Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Annick Vanclooster"'
Autor:
Ronit Shiri-Sverdlov, Inês Magro dos Reis, Yvonne Oligschlaeger, Tim Hendrikx, Dennis M. Meesters, Annick Vanclooster, Nele Vanhoutvin, Ger H. Koek, Marit Westerterp, Christoph J. Binder, David Cassiman, Tom Houben
Publikováno v:
Antioxidants, Vol 10, Iss 1, p 129 (2021)
As a mediator between lipid metabolism dysfunction, oxidative stress and inflammation, oxidized low-density lipoprotein (oxLDL) is a promising therapeutical target in a wide range of metabolic diseases. In mice, pneumococcal immunization increases an
Externí odkaz:
https://doaj.org/article/36dcda652b5347f298def4e713660ec5
Autor:
Heinz Zoller, Benedikt Schaefer, Annick Vanclooster, Bill Griffiths, Edouard Bardou-Jacquet, Elena Corradini, Graça Porto, John Ryan, Markus Cornberg
ispartof: JOURNAL OF HEPATOLOGY vol:77 issue:2 pages:479-502 status: published
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e3fb50990f641046a4fcd5146c9c7a6d
https://hdl.handle.net/11380/1280001
https://hdl.handle.net/11380/1280001
Autor:
Nele Vanhoutvin, Yvonne Oligschlaeger, Tom Houben, Christoph J. Binder, Marit Westerterp, David Cassiman, Tim Hendrikx, Annick Vanclooster, Ronit Shiri-Sverdlov, Ger H. Koek, Dennis M. Meesters, Inês Magro dos Reis
Publikováno v:
Antioxidants, 10(1):129. MDPI AG
Antioxidants, 10(1):129, 1-12. Multidisciplinary Digital Publishing Institute (MDPI)
Antioxidants, Vol 10, Iss 129, p 129 (2021)
Antioxidants
Volume 10
Issue 1
Antioxidants, 10(1):129, 1-12. Multidisciplinary Digital Publishing Institute (MDPI)
Antioxidants, Vol 10, Iss 129, p 129 (2021)
Antioxidants
Volume 10
Issue 1
As a mediator between lipid metabolism dysfunction, oxidative stress and inflammation, oxidized low-density lipoprotein (oxLDL) is a promising therapeutical target in a wide range of metabolic diseases. In mice, pneumococcal immunization increases an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cf9d8c8958dd352388bde948fa1b7bd5
https://research.rug.nl/en/publications/1e7eb386-a850-4270-ae43-27829627153c
https://research.rug.nl/en/publications/1e7eb386-a850-4270-ae43-27829627153c
Autor:
Evelien Gielen, Peter Witters, Annick Vanclooster, Michaël R. Laurent, Wouter Meersseman, David Cassiman, Eva Morava, Eveline Lefever
Publikováno v:
Journal of clinical densitometry : the official journal of the International Society for Clinical Densitometry. 23(3)
Background: Hypophosphatasia (HPP) is a rare metabolic bone disorder caused by mutations in the alkaline phosphatase (ALPL) gene, and characterized by low circulating alkaline phosphatase (ALP) levels and bone, muscle, dental and systemic manifestati
Therapeutic recommendations in HFE hemochromatosis for p.Cys282Tyr (C282Y/C282Y) homozygous genotype
Autor:
Sonia Distante, Ben Marris, Albert Altes, Alberto Piperno, Rodolfo D. Cançado, Paul C. Adams, Robert W. Evans, John Ryan, Graça Porto, Ioav Cabantchik, Emerência Teixeira, Annick Vanclooster, Dianne Prince, Desley White, Paulo Caleb Junior Lima Santos, Patricia J. Evans, Dorine W. Swinkels, Domenico Girelli, Mayka Sanchez, Gordon D. McLaren, Ketil Toska, Rolf Hultcrantz, Pierre Brissot, Brigitte Pineau, Elizabeta Nemeth, Peter Nielsen, Tomas Ganz, Nils Milman, Barbara Butzeck
Publikováno v:
Hepatology International
Although guidelines are available for hereditary hemochromatosis, a high percentage of the recommendations within them are not shared between the different guidelines. Our main aim is to provide an objective, simple, brief, and practical set of recom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a728a5d65c1e59cf0a3989bf3759033a
https://ora.ox.ac.uk/objects/uuid:dd16cf4c-126c-4bfb-9f6a-fb79ca535d8d
https://ora.ox.ac.uk/objects/uuid:dd16cf4c-126c-4bfb-9f6a-fb79ca535d8d
Autor:
David Cassiman, Stefan Ghysels, Erik M. Akkerman, Mario Maas, Ronald R. Peeters, Annick Vanclooster, Wouter Meersseman
Publikováno v:
Medical Research Archives.
Background and study aim: Dixon Quantitative Chemical Shift Imaging (QCSI) to measure lumbar spine bone marrow fat signal fraction (FF), is considered the ‘gold standard’ for the determination and follow up of bone involvement in type I Gaucher d
Publikováno v:
Gastroenterology, 153(3), 678-680.e2. Elsevier Saunders
Phlebotomy constitutes the established treatment for HFE-related hemochromatosis. Retrospective studies have suggested proton pump inhibitors (PPIs) reduce the need for phlebotomy in this population. We conducted a randomized controlled trial to prov
Autor:
Werner Van Steenbergen, Dorine W. Swinkels, David Cassiman, Mirian C. H. Janssen, Hub Wollersheim, Bert Aertgeerts, Joost P.H. Drenth, Annick Vanclooster
Publikováno v:
Clinics and Research in Hepatology and Gastroenterology, 39, 205-14
Clinics and Research in Hepatology and Gastroenterology, 39, 2, pp. 205-14
Clinics and Research in Hepatology and Gastroenterology, 39, 2, pp. 205-14
Item does not contain fulltext BACKGROUND AND OBJECTIVES: Hereditary haemochromatosis (HH) is the most prevalent genetic liver disease, with an incidence of 1/200 to 1/400 in the Caucasian population. HH patients are treated by family physicians as w
Autor:
Pieter Vermeersch, Karel Allegaert, K. Vande Kerckhove, Wouter Meersseman, A. Spraul, David Cassiman, Roland Devlieger, Annick Vanclooster, A. Meulemans
Publikováno v:
JIMD Reports ISBN: 9783642280955
A 19 year old woman with tyrosinaemia type 1 gave birth to a healthy girl after 41 weeks of gestation. Nitisinone was continued throughout the pregnancy (maternal levels 68-96 μmol/l, target level 30-60 μmol/l). Tyrosine levels during pregnancy wer