Literature DB >> 5947587

Anterior lenticonus and Alport's syndrome.

E J Arnott, M D Crawfurd, P J Toghill.   

Abstract

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Mesh:

Year:  1966        PMID: 5947587      PMCID: PMC506241          DOI: 10.1136/bjo.50.7.390

Source DB:  PubMed          Journal:  Br J Ophthalmol        ISSN: 0007-1161            Impact factor:   4.638


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  43 in total

1.  [ALPORT'S SYNDROME OR HEREDITARY CHRONIC NEPHRITIS].

Authors:  R PETERS
Journal:  Maandschr Kindergeneeskd       Date:  1964-01

2.  ANTERIOR LENTICONUS; REPORT OF AN UNUSUAL CASE.

Authors:  W W JOHNSTONE
Journal:  Am J Ophthalmol       Date:  1963-12       Impact factor: 5.258

3.  [HEREDITARY NEPHRITIS (ALPORT'S SYNDROME)].

Authors:  A ROSENKRANZ
Journal:  Ann Paediatr       Date:  1963

4.  [ALPORT'S SYNDROME OR HEREDITARY NEPHRITIS WITH DEAFNESS].

Authors:  A TILIAKOS; D VOULGARIDIS; J GIALAFOS
Journal:  Presse Med       Date:  1964-05-27       Impact factor: 1.228

5.  [ALPORT'S SYNDROME (HEREDITARY NEPHROPATHIES WITH DEAFNESS AND OCULAR CHANGES)].

Authors:  D PERRIN
Journal:  Ann Ocul (Paris)       Date:  1964-04

6.  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

7.  [Familial syndrome of nephropathy with deafness].

Authors:  J HAMBURGER; J CROSNIER; J LISSAC; J NAFFAH
Journal:  J Urol Medicale Chir       Date:  1956-03

8.  Partially sex-linked cominant inheritance of interstitial pyelonephritis.

Authors:  F E STEPHENS; G T PERKOFF; D A DOLOWITZ; F H TYLER
Journal:  Am J Hum Genet       Date:  1951-12       Impact factor: 11.025

9.  Familial hyperprolinemia, cerebral dysfunction and renal anomalies occurring in a family with hereditary nephropathy and deafness.

Authors:  I A Schafer; C R Scriver; M L Efron
Journal:  N Engl J Med       Date:  1962-07-12       Impact factor: 91.245

10.  Alport's syndrome of hereditary nephritis with deafness.

Authors:  D A WILLIAMSON
Journal:  Lancet       Date:  1961-12-16       Impact factor: 79.321

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  18 in total

1.  Lenticonus in spina bifida. A case report.

Authors:  R G Powell
Journal:  Br J Ophthalmol       Date:  1975-09       Impact factor: 4.638

Review 2.  Mendelian inheritance or transmissible agent? The lesson Kuru and the Australia antigen.

Authors:  P S Harper
Journal:  J Med Genet       Date:  1977-12       Impact factor: 6.318

Review 3.  Alport syndrome, basement membranes and collagen.

Authors:  C E Kashtan; M M Kleppel; R J Butkowski; A F Michael; A J Fish
Journal:  Pediatr Nephrol       Date:  1990-09       Impact factor: 3.714

4.  A mutation causing Alport syndrome with tardive hearing loss is common in the western United States.

Authors:  D F Barker; C J Pruchno; X Jiang; C L Atkin; E M Stone; J C Denison; P R Fain; M C Gregory
Journal:  Am J Hum Genet       Date:  1996-06       Impact factor: 11.025

5.  Alport syndrome with phenotypic marfanoid habitus: atypical case series.

Authors:  N Agrawal; D P Nayak; P Gupta; A Haripriya; P Bhuwania
Journal:  Eye (Lond)       Date:  2014-12-05       Impact factor: 3.775

Review 6.  Alport's syndrome.

Authors:  M A Crawfurd
Journal:  J Med Genet       Date:  1988-09       Impact factor: 6.318

7.  Hereditary nephritis.

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

8.  The use of ocular abnormalities to diagnose X-linked Alport syndrome in children.

Authors:  Ke Wei Zhang; Deb Colville; Rachel Tan; Colin Jones; Stephen I Alexander; Jeffrey Fletcher; Judy Savige
Journal:  Pediatr Nephrol       Date:  2008-03-15       Impact factor: 3.714

9.  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

10.  Developmental distribution of collagen IV isoforms and relevance to ocular diseases.

Authors:  Xiaoyang Bai; David J Dilworth; Yi-Chinn Weng; Douglas B Gould
Journal:  Matrix Biol       Date:  2009-03-09       Impact factor: 11.583

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