Literature DB >> 4045606

Recurrent hemolytic-uremic syndrome with the hypomorphic fast allele of the third component of complement.

R J Wyatt, D Jones, F B Stapleton, S Roy, T W Odom, R H McLean.   

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Year:  1985        PMID： 4045606     DOI： 10.1016/s0022-3476(85)80022-6

Source DB:  PubMed          Journal:  J Pediatr        ISSN： 0022-3476            Impact factor:   4.406


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  6 in total

1.  Familial, recurrent haemolytic-uraemic syndrome with hypocomplementaemia.

Authors:  J Zachwieja; K Strzykala; W Golda; J Maciejewski
Journal:  Pediatr Nephrol       Date:  1992-03       Impact factor: 3.714

2.  Recurrent haemolytic-uraemic syndrome with hypocomplementaemia: a case report.

Authors:  R Bogdanović; A Cvorić; V Nikolić; M Sindjić
Journal:  Pediatr Nephrol       Date:  1988-04       Impact factor: 3.714

3.  A clinicopathological study of 24 children with hemolytic uremic syndrome. A report of the Southwest Pediatric Nephrology Study Group.

Authors:  J C Argyle; R J Hogg; T J Pysher; F G Silva; R L Siegler
Journal:  Pediatr Nephrol       Date:  1990-01       Impact factor: 3.714

4.  Recurrent haemolytic uraemic syndrome and acquired hypomorphic variant of the third component of complement.

Authors:  A M Roodhooft; R H McLean; E Elst; K J Van Acker
Journal:  Pediatr Nephrol       Date:  1990-11       Impact factor: 3.714

Review 5.  Complement and glomerulonephritis--an update.

Authors:  R H McLean
Journal:  Pediatr Nephrol       Date:  1993-04       Impact factor: 3.714

6.  Hereditary partial deficiency of the third component of complement associated with minimal change nephrotic syndrome.

Authors:  J E Springate; R H McLean; J A Winkelstein; L G Feld
Journal:  Pediatr Nephrol       Date:  1987-10       Impact factor: 3.714
  6 in total

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