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

Year Number of Results
1991 1
1992 3
1993 1
1994 2
1996 2
1997 2
1998 3
1999 4
2000 1
2001 3
2002 1
2003 1
2004 4
2005 1
2006 2
2007 3
2008 2
2009 1
2010 2
2011 1
2012 1
2013 1
2017 3
2018 2
2019 1
2020 1
2021 4
2022 1
2023 1
2024 0

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51 results

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Page 1
Polyurethane-based drug delivery systems.
Cherng JY, Hou TY, Shih MF, Talsma H, Hennink WE. Cherng JY, et al. Among authors: talsma h. Int J Pharm. 2013 Jun 25;450(1-2):145-62. doi: 10.1016/j.ijpharm.2013.04.063. Epub 2013 Apr 28. Int J Pharm. 2013. PMID: 23632262 Review.
Making individualized drugs a reality.
Schellekens H, Aldosari M, Talsma H, Mastrobattista E. Schellekens H, et al. Among authors: talsma h. Nat Biotechnol. 2017 Jun;35(6):507-513. doi: 10.1038/nbt.3888. Epub 2017 Jun 5. Nat Biotechnol. 2017. PMID: 28581491 No abstract available.
Erratum: Making individualized drugs a reality.
Schellekens H, Aldosari M, Talsma H, Mastrobattista E. Schellekens H, et al. Among authors: talsma h. Nat Biotechnol. 2017 Aug 8;35(8):797. doi: 10.1038/nbt0817-797c. Nat Biotechnol. 2017. PMID: 28787402 No abstract available.
CRB1-Associated Retinal Dystrophies: A Prospective Natural History Study in Anticipation of Future Clinical Trials.
Nguyen XT, Talib M, van Schooneveld MJ, Wijnholds J, van Genderen MM, Schalij-Delfos NE, Klaver CCW, Talsma HE, Fiocco M, Florijn RJ, Ten Brink JB, Cremers FPM, Meester-Smoor MA, van den Born LI, Hoyng CB, Thiadens AAHJ, Bergen AA, Boon CJF. Nguyen XT, et al. Among authors: talsma he. Am J Ophthalmol. 2022 Feb;234:37-48. doi: 10.1016/j.ajo.2021.07.021. Epub 2021 Jul 25. Am J Ophthalmol. 2022. PMID: 34320374 Free article.
Autosomal Recessive NRL Mutations in Patients with Enhanced S-Cone Syndrome.
Littink KW, Stappers PTY, Riemslag FCC, Talsma HE, van Genderen MM, Cremers FPM, Collin RWJ, van den Born LI. Littink KW, et al. Among authors: talsma he. Genes (Basel). 2018 Jan 30;9(2):68. doi: 10.3390/genes9020068. Genes (Basel). 2018. PMID: 29385733 Free PMC article.
Defining inclusion criteria and endpoints for clinical trials: a prospective cross-sectional study in CRB1-associated retinal dystrophies.
Talib M, van Schooneveld MJ, Wijnholds J, van Genderen MM, Schalij-Delfos NE, Talsma HE, Florijn RJ, Ten Brink JB, Cremers FPM, Thiadens AAHJ, van den Born LI, Hoyng CB, Meester-Smoor MA, Bergen AA, Boon CJF. Talib M, et al. Among authors: talsma he. Acta Ophthalmol. 2021 May;99(3):e402-e414. doi: 10.1111/aos.14597. Epub 2021 Feb 2. Acta Ophthalmol. 2021. PMID: 33528094 Free PMC article.
Beyond nephronophthisis: Retinal dystrophy in the absence of kidney dysfunction in childhood expands the clinical spectrum of CEP83 deficiency.
Veldman BCF, Kuper WFE, Lilien M, Schuurs-Hoeijmakers JHM, Marcelis C, Phan M, Hettinga Y, Talsma HE, van Hasselt PM, Haijes HA. Veldman BCF, et al. Among authors: talsma he. Am J Med Genet A. 2021 Jul;185(7):2204-2210. doi: 10.1002/ajmg.a.62225. Epub 2021 May 3. Am J Med Genet A. 2021. PMID: 33938610 Free PMC article.
51 results