The homozygous leu variant of the factor XIII Val34Leu polymorphism as a risk factor for the manifestation of thrombotic microangiopathies.
Sucker, Christoph; Farokhzad, Firuseh; Kurschat, Christine; Grabensee, Bernd; Scharf, Rudiger E; Zotz, Rainer B; Maruhn-Debowski, Beate; Hetzel, Gerd R.
Clin Appl Thromb Hemost
; 15(2): 197-200, 2009 Mar-Apr.
Artigo em Inglês | MEDLINE | ID: mdl-17895511
Siblings with congenital thrombotic thrombocytopenic purpura.
Thrombotic thrombocytopenic purpura.
Kongenital trombotisk trombocytopenisk purpura.
Congenital and acquired ADAMTS13 deficiency: Two mechanisms, one patient.
Modified Ham test for atypical hemolytic uremic syndrome.
Acquired autoimmune thrombotic thrombocytopenic purpura.
A Severe Case of Congenital Thrombotic Thrombocytopenia Purpura Resulting From Compound Heterozygosity Involving a Novel ADAMTS13 Pathogenic Variant.
Inherited thrombotic thrombocytopenic purpura in children.
Long-Term Prevention of Congenital Thrombotic Thrombocytopenic Purpura in ADAMTS13 Knockout Mice by Sleeping Beauty Transposon-Mediated Gene Therapy.
ADAMTS13 and von Willebrand factor in thrombotic thrombocytopenic purpura.