Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Lutz Pelken"'
Autor:
Ulla Pechmann, Stefanie Weber, Daniel Lotan, Siegfried Waldegger, Shamima Rahman, Toshihiro Tajima, Hannsjoerg W. Seyberth, Lutz Pelken, Karl P. Schlingmann, Martin Konrad, San-Ging Shu, Daniel L. Metzger, David E. C. Cole, Martin Sassen, Maria Syrrou, Jeffrey J. Prebble, Kerstin Kusch
Publikováno v:
Journal of the American Society of Nephrology : JASN. 16(10)
Primary hypomagnesemia with secondary hypocalcemia is a rare autosomal recessive disorder characterized by profound hypomagnesemia associated with hypocalcemia. Pathophysiology is related to impaired intestinal absorption of magnesium accompanied by
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a17d0deffd266729057f9bd2e00c8c94
https://pubmed.ncbi.nlm.nih.gov/16107578
https://pubmed.ncbi.nlm.nih.gov/16107578
Autor:
J. Vormoor, Lutz Pelken, Heribert Jürgens, K L Schäfer, Cristian Rübe, Frans van Valen, Marc Hotfilder, Stephan Decker, Barbara Dockhorn-Dworniczak, G. Baersch
Publikováno v:
Pediatric research. 49(3)
Ewing tumors are a clinically heterogeneous group of childhood sarcomas that represent a paradigm for understanding solid tumor biology, as they are the first group of sarcomas for which a chromosome translocation has been characterized at the molecu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::79807756f3fcabd8406e8e0e80ede15e
https://pubmed.ncbi.nlm.nih.gov/11228258
https://pubmed.ncbi.nlm.nih.gov/11228258