Zobrazeno 1 - 10
of 253
pro vyhledávání: '"V, VAVROVA"'
Autor:
Stéphanie Bui, Thierry Bienvenu, Philippe Reix, Gabriel Bellon, Emanuelle Girodon, E. Deneuville, Isabelle Sermet-Gaudelus, Nathalie Stremmler, Albert Iron, Veronika Skalická, Michel Roussey, F. Huet, Delphine Roussel, Gérard Lenoir, M. Lebourgeois, V. Vavrova, Dorota Sands, Milan Macek, Aleksander Edelman, Jacques Sarles, Anne Munck, Isabelle Fajac
Publikováno v:
American Journal of Respiratory and Critical Care Medicine. 182:929-936
The diagnosis of cystic fibrosis (CF) is based on a characteristic clinical picture in association with a sweat chloride (Cl(-)) concentration greater than 60 mmol/L or the identification of two CF-causing mutations. A challenging problem is the sign
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::74a54144c48440c1a8fc6f8c97e6abeb
https://doi.org/10.1164/rccm.201003-0382oc
https://doi.org/10.1164/rccm.201003-0382oc
Autor:
J. Ticha, V. Vavrova, Jiri Kukacka, Karel Kotaska, Magdalena Kuzelova, M. Halacova, Richard Prusa
Publikováno v:
Journal of Clinical Pharmacy and Therapeutics. 33:409-417
SUMMARY Background and objective: Monitoring of renal function in cystic fibrosis (CF) patients is essential. The dosage regimen of amikacin is regularly modified according to the patient’s glomerular filtration rate (GFR). The aim of the study was
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b9cfc0591117af66dd2931633bc3c508
https://doi.org/10.1111/j.1365-2710.2008.00932.x
https://doi.org/10.1111/j.1365-2710.2008.00932.x
Publikováno v:
Journal of Inherited Metabolic Disease. 31:457-461
Genetic polymorphism of serum transferrin (Tf) was studied in order to differentiate between protein genetic variants and congenital disorders of glycosylation (CDG), further focusing on unusual findings.Screening of Tf hypoglycosylation was carried
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef8401fbafa8009c684037b71aaef176
https://doi.org/10.1007/s10545-008-0733-0
https://doi.org/10.1007/s10545-008-0733-0
Autor:
Anna Sediva, Milan Macek, Jitka Brazova, J. Bartosova, Kristyna Sismova, V. Vavrova, Hynek Lauschman
Publikováno v:
Clinical Immunology. 121:350-357
There is a significant phenotypic variance among cystic fibrosis (CF) patients. Due to the role of TGF-beta1 in fibrotic processes we investigated its role in CF pathogenesis. TGF-beta 1 codons 10 and 25 were genotyped in 118 Czech CF patients and 26
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2374113a5f576d76aa25acc88d0f94ad
https://doi.org/10.1016/j.clim.2006.08.015
https://doi.org/10.1016/j.clim.2006.08.015
Autor:
Ondrej Cinek, Petr Pohunek, Eshwar Mahenthiralingam, V. Vavrova, P. Drevinek, J. Bartosova, Sarka Vosahlikova
Publikováno v:
Journal of Medical Microbiology. 54:655-659
The morbidity and mortality rates in patients with cystic fibrosis (CF) are significantly affected by infections with Burkholderia cepacia complex. In a Czech CF Centre, the prevalence of the infection reached up to 30 %, with the majority of patient
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0c581e09cc917bdf008115d5ee32691f
https://doi.org/10.1099/jmm.0.46025-0
https://doi.org/10.1099/jmm.0.46025-0
Publikováno v:
Scopus-Elsevier
UNLABELLED 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, nutrit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::666cc932647d93412908df09b4841a7d
https://doi.org/10.1111/j.1651-2227.2001.tb02447.x
https://doi.org/10.1111/j.1651-2227.2001.tb02447.x
Publikováno v:
Allergy & Clinical Immunology International - Journal of the World Allergy Organization. 13:0067-0070
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f674214887a521e5f91489357378400c
https://doi.org/10.1027/0838-1925.13.2.67
https://doi.org/10.1027/0838-1925.13.2.67
Autor:
V. Vavrova, Veronika Skalická, Klara Dedeckova, Pavel Drevinek, Dana Zemkova, Libor Fila, T. Kucerova, Lucie Kalferstova, Oto Melter, J. Bartosova, Ondrej Cinek
Publikováno v:
Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society. 11(5)
Background Once the outbreak with Burkholderia cenocepacia ST32 was identified in the Prague cystic fibrosis (CF) centre, molecular tools were implemented into diagnostic routine in order to complement infection control measures with as accurate as p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a5fc8d86fcc1b308b5163a8699cdf180
https://pubmed.ncbi.nlm.nih.gov/22622026
https://pubmed.ncbi.nlm.nih.gov/22622026
Autor:
M. Proesmans, Steven P. Conway, V. Vavrova, K. De Boeck, Lena Hjelte, G. Canny, Burkhard Tümmler, Diana Bilton, S. Dumcius
Publikováno v:
Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society. 10
Pulmonary exacerbations represent a key outcome variable in clinical trials of cystic fibrosis (CF). As there is variation in the trigger for use of intravenous antibiotics compared to the use of oral antibiotics or new nebulised therapy for treatmen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6fa87a2bede8bd4fb7b85de8cbf7f168
https://pubmed.ncbi.nlm.nih.gov/21658647
https://pubmed.ncbi.nlm.nih.gov/21658647
Autor:
S. Dumcius, Niels Høiby, V. Vavrova, H. Kollberg, C. Bohmova, Lena Hjelte, Tacjana Pressler, Burkhard Tümmler, Steven P. Conway
Publikováno v:
Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society. 10
Chronic pulmonary infection with P. aeruginosa develops in most patients with cystic fibrosis (CF); by adulthood 80% of patients are infected and chronic P. aeruginosa infection is the primary cause of increased morbidity and mortality in CF. Chronic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8f7b1af5ed379892266b9aeb8c3a7dc7
https://pubmed.ncbi.nlm.nih.gov/21658646
https://pubmed.ncbi.nlm.nih.gov/21658646