Zobrazeno 1 - 10 of 268 pro vyhledávání: '"I. Walter-Sack"'
1
Basal and pulsatile secretion of human luteinizing hormone — New methods for the analysis of endocrine secretion processes
Autor: B. Runnebaum, I. Walter-Sack, T. N. Rabe, M. W. F. Schweizer
Publikováno v: Experimental and Clinical Endocrinology & Diabetes. 104:235-242
Serum concentrations of hormones show typical time-dependent patterns. The diurnal course of the serum concentrations of the luteinizing hormone (LH) was assessed in 35 healthy females monitoring individual concentrations every ten minutes for 24 hou
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4e92b0c0f5707b82893099564e3da2dd
https://doi.org/10.1055/s-0029-1211448
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3
Sekundäre Resistenz gegen Cumarinderivate bei einer Patientin mit Hyperkoagulabilitäts-Syndrom
Autor: I. Walter-Sack, Reinhard Ziegler, D. Maclachlan, O. Haisken, H. Kather, Peter P. Nawroth, K. Andrassy, C. Marburger, J. X. Devries
Publikováno v: DMW - Deutsche Medizinische Wochenschrift. 122:959-964
HISTORY AND CLINICAL FINDINGS A 23-year-old woman with deep (leg) vein thrombosis was hospitalised because the Quick value had not decreased despite administration of phenprocoumon. Two years previously she had sustained an anterior wall myocardial i
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::faf0fa670a9778157650144930ece14d
https://doi.org/10.1055/s-2008-1047715
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4
[Ethical and legal aspects of including patients unable to consent in acute therapy studies. Example of a medication study for the treatment of intracerebral hemorrhage--the Heidelberg procedure]
Autor: T, Steiner, I, Walter-Sack, J, Taupitz, W, Hacke, T, Strowitzki
Publikováno v: Deutsche medizinische Wochenschrift (1946). 133(15)
Clinical trials in patients who cannot sign an informed consent are only possible under certain circumstances. The present paper explains the legal prerequisites and ethic rationales, which may allow including patients in such a trial without having
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::e3a3a7281748dc3511272808754498bb
https://pubmed.ncbi.nlm.nih.gov/18382954
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5
[Drugs during pregnancy and breastfeeding: new risk categories--antibiotics as a model]
Autor: T, Bertsche, M, Haas, H, Oberwittler, W E, Haefeli, I, Walter-Sack
Publikováno v: Deutsche medizinische Wochenschrift (1946). 131(18)
In selecting drugs for treatment during pregnancy and breastfeeding it is essential to be certain of their safety. But categories are lacking that systematically relate the current state of knowledge of individual substances--rather than just drug cl
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::f3b9cc72cab9ffc7ad63ec88049b0eca
https://pubmed.ncbi.nlm.nih.gov/16673226
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7
[Consideration of drug absorption in customizing drug therapy]
Autor: I, Walter-Sack, W E, Haefeli
Publikováno v: Therapeutische Umschau. Revue therapeutique. 57(9)
The rate and extent of drug absorption from the small intestine are related to the release of the active ingredient from a dosage form, its solubility in the liquid phase of gastrointestinal contents, and the transport of the dissolved compound or th
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::1ce0d2001b672ad94aaf89f779cc35aa
https://pubmed.ncbi.nlm.nih.gov/11036435
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8
Heparin-mediated selective release of hepatocyte growth factor in humans
Autor: P B, Salbach, M, Brückmann, O, Turovets, J, Kreuzer, W, Kübler, I, Walter-Sack
Publikováno v: British journal of clinical pharmacology. 50(3)
The aim of this investigation was to compare the effects of standard (S) with low molecular weight (LMW) heparin on circulating levels of heparin-binding growth factors (HBGF), known to have angiogenic properties in humans.In two consecutive trials 1
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::b7d723ba6d551907f734016c05592dde
https://pubmed.ncbi.nlm.nih.gov/10971306
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10
Relationship between hepatic cytochrome P450 3A content and activity and the disposition of midazolam administered orally
Autor: C, Wandel, R H, Böcker, H, Böhrer, J X, deVries, W, Hofmann, K, Walter, B, Kleingeist, S, Neff, R, Ding, I, Walter-Sack, E, Martin
Publikováno v: Drug metabolism and disposition: the biological fate of chemicals. 26(2)
It was recently shown by others that the clearance of midazolam/kg body weight after iv administration correlates with hepatic cytochrome P450 (CYP or P450) 3A content in liver transplant patients. However, after po administration midazolam undergoes
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::38bfec341647be53d532bac009f20ced
https://pubmed.ncbi.nlm.nih.gov/9456296
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