Zobrazeno 1 - 10
of 20
pro vyhledávání: '"T. J. G. Gevers"'
Autor:
M A, Lantinga, R G L, de Sévaux, T J G, Gevers, W J G, Oyen, J W, de Fijter, D, Soonawala, R, Zietse, M, Salih, N F, Casteleijn, E M, Spithoven, E, Meijer, R T, Gansevoort, J P H, Drenth On Behalf Of The Dipak Consortium
Publikováno v:
The Netherlands Journal of Medicine. 76(5):226-234
BACKGROUND: Cyst infection may occur in autosomal dominant polycystic kidney disease (ADPKD) and autosomal dominant polycystic liver disease (ADPLD). Antimicrobial agents often fail to control infection, leading to invasive action. We aimed to identi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::95b3bedaf4f2a97b9b059c9e81b72ec5
https://hdl.handle.net/11370/bc360867-bdb4-4b82-9f52-c49ea5d76ff4
https://hdl.handle.net/11370/bc360867-bdb4-4b82-9f52-c49ea5d76ff4
Publikováno v:
Journal of Viral Hepatitis, 22, 12, pp. 965-73
Journal of Viral Hepatitis, 22, 965-73
Journal of Viral Hepatitis, 22, 965-73
Item does not contain fulltext Hepatitis E viral infection can lead to a chronic infection in immunocompromised patients, resulting in progressive liver disease and cirrhosis. Isolated cases have shown that treatment with ribavirin or pegylated inter
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c02ea63381832c8b83a62ac7685f65fd
https://hdl.handle.net/2066/152761
https://hdl.handle.net/2066/152761
Autor:
M, Chrispijn, F, Nevens, T J G, Gevers, R, Vanslembrouck, M G H, van Oijen, W, Coudyzer, A L, Hoffmann, H M, Dekker, R A, de Man, L, van Keimpema, J P H, Drenth
Publikováno v:
Alimentary pharmacologytherapeutics. 35(2)
Polycystic liver disease (PLD) is a phenotypical expression of autosomal dominant polycystic kidney disease and isolated polycystic liver disease. Somatostatin analogues, such as lanreotide, reduce polycystic liver volume.To establish long-term outco
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7975e36b65091837d5e7e82a0ac96905
https://pubmed.ncbi.nlm.nih.gov/22111942
https://pubmed.ncbi.nlm.nih.gov/22111942
Publikováno v:
The Netherlands journal of medicine. 69(9)
Autosomal dominant polycystic kidney disease (ADPKD) is a multisystem disorder. It is the most common genetic cause of end-stage renal disease. One frequent extra-renal manifestation is hepatic cyst formation. The majority of ADPKD patients develop c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5e236268634e9e98670b2132dcecca24
https://pubmed.ncbi.nlm.nih.gov/21978978
https://pubmed.ncbi.nlm.nih.gov/21978978
Autor:
Mironova, Maria1 (AUTHOR), Mahdi, Mohammed K.1 (AUTHOR), Bhatia, Jyoti2 (AUTHOR), Nielson, Rosemarie C.1 (AUTHOR), Doria, Cataldo3 (AUTHOR)
Publikováno v:
Case Reports in Gastrointestinal Medicine. 6/21/2021, p1-4. 4p.
Publikováno v:
ChemBioChem; Sep2023, Vol. 24 Issue 18, p1-8, 8p
Autor:
Gevers, Tom J.G.1, Nevens, Frederik2, Torres, Vicente E.3, Hogan, Marie C.3, Drenth, Joost P.H.1
Publikováno v:
Liver International. Apr2016, Vol. 36 Issue 4, p595-602. 8p.
Publikováno v:
Journal of Viral Hepatitis. Dec2015, Vol. 22 Issue 12, p965-973. 9p.
Autor:
Neijenhuis, M. K.1, Gevers, T. J. G.1, Nevens, F.2, Hogan, M. C.3, Torres, V. E.3, Kievit, W.4, Drenth, J. P. H.1
Publikováno v:
Alimentary Pharmacology & Therapeutics. Sep2015, Vol. 42 Issue 5, p591-598. 8p. 3 Charts.
Publikováno v:
Alimentary Pharmacology & Therapeutics. Feb2015, Vol. 41 Issue 3, p253-261. 9p. 2 Diagrams, 4 Charts, 1 Graph.