UGOLINI, SARA
UGOLINI, SARA
European Reference Network for Rare Vascular Diseases (VASCERN) position statement on cerebral screening in adults and children with hereditary haemorrhagic telangiectasia (HHT)
2020-01-01 Eker, O. F.; Boccardi, E.; Sure, U.; Patel, M. C.; Alicante, S.; Alsafi, A.; Coote, N.; Droege, F.; Dupuis, O.; Fialla, A. D.; Jones, B.; Kariholu, U.; Kjeldsen, A. D.; Lefroy, D.; Lenato, G. M.; Mager, H. J.; Manfredi, G.; Nielsen, T. H.; Pagella, F.; Post, M. C.; Rennie, C.; Sabba, C.; Suppressa, P.; Toerring, P. M.; Ugolini, S.; Buscarini, E.; Dupuis-Girod, S.; Shovlin, C. L.
Experience of an Italian reference laboratory for a rare disease: Hereditary Haemorragic Telangiectasia
2021-01-01 Olivieri, Carla; Pagella, FABIO GIUSEPPE MARIA; Plumitallo, Sara; Hladnik, Uroš; Buscarini, Elisabetta; Matti, Elina; Sbalchiero, Anna; Manfredi, Guido; Spinozzi, Giuseppe; DE SANDO, Elisabetta; Ugolini, Sara; Danesino, Cesare
FID Score: an effective tool in Hereditary Haemorrhagic Telangiectasia - related epistaxis
2020-01-01 Pagella, F.; Maiorano, E.; Matti, E.; Tinelli, C.; De Silvestri, A.; Ugolini, S.; Lizzio, R.; Olivieri, C.; Pusateri, A.; Spinozzi, G.
Hereditary Haemorrhagic Telangiectasia: evidence of a common ancestor in 19 families from Northern Italy
2021-01-01 Sbalchiero, A.; Abu Hweij, Y.; Mazza, T.; Buscarini, E.; Pagella, F.; Scotti, C.; Matti, E.; Manfredi, G.; Spinozzi, G.; Ugolini, S.; Olivieri, C.
Hereditary Haemorrhagic Telangiectasia: evidence of a common ancestor in 19 families from Northern Italy.
2021-01-01 Sbalchiero, Anna; ABU HWEIJ, Yasmin; Mazza, Tommaso; Buscarini, Elisabetta; Pagella, FABIO GIUSEPPE MARIA; Matti, Elina; Manfredi, Guido; Spinozzi, Giuseppe; Ugolini, Sara; Olivieri, Carla
The European Rare Disease Network for HHT Frameworks for management of hereditary haemorrhagic telangiectasia in general and speciality care
2022-01-01 Shovlin, C L; Buscarini, E; Sabbà, C; Mager, H J; Kjeldsen, A D; Pagella, F; Sure, U; Ugolini, S; Torring, P M; Suppressa, P; Rennie, C; Post, M C; Patel, M C; Nielsen, T H; Manfredi, G; Lenato, G M; Lefroy, D; Kariholu, U; Jones, B; Fialla, A D; Eker, O F; Dupuis, O; Droege, F; Coote, N; Boccardi, E; Alsafi, A; Alicante, S; Dupuis-Girod, S
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| European Reference Network for Rare Vascular Diseases (VASCERN) position statement on cerebral screening in adults and children with hereditary haemorrhagic telangiectasia (HHT) | 1-gen-2020 | Eker, O. F.; Boccardi, E.; Sure, U.; Patel, M. C.; Alicante, S.; Alsafi, A.; Coote, N.; Droege, F.; Dupuis, O.; Fialla, A. D.; Jones, B.; Kariholu, U.; Kjeldsen, A. D.; Lefroy, D.; Lenato, G. M.; Mager, H. J.; Manfredi, G.; Nielsen, T. H.; Pagella, F.; Post, M. C.; Rennie, C.; Sabba, C.; Suppressa, P.; Toerring, P. M.; Ugolini, S.; Buscarini, E.; Dupuis-Girod, S.; Shovlin, C. L. | |
| Experience of an Italian reference laboratory for a rare disease: Hereditary Haemorragic Telangiectasia | 1-gen-2021 | Olivieri, Carla; Pagella, FABIO GIUSEPPE MARIA; Plumitallo, Sara; Hladnik, Uroš; Buscarini, Elisabetta; Matti, Elina; Sbalchiero, Anna; Manfredi, Guido; Spinozzi, Giuseppe; DE SANDO, Elisabetta; Ugolini, Sara; Danesino, Cesare | |
| FID Score: an effective tool in Hereditary Haemorrhagic Telangiectasia - related epistaxis | 1-gen-2020 | Pagella, F.; Maiorano, E.; Matti, E.; Tinelli, C.; De Silvestri, A.; Ugolini, S.; Lizzio, R.; Olivieri, C.; Pusateri, A.; Spinozzi, G. | |
| Hereditary Haemorrhagic Telangiectasia: evidence of a common ancestor in 19 families from Northern Italy | 1-gen-2021 | Sbalchiero, A.; Abu Hweij, Y.; Mazza, T.; Buscarini, E.; Pagella, F.; Scotti, C.; Matti, E.; Manfredi, G.; Spinozzi, G.; Ugolini, S.; Olivieri, C. | |
| Hereditary Haemorrhagic Telangiectasia: evidence of a common ancestor in 19 families from Northern Italy. | 1-gen-2021 | Sbalchiero, Anna; ABU HWEIJ, Yasmin; Mazza, Tommaso; Buscarini, Elisabetta; Pagella, FABIO GIUSEPPE MARIA; Matti, Elina; Manfredi, Guido; Spinozzi, Giuseppe; Ugolini, Sara; Olivieri, Carla | |
| The European Rare Disease Network for HHT Frameworks for management of hereditary haemorrhagic telangiectasia in general and speciality care | 1-gen-2022 | Shovlin, C L; Buscarini, E; Sabbà, C; Mager, H J; Kjeldsen, A D; Pagella, F; Sure, U; Ugolini, S; Torring, P M; Suppressa, P; Rennie, C; Post, M C; Patel, M C; Nielsen, T H; Manfredi, G; Lenato, G M; Lefroy, D; Kariholu, U; Jones, B; Fialla, A D; Eker, O F; Dupuis, O; Droege, F; Coote, N; Boccardi, E; Alsafi, A; Alicante, S; Dupuis-Girod, S |