Neutral Lipid Storage Diseases: clinical/genetic features and natural history in a large cohort of Italian patients

E.M. Pennisi; M. Arca; E. Bertini; C. Bruno; D. Cassandrini; A. D'amico; M. Garibaldi; F. Gragnani; L. Maggi; R. Massa; S. Missaglia; L. Morandi; O. Musumeci; E. Pegoraro; E. Rastelli; F.M. Santorelli; E. Tasca; D. Tavian; A. Toscano; C. Angelini

doi:10.1186/s13023-017-0646-9

Neutral Lipid Storage Diseases: clinical/genetic features and natural history in a large cohort of Italian patients

E.M. Pennisi, M. Arca, E. Bertini, C. Bruno, D. Cassandrini, A. D'amico, M. Garibaldi, F. Gragnani, L. Maggi, R. Massa, S. Missaglia, L. Morandi, O. Musumeci, E. Pegoraro, E. Rastelli, F.M. Santorelli, E. Tasca, D. Tavian, A. Toscano, C. Angelini

Research output: Contribution to journal › Article › peer-review

Original language	Italian
Pages (from-to)	1-10
Number of pages	10
Journal	Orphanet Journal of Rare Diseases
Volume	12
Issue number	1
DOIs	https://doi.org/10.1186/s13023-017-0646-9
Publication status	Published - 2017

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10.1186/s13023-017-0646-9

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Pennisi, E. M., Arca, M., Bertini, E., Bruno, C., Cassandrini, D., D'amico, A., Garibaldi, M., Gragnani, F., Maggi, L., Massa, R., Missaglia, S., Morandi, L., Musumeci, O., Pegoraro, E., Rastelli, E., Santorelli, F. M., Tasca, E., Tavian, D., Toscano, A., & Angelini, C. (2017). Neutral Lipid Storage Diseases: clinical/genetic features and natural history in a large cohort of Italian patients. Orphanet Journal of Rare Diseases, 12(1), 1-10. https://doi.org/10.1186/s13023-017-0646-9

Neutral Lipid Storage Diseases: clinical/genetic features and natural history in a large cohort of Italian patients. / Pennisi, E.M.; Arca, M.; Bertini, E.; Bruno, C.; Cassandrini, D.; D'amico, A.; Garibaldi, M.; Gragnani, F.; Maggi, L.; Massa, R.; Missaglia, S.; Morandi, L.; Musumeci, O.; Pegoraro, E.; Rastelli, E.; Santorelli, F.M.; Tasca, E.; Tavian, D.; Toscano, A.; Angelini, C.

In: Orphanet Journal of Rare Diseases, Vol. 12, No. 1, 2017, p. 1-10.

Research output: Contribution to journal › Article › peer-review

Pennisi, EM, Arca, M, Bertini, E , Bruno, C , Cassandrini, D , D'amico, A, Garibaldi, M, Gragnani, F, Maggi, L, Massa, R, Missaglia, S, Morandi, L, Musumeci, O, Pegoraro, E, Rastelli, E, Santorelli, FM, Tasca, E, Tavian, D, Toscano, A & Angelini, C 2017, 'Neutral Lipid Storage Diseases: clinical/genetic features and natural history in a large cohort of Italian patients', Orphanet Journal of Rare Diseases, vol. 12, no. 1, pp. 1-10. https://doi.org/10.1186/s13023-017-0646-9

Pennisi, E.M. ; Arca, M. ; Bertini, E. ; Bruno, C. ; Cassandrini, D. ; D'amico, A. ; Garibaldi, M. ; Gragnani, F. ; Maggi, L. ; Massa, R. ; Missaglia, S. ; Morandi, L. ; Musumeci, O. ; Pegoraro, E. ; Rastelli, E. ; Santorelli, F.M. ; Tasca, E. ; Tavian, D. ; Toscano, A. ; Angelini, C. / Neutral Lipid Storage Diseases: clinical/genetic features and natural history in a large cohort of Italian patients. In: Orphanet Journal of Rare Diseases. 2017 ; Vol. 12, No. 1. pp. 1-10.

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