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

Year Number of Results
1986 1
1994 1
1998 1
1999 2
2000 1
2003 3
2004 1
2005 3
2006 1
2007 2
2008 3
2010 1
2011 1
2012 5
2013 4
2014 4
2015 6
2016 7
2017 4
2018 3
2019 2
2020 1
2021 5
2022 5
2023 6
2024 4

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73 results

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Page 1
Health systems for rare diseases: financial sustainability.
Iskrov G, Stefanov R, Ferrelli RM. Iskrov G, et al. Among authors: stefanov r. Ann Ist Super Sanita. 2019 Jul-Sep;55(3):270-275. doi: 10.4415/ANN_19_03_13. Ann Ist Super Sanita. 2019. PMID: 31553322 Free article. Review.
Access to orphan drugs - comparison across Balkan countries.
Pejcic AV, Iskrov G, Jakovljevic MM, Stefanov R. Pejcic AV, et al. Among authors: stefanov r. Health Policy. 2018 Jun;122(6):583-589. doi: 10.1016/j.healthpol.2018.04.009. Epub 2018 Apr 26. Health Policy. 2018. PMID: 29729905 Review.
Transposition and implementation of EU rare disease policy in Eastern Europe.
Pejcic AV, Iskrov G, Raycheva R, Stefanov R, Jakovljevic MM. Pejcic AV, et al. Among authors: stefanov r. Expert Rev Pharmacoecon Outcomes Res. 2017 Dec;17(6):557-566. doi: 10.1080/14737167.2017.1388741. Epub 2017 Oct 10. Expert Rev Pharmacoecon Outcomes Res. 2017. PMID: 28975845 Review.
National plans and strategies on rare diseases in Europe.
Taruscio D, Vittozzi L, Stefanov R. Taruscio D, et al. Among authors: stefanov r. Adv Exp Med Biol. 2010;686:475-91. doi: 10.1007/978-90-481-9485-8_26. Adv Exp Med Biol. 2010. PMID: 20824461 Review.
Genetic newborn screening and digital technologies: A project protocol based on a dual approach to shorten the rare diseases diagnostic path in Europe.
Garnier N, Berghout J, Zygmunt A, Singh D, Huang KA, Kantz W, Blankart CR, Gillner S, Zhao J, Roettger R, Saier C, Kirschner J, Schenk J, Atkins L, Ryan N, Zarakowska K, Zschüntzsch J, Zuccolo M, Müllenborn M, Man YS, Goodman L, Trad M, Chalandon AS, Sansen S, Martinez-Fresno M, Badger S, Walther van Olden R, Rothmann R, Lehner P, Tschohl C, Baillon L, Gumus G, Gross E, Stefanov R, Iskrov G, Raycheva R, Kostadinov K, Mitova E, Einhorn M, Einhorn Y, Schepers J, Hübner M, Alves F, Iskandar R, Mayer R, Renieri A, Piperkova A, Gut I, Beltran S, Matthiesen ME, Poetz M, Hansson M, Trollmann R, Agolini E, Ottombrino S, Novelli A, Bertini E, Selvatici R, Farnè M, Fortunato F, Ferlini A. Garnier N, et al. Among authors: stefanov r. PLoS One. 2023 Nov 22;18(11):e0293503. doi: 10.1371/journal.pone.0293503. eCollection 2023. PLoS One. 2023. PMID: 37992053 Free PMC article.
Outcome of renal transplantation in patients with non-Shiga toxin-associated hemolytic uremic syndrome: prognostic significance of genetic background.
Bresin E, Daina E, Noris M, Castelletti F, Stefanov R, Hill P, Goodship TH, Remuzzi G; International Registry of Recurrent and Familial HUS/TTP. Bresin E, et al. Among authors: stefanov r. Clin J Am Soc Nephrol. 2006 Jan;1(1):88-99. doi: 10.2215/CJN.00050505. Epub 2005 Nov 2. Clin J Am Soc Nephrol. 2006. PMID: 17699195 Review.
73 results