Ulc I - Search Results

1

Lack of male-female differences in disposition and esterase hydrolysis of ramipril to ramiprilat in healthy volunteers after a single oral dose.

Vree TB, Dammers E, Ulc I, Horkovics-Kovats S, Ryska M, Merkx, Ijsbrand. Vree TB, et al. Among authors: ulc i. ScientificWorldJournal. 2003 Dec 11;3:1332-43. doi: 10.1100/tsw.2003.124. ScientificWorldJournal. 2003. PMID: 14755115 Free article. Clinical Trial.

2

Differences between lovastatin and simvastatin hydrolysis in healthy male and female volunteers:gut hydrolysis of lovastatin is twice that of simvastatin.

Vree TB, Dammers E, Ulc I, Horkovics-Kovats S, Ryska M, Merkx I. Vree TB, et al. Among authors: ulc i. ScientificWorldJournal. 2003 Dec 11;3:1332-43. doi: 10.1100/tsw.2003.121. ScientificWorldJournal. 2003. PMID: 14755114 Free PMC article. Clinical Trial.

3

Lack of Male-Female Differences in Disposition and Esterase Hydrolysis of Ramipril to Ramiprilat in Healthy Volunteers after a Single Oral Dose.

Vree TB, Dammers E, Ulc I, Horkovics-Kovats S, Ryska M, Merkx I. Vree TB, et al. Among authors: ulc i. ScientificWorldJournal. 2003 Dec 11;3:1344-1358. doi: 10.1100/tsw.2003.122. eCollection 2003. ScientificWorldJournal. 2003. PMID: 29887764 Free PMC article.

4

Physicochemical pharmacokinetics as an optimization tool for generic development: A case study.

Horkovics-Kovats S, Ulč I, Vít L, Němec B, Rada V. Horkovics-Kovats S, et al. Among authors: ulc i. Eur J Pharm Sci. 2018 Jan 1;111:349-357. doi: 10.1016/j.ejps.2017.10.018. Epub 2017 Oct 13. Eur J Pharm Sci. 2018. PMID: 29032305 Clinical Trial.

5

Validated HPLC-MS-MS method for simultaneous determination of atorvastatin and 2-hydroxyatorvastatin in human plasma-pharmacokinetic study.

Borek-Dohalský V, Huclová J, Barrett B, Nemec B, Ulc I, Jelínek I. Borek-Dohalský V, et al. Among authors: ulc i. Anal Bioanal Chem. 2006 Sep;386(2):275-85. doi: 10.1007/s00216-006-0655-3. Epub 2006 Aug 22. Anal Bioanal Chem. 2006. PMID: 16924379

6

Pharmacokinetics and pharmacodynamics of two different landiolol formulations in a healthy Caucasian group.

Krumpl G, Ulc I, Trebs M, Kadlecová P, Hodisch J. Krumpl G, et al. Among authors: ulc i. Eur J Pharm Sci. 2016 Sep 20;92:64-73. doi: 10.1016/j.ejps.2016.06.022. Epub 2016 Jun 29. Eur J Pharm Sci. 2016. PMID: 27373605 Clinical Trial.

7

Pharmacokinetics of the novel oral prostacyclin receptor agonist selexipag in subjects with hepatic or renal impairment.

Kaufmann P, Cruz HG, Krause A, Ulč I, Halabi A, Dingemanse J. Kaufmann P, et al. Among authors: ulc i. Br J Clin Pharmacol. 2016 Aug;82(2):369-79. doi: 10.1111/bcp.12963. Epub 2016 May 10. Br J Clin Pharmacol. 2016. PMID: 27062188 Free PMC article. Clinical Trial.

8

Relative bioavailability of a pediatric dispersible tablet and adult film-coated tablet of macitentan in healthy volunteers.

Sidharta PN, Štěpánová R, Globig S, Ulč I, Csonka D. Sidharta PN, et al. Among authors: ulc i. Pharmacol Res Perspect. 2020 Apr;8(2):e00580. doi: 10.1002/prp2.580. Pharmacol Res Perspect. 2020. PMID: 32302056 Free PMC article. Clinical Trial.

9

Biocomparison Study of Adult and Paediatric Dose Strengths of the Prostacyclin Receptor Agonist Selexipag.

Boehler M, Bruderer S, Ulč I, Dingemanse J. Boehler M, et al. Among authors: ulc i. Eur J Drug Metab Pharmacokinet. 2018 Feb;43(1):115-120. doi: 10.1007/s13318-017-0424-z. Eur J Drug Metab Pharmacokinet. 2018. PMID: 28639216 Clinical Trial.

10

Pharmacokinetics and metabolism of [3H]-pipethiaden in healthy volunteers.

Plecitá Z, Spanĕl M, Ulc I, Rejŏlec V, Lapka R. Plecitá Z, et al. Among authors: ulc i. Eur J Drug Metab Pharmacokinet. 1992 Apr-Jun;17(2):89-92. doi: 10.1007/BF03188776. Eur J Drug Metab Pharmacokinet. 1992. PMID: 1425816

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