Zobrazeno 1 - 10 of 17 pro vyhledávání: '"Edwin M. Spithoven"'
1
Akademický článek
Association of plasma somatostatin with disease severity and progression in patients with autosomal dominant polycystic kidney disease
Autor: A. Lianne Messchendorp, Edwin M. Spithoven, Niek F. Casteleijn, Wendy A. Dam, Jacob van den Born, Wouter F. Tonnis, Carlo A. J. M. Gaillard, Esther Meijer, on behalf of the DIPAK Consortium
Publikováno v: BMC Nephrology, Vol 19, Iss 1, Pp 1-10 (2018)
Abstract Background Somatostatin (SST) inhibits intracellular cyclic adenosine monophosphate (cAMP) production and thus may modify cyst formation in autosomal dominant polycystic kidney disease (ADPKD). We investigated whether endogenous plasma SST c
Externí odkaz: https://doaj.org/article/5ffdb32fedf24b4aa7465562d43628c9
Zobrazit plný text záznamu
2
Akademický článek
Urinary Biomarkers to Identify Autosomal Dominant Polycystic Kidney Disease Patients With a High Likelihood of Disease Progression
Autor: A. Lianne Messchendorp, Esther Meijer, Wendy E. Boertien, Gerwin E. Engels, Niek F. Casteleijn, Edwin M. Spithoven, Monique Losekoot, Johannes G.M. Burgerhof, Dorien J.M. Peters, Ron T. Gansevoort
Publikováno v: Kidney International Reports, Vol 3, Iss 2, Pp 291-301 (2018)
The variable disease course of autosomal dominant polycystic kidney disease (ADPKD) makes it important to develop biomarkers that can predict disease progression, from a patient perspective and to select patients for renoprotective treatment. We ther
Externí odkaz: https://doaj.org/article/6fc726da32f847b0a64eb14f8c80f143
Zobrazit plný text záznamu
4
Effect of a Somatostatin Analogue on the Vasopressin Pathway in Patients With ADPKD
Autor: A. Lianne Messchendorp, Bart J. Kramers, Edwin M. Spithoven, Katrin Stade, Esther Meijer, Ron T. Gansevoort, Joost P.H. Drenth, Johan W. de Fijter, Folkert W. Visser, Jack F.M. Wetzels, Robert Zietse
Publikováno v: Kidney International Reports, 4, 1170-1174
Kidney International Reports, 4, 8, pp. 1170-1174
Kidney International Reports, 4(8), 1170-1174. ELSEVIER SCIENCE INC
Kidney International Reports
Contains fulltext : 209004.pdf (Publisher’s version ) (Open Access)
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::959ddce597bcfe97474f8ed7b350e064
http://hdl.handle.net/2066/209004
Zobrazit plný text záznamu
5
Urine and Plasma Osmolality in Patients with Autosomal Dominant Polycystic Kidney Disease: Reliable Indicators of Vasopressin Activity and Disease Prognosis?
Autor: Debbie Zittema, Stephan J. L. Bakker, Edwin M. Spithoven, Wendy E. Boertien, Niek F. Casteleijn, Joachim Struck, Ron T. Gansevoort, Carlo A. J. M. Gaillard, Esther Meijer
Publikováno v: American Journal of Nephrology, 41(3), 248-256. KARGER
Background: Vasopressin plays an essential role in osmoregulation, but has deleterious effects in patients with ADPKD. Increased water intake to suppress vasopressin activity has been suggested as a potential renoprotective strategy. This study inves
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::01d1fcd9e5b258df7d0b8618e9c8682d
https://doi.org/10.1159/000382081
Zobrazit plný text záznamu
6
The Association of Combined Total Kidney and Liver Volume with Pain and Gastrointestinal Symptoms in Patients with Later Stage Autosomal Dominant Polycystic Kidney Disease
Autor: Joost P.H. Drenth, Annemarie L. Messchendorp, Niek F. Casteleijn, Darius Soonawala, Ron T. Gansevoort, Maartje D A van Gastel, Tom J. G. Gevers, Dorien J.M. Peters, Robert Zietse, Hedwig M. A. D'Agnolo, Mahdi Salih, Folkert W. Visser, Edwin M. Spithoven, Hans de Fijter, Jack F.M. Wetzels
Publikováno v: American Journal of Nephrology, 46, 3, pp. 239-248
American Journal of Nephrology, 46(3), 239-248. Karger
American Journal of Nephrology, 46(3), 239-248. KARGER
American Journal of Nephrology, 46, 239-248
American Journal of Nephrology, 46(3), 239-248
Background: There is an ongoing debate if and how kidney and liver volume are associated with pain and gastrointestinal (GI) symptoms in autosomal dominant polycystic kidney disease (ADPKD) patients. Since both kidney and liver volume could interact,
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b48323e9e32a1c6c7240335f997ff2f1
https://hdl.handle.net/2066/177206
Zobrazit plný text záznamu
7
Nephrectomy in Autosomal Dominant Polycystic Kidney Disease: A Patient with Exceptionally Large, Still Functioning Kidneys
Autor: Edwin M. Spithoven, Roel Goldschmeding, Paul Berger, Niek F. Casteleijn
Publikováno v: Case Reports in Nephrology and Urology
Autosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary kidney disease. It is characterized by progressive cyst formation in both kidneys, often leading to end-stage kidney disease. Indications for surgical removal of an AD
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5158a76cca57c5025a4bfaa52cbc5149
https://doi.org/10.1159/000363378
Zobrazit plný text záznamu
8
Estimation of Total Kidney Volume in Autosomal Dominant Polycystic Kidney Disease
Autor: Edwin M. Spithoven, Maatje D.A. van Gastel, A. Lianne Messchendorp, Niek F. Casteleijn, Joost P.H. Drenth, Carlo A. Gaillard, Johan W. de Fijter, Esther Meijer, Dorien J.M. Peters, Peter Kappert, Remco J. Renken, Folkert W. Visser, Jack F.M. Wetzels, Robert Zietse, Ron T. Gansevoort, Hedwig d’Agnolo, Heleen Dekker, Joost Drenth, Tom J. Gevers, Hester Happé, Gert ter Horst, Remco Renken, H. Pieterman, Mahdi Salih, Darius Soonawala, Vicente E. Torres, M. Wasser, Marjolein van Buren, Nick Veeger, Marc Vervloet
Publikováno v: American Journal of Kidney Diseases, 66, 792-801
American Journal of Kidney Diseases, 66, 5, pp. 792-801
American Journal of Kidney Diseases, 66(5), 792-801. W.B. Saunders Ltd
American Journal of Kidney Diseases, 66(5), 792-801
American Journal of Kidney Diseases, 66(5), 792-801. W.B. Saunders
Spithoven, E M, van Gastel, M D, Messchendorp, A, Casteleijn, N F, Drenth, J P, Gaillard, C A J M, de Fijter, J W, Meijer, E, Peters, D J, Kappert, P, Renken, R J, Visser, F W, Wetzels, J F, Zietse, R & Gansevoort, R T 2015, ' Estimation of Total Kidney Volume in Autosomal Dominant Polycystic Kidney Disease ', American Journal of Kidney Diseases, vol. 66, no. 5, pp. 792-801 . https://doi.org/10.1053/j.ajkd.2015.06.017
American Journal of Kidney Diseases, 66(5), 792-801. W B SAUNDERS CO-ELSEVIER INC
Background: In autosomal dominant polycystic kidney disease (ADPKD), obtaining measured total kidney volume (mTKV) by magnetic resonance (MR) imaging and manual tracing is time consuming. Two alternative MR imaging methods have recently been proposed
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3731dc15e10cc5ed4372d52cb7b0b82c
http://hdl.handle.net/2066/152199
Zobrazit plný text záznamu
9
Bilateral cysts in the choroid plexus in a patient with autosomal dominant polycystic kidney disease
Autor: Edwin M. Spithoven, Niek F. Casteleijn, Mervyn D.I. Vergouwen, Ron T. Gansevoort, Maarten B. Rookmaaker
Publikováno v: Nephrology Dialysis Transplantation, 30(5), 859. Oxford University Press
Nephrology, Dialysis, Transplantation, 30(5), 859-861. Oxford University Press
Autosomal dominant polycystic kidney disease (ADPKD) is a genetic systemic disorder, which is associated with cyst formation in several organs, renal function decline and a higher prevalence of intracranial aneurysms. We report a 52-year-old, otherwi
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d319b67a881405ca07cfd7244e218e59
https://dspace.library.uu.nl/handle/1874/331569
Zobrazit plný text záznamu

Vyhledávací nástroje:

Upřesnit hledání

Omezení vyhledávání
Plný text Recenzováno Digitální knihovna AV ČR
Zdroje