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Genetic analysis and functional characterization of novel mutations in a series of patients with atypical hemolytic uremic syndrome.
Szarvas, Nóra; Szilágyi, Ágnes; Csuka, Dorottya; Takács, Beáta; Rusai, Krisztina; Müller, Thomas; Arbeiter, Klaus; Réti, Marienn; Haris, Ágnes; Wagner, László; Török, Szilárd; Kelen, Kata; Szabó, Attila J; Reusz, György S; Morgan, B Paul; Prohászka, Zoltán.
Affiliation
  • Szarvas N; 3rd Department of Internal Medicine, Semmelweis University, Budapest, Hungary.
  • Szilágyi Á; 3rd Department of Internal Medicine, Semmelweis University, Budapest, Hungary.
  • Csuka D; 3rd Department of Internal Medicine, Semmelweis University, Budapest, Hungary.
  • Takács B; 3rd Department of Internal Medicine, Semmelweis University, Budapest, Hungary.
  • Rusai K; Department of Pediatrics, Medical University Vienna, Austria.
  • Müller T; Department of Pediatrics, Medical University Vienna, Austria.
  • Arbeiter K; Department of Pediatrics, Medical University Vienna, Austria.
  • Réti M; Department of Hematology and Stem Cell Transplantation, St. István and St. László Hospital, Budapest, Hungary.
  • Haris Á; Department of Nephrology, St. Margit Hospital, Budapest, Hungary.
  • Wagner L; Department of Transplantation and Surgery, Semmelweis University, Budapest, Hungary.
  • Török S; Department of Transplantation and Surgery, Semmelweis University, Budapest, Hungary.
  • Kelen K; 1st Department of Pediatrics, Semmelweis University, Budapest, Hungary.
  • Szabó AJ; 1st Department of Pediatrics, Semmelweis University, Budapest, Hungary.
  • Reusz GS; 1st Department of Pediatrics, Semmelweis University, Budapest, Hungary.
  • Morgan BP; Complement Biology Group, Institute of Infection and Immunity, School of Medicine, Cardiff University, Cardiff, UK.
  • Prohászka Z; 3rd Department of Internal Medicine, Semmelweis University, Budapest, Hungary. Electronic address: prohaszka.zoltan@med.semmelweis-univ.hu.
Mol Immunol ; 71: 10-22, 2016 Mar.
Article in En | MEDLINE | ID: mdl-26826462
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Complement Factor H / Genetic Predisposition to Disease / Atypical Hemolytic Uremic Syndrome / Mutation Type of study: Prognostic_studies / Risk_factors_studies Limits: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male / Middle aged / Newborn Language: En Journal: Mol Immunol Year: 2016 Document type: Article Affiliation country: Hungary Country of publication: United kingdom
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Complement Factor H / Genetic Predisposition to Disease / Atypical Hemolytic Uremic Syndrome / Mutation Type of study: Prognostic_studies / Risk_factors_studies Limits: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male / Middle aged / Newborn Language: En Journal: Mol Immunol Year: 2016 Document type: Article Affiliation country: Hungary Country of publication: United kingdom