Zobrazeno 1 - 10
of 67
pro vyhledávání: '"Agnieszka Zmysłowska"'
Autor:
Aneta Nitsch-Osuch, Piotr Jankowski, Joanna Kokoszka-Paszkot, Ernest Kuchar, Agnieszka Mastalerz-Migas, Przemysław Mitkowski, Jacek Wysocki, Agnieszka Zmysłowska, Adam Antczak
Publikováno v:
Family Medicine & Primary Care Review, Vol 26, Iss 1, Pp 116-122 (2024)
Annual vaccination is the most effective protection against influenza and its serious complications. It is especially important for people at high risk of severe course of the disease and serious complications: individuals with specific chronic medic
Externí odkaz:
https://doaj.org/article/d6c341bf1c7f4f6a9f3cb5dd6ef980c6
Autor:
Krzysztof Jeziorny, Ewa Zmyslowska-Polakowska, Krystyna Wyka, Aleksandra Pyziak-Skupień, Maciej Borowiec, Agnieszka Szadkowska, Agnieszka Zmysłowska
Publikováno v:
Bone Reports, Vol 17, Iss , Pp 101600- (2022)
Objectives: Causative variants in genes responsible for Alström syndrome (ALMS) and Bardet-Biedl syndrome (BBS) cause damage to primary cilia associated with correct functioning of cell signaling pathways in many tissues. Despite differences in gene
Externí odkaz:
https://doaj.org/article/7f9bc60f38584dc59b1501554cb38bde
Autor:
Arleta Waszczykowska, Agnieszka Zmysłowska, Marcin Braun, Marilin Ivask, Sulev Koks, Piotr Jurowski, Wojciech Młynarski
Publikováno v:
Diagnostics, Vol 10, Iss 9, p 607 (2020)
Background: Wolfram syndrome (WFS, OMIM: #222300) is an ultrarare autosomal recessive disorder characterized by diabetes insipidus, diabetes mellitus, optic nerve atrophy and deafness. It has been reported that the average retinal thickness in WFS pa
Externí odkaz:
https://doaj.org/article/15bfab7a77514f119bc7deeac43d19a4
Autor:
Magdalena Kołodziej, Arleta Waszczykowska, Irmina Korzeniewska-Dyl, Aleksandra Pyziak-Skupien, Konrad Walczak, Dariusz Moczulski, Piotr Jurowski, Wojciech Młynarski, Agnieszka Szadkowska, Agnieszka Zmysłowska
Publikováno v:
Diagnostics, Vol 9, Iss 3, p 105 (2019)
The aim of the study was to analyze the thickness of individual retinal layers in patients with type 1 diabetes (T1D) in comparison to the control group and in relation to markers of diabetes metabolic control. The study group consisted of 111 patien
Externí odkaz:
https://doaj.org/article/f7f45870a6814444967cac0b42e026df
Autor:
Marcin Braun, Bartlomiej Tomasik, Ewa Wrona, Wojciech Fendler, Przemyslawa Jarosz-Chobot, Agnieszka Szadkowska, Agnieszka Zmysłowska, Jayne Wilson, Wojciech Mlynarski
Publikováno v:
Journal of Diabetes Research, Vol 2016 (2016)
Introduction. It remains unclear how HbA1c recommendations influence metabolic control of paediatric patients with type 1 diabetes mellitus. To evaluate this we compared reported HbA1c with guideline thresholds. Materials and Methods. We searched sys
Externí odkaz:
https://doaj.org/article/d69d391f357548729aee4dca75ed9fad
Autor:
Urszula Smyczynska, Marcin Stanczak, Miljan Kuljanin, Aneta Włodarczyk, Ewelina Stoczynska-Fidelus, Joanna Taha, Bartłomiej Pawlik, Maciej Borowiec, Joseph D. Mancias, Wojciech Mlynarski, Piotr Rieske, Wojciech Fendler, Agnieszka Zmysłowska
Publikováno v:
Genes; Volume 13; Issue 12; Pages: 2370
Alström syndrome (ALMS) and Bardet–Biedl syndrome (BBS) are rare genetic diseases with a number of common clinical features ranging from early-childhood obesity and retinal degeneration. ALMS and BBS belong to the ciliopathies, which are known to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::766f3c3ffc799869a7c13366aa04ab41
Autor:
Magdalena Lebiedzinska-Arciszewska, Bartlomiej Pawlik, Piotr Rieske, Joanna Taha, Wojciech Fendler, Hanna Nieznanska, Miljan Kuljanin, Aneta Wlodarczyk, Dominika Michałek, Agnieszka Zmysłowska, Beata Małachowska, Joseph D. Mancias, Wojciech Młynarski, Marcin Stanczak, Maciej Borowiec, Mariusz R. Wieckowski, Dagmara Grot
Publikováno v:
Cell Communication and Signaling, Vol 19, Iss 1, Pp 1-14 (2021)
Cell Communication and Signaling : CCS
Cell Communication and Signaling : CCS
Background Wolfram syndrome (WFS) is a rare autosomal recessive syndrome in which diabetes mellitus and neurodegenerative disorders occur as a result of Wolframin deficiency and increased ER stress. In addition, WFS1 deficiency leads to calcium homeo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::79d969bef511c2898189cf414590f38a
https://doaj.org/article/e9ae24e4ded347729d7a31887a6ccfdf
https://doaj.org/article/e9ae24e4ded347729d7a31887a6ccfdf
Autor:
Maciej Borowiec, Agnieszka Zmysłowska, Krzysztof Jeziorny, Krystyna Wyka, Agnieszka Szadkowska
Publikováno v:
Pediatric Diabetes. 22:3-32
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4d92a9639c8451a591f1cdc0a7ea5abf
https://doi.org/10.1111/pedi.13268
https://doi.org/10.1111/pedi.13268
Publikováno v:
Endocrine
Aims Maturity‐onset diabetes of the young (MODY) is one of the rare monogenic forms of diabetes. To date, about 12 genes in the scientific literature are closely related to the occurrence of the disease phenotype. However, there is still a high pre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fbbe77538e52a64d285eb672284ce5ec
https://doi.org/10.1007/s12020-021-02753-7
https://doi.org/10.1007/s12020-021-02753-7
Autor:
Sulev Kõks, Arleta Waszczykowska, Emil Zielonka, Marcin Braun, Wojciech Młynarski, Piotr Jurowski, Marilin Ivask, Agnieszka Zmysłowska
Publikováno v:
American Journal of Ophthalmology. 217:140-151
Purpose To evaluate corneal morphology among patients with Wolfram syndrome (WFS). Design Comparative observational longitudinal case series of WFS patients with a laboratory approach in the WFS1 gene knockout (Wfs1KO) mouse model. Methods A group of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b1c901d9b1303da8f1636f82d18c197d
https://doi.org/10.1016/j.ajo.2020.04.012
https://doi.org/10.1016/j.ajo.2020.04.012