Hemolytic-uremic syndrome: hereditary forms and forms associated with hereditary diseases.

Advances in nephrology from the Necker Hospital

Volumn 30, Issue , 2000, Pages 261-280

  Niaudet, P ^a   Gagnadoux, M F ^a   Broyer, M ^a   Salomon, R ^a  

^a UNIVERSITÉ PARIS DESCARTES   (France)

Author keywords

[No Author keywords available]

Indexed keywords

5 METHYLTETRAHYDROFOLATE HOMOCYSTEINE METHYLTRANSFERASE; COMPLEMENT; COMPLEMENT FACTOR H; COMPLEMENT FACTOR H, HUMAN; CYANOCOBALAMIN;

DOMINANT GENE; GENETIC DISORDER; GENETICS; HEMOLYTIC UREMIC SYNDROME; HUMAN; INBORN ERROR OF METABOLISM; METABOLISM; MUTATION; PHYSIOLOGY; RECESSIVE GENE; REVIEW;

5-METHYLTETRAHYDROFOLATE-HOMOCYSTEINE S-METHYLTRANSFERASE; COMPLEMENT FACTOR H; COMPLEMENT SYSTEM PROTEINS; GENES, DOMINANT; GENES, RECESSIVE; GENETIC DISEASES, INBORN; HEMOLYTIC-UREMIC SYNDROME; HUMANS; METABOLISM, INBORN ERRORS; MUTATION; VITAMIN B 12;

EID: 0034566801     PISSN: 00845957     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review

References (118)