Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Wojciech Jańczyk"'
Autor:
Wojciech Jańczyk, Joanna B. Bierła, Ilona Trojanowska, Aldona Wierzbicka-Rucińska, Bożena Cukrowska, Piotr Socha
Publikováno v:
Diagnostics, Vol 13, Iss 4, p 768 (2023)
Autoantibodies occur in healthy subjects as well as in children with Wilson’s disease (WD), but their prevalence and significance are unknown. Thus, we aimed to assess the prevalence of autoantibodies and autoimmune markers, and their relationship
Externí odkaz:
https://doaj.org/article/e037af047d674f33983d61071b9fef6f
Autor:
Joanna B. Trojanek, Jacek Michałkiewicz, Renata Grzywa-Czuba, Wojciech Jańczyk, Lidia Gackowska, Izabela Kubiszewska, Anna Helmin-Basa, Aldona Wierzbicka-Rucińska, Mieczysław Szalecki, Piotr Socha
Publikováno v:
Mediators of Inflammation, Vol 2020 (2020)
Gene expression profiles of matrix metalloproteinases (MMPs) and their tissue inhibitors (TIMPs) were evaluated in peripheral blood leukocytes of children with nonalcoholic fatty liver disease (NAFLD). Gene expression patterns were correlated with th
Externí odkaz:
https://doaj.org/article/20bfd01562d3454c8a3c596457f20653
Autor:
Dorota Wicher, Irena Jankowska, Patryk Lipiński, Paulina Szymańska-Rożek, Jakub Kmiotek, Wojciech Jańczyk, Jacek Rubik, Krystyna Chrzanowska, Piotr Socha
Publikováno v:
Frontiers in Pediatrics, Vol 6 (2019)
Introduction: Congenital hepatic fibrosis (CHF) is invariably present in all patients with autosomal recessive polycystic kidney disease (ARPKD) but is usually clinically asymptomatic. The portal hypertension in the course of CHF develops and progres
Externí odkaz:
https://doaj.org/article/ed43dae0146d4f50ada514bf7525034b
Autor:
Jake P Mann, Anita CE Vreugdenhil, Aglaia Zellos, Aleksander Krag, Anastasia Konidari, Anna Alisi, Bart Koot, Benno Kohlmaier, Christian A Hudert, Christos Tzivinikos, Cigdem Arikan, Corina Pienar, Deirdre Kelly, Eberhard Lurz, Elvira Verduci, Emanuele Nicastro, Emer Fitzpatrick, Giuseppe Indolfi, Giusy Ranucci, Henedina Antunes, Idoia Labayen, Irene Degrassi, Jan Melek, Jernej Brecelj, Jiri Bronsky, Judith Lubrecht, Kimberley Brook, Maria Fotoulaki, Maria Rogalidou, Marianne Samyn, Natalia Zavhorodnia, Norman Junge, Olha Zavhorodnia, Phil Newsome, Ruth DeBruyne, Sander Lefere, Stephenne Xavier, Thomas Berg, Tudor Lucian, Virginie Frings, Wojciech Jańczyk, Ulli Baumann
Publikováno v:
The Lancet Gastroenterology and Hepatology. Elsevier Limited
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b88592ef750705bbcff171fc123d52ec
http://www.scopus.com/inward/record.url?scp=85153324119&partnerID=8YFLogxK
http://www.scopus.com/inward/record.url?scp=85153324119&partnerID=8YFLogxK
Autor:
Renata Grzywa-Czuba, Joanna Trojanek, Izabela Kubiszewska, Piotr Socha, Jacek Michałkiewicz, Wojciech Jańczyk, Mieczysław Szalecki, Lidia Gackowska, Aldona Wierzbicka-Rucińska, Anna Helmin-Basa
Publikováno v:
Mediators of Inflammation
Mediators of Inflammation, Vol 2020 (2020)
Mediators of Inflammation, Vol 2020 (2020)
Gene expression profiles of matrix metalloproteinases (MMPs) and their tissue inhibitors (TIMPs) were evaluated in peripheral blood leukocytes of children with nonalcoholic fatty liver disease (NAFLD). Gene expression patterns were correlated with th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::03328311d0063f8b06855442a65f0340
https://doi.org/10.1155/2020/8327945
https://doi.org/10.1155/2020/8327945
Autor:
Indra van Mourik, Anita Vreugdenhil, Valerio Nobili, Deirdre Kelly, Claude Marcus, Wojciech Jańczyk, Sanjay Rajwal, Thomas Casswall, Gabriele Noble-Jamieson, Béatrice Dubern, Florence Lacaille, Jake P. Mann, Myriam Dabbas, Stephen O'Rahilly, Quentin M. Anstee, Piotr Socha, Ulrich Baumann, David B. Savage
Publikováno v:
Contemporary Clinical Trials, 75, 67-71. Elsevier Science
Non-alcoholic fatty liver disease (NAFLD) is the most common liver disorder in children and has the potential to progress to advanced fibrosis/cirrhosis, end-stage liver disease and hepatocellular carcinoma. However, the natural history of the condit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0603dcc810d881d44d8daec9d979dd50
https://doi.org/10.1016/j.cct.2018.11.003
https://doi.org/10.1016/j.cct.2018.11.003
Autor:
Bożena Cukrowska, Aldona Wierzbicka-Rucińska, Piotr Socha, Ewa Konopka, Wojciech Jańczyk, Łukasz Obrycki, Ewelina Kanarek, Sebastian Więckowski, Joanna Bierła, Jędrzej Sarnecki
Publikováno v:
Journal of pediatric gastroenterology and nutrition. 73(4)
OBJECTIVES Wilson disease (WD) is a copper metabolism disorder with toxic copper accumulation in the liver leading to liver steatosis or fibrosis. In vitro studies suggest that fatty acid-binding protein 1 (L-FABP) and lipid droplet-associated protei
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4a92d29af970726ee608c4043b920800
https://pubmed.ncbi.nlm.nih.gov/33908738
https://pubmed.ncbi.nlm.nih.gov/33908738
Autor:
Hartmut Schmidt, Anna Hüsing-Kabar, Magdalena Naorniakowska, Diana Kamińska, Piotr Socha, Anna Wiernicka, Wojciech Jańczyk, Maciej Dądalski
Publikováno v:
Journal of Pediatric Gastroenterology & Nutrition. 65:555-560
The aim of the study was to analyze the clinical presentations, diagnosis, and treatment of patients ages ≤5 years with early onset Wilson disease (WD).Data from 143 pediatric patients with WD treated at our center between January 1996 and November
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::541528df302af273fe6de497c8b70e05
https://doi.org/10.1097/mpg.0000000000001700
https://doi.org/10.1097/mpg.0000000000001700
Autor:
Thomas Scheper, Dilek Dayanakli, Dimietrios Bogdanos, Kai Fechner, Marek Woynarowski, Bożena Cukrowska, Simon D. Lytton, Dieter Abendroth, Marcin Osiecki, Dietmar Fuchs, Sabine Kramp, Chelsea Bentow, MałgorzataWoźniak, Maria Goliszek, Aldona Wierzbicka, Piotr Socha, Wojciech Jańczyk, Michael Mahler
Publikováno v:
Immunologic research. 67(1)
The impairment of regulatory T cells (Tregs) is a characteristic feature of autoimmune hepatitis (AIH), and the degradation of tryptophan (Trp) to kynurenine (Kyn), by gamma interferon-induced indoleamine-2,3-dioxygenase-1 (IDO-1), is a central metab
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::81bd6c060f2113d280b7331722f0ffd1
https://pubmed.ncbi.nlm.nih.gov/30666511
https://pubmed.ncbi.nlm.nih.gov/30666511
Autor:
Jacek Rubik, Irena Jankowska, Patryk Lipiński, Dorota Wicher, Krystyna Chrzanowska, Piotr Socha, Jakub Kmiotek, Wojciech Jańczyk, Paulina Szymańska-Rożek
Publikováno v:
Frontiers in Pediatrics
Frontiers in Pediatrics, Vol 6 (2019)
Frontiers in Pediatrics, Vol 6 (2019)
Introduction: Congenital hepatic fibrosis (CHF) is invariably present in all patients with autosomal recessive polycystic kidney disease (ARPKD) but is usually clinically asymptomatic. The portal hypertension in the course of CHF develops and progres
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fc552aa5e626476f7fbac824e5f3a601
https://doi.org/10.3389/fped.2018.00422
https://doi.org/10.3389/fped.2018.00422