Zobrazeno 1 - 10
of 87
pro vyhledávání: '"Nauck, Markus"'
Autor:
Kim, Hyon Suk, Chen, Xinyue, Xu, Min, Yan, Cunling, Liu, Yali, Deng, Haohui, Hoang, Bui Huu, Thuy, Pham Thi Thu, Wang, Terry, Yan, Yiwen, Zeng, Zhen, Gencay, Mikael, Westergaard, Gaston, Pabinger, Stephan, Kriegner, Albert, Nauck, Markus, Seffner, Anja, Gohl, Peter, Hübner, Kirsten, Kaminski, Wolfgang E.
Publikováno v:
In Journal of Clinical Virology June 2018 103:48-56
Autor:
Gencay, Mikael, Vermeulen, Marion, Neofytos, Dionysis, Westergaard, Gaston, Pabinger, Stephan, Kriegner, Albert, Seffner, Anja, Gohl, Peter, Huebner, Kirsten, Nauck, Markus, Kaminski, Wolfgang E.
Publikováno v:
In Journal of Clinical Virology April 2018 101:38-43
Autor:
Roth, Michael, Nauck, Markus, Tamm, Michael, Perruchoud, Andre P., Ziesche, Rolf, Blck, Lutz H.
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, 1995 Feb . 92(5), 1312-1316.
Externí odkaz:
https://www.jstor.org/stable/2366772
Autor:
Ziesche, Rolf, Roth, Michael, Papakonstantinou, Eleni, Nauck, Markus, Horl, Walter H., Kashgarian, Michael, Block, Lutz H.
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, 1994 Jan 01. 91(1), 301-305.
Externí odkaz:
https://www.jstor.org/stable/2363788
Autor:
Arndt, Torsten, Guessregen, Brunhilde, Hallermann, Dörte, Nauck, Markus, Terjung, Dirk, Weckesser, Holger
Publikováno v:
In Forensic Science International 2008 175(1):27-30
Publikováno v:
In Clinica Chimica Acta 2006 372(1):184-187
Autor:
Pilz, Stefan, Maerz, Winfried, Weihrauch, Gisela, Sargsyan, Karine, Almer, Gunter, Nauck, Markus, Boehm, Bernhard O., Winkelmann, Bernhard R., Mangge, Harald
Publikováno v:
In Clinica Chimica Acta 2006 364(1):251-255
Autor:
Eisenberger Tobias, Slim Rima, Mansour Ahmad, Nauck Markus, Nürnberg Gudrun, Nürnberg Peter, Decker Christian, Dafinger Claudia, Ebermann Inga, Bergmann Carsten, Bolz Hanno
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 7, Iss 1, p 59 (2012)
Abstract Background Usher syndrome (USH) is an autosomal recessive genetically heterogeneous disorder with congenital sensorineural hearing impairment and retinitis pigmentosa (RP). We have identified a consanguineous Lebanese family with two affecte
Externí odkaz:
https://doaj.org/article/e2f4483210944afc8241d9b2871bc3f1
Autor:
Scharnagl, Hubert *, Schliack, Michael, Löser, Roland, Nauck, Markus, Gierens, Hedi, Jeck, Nikola, Wieland, Heinrich, Groß, Werner, März, Winfried
Publikováno v:
In Atherosclerosis 2000 153(1):69-80
Autor:
Nauck, Markus S. *, Scharnagl, Hubert, Nissen, Henrik, Schürmann, Christine, Mattern, Dirk, Nauck, Matthias A., Wieland, Heinrich, März, Winfried
Publikováno v:
In Atherosclerosis 2000 151(2):525-534