Rezultati - Thomas Giner

  • Showing 1 - 5 results of 5
Refine Results
  1. 1
    Complement Factor H-Antibody–Associated Hemolytic Uremic Syndrome: Pathogenesis, Clinical Presentation, and Treatment

    Complement Factor H-Antibody–Associated Hemolytic Uremic Syndrome: Pathogenesis, Clinical Presentation, and Treatment od Thomas Giner, Mihály Józsi, Johannes Hofer

    Izdano 2014
    Polni tekst
    Revisão
    Dodaj v priljubljene
    Shranjeno v:
  2. 2
    Extra-Renal Manifestations of Complement-Mediated Thrombotic Microangiopathies

    Extra-Renal Manifestations of Complement-Mediated Thrombotic Microangiopathies od Johannes Hofer, Alejandra Rosales, Caroline Fischer, Thomas Giner

    Izdano 2014
    Polni tekst Polni tekst
    Revisão
    Dodaj v priljubljene
    Shranjeno v:
  3. 3
    Need for Long-term Follow-up in Enterohemorrhagic Escherichia coli–Associated Hemolytic Uremic Syndrome Due to Late-Emerging Sequelae

    Need for Long-term Follow-up in Enterohemorrhagic Escherichia coli–Associated Hemolytic Uremic Syndrome Due to Late-Emerging Sequelae od Alejandra Rosales, Johannes Hofer, Lothar‐Bernd Zimmerhackl, Therese Jungraithmayr, Magdalena Riedl, Thomas Giner, Alexander Strasak, Dorothea Orth‐Höller, Reinhard Würzner, Helge Karch

    Izdano 2012
    Polni tekst
    Artigo
    Dodaj v priljubljene
    Shranjeno v:
  4. 4
    Complement Factor H–Related Protein 1 Deficiency and Factor H Antibodies in Pediatric Patients with Atypical Hemolytic Uremic Syndrome

    Complement Factor H–Related Protein 1 Deficiency and Factor H Antibodies in Pediatric Patients with Atypical Hemolytic Uremic Syndrome od Johannes Hofer, Andreas Janecke, Lothar Bernd Zimmerhackl, Magdalena Riedl, Alejandra Rosales, Thomas Giner, Gérard Cortina, Carola J. Haindl, Barbara Petzelberger, Miriam Pawlik, Verena Jeller, Udo Vester, Bettina Gadner, Michael van Husen, Michael L. Moritz, Reinhard Würzner, Therese Jungraithmayr

    Izdano 2012
    Polni tekst
    Artigo
    Dodaj v priljubljene
    Shranjeno v:
  5. 5
    Deficiency of the sphingosine-1-phosphate lyase SGPL1 is associated with congenital nephrotic syndrome and congenital adrenal calcifications

    Deficiency of the sphingosine-1-phosphate lyase SGPL1 is associated with congenital nephrotic syndrome and congenital adrenal calcifications od Andreas Janecke, Ruijuan Xu, Elisabeth Steichen‐Gersdorf, Siegfried Waldegger, Andreas Entenmann, Thomas Giner, Iris M. Krainer, Lukas A. Huber, Michael W. Hess, Yaacov Frishberg, Hila Barash, Shay Tzur, Nira Schreyer‐Shafir, Rivka Sukenik‐Halevy, Tania Zehavi, Annick Raas‐Rothschild, Cungui Mao, Thomas Müller

    Izdano 2017
    Polni tekst
    Artigo
    Dodaj v priljubljene
    Shranjeno v:

Iskalna orodja: