Complement Regulatory Genetic Mutations in the Setting of Autoimmune Thrombotic Thrombocytopenic Purpura: A Case Series.

Atrash, Shebli; Sasapu, Appalanaidu; Pandey, Soumya; Cottler-Fox, Michele; Motwani, Pooja

Atrash, Shebli; Sasapu, Appalanaidu; Pandey, Soumya; Cottler-Fox, Michele; Motwani, Pooja.

Afiliación

Atrash S; Division of Hematology, Levine Cancer Institute, Carolinas HealthCare System, Charlotte, NC.
Sasapu A; Department of Medicine, Division of Hematology/Oncology, University of Arkansas for Medical Sciences, Little Rock.
Pandey S; Department of Medicine, Division of Hematology/Oncology, University of Arkansas for Medical Sciences, Little Rock.
Cottler-Fox M; Department of Pathology, University of Arkansas for Medical Sciences, Little Rock.
Motwani P; Department of Pathology, University of Arkansas for Medical Sciences, Little Rock.

Mayo Clin Proc Innov Qual Outcomes ; 2(1): 69-73, 2018 Mar.

Article en En | MEDLINE | ID: mdl-30225434

Palabras clave

ADAMTS13, disintegrin and metalloproteinase with a thrombospondin type 1 motif, member 13; BU, Bethesda units; CF, complement factor; CFHR, complement factor Hrelated; HUS, hemolytic uremic syndrome; TMA, thrombotic microangiopathy; TPE, therapeutic plasma exchange; TTP, thrombotic thrombocytopenic purpura; aHUS, atypical hemolytic uremic syndrome; iTTP, autoimmune thrombotic thrombocytopenic purpura

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Texto completo: 1 Bases de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: Mayo Clin Proc Innov Qual Outcomes Año: 2018 Tipo del documento: Article País de afiliación: Nueva Caledonia

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