Zobrazeno 1 - 10
of 351
pro vyhledávání: '"Joost P H, Drenth"'
Autor:
Gijs Kemper, Christian Gerges, Erik J. Schoon, Ramon-Michel Schreuder, Ruud R. W. Schrauwen, Ludger S. M. Epping, Torsten Beyna, Joost P. H. Drenth, Ufuk Gündug, Peter D. Siersema, Erwin J. M. van Geenen, the ENDOCARE study group
Publikováno v:
Trials, Vol 25, Iss 1, Pp 1-7 (2024)
Abstract Background Nowadays, large benign lateral spreading lesions (LSLs) and sessile polyps in the colorectum are mostly resected by endoscopic mucosal resection (EMR). A major drawback of EMR is the polyp recurrence rate of up to 20%. Snare tip s
Externí odkaz:
https://doaj.org/article/8fb8fb27984743f0ac8d88eb91d92afa
Autor:
Anna E. C. Stoelinga, Maarten E. Tushuizen, Wilbert B. van den Hout, Mar D. M. Rodriguez Girondo, Elsemieke S. de Vries, Amar D. Levens, Dirk-Jan A. R. Moes, Tom J. G. Gevers, Suzanne van der Meer, Hans T. Brouwer, Hendrik J. M. de Jonge, Ynte S. de Boer, Ulrich H. W. Beuers, Adriaan J. van der Meer, Aad P. van den Berg, Maureen M. J. Guichelaar, Joost P. H. Drenth, Bart van Hoek, on behalf of the Dutch Autoimmune Hepatitis Group
Publikováno v:
Trials, Vol 25, Iss 1, Pp 1-11 (2024)
Abstract Background Autoimmune hepatitis (AIH) is a rare, chronic inflammatory disease of the liver. The treatment goal is reaching complete biochemical response (CR), defined as the normalisation of aspartate and alanine aminotransferases and immuno
Externí odkaz:
https://doaj.org/article/e9871b3711e44943a5adbb67b77352b2
Autor:
Romée J. A. L. M. Snijders, Anna E. C. Stoelinga, Tom J. G. Gevers, Simon Pape, Maaike Biewenga, Robert C. Verdonk, Hendrik J. M. de Jonge, Jan Maarten Vrolijk, Sjoerd F. Bakker, Thomas Vanwolleghem, Ynto S. de Boer, Martine A. M. C. Baven Pronk, Ulrich H. W. Beuers, Adriaan J. van der Meer, Nicole M. F. van Gerven, Marijn G. M. Sijtsma, Bart J. Verwer, Ingrid A. M. Gisbertz, Maartje Bartelink, Floris F. van den Brand, Kerem Sebib Korkmaz, Aad P. van den Berg, Maureen M. J. Guichelaar, Khalida Soufidi, Amar D. Levens, Bart van Hoek, Joost P. H. Drenth, on behalf of the Dutch Autoimmune Hepatitis Working Group
Publikováno v:
Trials, Vol 23, Iss 1, Pp 1-13 (2022)
Abstract Background Currently, the standard therapy for autoimmune hepatitis (AIH) consists of a combination of prednisolone and azathioprine. However, 15% of patients are intolerant to azathioprine which necessitates cessation of azathioprine or cha
Externí odkaz:
https://doaj.org/article/94c4694744e64d888bdd6fba2110a79f
Autor:
Daan W. Von den Hoff, Floor A. C. Berden, Joost P. H. Drenth, Arnt F. A. Schellekens, HepNed, NISPA
Publikováno v:
Addiction Science & Clinical Practice, Vol 17, Iss 1, Pp 1-7 (2022)
Abstract Background People who use drugs (PWUD) are at high risk for hepatitis C virus (HCV) infection and its complications. Given the high prevalence rate of HCV in PWUD, the World Health Organization (WHO) emphasizes PWUD as a target population fo
Externí odkaz:
https://doaj.org/article/5512f6b01f404c8f8571d739aec06c77
Publikováno v:
Genes, Vol 14, Iss 9, p 1755 (2023)
α-1,2-mannosyltransferase (ALG9) germline variants are linked to autosomal dominant polycystic kidney disease (ADPKD). Many individuals affected with ADPKD possess polycystic livers as a common extrarenal manifestation. We performed whole exome sequ
Externí odkaz:
https://doaj.org/article/8c7fed95add843cb8e67fe22737115da
Autor:
Melissa M. Boerrigter, René H. M. te Morsche, Hanka Venselaar, Nikki Pastoors, Anja M. Geerts, Anne Hoorens, Joost P. H. Drenth
Publikováno v:
Genes, Vol 14, Iss 8, p 1652 (2023)
Protein-truncating variants in α-1,3-glucosyltransferase (ALG8) are a risk factor for a mild cystic kidney disease phenotype. The association between these variants and liver cysts is limited. We aim to identify pathogenic ALG8 variants in our cohor
Externí odkaz:
https://doaj.org/article/777193cc9832447997d23b05e15c50ba
Autor:
Lotty Hooft, Pauline Heus, Gert P Westert, Rudolf B Kool, Suzanne E Geerlings, Janwillem Kocks, Prabath W B Nanayakkara, Tessa Rietbergen, Leti van Bodegom-Vos, Simone A van Dulmen, Eva W Verkerk, Corina de Jong, Bart J Laan, JOOST P H DRENTH, Marlies Wakkee, Aniek de Coninck, Harry C Schouten, Evelien I T de Schepper, Saskia F van Vugt, Renuka S Bindraban, Sven van Egmond, Judith J de Jong
Publikováno v:
BMJ Open Quality, Vol 11, Iss 3 (2022)
Background Reducing the overuse of care that is proven to be of low value increases the quality and safety of care. We aimed to identify lessons for reducing low-value care by looking at: (1) The effects of eight de-implementation projects. (2) The b
Externí odkaz:
https://doaj.org/article/765a305c91e64bc9b65399547acc336e
Autor:
Floris M. Thunnissen, Daan J. Comes, Remy W. F. Geenen, Deniece Riviere, Carmen S. S. Latenstein, Marten A. Lantinga, Henk J. Schers, Cornelis J. H. M. van Laarhoven, Joost P. H. Drenth, Femke Atsma, Philip R. de Reuver
Publikováno v:
Journal of Clinical Medicine, Vol 12, Iss 12, p 4162 (2023)
This study aimed to quantify the confirmation of gallstones on ultrasound (US) in patients with suspicion of gallstone disease. To aid general practitioners (GPs) in diagnostic workup, a model to predict gallstones was developed. A prospective cohort
Externí odkaz:
https://doaj.org/article/73bcf83951f0472ea558bc6fd7ecd7a7
Autor:
Koen C. van Son, Lars Verschuren, Roeland Hanemaaijer, Helen Reeves, R. Bart Takkenberg, Joost P. H. Drenth, Maarten E. Tushuizen, Adriaan G. Holleboom
Publikováno v:
Cancers, Vol 15, Iss 4, p 1308 (2023)
Hepatocellular carcinoma (HCC) in the setting of non-alcoholic fatty liver disease (NAFLD)-related cirrhosis and even in the pre-cirrhotic state is increasing in incidence. NAFLD-related HCC has a poor clinical outcome as it is often advanced at diag
Externí odkaz:
https://doaj.org/article/91b49efabd2a42de965ddbd396fb92b3
Autor:
Liyanne F. M. van de Laarschot, René H. M. te Morsche, Alexander Hoischen, Hanka Venselaar, Hennie M. Roelofs, Wybrich R. Cnossen, Jesus M. Banales, Ronald Roepman, Joost P. H. Drenth
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-11 (2020)
Abstract Background Polycystic liver disease (PLD) is an inherited disorder characterized by numerous cysts in the liver. Autosomal dominant polycystic kidney and liver disease (ADPKD and ADPLD, respectively) have been linked to pathogenic GANAB vari
Externí odkaz:
https://doaj.org/article/c710959f5f25452a936f4f4f95599345