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Validation of Polish-Language Questionnaires for Assessing the Quality of Life of Patients with Primary Ciliary Dyskinesia (PCD-QOL).
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- Advances in Respiratory Medicine (MDPI), 2024, v. 92, n. 4, p. 254, doi. 10.3390/arm92040025
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- Article
Increased aminotransferases do not necessarily mean hepatotoxicity of CFTR modulator therapy.
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- Clinical & Experimental Hepatology, 2023, v. 9, n. 4, p. 405, doi. 10.5114/ceh.2023.132264
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- Article
Fat-Soluble Vitamins in Standard vs. Liposomal Form Enriched with Vitamin K2 in Cystic Fibrosis: A Randomized Multi-Center Trial.
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- 2022
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- Abstract
Fat-Soluble Vitamin Supplementation Using Liposomes, Cyclodextrins, or Medium-Chain Triglycerides in Cystic Fibrosis: A Randomized Controlled Trial.
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- Nutrients, 2021, v. 13, n. 12, p. 4554, doi. 10.3390/nu13124554
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- Article
Leukocyte Telomere Length Is Not Reduced in Children and Adults with Cystic Fibrosis but Associates with Clinical Characteristics—A Cross-Sectional Study.
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- Journal of Clinical Medicine, 2021, v. 10, n. 4, p. 590, doi. 10.3390/jcm10040590
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- Article
Anthropometric measurements, nutritional status and body composition in children with cystic fibrosis - the prospective study.
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- European Journal of Translational & Clinical Medicine, 2020, v. 3, n. 1, p. 34, doi. 10.31373/ejtcm/120582
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- Article
The evaluation of α-tocopherol concentration instead of α-tocopherol:cholesterol ratio in adult cystic fibrosis patients results in the overestimation of vitamin E deficiency.
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- Journal of Medical Science, 2019, p. 21, doi. 10.20883/jms.313
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- Article
Serum Phospholipid Fatty Acid Composition in Cystic Fibrosis Patients with and without Liver Cirrhosis.
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- Annals of Nutrition & Metabolism, 2017, v. 71, n. 1/2, p. 91, doi. 10.1159/000477913
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- Article
Increased Soluble VCAM-1 and Normal P-Selectin in Cystic Fibrosis: a Cross-Sectional Study.
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- Lung, 2017, v. 195, n. 4, p. 445, doi. 10.1007/s00408-017-0029-y
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- Article
VITAMIN A STATUS AND ITS DETERMINANTS IN PATIENTS WITH CYSTIC FIBROSIS.
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- Acta Scientiarum Polonorum. Technologia Alimentaria, 2017, v. 16, n. 3, p. 345, doi. 10.17306/J.AFS.2017.0473
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- Article
Mild CFTR mutations and genetic predisposition to lactase persistence in cystic fibrosis.
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- European Journal of Human Genetics, 2011, v. 19, n. 7, p. 748, doi. 10.1038/ejhg.2011.36
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- Article