Severe deficiency of the specific von Willebrand factor-cleaving protease (ADAMTS 13) activity in a subgroup of children with atypical hemolytic uremic syndrome

Author:

Veyradier Agnès,Obert Bernadette,Haddad Elie,Cloarec Sylvie,Nivet Hubert,Foulard Michel,Lesure François,Delattre Pierre,Lakhdari Mustapha,Meyer Dominique,Girma Jean-Pierre,Loriat Chantal

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology and Child Health

Reference39 articles.

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2. Thrombotic microangiopathy, hemolytic-uremic syndrome, and thrombotic thrombocytopenic purpura;Ruggenenti;Kidney Int,2001

3. Atypical hemolytic-uremic syndrome: A comparison with postdiarrheal disease;Siegler;J Pediatr,1996

4. Heterogeneity of atypical haemolytic uraemic syndrome;Neuhaus;Arch Dis Child,1997

5. Remethylation defects: Guidelines for clinical diagnosis and treatment;Ogier de Baulny;Eur J Pediatr,1998

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