILDHOOD.

J G ELLIS, S J YAFFE.   

Abstract

Entities:  

Keywords:  ALPORT'S SYNDROME; CHILD; DEAFNESS; GENETICS, HUMAN; HEMATURIA; NEPHRITIS

Mesh：

Year:  1964        PMID： 14165881      PMCID： PMC1515499     

Source DB:  PubMed          Journal:  Calif Med        ISSN： 0008-1264


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  5 in total

1.  Hereditary nephropathy, deafness and renal foam cells.

Authors:  R E WHALEN; S HUANG; E PESCHEL; H D McINTOSH
Journal:  Am J Med       Date:  1961-08       Impact factor: 4.965

2.  A follow-up study of hereditary chronic nephritis.

Authors:  G T PERKOFF; C A NUGENT; D A DOLOWITZ; F E STEPHENS; W H CARNES; F H TYLER
Journal:  AMA Arch Intern Med       Date:  1958-11

3.  Hereditary renal disease associated with nerve deafness and ocular lesions.

Authors:  R B GOLDBLOOM; F C FRASER; D WAUGH; M ARONOVITCH; F W WIGLESWORTH
Journal:  Pediatrics       Date:  1957-08       Impact factor: 7.124

4.  Congenital hereditary hematuria.

Authors:  G C REYERSBACH; A M BUTLER
Journal:  N Engl J Med       Date:  1954-09-02       Impact factor: 91.245

5.  A clinical study of hereditary interstitial pyelonephritis.

Authors:  G T PERKOFF; F E STEPHENS; D A DOLOWITZ; F H TYLER
Journal:  AMA Arch Intern Med       Date:  1951-08
  5 in total
  1 in total

1.  Anterior lenticonus and Alport's syndrome.

Authors:  E J Arnott; M D Crawfurd; P J Toghill
Journal:  Br J Ophthalmol       Date:  1966-07       Impact factor: 4.638
  1 in total

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