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Titlebook: Klinische Mikrobiologie für den Urologen; Ein Leitfaden für da Holger Blenk,Alfons G. Hofstetter,Winfried Vahlens Book 1997 Springer-Verlag

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發(fā)表于 2025-3-25 07:01:17 | 只看該作者
,Bezugsquellen für Labormaterial, N?hrmedien, Reagenzien,
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發(fā)表于 2025-3-25 20:16:37 | 只看該作者
Holger Blenk,Alfons G. Hofstetter,Kurt G. Naber,Winfried Vahlensieck Jr.ence, thyroid hormone actions are impaired at the tissue level. The phenotypic manifestations of RTHβ and RTHα are to some extent correlated with the degree of disruption and the tissue distribution of the TRs being characterized by variable coexistence of hypothyroid or thyrotoxic manifestations in
26#
發(fā)表于 2025-3-26 01:44:51 | 只看該作者
Holger Blenk,Alfons G. Hofstetter,Kurt G. Naber,Winfried Vahlensieck Jr. fails to operate the normal function of AVP-V2R-AQP2 system, it can result in various diseases such as diabetes insipidus (DI) or nephrogenic syndrome of inappropriate diuresis (NSIAD). The DI is characterized by excessive production of hyposmotic urine (“insipidus” means tasteless) due to the inab
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28#
發(fā)表于 2025-3-26 12:25:45 | 只看該作者
Holger Blenk,Alfons G. Hofstetter,Kurt G. Naber,Winfried Vahlensieck Jr. fails to operate the normal function of AVP-V2R-AQP2 system, it can result in various diseases such as diabetes insipidus (DI) or nephrogenic syndrome of inappropriate diuresis (NSIAD). The DI is characterized by excessive production of hyposmotic urine (“insipidus” means tasteless) due to the inab
29#
發(fā)表于 2025-3-26 15:30:07 | 只看該作者
Holger Blenk,Alfons G. Hofstetter,Kurt G. Naber,Winfried Vahlensieck Jr.her hand, undiagnosed, hormonally active Pheos may lead to severe, or even lethal, consequences. This chapter will summarize our recent knowledge about the genetics of Pheo/PGL, focusing on tumor syndromes where Pheo/PGLs are among the main manifestations.
30#
發(fā)表于 2025-3-26 17:23:33 | 只看該作者
Holger Blenk,Alfons G. Hofstetter,Kurt G. Naber,Winfried Vahlensieck Jr.d cornea, while POAG involves a block in the trabecular meshwork due to malfunction. PCG (also known as buphthalmos) is a rare form of developmental glaucoma which occurs due to defects in the development of the trabecular meshwork (TM), in the absence of any other ocular anomalies.
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