Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Iwona Chaberska"'
Autor:
Iwona Chaberska, Aleksandra Feruś, Julia Lipska, Monika Turek, Klara Wojciechowska, Karolina Piątkowska, Aleksandra Jaroń, Katarzyna Jastrzębska
Publikováno v:
Quality in Sport, Vol 19 (2024)
Objective: The study aims to investigate the impact of various supplements, namely selenium, vitamin D, zinc, magnesium, vitamin A, iodine, L-carnitine, and proteolytic enzymes, on the management of hypothyroidism, with a particular focus on Hashimot
Externí odkaz:
https://doaj.org/article/c40210532b89489b8bad76867e1a8eaa
Autor:
Monika Turek, Klara Wojciechowska, Karolina Piątkowska, Aleksandra Jaroń, Katarzyna Jastrzębska, Iwona Chaberska, Aleksandra Feruś, Julia Lipska
Publikováno v:
Quality in Sport, Vol 18 (2024)
Introduction: Systemic lupus erythematosus (SLE) is a chronic autoimmune disease, often affecting women of childbearing age, with periods of exacerbations and remissions. SLE can impact multiple organs, causing a range of clinical symptoms. Neuropsyc
Externí odkaz:
https://doaj.org/article/ba60a2afdfe44239872b6d4a98889fa0
Autor:
Aleksandra Jaroń, Katarzyna Jastrzębska, Klara Wojciechowska, Monika Turek, Iwona Chaberska, Aleksandra Feruś, Julia Lipska, Karolina Piątkowska
Publikováno v:
Quality in Sport, Vol 17 (2024)
Introduction and aim of study: Obesity is a chronic disease associated with numerous health complications, and the number of patients is steadily increasing. Pharmacological methods for treating obesity are becoming increasingly popular. This paper a
Externí odkaz:
https://doaj.org/article/57a88aaa353e4463b80ccb7efa6acb5d
Autor:
Paweł Turski, Iwona Chaberska, Piotr Szukało, Paulina Pyska, Łukasz Milanowski, Stanisław Szlufik, Monika Figura, Dorota Hoffman-Zacharska, Joanna Siuda, Dariusz Koziorowski
Publikováno v:
Frontiers in Neuroscience, Vol 16 (2022)
Parkinson’s disease (PD) is a heterogenous neurodegenerative disorder. Genetic factors play a significant role, especially in early onset and familial cases. Mutations are usually found in the LRRK2 gene, but their importance varies. Some mutations
Externí odkaz:
https://doaj.org/article/928f1942ec6f4bd49fac8f1c61a6abc1