Taruscio D - Search Results

1

Quality of life assessment in a sample of patients affected by Prader-Willi syndrome.

Caliandro P, Grugni G, Padua L, Kodra Y, Tonali P, Gargantini L, Ragusa L, Crinò A, Taruscio D. Caliandro P, et al. Among authors: taruscio d. J Paediatr Child Health. 2007 Dec;43(12):826-30. doi: 10.1111/j.1440-1754.2007.01200.x. Epub 2007 Sep 4. J Paediatr Child Health. 2007. PMID: 17803668

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

The social burden and quality of life of patients with haemophilia in Italy.

Kodra Y, Cavazza M, Schieppati A, De Santis M, Armeni P, Arcieri R, Calizzani G, Fattore G, Manzoli L, Mantovani L, Taruscio D. Kodra Y, et al. Among authors: taruscio d. Blood Transfus. 2014 Apr;12 Suppl 3(Suppl 3):s567-75. doi: 10.2450/2014.0042-14s. Blood Transfus. 2014. PMID: 24922297 Free PMC article.

9

Current status of Italian Registries on inherited bleeding disorders.

Hassan HJ, Morfini M, Taruscio D, Abbonizio F, Giampaolo A, Kodra Y, Oliovecchio E, Vittozzi L. Hassan HJ, et al. Among authors: taruscio d. Blood Transfus. 2014 Apr;12 Suppl 3(Suppl 3):s576-81. doi: 10.2450/2014.0017-14s. Blood Transfus. 2014. PMID: 24922298 Free PMC article. No abstract available.

10

National registries of rare diseases in Europe: an overview of the current situation and experiences.

Taruscio D, Vittozzi L, Choquet R, Heimdal K, Iskrov G, Kodra Y, Landais P, Posada M, Stefanov R, Steinmueller C, Swinnen E, Van Oyen H. Taruscio D, et al. Public Health Genomics. 2015;18(1):20-5. doi: 10.1159/000365897. Epub 2014 Sep 9. Public Health Genomics. 2015. PMID: 25228300

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