Zobrazeno 1 - 10
of 353
pro vyhledávání: '"V, Vávrová"'
Publikováno v:
Metalurgija, Vol 53, Iss 1, Pp 85-88 (2014)
The article describes the possibilities of using the pupillary light reflex for subconscious ascertainment of consumer preferences also in technical, industrial sectors. It describes the essence and use of pupillometry in marketing, types of pupillom
Externí odkaz:
https://doaj.org/article/bb95b622e94f4e66b398e07792b8d170
Publikováno v:
Casopis lekaru ceskych. 143(3)
Once-daily administration of aminoglykosides is routinely used, but comparative efficacy data for patients with cystic fibrosis are not available.The aim of the this study was to compare the predicted pharmacodynamic (PD) activity of amikacin at 28 m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::99adecfdd7e03187cd134592f677daf7
https://pubmed.ncbi.nlm.nih.gov/15134039
https://pubmed.ncbi.nlm.nih.gov/15134039
Autor:
K, Sídlová, V, Skalická, K, Kotaska, M, Pechová, M, Chada, J, Bartosová, Z, Hríbal, J, Nevoral, V, Vávrová, R, Průsa
Publikováno v:
Physiological research. 52(3)
The aim of the study was to evaluate serum a-glutathione S-transferase (s-GSTA) levels in patients with cystic fibrosis (CF) and to compare s-GSTA with other liver function tests and with a hepatic ultrasound scan (US). The cytosolic enzyme, alpha-gl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::28d7caa87dd3f283a9cee02a0bcb117e
https://pubmed.ncbi.nlm.nih.gov/12790769
https://pubmed.ncbi.nlm.nih.gov/12790769
Autor:
A, Sedivá, R, Lischke, J, Simonek, J, Tkaczyk, V, Vávrová, J, Bartosová, P, Pohunek, J, Bartůnková, P, Pafko
Publikováno v:
Medical science monitor : international medical journal of experimental and clinical research. 7(6)
In the current study we focused on changes in the immune parameters of patients with CF after lung transplantation (Tx), with particular emphasis on the interaction of the immune system, infection, the autoimmune phenomenon observed in some CF patien
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::102c3c90e3e700e76e5224902dfc363d
https://pubmed.ncbi.nlm.nih.gov/11687733
https://pubmed.ncbi.nlm.nih.gov/11687733
Publikováno v:
Acta paediatrica (Oslo, Norway : 1992). 90(8)
Patients with cystic fibrosis (CF) are underweight and growth retarded. This study tested the link between serum insulin-like growth factor-I (IGF-I) and insulin-like growth factor-binding protein-3 (IGFBP-3) levels and body height, nutritional statu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::05846cbf64047a24374b8da6c408ed71
https://pubmed.ncbi.nlm.nih.gov/11529532
https://pubmed.ncbi.nlm.nih.gov/11529532
Autor:
V, Vávrová, D, Zemková, J, Bartosová, A, Zapletal, L, Smolíková, A, Krebsová, M, Koudová, M, Macek
Publikováno v:
Casopis lekaru ceskych. 138(21)
Cystic fibrosis (CF) is no longer a childhood disease. Since the identification of the gene in 1989 research has made advances and changed views on the pathogenesis, diagnosis and treatment. The objective of the present work is to make doctors treati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ed148f3782210ffe3e7882ef324131ab
https://pubmed.ncbi.nlm.nih.gov/10746022
https://pubmed.ncbi.nlm.nih.gov/10746022
Autor:
T. Dörk, M. Macek Jr, F. Mekus, B. Tümmler, J. Tzountzouris, T. Casals, A. Krebsová, M. Koudová, I. Sakmaryová, M. Macek Sr, V. Vávrová, D. Zemková, E. Ginter, N.V. Petrova, T. Ivaschenko, V. Baranov, M. Witt, A. Pogorzelski, J. Bal, C. Zékanowsky, K. Wagner, M. Stuhrmann, I. Bauer, H.H. Seydewitz, T. Neumann, S. Jakubiczka, C. Kraus, B. Thamm, M. Nechiporenko, L. Livshits, N. Mosse, G. Tsukerman, L. Kadási, M. Ravnik-Glavač, D. Glavač, R. Komel, K. Vouk, V. Kučinskas, A. Krumina, M. Teder, S. Kocheva, G.D. Efremov, T. Onay, B. Kirdar, G. Malone, M. Schwarz, Z. Zhou, K.J. Friedman, S. Carles, M. Claustres, D. Bozon, C. Verlingue, C. Férec, M. Tzetis, E. Kanavakis, H. Cuppens, C. Bombieri, P.F. Pignatti, F. Sangiuolo, A. Jordanova, J. Kusic, D. Radojkovič, J. Sertić, D. Richter, A. Stavljenić Rukavina, E. Bjorck, B. Strandvik, H. Cardoso, M. Montgomery, B. Nakielna, D. Hughes, X. Estivill, I. Aznarez, E. Tullis, L.-C. Tsui, J. Zielenski
Publikováno v:
Scopus-Elsevier
We report a large genomic deletion of the cystic fibrosis transmembrane conductance regulator (CFTR) gene, viz., a deletion that is frequently observed in Central and Eastern Europe. The mutation, termed CFTRdele2, 3(21 kb), deletes 21, 080 bp spanni
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::08016ea87f1ed7bb9a372f37e3116267
https://www.bib.irb.hr/233049
https://www.bib.irb.hr/233049
Autor:
V, Vávrová
Publikováno v:
Ceskoslovenska pediatrie. 49(1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::af06f6c65b8f1a55fa93b10b3f16617f
https://pubmed.ncbi.nlm.nih.gov/8124751
https://pubmed.ncbi.nlm.nih.gov/8124751
Publikováno v:
Casopis lekaru ceskych. 129(22)
The authors describe their experience with the prenatal genetic diagnosis of cystic fibrosis (CF), using DNA analysis in the first trimester of pregnancy in three families with a 25% risk of CF. The authors examined polymorphisms of probes J3.11, met
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9790695119ad1f6bde3c975338555084
https://pubmed.ncbi.nlm.nih.gov/1973632
https://pubmed.ncbi.nlm.nih.gov/1973632
Autor:
M, Macek, I, Boehm, L, Arnold, J, Smrt, R, Duspivová, V, Vávrová, Z, Sedlácek, K, Sperling, J, Schmidtke
Publikováno v:
Czechoslovak medicine. 13(4)
The authors report their experience with about two thousand DNA amplifications by polymerase chain reaction (PCR) in prenatal diagnosis of cystic fibrosis. The method is demonstrated on examples of diagnostic informativity and prenatal diagnosis exam
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8b2f6395ff844360b96a68f374f5a584
https://pubmed.ncbi.nlm.nih.gov/1981984
https://pubmed.ncbi.nlm.nih.gov/1981984