Zobrazeno 1 - 10
of 43
pro vyhledávání: '"Halina Cichoz-Lach"'
Autor:
Anna Rycyk-Bojarzynska, Beata Kasztelan-Szczerbinska, Halina Cichoz-Lach, Agata Surdacka, Jacek Rolinski
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 14, p 7597 (2024)
Neutrophils release neutrophil extracellular traps (NETs) as a defense strategy in response to broad-spectrum infections and sterile triggers. NETs consist of a DNA scaffold decorated with antimicrobial peptides (AMPs) and enzymatically active protea
Externí odkaz:
https://doaj.org/article/765842b1cb744443a868ed6fb39921ea
Publikováno v:
Folia Medica, Vol 64, Iss 4, Pp 693-696 (2022)
We report a rare case of Peutz-Jeghers syndrome (PJS) in a 35-year-old female. The patient was diagnosed with PJS when she was 11 years old. She has remained under observation since then. We strongly believe that PJS is a very rare diagnosis. However
Externí odkaz:
https://doaj.org/article/96b7644a715b46c0b62d155304a7b843
Autor:
Beata Kasztelan-Szczerbinska, Bartosz Zygo, Anna Rycyk-Bojarzynska, Agata Surdacka, Jacek Rolinski, Halina Cichoz-Lach
Publikováno v:
PLoS ONE, Vol 18, Iss 1, p e0280068 (2023)
BackgroundImmune dysregulation and neutrophil infiltration are hallmarks of alcohol-related liver disease (ALD). Our objective was to evaluate the blood profile of neutrophil-derived mediators [neutrophil elastase (NE), myeloperoxidase (MPO), alpha1-
Externí odkaz:
https://doaj.org/article/efe4f8c3086644a2bb655a7f1ee0527a
Publikováno v:
Journal of Education, Health and Sport, Vol 12, Iss 2 (2022)
Introduction Inflammatory bowel disease (IBD) in most cases is classified into Crohn’s disease (CD) or ulcerative colitis (UC). It appears in 25-35 years of age and the second peak is after fifties. It is very rare to recognize it in the elderly.
Externí odkaz:
https://doaj.org/article/b3b57d31485e4ff2a07a756401516c08
Autor:
Beata Kasztelan-Szczerbinska, Anna Rycyk-Bojarzynska, Agnieszka Szczerbinska, Halina Cichoz-Lach
Publikováno v:
Nutrients, Vol 15, Iss 3, p 760 (2023)
Primary biliary cholangitis (PBC), and primary sclerosing cholangitis (PSC) are rare immune-related cholangiopathies with still poorly explained pathogenesis. Although triggers of chronic inflammation with subsequent fibrosis that affect cholangiocyt
Externí odkaz:
https://doaj.org/article/208b45e57f60431c970e5db57784d612
Publikováno v:
Journal of Education, Health and Sport, Vol 9, Iss 1, Pp 234-240 (2019)
One of programmed cell death types, netosis, discovered in ’96, was first described by Zychlinsky et al. and has gained elevating popularity among many researchers. It is a process occurring in order to catch pathogens into a trap and kill them. Th
Externí odkaz:
https://doaj.org/article/fdf67b46021e4965b1e7214dc6d41b57
Publikováno v:
Medicina, Vol 58, Iss 3, p 333 (2022)
Osler-Weber-Rendu disease, also known as hereditary hemorrhagic telangiectasia (HHT), is a rare, autosomal dominant condition that affects approximately 1 in 5000 patients causing abnormal blood vessel formation. HHT patients have mucocutaneous telan
Externí odkaz:
https://doaj.org/article/de10fb3afd424a95bc6881a49a39b0f0
Publikováno v:
PeerJ, Vol 7, p e7855 (2019)
Refractory ascites (RA) refers to ascites that cannot be mobilized or that has an early recurrence that cannot be prevented by medical therapy. Every year, 5–10% of patients with liver cirrhosis and with an accumulation of fluid in the peritoneal c
Externí odkaz:
https://doaj.org/article/083e3090fba04f77a55376e5c0517d90
Autor:
Beata Kasztelan-Szczerbinska, Agata Surdacka, Maria Slomka, Jacek Rolinski, Krzysztof Celinski, Halina Cichoz-Lach, Agnieszka Madro, Mariusz Szczerbinski
Publikováno v:
Mediators of Inflammation, Vol 2014 (2014)
Angiogenesis is believed to be implicated in the pathogenesis of alcoholic liver disease (ALD). We aimed to explore the usefulness and accuracy of plasma angiogenic biomarkers for noninvasive evaluation of the severity of liver failure and ALD outcom
Externí odkaz:
https://doaj.org/article/08758e1037474d97a020e19570b3b2f1
Publikováno v:
Folia medica. 64(4)
We report a rare case of Peutz-Jeghers syndrome (PJS) in a 35-year-old female. The patient was diagnosed with PJS when she was 11 years old. She has remained under observation since then. We strongly believe that PJS is a very rare diagnosis. However
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0cc91d63c135f33de677f0d29856a8b3
https://pubmed.ncbi.nlm.nih.gov/36045464
https://pubmed.ncbi.nlm.nih.gov/36045464