Zobrazeno 1 - 10
of 55
pro vyhledávání: '"Mikołaj Teisseyre"'
Autor:
Dominika Kaps-Kopiec, Andrzej Pławski, Magdalena Badura-Stronka, Mikołaj Teisseyre, Maciej Dądalski, Joanna Cielecka-Kuszyk, Joanna Pawłowska
Publikováno v:
Pediatria Polska, Vol 96, Iss 1, Pp 71-76 (2021)
Germline mutations in the SMAD4 gene cause juvenile polyposis syndrome and hereditary haemorrhagic telangiectasia. In some cases, the coexistence of these 2 syndromes can be observed among probands with the mutation in the SMAD4 gene. A combined synd
Externí odkaz:
https://doaj.org/article/7cde975bf83140edbd818c88296bfee8
Autor:
Dorota Wicher, Ryszard Grenda, Mikołaj Teisseyre, Marek Szymczak, Paulina Halat-Wolska, Dorota Jurkiewicz, Max Christoph Liebau, Elżbieta Ciara, Małgorzata Rydzanicz, Joanna Kosińska, Krystyna Chrzanowska, Irena Jankowska
Publikováno v:
Frontiers in Pediatrics, Vol 8 (2020)
Purpose: Liver involvement in autosomal recessive polycystic kidney disease (ARPKD) leads to the development of portal hypertension and its complications. The aim of this study was to analyze the occurrence of the portal hypertension and its clinical
Externí odkaz:
https://doaj.org/article/fb237a9d3c49455ab3a365985f97454c
Autor:
Marek Stefanowicz, Joanna Pawłowska, Jarosław Kierkuś, Maciej Dądalski, Irena Jankowska, Marcin Osiecki, Mikołaj Teisseyre, Dorota Jarzębicka, Małgorzata Woźniak, Piotr Czubkowski
Publikováno v:
Transplantation Proceedings. 53:244-249
Background Primary sclerosing cholangitis (PSC) and autoimmune sclerosing cholangitis (ASC) are often associated with ulcerative colitis (UC). The impact on the course of UC remains unclear, and up-to-date evidence in pediatric populations is scarce.
Autor:
Piotr Kaliciński, Joanna Pawłowska, Marek Szymczak, Małgorzata Markiewicz-Kijewska, Dorota Jarzębicka, Małgorzata Rurarz, Kazimierz Janiszewski, Jan Pertkiewicz, Irena Jankowska, Piotr Czubkowski, Mikołaj Teisseyre, Diana Kamińska
Publikováno v:
Annals of Transplantation
BACKGROUND Biliary strictures (BS) are frequent after pediatric liver transplantation (LTx) and in spite of ongoing progress, they remain a significant cause of morbidity. In children, the majority of reconstruction is hepatico-jejunal anastomosis (H
Autor:
Maciej Dądalski, Violetta Wojno, Mikołaj Teisseyre, Emil Plowiecki, Marek Woynarowski, Leszek Hurkała
Publikováno v:
Journal of Pediatric Gastroenterology & Nutrition. 64:696-700
This article presents the results of endoscopic treatment for recurrent postcorrosive esophageal stenosis with a tube-stent developed at our institution. The tube-stent was implanted in 5 children with corrosive esophageal injury at the age of 2 to 8
Autor:
Piotr Socha, Piotr Kaliciński, Mikołaj Teisseyre, Irena Jankowska, Agnieszka Bakuła, Olga Niewiadomska, Joanna Pawłowska
Publikováno v:
Transplantation Proceedings. 48:3323-3327
Background α1-Antitrypsin deficiency (ATD) is the most common genetic cause of liver injury in young children. Asymptomatic hepatitis is observed in most patients. However, the course of liver disease due to ATD is unpredictable, and some children d
Autor:
I. Celine Hanson, Nedim Hadzic, Gustavo Kusminsky, Francesca Ferrua, Matías Oleastro, Isabelle Meyts, Giorgia Bucciol, Jacques Pirenne, Paola Quarello, M. Teresa de la Morena, Andrzej Lange, Marek Stefanowicz, Nizar Mahlaoui, Francesco Tandoi, Z Nademi, Pier Luigi Calvo, Elena Soncini, Fulvio Porta, Troy R. Torgerson, Andrew J. Cant, Teresa Espanol, Marcelo Silva, Andrew R. Gennery, Sarah K. Nicholas, Benedicte Neven, Beata Wolska-Kuśnierz, Katja G. Weinacht, Paul Veys, Fanny Lanternier, Miguel Galicchio, Despina Moshous, J. David M. Edgar, Mary Slatter, Mikołaj Teisseyre
Liver disease in X-linked hyper IgM syndrome (XHIGM) is an important predictor of mortality. In case liver transplantation (LT) is required, a survival benefit is observed when LT is combined with HSCT. ispartof: JOURNAL OF ALLERGY AND CLINICAL IMMUN
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::47b33dc1fa6504d7faeb91aa6bf94066
https://lirias.kuleuven.be/handle/123456789/633572
https://lirias.kuleuven.be/handle/123456789/633572
Autor:
Dorota Dudka, Ewa Najberg, Rafał Śnitko, Agnieszka Ochocińska, Mikołaj Teisseyre, Roman Janas, Jarosław Kierkuś
Publikováno v:
Journal of Gastroenterology and Hepatology. 29:1883-1889
Background Neutrophil gelatinase-associated lipocalin (NGAL) is a 25 kDa glycoprotein present in the bodily fluids and tissues. It is secreted by neutrophils, epithelial cells, hepatocytes and adipocytes, and its expression is highly increased in res
Autor:
Jerzy Socha, Mikołaj Teisseyre, Joanna Pawłowska, Józef Ryżko, Paweł Płudowski, Hor Ismail, Elzbieta Karczmarewicz, Roman S. Lorenc, Ewa Skorupa, Edyta Kryskiewicz, Piotr Kaliciński
Publikováno v:
Journal of Clinical Densitometry. 15:233-240
Bone disorders are common in children with end-stage liver diseases, especially those associated with cholestasis. Abnormal hepatocyte function, disordered vitamin D metabolism and calcium-phosphorous homeostasis, malnutrition, and immunosuppressive
Autor:
Joanna Pawłowska, Piotr Czubkowski, Diana Kamińska, Mikołaj Teisseyre, M Markiewicz, Józef Ryżko, Irena Jankowska
Publikováno v:
Pediatric Transplantation. 16:E261-E264
TMA is a rare complication of tacrolimus. Disruption of endothelial cells, platelet aggregation, and intravascular mechanical fragmentation of red cells are core mechanisms of injury; however, exact pathways of toxicity are not clear. The clinical pr