Taruscio D - Search Results

1

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

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

Tackling rare diseases at European level: why do we need a harmonized framework?

Taruscio D, Trama A, Stefanov R. Taruscio D, et al. Folia Med (Plovdiv). 2007;49(1-2):59-67. Folia Med (Plovdiv). 2007. PMID: 18018471

4

[Folic acid and congenital malformation: scientific evidence and public health strategies].

Salerno P, Bianchi F, Pierini A, Baldi F, Carbone P, Mantovani A, Taruscio D. Salerno P, et al. Among authors: taruscio d. Ann Ig. 2008 Nov-Dec;20(6):519-30. Ann Ig. 2008. PMID: 19238877 Review. Italian.

5

National plans and strategies on rare diseases in Europe.

Taruscio D, Vittozzi L, Stefanov R. Taruscio D, et al. 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.

6

Rare diseases and orphan drugs.

Taruscio D, Capozzoli F, Frank C. Taruscio D, et al. Ann Ist Super Sanita. 2011;47(1):83-93. doi: 10.4415/ANN_11_01_17. Ann Ist Super Sanita. 2011. PMID: 21430345 Free article. Review.

7

[Congenital malformations in Italy. A network to monitor the phenomenon].

Carbone P, Taruscio D, Bianchi F, Calzolari E, Scarano G; Coordinamento Nazionale dei Registri delle Malformazioni Congenite. Carbone P, et al. Among authors: taruscio d. Epidemiol Prev. 2011 Sep-Dec;35(5-6 Suppl 2):90-1. Epidemiol Prev. 2011. PMID: 22166874 Free article. Italian. No abstract available.

8

The need for worldwide policy and action plans for rare diseases.

Forman J, Taruscio D, Llera VA, Barrera LA, Coté TR, Edfjäll C, Gavhed D, Haffner ME, Nishimura Y, Posada M, Tambuyzer E, Groft SC, Henter JI; International Conference for Rare Diseases and Orphan Drugs (ICORD). Forman J, et al. Among authors: taruscio d. Acta Paediatr. 2012 Aug;101(8):805-7. doi: 10.1111/j.1651-2227.2012.02705.x. Epub 2012 May 11. Acta Paediatr. 2012. PMID: 22519914 Free PMC article.

9

Newborn screening programmes in Europe; arguments and efforts regarding harmonization. Part 2. From screening laboratory results to treatment, follow-up and quality assurance.

Burgard P, Rupp K, Lindner M, Haege G, Rigter T, Weinreich SS, Loeber JG, Taruscio D, Vittozzi L, Cornel MC, Hoffmann GF. Burgard P, et al. Among authors: taruscio d. J Inherit Metab Dis. 2012 Jul;35(4):613-25. doi: 10.1007/s10545-012-9484-z. Epub 2012 Apr 28. J Inherit Metab Dis. 2012. PMID: 22544437

10

A framework to start the debate on neonatal screening policies in the EU: an Expert Opinion Document.

Cornel MC, Rigter T, Weinreich SS, Burgard P, Hoffmann GF, Lindner M, Gerard Loeber J, Rupp K, Taruscio D, Vittozzi L. Cornel MC, et al. Among authors: taruscio d. Eur J Hum Genet. 2014 Jan;22(1):12-7. doi: 10.1038/ejhg.2013.90. Epub 2013 May 8. Eur J Hum Genet. 2014. PMID: 23652378 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

231 results

Search Page

Filters