Zobrazeno 11 - 20
of 181
pro vyhledávání: '"Dorota Sands"'
Publikováno v:
Journal of Clinical Medicine, Vol 10, Iss 21, p 4884 (2021)
(1) Background: Pulmonary exacerbation (PEx) is one of the main factors affecting the quality of life and life expectancy in patients with cystic fibrosis (CF). Our study aimed to evaluate the change in selected pulmonary function parameters, includi
Externí odkaz:
https://doaj.org/article/b8e86f3e8b7e45c898b365114ff9f851
Publikováno v:
Folia Histochemica et Cytobiologica, Vol 48, Iss 3, Pp 358-365 (2010)
Infants with positive CF newborn screening (NBS) results are called to a CF Centre for verification. Those, in whom the sweat test is elevated, undergo further medical procedures. The aim of our study was to evaluate the applicability of Nanoduct - a
Externí odkaz:
https://doaj.org/article/9c3e528ffeff405d97424d8f4a9a0f39
Publikováno v:
Folia Histochemica et Cytobiologica, Vol 48, Iss 2, Pp 185-190 (2010)
Malnutrition, delayed growth and puberty are commonly observed in children suffering from cystic fibrosis. The aim of this study was to assess the age of menarche in girls with CF using status quo analysis. The relationship between types of CFTR muta
Externí odkaz:
https://doaj.org/article/f5730d7f954f42d3bc811ba889d7dc4e
Publikováno v:
Folia Histochemica et Cytobiologica, Vol 45, Iss 3, Pp 165-168 (2007)
Cystic fibrosis (CF) is genetically determined illness, which is caused by the mutation in the CFTR gene. CFTR protein is also expressed in epithelial cells of parotid glands, therefore parotid glands are also affected in CF patients. Cathepsin D is
Externí odkaz:
https://doaj.org/article/be8d17942af14b57a8530e201fe302d5
Publikováno v:
Folia Histochemica et Cytobiologica, Vol 48, Iss 1, Pp 163-165 (2010)
The different clinical manifestations of cystic fibrosis, with variable intensity and timing, often delay the diagnosis of this genetic autosomal recessive disorder. Many countries have introduced newborn screening for cystic fibrosis to facilitate d
Externí odkaz:
https://doaj.org/article/4d4c3fce7724411d83faa00bcb6c369c
Autor:
Ida Chiara Guerrera, Giuseppe Astarita, Jean-Philippe Jais, Dorota Sands, Anna Nowakowska, Julien Colas, Isabelle Sermet-Gaudelus, Martin Schuerenberg, Daniele Piomelli, Aleksander Edelman, Mario Ollero
Publikováno v:
PLoS ONE, Vol 4, Iss 11, p e7735 (2009)
The aim of this study was to search for lipid signatures in blood plasma from cystic fibrosis (CF) patients using a novel MALDI-TOF-ClinProTools strategy, initially developed for protein analysis, and thin layer chromatography coupled to MALDI-TOF (T
Externí odkaz:
https://doaj.org/article/21a3935d2dab4a2a9288ca171f03f90a
Autor:
Marek Gacko, Anetta Sulewska, Alicja Karwowska, Alina Minarowska, Dorota Sands, Łukasz Minarowski, Elzbieta Chyczewska
Publikováno v:
Folia Histochemica et Cytobiologica, Vol 46, Iss 2, Pp 245-246 (2008)
Thiocyanates (SCN-) are ubiquitous in nature. There are indispensable part of host defense system that act as a substrate for lactoperoxidase (LPO). In our study we present initial data on SCN- concentration in saliva of CF patients in comparison to
Externí odkaz:
https://doaj.org/article/4011d928e1a64c709599e055de66ab25
Autor:
Anne Munck, Daria O Berger, Kevin W Southern, Carla Carducci, Karin M de Winter-de Groot, Silvia Gartner, Nataliya Kashirskaya, Barry Linnane, Marijke Proesmans, Dorota Sands, Olaf Sommerburg, Carlo Castellani, Jürg Barben, Sabine Renner, Max Zeyda, Elke de Wachter, Luc Regal, Felix Votava, Andrea Holubova, Marianne Skov, Tessa Morgan, Paul Bregeaut, Loretta O'Grady, Ines Bucci, Stefano Pantano, Simonetta Simonetti, Domenica De Venuto, Donatello Salvatore, Nicola Perrotti, Mimma Caloiero, Giuseppe Castaldo, Antonella Tosco, Francesca Righetti, Giovanna Pisi, Fiorella Battistini, Antonio Angeloni, Giuseppe Cimino, Giovanni Fiocchi, Antonella Angiolillo, Michela Cassanello, Luisella Alberti, Laura E Claut, Raffaele Badolato, Enza Pavanello, Benedetta Fabrizzi, Elisabetta Bignamini, Anna Cardillo, Mariangela Lombardo, Letizia Cocciadiferro, Lisa Termini, Daniela Dolce, Vito Terlizzi, Anna Tamanini, Francesca Pauro, Giancarlo la Marca, Elina Aleksejeva, Dita Gaidule-Logina, Stoika Fustik, Violeta Anastasovska, Marelle Bouva, Alastair Reid, Jennifer Cundick, Emma Lundman, Egil Bakkeheim, Katarzyna Zybert, Mariusz Oltarzewski, Laura Vilarinho, Victoria Sherman, Elena Kondratyeva, Sarah Smith, Gordana Vilotijevic Dautovic, Maria Knapkova, Zuzana Mydlova, Rosa Mª López, Valle Velasco, Felicitas Díaz Flores, Cristóbal Colón Mejeras, Eva SL Pedersen, Ugur Ozcelik, Bulent Karadag, Halyna Makukh, Moat Stuart
European CF Society Neonatal Screening Working Group (ECFS NSWG): Sabine Renner , Max Zeyda , Elke de Wachter , Luc Regal , Felix Votava, Andrea Holubova, Marianne Skov , Tessa Morgan, Paul Bregeaut , Loretta O'Grady, Ines Bucci , Stefano Pantano , S
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c1280e533a22801c54cb7ddf56c1b22d
https://hdl.handle.net/11424/290369
https://hdl.handle.net/11424/290369
Autor:
Jürg Barben, Nataliya Kashirskaya, Anne Munck, Kevin W Southern, Olaf Sommerburg, Barry Linnane, Dorota Sands, Silvia Gartner, Sarah Mayell, Marijke Proesmans, Carlo Castellani, Karin M. de Winter-de Groot
Publikováno v:
Journal of Cystic Fibrosis. 20:820-823
Autor:
Dorota Sands, Justyna Milczewska, Katarzyna Walicka-Serzysko, Andrzej Pogorzelski, Szczepan Cofta, Wojciech Skorupa
Publikováno v:
Forum Zakażeń. 12:163-173
Przewlekła choroba oskrzelowo-płucna, której postęp spowodowany jest przewlekłymi zakażeniami, stanowi główną przyczynę hospitalizacji i śmierci osób chorych na mukowiscydozę. Wśród bakterii najczęściej powodujących przewlekłe zaka