Superiority of Laparoscopic Gastrojejunostomy Combined With Multimodality Therapy for Gastric Outlet Obstruction Caused by Advanced Gastric Cancer

Autor: Chuandong Wang, Xiaojuan Zhang, Shengtao Lin, Changshun Yang, BiaoHuan Zhou, Yulong Mi, Rong Ye, Yifan Chen, Weijie Chen, Xiaojun Lin, Song Tan, Yuhang Zhou, Weihua Li

Publikováno v: Frontiers in Oncology, Vol 12 (2022)

BackgroundData are limited concerning the survival outcomes of patients with gastric outlet obstruction (GOO) caused by advanced gastric cancers according to laparoscopic gastrojejunostomy (LGJ) combined with multimodality therapy (MMT). Therefore, t

Externí odkaz: https://doaj.org/article/5e8f9fc4db1a4a64b0568dfe0e93ab8a

Liver Phenotypes of European Adults Heterozygous or Homozygous for Pi∗Z Variant of AAT (Pi∗MZ vs Pi∗ZZ genotype) and Noncarriers

Autor: Mattias Mandorfer, Nadine T. Gaisa, Christian Trautwein, Jef Verbeek, Helmut Denk, Daniel Neureiter, Elmar Aigner, Julia Kümpers, Heinz Zoller, Barbara Burbaum, LS Moeller, Heike Bantel, Olivier Govaere, Federica Benini, Joanna Chorostowska-Wynimko, Aleksander Krag, Frank Lammert, Jacob George, Katharina Wöran, Thomas Reiberger, Georg Lurje, Marla Gutberlet, Felix Stickel, Lisa Bewersdorf, Michael Trauner, Mohammed Eslam, V Woditsch, Sabina Janciauskiene, Tania Roskams, V Pereira, Johannes Haybaeck, J. Voss, Karim Hamesch, C Lindhauer, Annika Gross, Andreas Geier, Mònica Pons, Malin Fromme, Alexander Teumer, Quentin M. Anstee, Joan Genescà, Matthias C. Reichert, Biaohuan Zhou, Pawel Kuca, Marcin Krawczyk, Carolin V. Schneider, Pavel Strnad, Timm Dirrichs, Christian Datz, Joana Carvão, Robert Bals, Frederik Nevens, Benedikt Schäfer

Publikováno v: Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Schneider, C V, Hamesch, K, Gross, A, Mandorfer, M, Moeller, L S, Pereira, V, Pons, M, Kuca, P, Reichert, M C, Benini, F, Burbaum, B, Voss, J, Gutberlet, M, Woditsch, V, Lindhauer, C, Fromme, M, Kümpers, J, Bewersdorf, L, Schäfer, B, Eslam, M, Bals, R, Janciauskiene, S, Carvão, J, Neureiter, D, Zhou, B, Wöran, K, Bantel, H, Geier, A, Dirrichs, T, Stickel, F, Teumer, A, Verbeek, J, Nevens, F, Govaere, O, Krawczyk, M, Roskams, T, Haybaeck, J, Lurje, G, Chorostowska-Wynimko, J, Genesca, J, Reiberger, T, Zoller, H, Lammert, F, Krag, A, George, J, Anstee, Q M, Trauner, M, Datz, C, Gaisa, N T, Denk, H & European Alpha-1 Liver Study Group 2020, ' Liver Phenotypes of European Adults Heterozygous or Homozygous for Pi∗Z Variant of AAT (Pi∗MZ vs Pi∗ZZ genotype) and Noncarriers ', Gastroenterology, vol. 159, no. 2, pp. 534-548.e11 . https://doi.org/10.1053/j.gastro.2020.04.058

BACKGROUND & AIMS: Homozygosity for the Pi∗Z variant of the gene that encodes the alpha-1 antitrypsin peptide (AAT), called the Pi∗ZZ genotype, causes a liver and lung disease called alpha-1 antitrypsin deficiency. Heterozygosity (the Pi∗MZ gen

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d59dc7827cb0387e946e44ea0d463025

HINT2 downregulation promotes colorectal carcinoma migration and metastasis

Autor: Huan Wang, Shaoxin Cai, Weihua Li, Biaohuan Zhou, Le Wang, Changshun Yang

Publikováno v: Oncotarget

// Weihua Li 1, * , Shaoxin Cai 1, * , Le Wang 1 , Changshun Yang 1 , Biaohuan Zhou 1 , Huan Wang 1 1 Department of Surgical Oncology, Fujian Provincial Clinical College, Fujian Medical University, Fuzhou 350001, China * These authors contributed equ

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb3e2582c0893f67f2c42634cf23bb25
https://doi.org/10.18632/oncotarget.14587

Liver Fibrosis and Metabolic Alterations in Adults With alpha-1-antitrypsin Deficiency Caused by the Pi*ZZ Mutation

Autor: Karim Hamesch, I. Spivak, Sabina Janciauskiene, LS Moeller, Mario Bento-Miranda, Frank Lammert, Malin Fromme, Mònica Pons, Rodrigo Liberal, Pavel Strnad, Josef van Helden, Biaohuan Zhou, Michael Trauner, Eray Yagmur, Rui Gaspar, M Wetzel, Jan Stolk, Joan Genescà, Ravi Mahadeva, Rembert Koczulla, Carolin V. Schneider, A Arslanow, Thomas Reiberger, Aleksander Krag, William J.H. Griffiths, J. Voss, Nurdan Guldiken, Elmar Aigner, Christian Trautwein, Dalila Costa, Robert Bals, V Pereira, C Lindhauer, V Woditsch, Benedikt Schaefer, Carolina Simões, Heinz Zoller, Felix Stickel, Britta Siegmund, Marc Miravitlles, Matthias C. Reichert, Grace E. Dolman, Wolfgang Gleiber, Danilo Bzdok, Verena Knipel, Miriam Barrecheguren, Luís Maia, Mattias Mandorfer, Wolfram Windisch

Publikováno v: Hamesch, K, Mandorfer, M, Pereira, V M, Moeller, L S, Pons, M, Dolman, G E, Reichert, M C, Schneider, C V, Woditsch, V, Voss, J, Lindhauer, C, Fromme, M, Spivak, I, Guldiken, N, Zhou, B, Arslanow, A, Schaefer, B, Zoller, H, Aigner, E, Reiberger, T, Wetzel, M, Siegmund, B, Simões, C, Gaspar, R, Maia, L, Costa, D, Bento-Miranda, M, van Helden, J, Yagmur, E, Bzdok, D, Stolk, J, Gleiber, W, Knipel, V, Windisch, W, Mahadeva, R, Bals, R, Koczulla, R, Barrecheguren, M, Miravitlles, M, Janciauskiene, S, Stickel, F, Lammert, F, Liberal, R, Genesca, J, Griffiths, W J, Trauner, M, Krag, A, Trautwein, C, Strnad, P & European Alpha1-Liver Study Group 2019, ' Liver Fibrosis and Metabolic Alterations in Adults With alpha-1-antitrypsin Deficiency Caused by the Pi*ZZ Mutation ', Gastroenterology, vol. 157, no. 3, pp. 705-719.e18 . https://doi.org/10.1053/j.gastro.2019.05.013
Gastroenterology, 157(3), 705-+. W B SAUNDERS CO-ELSEVIER INC

Background & Aims Alpha-1 antitrypsin deficiency (AATD) is among the most common genetic disorders. Severe AATD is caused by a homozygous mutation in the SERPINA1 gene that encodes the Glu342Lys substitution (called the Pi*Z mutation, Pi*ZZ genotype)

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c589f8fd0ed2d082da4edb5e1cc42717
https://doi.org/10.1053/j.gastro.2019.05.013