Zobrazeno 1 - 10
of 124
pro vyhledávání: '"Lothar Bernd Zimmerhackl"'
Autor:
Magdalena Riedl, Verena Jeller, Reinhard Würzner, Lambert P. van den Heuvel, Günter Weiss, Alejandra Rosales, Tanja Maier, Karsten Häffner, Thomas Giner, Therese Jungraithmayr, Johannes Hofer, Ulrike Walden, Dorothea Heininger, Lothar Bernd Zimmerhackl, Giacomo D. Simonetti
Publikováno v:
Journal of Immunological Methods, 435, 60-67
Journal of Immunological Methods, 435, pp. 60-67
Journal of Immunological Methods, 435, pp. 60-67
Atypical hemolytic uremic syndrome (aHUS) is a devastating disease characterized by thrombus formation in the microvasculature and is associated with complement dysregulation. The recommended treatment is eculizumab, an humanized monoclonal antibody,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4359be348eba088f097c58c9bde4422e
https://doi.org/10.1016/j.jim.2016.05.009
https://doi.org/10.1016/j.jim.2016.05.009
Publikováno v:
Journal of Pediatric Infectious Diseases. :111-114
Despite advances in the management of severe sepsis, the mortality rate of septic shock in children and adults remains high. Meningococcal disease is the leading cause of sepsis affecting previously healthy children and young adults. In a septic infe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a7ac624ea3a5973a13c1bff2d519134e
https://doi.org/10.1055/s-0035-1557072
https://doi.org/10.1055/s-0035-1557072
Autor:
Alejandra, Rosales, Johannes, Hofer, Lothar-Bernd, Zimmerhackl, Therese C, Jungraithmayr, Magdalena, Riedl, Thomas, Giner, Alexander, Strasak, Dorothea, Orth-Höller, Reinhard, Würzner, Helge, Karch, R, Würzner
Publikováno v:
Clinical Infectious Diseases. 54:1413-1421
BACKGROUND The aim of this study was to evaluate the long-term prognosis of children with hemolytic uremic syndrome (HUS). METHODS Over a 6-year period, 619 pediatric patients with the clinical diagnosis of HUS were registered in Austria and Germany,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::27bf4181a99d1c6ae28e931795382c51
https://doi.org/10.1093/cid/cis196
https://doi.org/10.1093/cid/cis196
Autor:
Lothar Bernd Zimmerhackl, Therese Jungraithmayr, Matthias Frosch, Martina Prelog, Johannes Elias, Ulrich Vogel, Johannes Hofer, Manuela Zlamy
Publikováno v:
Pediatric Transplantation. 16:E246-E250
We report successful kidney transplantation in a 10-yr-old boy with aHUS and heterozygous factor H mutation using the terminal complement inhibitor eculizumab to avoid recurrence of aHUS in the renal graft. Vaccination against meningococcus C (Men C)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e047908f8c662caac300149ce9de19c5
https://doi.org/10.1111/j.1399-3046.2011.01585.x
https://doi.org/10.1111/j.1399-3046.2011.01585.x
Autor:
Lutz T. Weber, Eileen Tsai, Dirk Kuypers, Burkhard Tönshoff, Lothar Bernd Zimmerhackl, Elias David-Neto, Jens Goebel, Alexander A. Vinks, Guido Filler, Robert B. Ettenger, Teun van Gelder
Publikováno v:
Transplantation Reviews, 25(2), 78-89. W.B. Saunders
Mycophenolate mofetil (MMF) is widely used for maintenance immunosuppressive therapy in pediatric renal and heart transplant recipients. Children undergo developmental changes (ontogeny) of drug disposition, which may affect drug metabolism of the ac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8fde06f49ac14a4f5184867852143e3a
https://pure.eur.nl/en/publications/a7cbe2f4-4280-4cdd-ace4-88e26832518e
https://pure.eur.nl/en/publications/a7cbe2f4-4280-4cdd-ace4-88e26832518e
Publikováno v:
Klinische Pädiatrie. 222:302-307
BACKGROUND: Lyme neuroborreliosis (LNB) is the second most common manifestation of Borrelia burgdorferi sensu lato (s. l.) infection in Europe. LNB is difficult to differentiate from other aetiologies of aseptic meningitis. Diagnostic criteria for LN
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3bbabc305bca82dd9f036a451ec14158
https://doi.org/10.1055/s-0030-1249091
https://doi.org/10.1055/s-0030-1249091
Autor:
Gerda Falkensammer, Andrea Griesmacher, Gerhard Luef, Markus Rauchenzauner, Wolfgang Högler, Lothar-Bernd Zimmerhackl, Edda Haberlandt, Tobias Tatarczyk, Alexander Strasak
Publikováno v:
Developmental Medicine & Child Neurology. 52:283-288
Aim The aim of this study was to determine the influence of chronic monotherapy with antiepileptic drugs (AEDs) on vitamin D levels, bone metabolism, and body composition. Method Eighty-five children (38 males, 47 females; mean age 12y 5mo, SD 3y 4mo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a021c2cb69872d6a9cbd3aadc1df13c3
https://doi.org/10.1111/j.1469-8749.2009.03402.x
https://doi.org/10.1111/j.1469-8749.2009.03402.x
Publikováno v:
Pediatric Transplantation. 14:41-47
Reports about efficacy and safety of live-virus attenuated vaccines in patients before and after transplantation are mainly based on small patient numbers, making general recommendations for this patient population difficult. Children and adults as w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::12648814a03c0967ff716b2bd28ea999
https://doi.org/10.1111/j.1399-3046.2009.01204.x
https://doi.org/10.1111/j.1399-3046.2009.01204.x
Autor:
Elisabeth Steichen, Deborah J G Mackay, Barbara Wiedemann, Julia Koehle, Dagmar Meraner, Lothar-Bernd Zimmerhackl, Sarah E. Flanagan, Sian Ellard, Edith Schober, Andrew T. Hattersley, Thomas Waldhoer, Sabine E. Hofer
Publikováno v:
Pediatric Diabetes. 11:18-23
Background: Neonatal diabetes mellitus (NDM) is a rare monogenic form of diabetes which is diagnosed in the first 6 months of life. Several studies in the last few years provide information on genetic causes for NDM. Objective: The aim of this study
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7169ca71f3dd9ebe3ad3a42c9b9b0296
https://doi.org/10.1111/j.1399-5448.2009.00530.x
https://doi.org/10.1111/j.1399-5448.2009.00530.x
Autor:
Lothar Bernd Zimmerhackl, Verena Fally, Karl Lhotta, Véronique Frémeaux-Bacchi, Reinhard Würzner, Johanna Scheiring, Gert Mayer, Thomas Giner, Andreas R. Janecke, Barbara Petzlberger
Publikováno v:
Clinical Journal of the American Society of Nephrology. 4:1356-1362
Background and objectives: Atypical hemolytic uremic syndrome (aHUS) is associated with mutations in genes encoding complement-regulatory proteins factor H, I and B and membrane cofactor protein. Recently, heterozygous gain-of-function mutations in t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::83019115f84c686a40dbb137e6e1e00b
https://doi.org/10.2215/cjn.06281208
https://doi.org/10.2215/cjn.06281208