Výsledky vyhľadávania - "Cystic Fibrosis physiopathology"

Lung structural and functional impairments in young children with cystic fibrosis diagnosed following newborn screening – A nationwide observational study

Autori: Bettina S. Frauchiger Corin Willers Jasna Cotting a ďalší

Prispievatelia: Bettina S. Frauchiger Corin Willers Jasna Cotting a ďalší

Zdroj: Journal of cystic fibrosis, vol. 23, no. 5, pp. 910-917
Frauchiger, Bettina S; Willers, Corin; Cotting, Jasna; Kieninger, Elisabeth; Korten, Insa; Casaulta, Carmen; Salem, Yasmin; Stranzinger, Enno; Brabandt, Ben; Usemann, Jakob; Regamey, Nicolas; Kuhn, Alena; Blanchon, Sylvain; Rochat, Isabelle; Bauman, Grzegorz; Müller-Suter, Dominik; Moeller, Alexander; Latzin, Philipp; Ramsey, Kathryn A (2024). Lung structural and functional impairments in young children with cystic fibrosis diagnosed following newborn screening-A nationwide observational study. Journal of cystic fibrosis, 23(5), pp. 910-917. Elsevier 10.1016/j.jcf.2024.05.010 <http://dx.doi.org/10.1016/j.jcf.2024.05.010>

Predmety: Male, Cystic Fibrosis, Infant, Newborn, 610 Medicine & health, Magnetic Resonance Imaging, Respiratory Function Tests, 3. Good health, Neonatal Screening, Child, Preschool, Humans, Cystic Fibrosis/physiopathology, Cystic Fibrosis/complications, Cystic Fibrosis/diagnosis, Neonatal Screening/methods, Female, Magnetic Resonance Imaging/methods, Child, Respiratory Function Tests/methods, Switzerland/epidemiology, Lung/physiopathology, Lung/diagnostic imaging, Children, Cystic fibrosis, Lung clearance index, Magnetic resonance imaging, Multiple breath washout, Lung, Switzerland

Popis súboru: application/pdf

Prístupová URL adresa: https://pubmed.ncbi.nlm.nih.gov/38926017
http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_B8C300EAC7711
https://serval.unil.ch/resource/serval:BIB_B8C300EAC771.P001/REF.pdf
https://serval.unil.ch/notice/serval:BIB_B8C300EAC771
https://boris.unibe.ch/198161/

Impact of COVID-19 infection on lung function and nutritional status amongst individuals with cystic fibrosis: A global cohort study: A global cohort study

Autori: Semenchuk, Julie Naito, Yumi Charman, Susan a ďalší

Prispievatelia: Semenchuk, Julie Naito, Yumi Charman, Susan a ďalší

Zdroj: Journal of Cystic Fibrosis, 23, 5, pp. 815-822
Journal of cystic fibrosis, Vol. 23, no.5, p. 815-822 (2024)
Journal of Cystic Fibrosis
Journal of cystic fibrosis, vol. 23, no. 5, pp. 815-822
JOURNAL OF CYSTIC FIBROSIS
Semenchuk, J, Naito, Y, Charman, S C, Carr, S B, Cheng, S Y, Marshall, B C, Faro, A, Elbert, A, Gutierrez, H H, Goss, C H, Karadag, B, Burgel, P R, Colombo, C, Salvatore, M, Padoan, R, Daneau, G, Harutyunyan, S, Kashirskaya, N, Kirwan, L, Middleton, P G, Ruseckaite, R, de Monestrol, I, Naehrlich, L, Mondejar-Lopez, P, Jung, A, van Rens, J, Bakkeheim, E, Orenti, A, Zomer-van Ommen, D, da Silva-Filho, L V RF, Fernandes, F F, Zampoli, M, Stephenson, A L & on behalf of the Global CF Registry Collaboration 2024, 'Impact of COVID-19 infection on lung function and nutritional status amongst individuals with cystic fibrosis : A global cohort study', Journal of Cystic Fibrosis, vol. 23, no. 5, pp. 815-822. https://doi.org/10.1016/j.jcf.2024.07.019

Predmety: Pulmonary and Respiratory Medicine, Male, Adult, Cystic Fibrosis, Nutritional Status, CHILDREN, SARS-COV-2 INFECTION, Cystic fibrosis, Body Mass Index, PEOPLE, Forced Expiratory Volume, Medicine and Health Sciences, Humans, Paediatrics - Radboud University Medical Center, Pediatrics, Perinatology, and Child Health, Retrospective Studies, [SDV.MHEP.ME] Life Sciences [q-bio]/Human health and pathology/Emerging diseases, 2. Zero hunger, ddc:610, SARS-CoV-2, COVID-19, Coronavirus, VDP::Medical disciplines: 700::Health sciences: 800, Respiratory Function Tests, 3. Good health, [SDV.SPEE] Life Sciences [q-bio]/Santé publique et épidémiologie, [SDV.MHEP.MI] Life Sciences [q-bio]/Human health and pathology/Infectious diseases, [SDV.MHEP.PSR] Life Sciences [q-bio]/Human health and pathology/Pulmonology and respiratory tract, Female, Cystic Fibrosis/physiopathology, Cystic Fibrosis/complications, COVID-19/physiopathology, COVID-19/complications, COVID-19/epidemiology, Respiratory Function Tests/methods

Popis súboru: application/pdf

Prístupová URL adresa: https://pubmed.ncbi.nlm.nih.gov/39191560
https://dspace.library.uu.nl/handle/1874/458466
https://hdl.handle.net/2066/310541
https://repository.ubn.ru.nl//bitstream/handle/2066/310541/310541.pdf
https://hdl.handle.net/2078.1/301526
https://hdl.handle.net/11250/3182926
https://serval.unil.ch/resource/serval:BIB_4FBFDD398F1F.P001/REF.pdf
https://serval.unil.ch/notice/serval:BIB_4FBFDD398F1F
http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_4FBFDD398F1F7
https://biblio.ugent.be/publication/01JAASPKV4YCTP8AY19FY06FYW
https://biblio.ugent.be/publication/01JAASPKV4YCTP8AY19FY06FYW/file/01JAASWRWC0E0D3AEKHK9WEM36
http://hdl.handle.net/1854/LU-01JAASPKV4YCTP8AY19FY06FYW
http://doi.org/10.1016/j.jcf.2024.07.019

A longitudinal study assessing the impact of elexacaftor/tezacaftor/ivacaftor on gut transit and function in people with cystic fibrosis using magnetic resonance imaging (MRI)

Autori: Alexander Yule Christabella Ng Arantxa Recto a ďalší

Zdroj: Journal of cystic fibrosis, vol. 23, no. 5, pp. 984-990
Yule, A, Ng, C, Recto, A, Lockwood, F, Dellschaft, N S, Hoad, C L, Zagoya, C, Mainz, J G, Major, G, Barr, H L, Gowland, P A, Stewart, I, Marciani, L, Spiller, R C & Smyth, A R 2024, 'A longitudinal study assessing the impact of elexacaftor/tezacaftor/ivacaftor on gut transit and function in people with cystic fibrosis using magnetic resonance imaging (MRI)', Journal of Cystic Fibrosis, vol. 23, no. 5, pp. 984-990. https://doi.org/10.1016/j.jcf.2024.08.001

Predmety: Male, Adult, Indoles, Cystic Fibrosis, Adolescent, Pyridines, Humans, Cystic Fibrosis/drug therapy, Cystic Fibrosis/physiopathology, Female, Magnetic Resonance Imaging/methods, Benzodioxoles/therapeutic use, Gastrointestinal Transit/drug effects, Longitudinal Studies, Prospective Studies, Aminophenols/therapeutic use, Pyrazoles/therapeutic use, Pyrazoles/pharmacology, Indoles/therapeutic use, Drug Combinations, Chloride Channel Agonists/therapeutic use, Quinolones/therapeutic use, Pyridines/therapeutic use, Pyridines/pharmacology, Cystic Fibrosis Transmembrane Conductance Regulator, Child, Quinolines/therapeutic use, Quinolines/pharmacology, Young Adult, Pyrrolidines/therapeutic use, CF, CFTR modulator, Cystic fibrosis, ETI, GI, MRI, elexacaftor/tezacaftor/ivacaftor, gastrointestinal, gut, magnetic resonance imaging, name=Pediatrics, Quinolones, Aminophenols, name=Pulmonary and Respiratory Medicine, Benzodioxoles, Gastrointestinal Transit, Chloride Channel Agonists, Perinatology, Magnetic Resonance Imaging, and Child Health, name=Pediatrics, Perinatology, and Child Health, Pyrazoles

Popis súboru: application/pdf

Prístupová URL adresa: https://pubmed.ncbi.nlm.nih.gov/39242338
http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_3D663DEB2F8C5
https://serval.unil.ch/notice/serval:BIB_3D663DEB2F8C
https://serval.unil.ch/resource/serval:BIB_3D663DEB2F8C.P001/REF.pdf
https://pure.qub.ac.uk/en/publications/07614c4d-4a86-4855-8799-bf0645425487

The Long-Term Uptake of Home Spirometry in Regular Cystic Fibrosis Care:Retrospective Multicenter Observational Study

Autori: Bertram, Pia Oppelaar, Martinus C Bannier, Michiel Age a ďalší

Zdroj: Bertram, P, Oppelaar, M C, Bannier, M A, Reijers, M H, van der Vaart, H, van der Meer, R, Altenburg, J, Conemans, L, Rottier, B L, Nuijsink, M, van den Wijngaart, L S, Merkus, P J & Roukema, J 2025, 'The Long-Term Uptake of Home Spirometry in Regular Cystic Fibrosis Care : Retrospective Multicenter Observational Study', Journal of Medical Internet Research, vol. 27, e60689. https://doi.org/10.2196/60689

Predmety: Adolescent, Adult, Child, Female, Humans, Male, Young Adult, Cystic Fibrosis/physiopathology, Home Care Services/statistics & numerical data, Netherlands, Retrospective Studies, Spirometry/methods

Popis súboru: application/pdf

Relation: info:eu-repo/semantics/altIdentifier/pmid/39788554; info:eu-repo/semantics/altIdentifier/hdl/https://hdl.handle.net/11370/5f42b9e2-7e75-4e35-b13a-bf0bc7838e32; info:eu-repo/semantics/altIdentifier/pissn/1438-8871

Dostupnosť: https://hdl.handle.net/11370/5f42b9e2-7e75-4e35-b13a-bf0bc7838e32
https://research.rug.nl/en/publications/5f42b9e2-7e75-4e35-b13a-bf0bc7838e32
https://doi.org/10.2196/60689
https://pure.rug.nl/ws/files/1224212308/jmir-2025-1-e60689.pdf
https://www.scopus.com/pages/publications/85214843659

Accuracy, Reproducibility, and Responsiveness to Treatment of Home Spirometry in Cystic Fibrosis: Multicenter, Retrospective, Observational Study: Multicenter, Retrospective, Observational Study

Autori: Martinus C Oppelaar Hanneke AC van Helvoort Michiel AGE Bannier a ďalší

Zdroj: J Med Internet Res
Journal of Medical Internet Research, Vol 26, p e60892 (2024)
Journal of Medical Internet Research, 26, pp. e60892

Predmety: Male, Adult, Indoles, pediatrics, Spirometry/methods, Cystic Fibrosis, Adolescent, Computer applications to medicine. Medical informatics, Vital Capacity, digital health, R858-859.7, morbidity, cystic fibrosis, pulmonary infections, Young Adult, 03 medical and health sciences, 0302 clinical medicine, telespirometry, Forced Expiratory Volume, Humans, Paediatrics - Radboud University Medical Center, Child, remote monitoring, Retrospective Studies, mobile phone, Original Paper, reliability, telemonitoring, Spirometry/methods statistics & numerical data, Reproducibility of Results, Cystic Fibrosis/physiopathology, chronic respiratory disease, mortality, Cystic Fibrosis/physiopathology therapy drug therapy, chronic pulmonary inflammation, Spirometry, Female, Public aspects of medicine, RA1-1270, Pulmonary Diseases - Radboud University Medical Center, hereditary, Indoles/therapeutic use

Prístupová URL adresa: https://pubmed.ncbi.nlm.nih.gov/39626236
https://doaj.org/article/f575d1b330214ada983f764d0fe75f87
https://hdl.handle.net/https://repository.ubn.ru.nl/handle/2066/313320
https://doi.org/10.2196/60892
https://research.rug.nl/en/publications/a65eefca-6439-4497-8fa6-72ac1d03cff1
https://doi.org/10.2196/60892
https://hdl.handle.net/11370/a65eefca-6439-4497-8fa6-72ac1d03cff1
https://cris.maastrichtuniversity.nl/en/publications/ee5019f5-de12-463e-8e1d-3cbf67332c8c
https://doi.org/10.2196/60892
https://pure.amsterdamumc.nl/en/publications/c2a2e4ee-4ab2-46fd-85ad-e71f494a2355
https://doi.org/10.2196/60892
https://hdl.handle.net/2066/313320
https://repository.ubn.ru.nl//bitstream/handle/2066/313320/313320.pdf

Respiratory symptoms do not reflect functional impairment in early CF lung disease

Autori: Insa Korten Marc-Alexander Oestreich Urs Frey a ďalší

Prispievatelia: Insa Korten Marc-Alexander Oestreich Urs Frey a ďalší

Zdroj: Journal of cystic fibrosis, vol. 20, no. 6, pp. 957-964
Korten, Insa; Oestreich, Marc-Alexander; Frey, Urs; Moeller, Alexander; Jung, Andreas; Spinas, Renate; Mueller-Suter, Dominik; Trachsel, Daniel; Rochat, Isabelle; Spycher, Ben; Latzin, Philipp; Casaulta, Carmen; Ramsey, Kathryn (2021). Respiratory symptoms do not reflect functional impairment in early CF lung disease. Journal of cystic fibrosis, 20(6), pp. 957-964. Elsevier 10.1016/j.jcf.2021.04.006 <http://dx.doi.org/10.1016/j.jcf.2021.04.006>

Predmety: Male, Cystic Fibrosis, Infant, 610 Medicine & health, Respiratory Function Tests, 3. Good health, 03 medical and health sciences, 0302 clinical medicine, Respiratory Rate, 10036 Medical Clinic, 2740 Pulmonary and Respiratory Medicine, 360 Social problems & social services, Predictive Value of Tests, Case-Control Studies, Humans, Female, 2735 Pediatrics, Perinatology and Child Health, Prospective Studies, Cystic Fibrosis/physiopathology, Cohort study, Cystic fibrosis, Healthy controls, Infancy, Respiratory symptoms

Popis súboru: application/pdf; PIIS1569199321001168.pdf - application/pdf

Prístupová URL adresa: http://www.cysticfibrosisjournal.com/article/S1569199321001168/pdf
https://pubmed.ncbi.nlm.nih.gov/34088612
https://www.cysticfibrosisjournal.com/article/S1569199321001168/pdf
https://www.sciencedirect.com/science/article/abs/pii/S1569199321001168
https://www.sciencedirect.com/science/article/pii/S1569199321001168
https://www.cysticfibrosisjournal.com/article/S1569-1993(21)00116-8/fulltext
https://pubmed.ncbi.nlm.nih.gov/34088612/
https://europepmc.org/article/MED/34088612
https://serval.unil.ch/resource/serval:BIB_2F084B7CBAA8.P001/REF.pdf
https://serval.unil.ch/notice/serval:BIB_2F084B7CBAA8
http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_2F084B7CBAA84
https://boris.unibe.ch/159015/
https://www.zora.uzh.ch/id/eprint/216769/
https://doi.org/10.5167/uzh-216769

Gastric emptying and lingual lipase activity in cystic fibrosis

Autori: Roulet, M. Weber, A. M. Paradis, Y. a ďalší

Predmety: Adolescent Butter Cystic Fibrosis/*physiopathology *Gastric Emptying Gastric Juice/secretion Glycerides/metabolism Humans Lipase/*metabolism Lipolysis Pancreas/physiopathology Tongue/*enzymology

Relation: Pediatric Research; https://iris.unil.ch/handle/iris/215951; serval:BIB_BD12E4D30B8D; A1980KV14000018; 7208153

Dostupnosť: https://iris.unil.ch/handle/iris/215951

False normal Lung Clearance Index in infants with cystic fibrosis due to software algorithms.

Autori: Anagnostopoulou, P. Yammine, S. Schmidt, A. a ďalší

Predmety: Algorithms, Case-Control Studies, Cystic Fibrosis/physiopathology, Female, Humans, Infant, Male, Reference Values, Respiratory Function Tests/instrumentation, Respiratory Function Tests/methods, Software

Relation: Pediatric Pulmonology; https://iris.unil.ch/handle/iris/207611; serval:BIB_754AFE740570; 000363287800005

Dostupnosť: https://iris.unil.ch/handle/iris/207611
https://doi.org/10.1002/ppul.23256

Bone mineral content in cystic fibrosis patients: correlation with fat-free mass.

Autori: Salamoni, F. Roulet, M. Gudinchet, F. a ďalší

Predmety: Adolescent, Adult, Anthropometry, Body Composition/physiology, Bone Density/physiology, Child, Cystic Fibrosis/genetics, Cystic Fibrosis/physiopathology, Diet, Female, Humans, Lumbar Vertebrae/physiopathology, Male, Mutation, Puberty/physiology

Relation: Archives of Disease in Childhood; https://iris.unil.ch/handle/iris/201573; serval:BIB_8FDA200FED2E; A1996UF64400007; 8669931

Dostupnosť: https://iris.unil.ch/handle/iris/201573
https://doi.org/10.1136/adc.74.4.314

Bio-electrical impedance analysis for estimation of fat-free mass and muscle mass in cystic fibrosis patients.

Autori: Spicher, V. Roulet, M. Schaffner, C. a ďalší

Predmety: Adipose Tissue, Adolescent, Adult, Body Composition, Child, Cystic Fibrosis/physiopathology, Electric Impedance, Female, Humans, Male, Muscles, Nutritional Status, Skinfold Thickness

Relation: European Journal of Pediatrics; https://iris.unil.ch/handle/iris/195807; serval:BIB_AD484D6945A5; A1993KM32200012; 8444248

Dostupnosť: https://iris.unil.ch/handle/iris/195807
https://doi.org/10.1007/BF01956149

Electrogastrography reveals post-prandial gastric dysmotility in children with cystic fibrosis

Autori: Schappi, M. G. Roulet, M. Rochat, T. a ďalší

Predmety: Adolescent Case-Control Studies Child Child, Preschool Cisapride/*administration & dosage Cystic Fibrosis/*physiopathology Electrophysiology Female *Gastric Emptying/drug effects/physiology Gastrointestinal Agents/*administration & dosage Gastrointestinal Motility/physiology Humans Infant Male Postprandial Period Stomach/physiopathology Time Factors

Relation: Journal of Pediatric Gastroenterology and Nutrition; https://iris.unil.ch/handle/iris/142790; serval:BIB_D30916803EE0; 000223570600005

Dostupnosť: https://iris.unil.ch/handle/iris/142790

Deep learning-based segmentation of the lung in MR-images acquired by a stack-of-spirals trajectory at ultra-short echo-times

Autori: Weng, Andreas M. Heidenreich, Julius F. Metz, Corona a ďalší

Zdroj: BMC Med Imaging
BMC Medical Imaging, Vol 21, Iss 1, Pp 1-11 (2021)

Predmety: ddc:610, Image segmentation, Lung Neoplasms, Cystic Fibrosis, Research, Respiration, Deep learning, Pneumonia, Lung Neoplasms/diagnostic imaging [MeSH], Deep Learning [MeSH], Humans [MeSH], MRI, Lung/diagnostic imaging [MeSH], Lung, Lung/physiology [MeSH], Neural Networks, Computer [MeSH], Respiration [MeSH], Pneumonia/diagnostic imaging [MeSH], Cystic Fibrosis/physiopathology [MeSH], Case-Control Studies [MeSH], Magnetic Resonance Imaging/methods [MeSH], Cystic Fibrosis/diagnostic imaging [MeSH], Magnetic Resonance Imaging, 3. Good health, 03 medical and health sciences, Deep Learning, 0302 clinical medicine, Case-Control Studies, Medical technology, Humans, Neural Networks, Computer, R855-855.5

Popis súboru: application/pdf

Prístupová URL adresa: https://bmcmedimaging.biomedcentral.com/track/pdf/10.1186/s12880-021-00608-1
https://pubmed.ncbi.nlm.nih.gov/33964892
https://doaj.org/article/2efb463fc97d4d4292416e1be37dbd78
https://repository.publisso.de/resource/frl:6462667
https://opus.bibliothek.uni-wuerzburg.de/files/26052/s12880-021-00608-1.pdf
https://opus.bibliothek.uni-wuerzburg.de/frontdoor/index/index/docId/26052
https://nbn-resolving.org/urn:nbn:de:bvb:20-opus-260520
https://doi.org/10.1186/s12880-021-00608-1

Salivary lipids: A review

Autori: Mateusz Maciejczyk Jan Matczuk Małgorzata Żendzian-Piotrowska a ďalší

Zdroj: Advances in Clinical and Experimental Medicine. 26:1021-1029

Predmety: Sjogren's syndrome - metabolism, Cystic fibrosis - physiopathology, Cystic fibrosis - metabolism, Diabetes mellitus - physiopathology, Cystic Fibrosis, Lipid Metabolism, Saliva - metabolism, Sjogren's syndrome - physiopathology, Salivary Glands, Diabetes mellitus - metabolism, 03 medical and health sciences, Lipid metabolism, Sjogren's Syndrome, 0302 clinical medicine, Diabetes Mellitus, Animals, Humans, Saliva, Salivation, Salivary glands - metabolism

Prístupová URL adresa: https://pubmed.ncbi.nlm.nih.gov/29068606
http://europepmc.org/abstract/MED/29068606
https://www.ncbi.nlm.nih.gov/pubmed/29068606
https://advances.umw.edu.pl/en/article/2017/26/6/1023/
https://pubmed.ncbi.nlm.nih.gov/29068606/
http://www.advances.umed.wroc.pl/en/article/2017/26/6/1023/

'Back to the future.': a word from the editor.

Autori: Rossier, B.

Predmety: Animals, Cystic Fibrosis/physiopathology, Disease Models, Animal, Humans, Kidney Diseases/physiopathology, Mice, Physiology/trends

Relation: Pflügers Archiv European Journal of Physiology; https://iris.unil.ch/handle/iris/58394; serval:BIB_2895062A2504; 000181365600001

Dostupnosť: https://iris.unil.ch/handle/iris/58394
https://doi.org/10.1007/s00424-002-0949-z

Multiple breath washout: clinical benefit in cystic fibrosis / Multiple breath washout: klinisk nytta vid cystisk fibros

Autori: Lindblad, Anders Svedberg, Marcus

Zdroj: Allergi i Praxis. (2):40

Decreased renal accumulation of aminoglycoside reflects defective receptor-mediated endocytosis in cystic fibrosis and Dent’s disease

Autori: Claudia Raggi Teresinha Leal Olivier Devuyst a ďalší

Prispievatelia: Claudia Raggi Teresinha Leal Olivier Devuyst a ďalší

Zdroj: Pflügers Archiv-European Journal of Physiology
Pflugers Archiv European Journal of Physiology

Predmety: 0301 basic medicine, Cystic Fibrosis, Kidney Tubules, Proximal/cytology/metabolism, Cystic Fibrosis Transmembrane Conductance Regulator, 610 Medicine & health, Urologie & néphrologie, 1308 Clinical Biochemistry, Kidney, Sciences de la santé humaine, 10052 Institute of Physiology, Kidney Tubules, Proximal, Mice, 03 medical and health sciences, 2737 Physiology (medical), Gentamicins/metabolism, Chloride Channels, 11554 Zurich Center for Integrative Human Physiology (ZIHP), Animals, Humans, Urology & nephrology, Human health sciences, Cells, Cultured, Chloride Channels/genetics/metabolism, Dent Disease, Mice, Knockout, 0303 health sciences, Anti-Bacterial Agents/metabolism, Cystic Fibrosis Transmembrane Conductance Regulator/genetics/metabolism, 1314 Physiology, Cystic Fibrosis/physiopathology, Endocytosis, Anti-Bacterial Agents, 3. Good health, Mice, Inbred C57BL, Kidney/metabolism, Dent Disease/physiopathology, Aminoglycosides, Aminoglycosides/metabolism, 570 Life sciences, biology, Gentamicins, Endocytosis/physiology

Popis súboru: Raggi_et_al_Increased_Renal_Clearance.pdf - application/pdf; ZORA_NL_53205.pdf - application/pdf

Prístupová URL adresa: https://www.zora.uzh.ch/id/eprint/53205/13/ZORA_NL_53205.pdf
https://pubmed.ncbi.nlm.nih.gov/21927812
https://core.ac.uk/display/13501323
https://link.springer.com/article/10.1007/s00424-011-1026-2
https://europepmc.org/article/MED/21927812
https://www.ncbi.nlm.nih.gov/pubmed/21927812
https://orbi.uliege.be/handle/2268/134447
https://link.springer.com/10.1007/s00424-011-1026-2
https://hdl.handle.net/2268/134447
https://doi.org/10.1007/s00424-011-1026-2
http://doc.rero.ch/record/309589/files/424_2011_Article_1026.pdf
https://www.zora.uzh.ch/id/eprint/53205/
https://doi.org/10.5167/uzh-53205

Mild CFTR mutations and genetic predisposition to lactase persistence in cystic fibrosis

Autori: Mądry, E. Fidler, E. Sobczyńska-Tomaszewska, A. a ďalší

Zdroj: European Journal of Human Genetics. 19(7):748-752

Predmety: Adult, Male, Adolescent, Genotype, Lactase - genetics, Gene frequency - genetics, lactose malabsorption, cystic fibrosis, Mutation - genetics, LCT polymorphism, CFTR mutations, hypolactasia, single nucleotide - genetics, Humans, Polymorphism, Child, Lactose intolerance - genetics, Alleles, Genetic predisposition to disease - genetics, Cystic fibrosis - physiopathology, Lactase - metabolism, lactose intolerance, Cystic fibrosis transmembrane conductance regulator - genetics, Young adult, Female, Cystic fibrosis - genetics

Prístupová URL adresa: https://www.nature.com/articles/ejhg201136.pdf

CFTR and defective endocytosis: new insights in the renal phenotype of cystic fibrosis

Autori: JOURET, François Devuyst, Olivier

Zdroj: Pflügers Archiv-European Journal of Physiology; Vol 457
Pflügers Archiv-European Journal of Physiology
Pflugers Archiv European Journal of Physiology

Predmety: 0301 basic medicine, Anatomie (cytologie, histologie, embryologie...) & physiologie, 0303 health sciences, Cystic Fibrosis, Chloride Channels/physiology, Kidney Tubules, Proximal/physiopathology, Cystic Fibrosis Transmembrane Conductance Regulator, Cystic Fibrosis/physiopathology, Anatomy (cytology, histology, embryology...) & physiology, Kidney, Life sciences, Endocytosis, 3. Good health, Kidney Tubules, Proximal, Mice, 03 medical and health sciences, Chloride Channels, Sciences du vivant, Animals, Humans, Endocytosis/physiology, Cystic Fibrosis Transmembrane Conductance Regulator/genetics/physiology, Kidney/physiopathology

Prístupová URL adresa: https://orbi.uliege.be/bitstream/2268/134474/1/PflugersArch_2009.pdf
https://pubmed.ncbi.nlm.nih.gov/18839205
https://orbi.ulg.ac.be/bitstream/2268/134474/1/PflugersArch_2009.pdf
https://link.springer.com/article/10.1007%2Fs00424-008-0594-2
https://pubmed.ncbi.nlm.nih.gov/18839205/
https://rd.springer.com/article/10.1007/s00424-008-0594-2
http://orbi.ulg.ac.be/bitstream/2268/134474/1/PflugersArch_2009.pdf
https://www.ncbi.nlm.nih.gov/pubmed/18839205
https://hdl.handle.net/2268/134474
https://doi.org/10.1007/s00424-008-0594-2

Expression and localization of cystic fibrosis transmembrane conductance regulator in the rat endocrine pancreas

Autori: Boom, Alain Lybaert, Pascale Pollet, Jean-François a ďalší

Zdroj: Endocrine. 32:197-205

Predmety: Glucagon-Secreting Cells -- cytology, 0301 basic medicine, Cystic Fibrosis, Cystic Fibrosis Transmembrane Conductance Regulator -- immunology, Cells, Wistar, Cystic Fibrosis Transmembrane Conductance Regulator, Antibodies, Cystic fibrosis, Islets of Langerhans -- cytology, Islets of Langerhans -- metabolism, Epitopes, Islets of Langerhans, 03 medical and health sciences, Diabetes Mellitus, Animals, RNA, Messenger, Cystic Fibrosis -- complications, Cystic Fibrosis -- physiopathology, CFTR, Rats, Wistar, Cells, Cultured, 0303 health sciences, Monoclonal -- immunology, Cultured, Diabetes Mellitus -- physiopathology, Antibodies, Monoclonal, Sciences bio-médicales et agricoles, Glucagon, Glucagon-Secreting Cells -- metabolism, Rats, 3. Good health, Cystic Fibrosis Transmembrane Conductance Regulator -- metabolism, Messenger -- metabolism, Epitopes -- immunology, Glucagon-Secreting Cells, RNA, Alpha and beta cells, Female, Cystic Fibrosis Related Diabetes (CFRD), Monoclonal -- metabolism, Diabetes Mellitus -- etiology

Popis súboru: 1 full-text file(s): application/pdf

Prístupová URL adresa: https://pubmed.ncbi.nlm.nih.gov/18040894
https://core.ac.uk/display/8852833
https://link.springer.com/article/10.1007/s12020-007-9026-x/fulltext.html
https://pubmed.ncbi.nlm.nih.gov/18040894/
https://www.ncbi.nlm.nih.gov/pubmed/18040894
https://difusion.ulb.ac.be/vufind/Record/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/147562/Details
https://link.springer.com/article/10.1007%2Fs12020-007-9026-x

Peripheral airway involvement in CF and asthma compared by inert gas washout

Autori: Gustafsson, Per M., 1952

Zdroj: Pediatr Pulmonol. 42(2):168-76

Predmety: Dermatology and Venereal Diseases, Dermatologi och venereologi, Medical and Health Sciences, Medicin och hälsovetenskap, Adolescent, Adult, Asthma/*physiopathology, Breath Tests, Bronchodilator Agents/*pharmacology, Child, Cystic Fibrosis/*physiopathology, Female, Forced Expiratory Volume/drug effects/physiology, Humans, Lung/*physiology, Male, Noble Gases, Pulmonary Ventilation/drug effects/*physiology, Respiration/*drug effects, Respiratory Dead Space, Spirometry, Vital Capacity/drug effects

Prístupová URL adresa: https://gup.ub.gu.se/publication/55104