Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Kristina Moeller"'
Autor:
Tomáš Seeman, Kristina Moeller, Shivani Joshi, Trine Korsgaard, Søren Rittig, Ludmila Podracka, Hans Eiberg, René Frydensbjerg Andersen
Publikováno v:
Korsgaard, T, Joshi, S, Andersen, R F, Moeller, K, Seeman, T, Podracká, L, Eiberg, H & Rittig, S 2020, ' Human leukocyte antigen association with familial steroid-sensitive nephrotic syndrome ', European Journal of Pediatrics, vol. 179, no. 9, pp. 1481-1486 . https://doi.org/10.1007/s00431-020-03634-3
Steroid-sensitive nephrotic syndrome (SSNS) is the most common form of nephrotic syndrome in childhood. Cases with the familial occurrence of SSNS suggest that genetics may play a role in the disease. Human leucocyte antigen (HLA) alleles have been a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e5a43ae45477d337deb39fff97ea9ad8
https://doi.org/10.1007/s00431-020-03634-3
https://doi.org/10.1007/s00431-020-03634-3
Autor:
Christina Nießl, Anne-Laure Boulesteix, Jun Oh, Katja Palm, Peter Schlingmann, Simone Wygoda, Dieter Haffner, Elke Wühl, Burkhard Tönshoff, Anja Buescher, Heiko Billing, Bernd Hoppe, Matthias Zirngibl, Matthias Kettwig, Kristina Moeller, Birgit Acham-Roschitz, Klaus Arbeiter, Martin Bald, Marcus Benz, Matthias Galiano, Ulrike John-Kroegel, Guenter Klaus, Daniela Marx-Berger, Katja Moser, Dirk Mueller, Ludwig Patzer, Martin Pohl, Barbara Seitz, Ulrike Treikauskas, Rodo O. von Vigier, William Allen Gahl, Katharina Hohenfellner
Infantile nephropathic cystinosis, due to impaired transport of cystine out of lysosomes, occurs with an incidence of 1 in 100–200,000 live births. It is characterized by renal Fanconi syndrome in the first year of life and glomerular dysfunction p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f153907d5bb7c1cde126a1c1be60a4b3
https://www.ncbi.nlm.nih.gov/pubmed/35835062
https://www.ncbi.nlm.nih.gov/pubmed/35835062
