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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1981 2
1990 1
1991 1
1995 4
1996 1
1997 1
1998 2
2000 2
2001 1
2002 1
2003 4
2004 4
2005 2
2006 2
2009 3
2011 1
2012 1
2014 1
2015 1
2017 2
2018 1
2021 2
2024 0

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39 results

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Page 1
Lumasiran, an RNAi Therapeutic for Primary Hyperoxaluria Type 1.
Garrelfs SF, Frishberg Y, Hulton SA, Koren MJ, O'Riordan WD, Cochat P, Deschênes G, Shasha-Lavsky H, Saland JM, Van't Hoff WG, Fuster DG, Magen D, Moochhala SH, Schalk G, Simkova E, Groothoff JW, Sas DJ, Meliambro KA, Lu J, Sweetser MT, Garg PP, Vaishnaw AK, Gansner JM, McGregor TL, Lieske JC; ILLUMINATE-A Collaborators. Garrelfs SF, et al. Among authors: van t hoff wg. N Engl J Med. 2021 Apr 1;384(13):1216-1226. doi: 10.1056/NEJMoa2021712. N Engl J Med. 2021. PMID: 33789010 Clinical Trial.
Molecular developments in renal tubulopathies.
Van'T Hoff WG. Van'T Hoff WG. Arch Dis Child. 2000 Sep;83(3):189-91. doi: 10.1136/adc.83.3.189. Arch Dis Child. 2000. PMID: 10952627 Free PMC article. Review. No abstract available.
Phase 1/2 Study of Lumasiran for Treatment of Primary Hyperoxaluria Type 1: A Placebo-Controlled Randomized Clinical Trial.
Frishberg Y, Deschênes G, Groothoff JW, Hulton SA, Magen D, Harambat J, Van't Hoff WG, Lorch U, Milliner DS, Lieske JC, Haslett P, Garg PP, Vaishnaw AK, Talamudupula S, Lu J, Habtemariam BA, Erbe DV, McGregor TL, Cochat P; study collaborators. Frishberg Y, et al. Among authors: van t hoff wg. Clin J Am Soc Nephrol. 2021 Jul;16(7):1025-1036. doi: 10.2215/CJN.14730920. Epub 2021 May 13. Clin J Am Soc Nephrol. 2021. PMID: 33985991 Free PMC article. Clinical Trial.
EUNEFRON, the European Network for the Study of Orphan Nephropathies.
Devuyst O, Meij I, Jeunemaitre X, Ronco P, Antignac C, Christensen EI, Knoers NV, Levtchenko EN, Deen PM, Müller D, Wagner CA, Rampoldi L, van't Hoff WG; EUNEFRON consortium. Devuyst O, et al. Among authors: van t hoff wg. Nephrol Dial Transplant. 2009 Jul;24(7):2011-5. doi: 10.1093/ndt/gfp095. Epub 2009 Mar 4. Nephrol Dial Transplant. 2009. PMID: 19264741 Free article. No abstract available.
Cysteamine toxicity in patients with cystinosis.
Besouw MT, Bowker R, Dutertre JP, Emma F, Gahl WA, Greco M, Lilien MR, McKiernan J, Nobili F, Schneider JA, Skovby F, van den Heuvel LP, Van't Hoff WG, Levtchenko EN. Besouw MT, et al. Among authors: van t hoff wg. J Pediatr. 2011 Dec;159(6):1004-11. doi: 10.1016/j.jpeds.2011.05.057. Epub 2011 Jul 23. J Pediatr. 2011. PMID: 21784456
Simultaneous sequencing of 37 genes identified causative mutations in the majority of children with renal tubulopathies.
Ashton EJ, Legrand A, Benoit V, Roncelin I, Venisse A, Zennaro MC, Jeunemaitre X, Iancu D, Van't Hoff WG, Walsh SB, Godefroid N, Rotthier A, Del Favero J, Devuyst O, Schaefer F, Jenkins LA, Kleta R, Dahan K, Vargas-Poussou R, Bockenhauer D. Ashton EJ, et al. Among authors: van t hoff wg. Kidney Int. 2018 Apr;93(4):961-967. doi: 10.1016/j.kint.2017.10.016. Epub 2018 Feb 15. Kidney Int. 2018. PMID: 29398133 Free article.
Clinical and molecular aspects of distal renal tubular acidosis in children.
Besouw MTP, Bienias M, Walsh P, Kleta R, Van't Hoff WG, Ashton E, Jenkins L, Bockenhauer D. Besouw MTP, et al. Among authors: van t hoff wg. Pediatr Nephrol. 2017 Jun;32(6):987-996. doi: 10.1007/s00467-016-3573-4. Epub 2017 Feb 10. Pediatr Nephrol. 2017. PMID: 28188436 Free article.
39 results