Taruscio D - Search Results

1

The EuRRECa Project as a Model for Data Access and Governance Policies for Rare Disease Registries That Collect Clinical Outcomes.

Ali SR, Bryce J, Tan LE, Hiort O, Pereira AM, van den Akker ELT, Appelman-Dijkstra NM, Bertherat J, Cools M, Dekkers OM, Kodra Y, Persani L, Smyth A, Smythe C, Taruscio D, Ahmed SF. Ali SR, et al. Among authors: taruscio d. Int J Environ Res Public Health. 2020 Nov 25;17(23):8743. doi: 10.3390/ijerph17238743. Int J Environ Res Public Health. 2020. PMID: 33255540 Free PMC article. Review.

2

Access to and quality of health and social care for rare diseases: patients' and caregivers' experiences.

Kodra Y, Morosini PR, Petrigliano R, Agazio E, Salerno P, Taruscio D. Kodra Y, et al. Among authors: taruscio d. Ann Ig. 2007 Mar-Apr;19(2):153-60. Ann Ig. 2007. PMID: 17547220

3

[Accessibility and quality of Italian health and social services: the experiences of patients with neurofibromatosis type 1 and of their relatives].

Kodra Y, Salerno P, Agazio E, Mirabella F, Taruscio D. Kodra Y, et al. Among authors: taruscio d. Ann Ig. 2007 Sep-Oct;19(5):443-50. Ann Ig. 2007. PMID: 18210774 Italian.

4

Health-related quality of life in patients with neurofibromatosis type 1. A survey of 129 Italian patients.

Kodra Y, Giustini S, Divona L, Porciello R, Calvieri S, Wolkenstein P, Taruscio D. Kodra Y, et al. Among authors: taruscio d. Dermatology. 2009;218(3):215-20. doi: 10.1159/000187594. Epub 2008 Dec 17. Dermatology. 2009. PMID: 19088462

5

Mortality associated with neurofibromatosis type 1: a study based on Italian death certificates (1995-2006).

Masocco M, Kodra Y, Vichi M, Conti S, Kanieff M, Pace M, Frova L, Taruscio D. Masocco M, et al. Among authors: taruscio d. Orphanet J Rare Dis. 2011 Mar 25;6:11. doi: 10.1186/1750-1172-6-11. Orphanet J Rare Dis. 2011. PMID: 21439034 Free PMC article.

6

[Rare diseases. A national network to benefit early diagnosis and more effective therapies].

Taruscio D, Kodra Y. Taruscio D, et al. Epidemiol Prev. 2011 Sep-Dec;35(5-6 Suppl 2):92-3. Epidemiol Prev. 2011. PMID: 22166875 Free article. Italian. No abstract available.

7

Classification and codification of rare diseases.

Kodra Y, Fantini B, Taruscio D. Kodra Y, et al. Among authors: taruscio d. J Clin Epidemiol. 2012 Sep;65(9):1026-7. doi: 10.1016/j.jclinepi.2012.02.014. Epub 2012 Apr 20. J Clin Epidemiol. 2012. PMID: 22521575 No abstract available.

8

Editorial.

Taruscio D. Taruscio D. Public Health Genomics. 2013;16(6):257-8. doi: 10.1159/000355926. Epub 2014 Feb 3. Public Health Genomics. 2013. PMID: 24503585 No abstract available.

9

EUROPLAN: a project to support the development of national plans on rare diseases in Europe.

Taruscio D, Gentile AE, De Santis M, Ferrelli RM, Posada de la Paz M, Hens M, Huizer J, Fregonese L, Stefanov R, Bottarelli V, Weinman A, Le Cam Y, Gavhed D, Mincarone P, Bushby K, Frazzica RG, Donati C, Vittozzi L, Jessop E. Taruscio D, et al. Public Health Genomics. 2013;16(6):278-87. doi: 10.1159/000355932. Epub 2014 Feb 3. Public Health Genomics. 2013. PMID: 24503588

10

The current situation and needs of rare disease registries in Europe.

Taruscio D, Gainotti S, Mollo E, Vittozzi L, Bianchi F, Ensini M, Posada M. Taruscio D, et al. Public Health Genomics. 2013;16(6):288-98. doi: 10.1159/000355934. Epub 2014 Feb 3. Public Health Genomics. 2013. PMID: 24503589

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