Ives J - Search Results

1

The efficacy and safety of 200 days valganciclovir cytomegalovirus prophylaxis in high-risk kidney transplant recipients.

Humar A, Lebranchu Y, Vincenti F, Blumberg EA, Punch JD, Limaye AP, Abramowicz D, Jardine AG, Voulgari AT, Ives J, Hauser IA, Peeters P. Humar A, et al. Among authors: ives j. Am J Transplant. 2010 May;10(5):1228-37. doi: 10.1111/j.1600-6143.2010.03074.x. Epub 2010 Mar 26. Am J Transplant. 2010. PMID: 20353469 Free article. Clinical Trial.

2

Extended valganciclovir prophylaxis in D+/R- kidney transplant recipients is associated with long-term reduction in cytomegalovirus disease: two-year results of the IMPACT study.

Humar A, Limaye AP, Blumberg EA, Hauser IA, Vincenti F, Jardine AG, Abramowicz D, Ives JA, Farhan M, Peeters P. Humar A, et al. Transplantation. 2010 Dec 27;90(12):1427-31. doi: 10.1097/tp.0b013e3181ff1493. Transplantation. 2010. PMID: 21197713 Clinical Trial.

3

Cytomegalovirus resistance in solid organ transplant recipients treated with intravenous ganciclovir or oral valganciclovir.

Boivin G, Goyette N, Rollag H, Jardine AG, Pescovitz MD, Asberg A, Ives J, Hartmann A, Humar A. Boivin G, et al. Among authors: ives j. Antivir Ther. 2009;14(5):697-704. Antivir Ther. 2009. PMID: 19704173 Clinical Trial.

4

Valganciclovir dosing according to body surface area and renal function in pediatric solid organ transplant recipients.

Vaudry W, Ettenger R, Jara P, Varela-Fascinetto G, Bouw MR, Ives J, Walker R; Valcyte WV16726 Study Group. Vaudry W, et al. Among authors: ives j. Am J Transplant. 2009 Mar;9(3):636-43. doi: 10.1111/j.1600-6143.2008.02528.x. Am J Transplant. 2009. PMID: 19260840 Free article. Clinical Trial.

5

Incidence of cytomegalovirus UL97 and UL54 amino acid substitutions detected after 100 or 200 days of valganciclovir prophylaxis.

Boivin G, Goyette N, Farhan M, Ives J, Elston R. Boivin G, et al. Among authors: ives j. J Clin Virol. 2012 Mar;53(3):208-13. doi: 10.1016/j.jcv.2011.12.019. Epub 2012 Jan 10. J Clin Virol. 2012. PMID: 22237003 Clinical Trial.

6

Recombinant phenotyping of cytomegalovirus sequence variants detected after 200 or 100 days of valganciclovir prophylaxis.

Chou S, Marousek G, Boivin G, Goyette N, Farhan M, Ives JA, Elston R. Chou S, et al. Transplantation. 2010 Dec 27;90(12):1409-13. doi: 10.1097/TP.0b013e3181fdd9d2. Transplantation. 2010. PMID: 21030903 Clinical Trial.

7

Incidence and characterization of cytomegalovirus resistance mutations among pediatric solid organ transplant patients who received valganciclovir prophylaxis.

Martin M, Goyette N, Ives J, Boivin G. Martin M, et al. Among authors: ives j. J Clin Virol. 2010 Apr;47(4):321-4. doi: 10.1016/j.jcv.2010.01.009. Epub 2010 Feb 6. J Clin Virol. 2010. PMID: 20138805

8

Tolerability of up to 200 days of prophylaxis with valganciclovir oral solution and/or film-coated tablets in pediatric kidney transplant recipients at risk of cytomegalovirus disease.

Varela-Fascinetto G, Benchimol C, Reyes-Acevedo R, Genevray M, Bradley D, Ives J, Silva HT Jr. Varela-Fascinetto G, et al. Among authors: ives j. Pediatr Transplant. 2017 Feb;21(1). doi: 10.1111/petr.12833. Epub 2016 Oct 17. Pediatr Transplant. 2017. PMID: 27753183 Clinical Trial.

9

Pharmacokinetics of oral valganciclovir solution and intravenous ganciclovir in pediatric renal and liver transplant recipients.

Pescovitz MD, Ettenger RB, Strife CF, Sherbotie JR, Thomas SE, McDiarmid S, Bartosh S, Ives J, Bouw MR, Bucuvalas J. Pescovitz MD, et al. Among authors: ives j. Transpl Infect Dis. 2010 Jun;12(3):195-203. doi: 10.1111/j.1399-3062.2009.00478.x. Epub 2009 Dec 4. Transpl Infect Dis. 2010. PMID: 20002356 Free article. Clinical Trial.

10

Pharmacokinetics and Safety of Valganciclovir in Pediatric Heart Transplant Recipients 4 Months of Age and Younger.

Bradley D, Moreira S, Subramoney V, Chin C, Ives J, Wang K; Valcyte NP22523 Study Team. Bradley D, et al. Among authors: ives j. Pediatr Infect Dis J. 2016 Dec;35(12):1324-1328. doi: 10.1097/INF.0000000000001317. Pediatr Infect Dis J. 2016. PMID: 27580058

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