Zobrazeno 1 - 10
of 138
pro vyhledávání: '"Laverda Am"'
Autor:
Suppiej, A, Gentilomo, C, Saracco, P, Sartori, S, Agostini, M, Bagna, R, Bassi, B, Giordano, P, Grassi, M, Guzzetta, A, Lasagni, D, Luciani, M, Molinari, Ac, Palmieri, A, Putti, Mc, Ramenghi, La, Rota, Ll, Sperlì, D, Laverda, Am, Simioni, P(1), Collaborators: Angriman M, Stroke working group of the Italian Registry of Pediatric Thrombosis., Aru, Ab, Barisone, E, Bartalena, L, Berta, M, Bertoni, E, Cancarini, P, Cavaliere, E, Celle, Me, Cerbone, Am, Cesaroni, E, Dalla Via, L, Dell'Oro, Mg, Di Rosa, G, Ferrari, Gm, Fiori, S, Gaffuri, M, Gallina, Mr, Gimmillaro, A, Grandone, E, Ladogana, S, Laforgia, N, La Piana, R, Maschio, F, Miniero, R, Nosadini, M, Panzeri, D, Petrucci, A, Piersigilli, F, Sala, D, Sangermani, R, Santoro, N, Tufano, A, Ventura, G, Vittorini, R.
SummaryData from large case series of children with cerebral thrombotic events are pivotal to improve prevention, early recognition and treatment of these conditions. The Italian Registry of Pediatric Thrombosis (R. I. T. I.) was established in 2007
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cf5f7d56aad7d16d25eab12c0081d5ee
http://hdl.handle.net/11568/785573
http://hdl.handle.net/11568/785573
Autor:
Baggio, L, Sartori, S, Nosadini, M, Gentilomo, C, Saracco, P, Agostini, M, Bassi, B, Palmieri, A, Laverda, Am, Simioni, P, Suppiej, A, per il GIRTI (Gruppo Italiano Registro Trombosi Infantili)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3709::b4d3163cface8ef954f963b891403e35
http://hdl.handle.net/11392/2405876
http://hdl.handle.net/11392/2405876
Autor:
Gentilomo, C, Saracco, P, Bagna, R, Bassi, B, Agostini, M, Giordano, P, Ramenghi, La, Molinari, Ac, Laverda, Am, Grassi, M, Putti, Mc, Suppiej, A, Sartori, S, Simioni, P
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3709::0c0518cd7f7c01f8a3b4e87b37144d9b
http://hdl.handle.net/11392/2387965
http://hdl.handle.net/11392/2387965
Autor:
Bassi, Bianca, Gentilomo, C, Saracco, P, Lorenzon, E, Laverda, Am, Battini, R, Agostini, M, Bagna, R, Giordano, P, Molinari, C, Ramenghi, L, Simioni, P, Gruppo italiano per il registro trombosi infantili GIRTI
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______970::996b6e08573322c6cdf953de2e4ab6b8
http://hdl.handle.net/2318/139581
http://hdl.handle.net/2318/139581
Autor:
Paola Drigo, M. A. Battaglia, Pier Antonio Battistella, G. L. Casara, Agnese Suppiej, R. Casellato, Laverda Am
Publikováno v:
Child's Nervous System. 9:84-87
Four children with congenital muscular dystrophy (CMD), eye and brain abnormalities are described. Their clinical and neuroradiological features are compatible with a diagnosis of Walker-Warburg syndrome (WWS), according to the criteria proposed by D
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e780203e6af220db9eb5601f19c684bc
https://doi.org/10.1007/bf00305313
https://doi.org/10.1007/bf00305313
Autor:
Paola Drigo, Maria Rosaria Stabile, Pier Antonio Battistella, Giovanni Cecchetto, Laverda Am, C. Zorzi, Piergiorgio Gamba, F. Martinello, Emilia Ferruzza, C. Previtera, Carla Carollo, Corrado Angelini, Carlo P. Trevisan
Publikováno v:
Rivista di Neuroradiologia. 5:39-42
La forma tipica di distrofia muscolare congenita (DMC) è ritenuta priva di alterazioni cerebrali, a differenza della sua variante giapponese che oltre all'interessamento muscolare presenta un imponente coinvolgimento del sistema nervoso centrale con
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::99090b616e1d0d9046fb9df59dd597a8
https://doi.org/10.1177/19714009920050s107
https://doi.org/10.1177/19714009920050s107
Autor:
Cantagrel, V, Silhavy, Jl, Bielas, S, Swistun, D, Marsh, Se, Bertrand, J, Audollent, S, Attié Bitach, T, Holden, Kr, Dobyns, Wb, Traver, D, Al Gazali, L, Ali, Br, Lindner, Th, Caspary, T, Otto, Ea, Hildebrandt, F, Glass, Ia, Logan, Cv, Johnson, Ca, Bennett, C, Brancati, F, Grattan Smith, P, Leventer, J, Van Coster, R, Dias, K, Moco, C, Moreira, Ae Kim, C, Akiss, A, Maegawa, G, Abdel Salam GMH, Abdel Aleem, A, Zaki, Ms, Marti, I, Quijano Roy, S, de Lonlay, P, Verloes A, A., Touraine, R, Koenig, M, Lagier Tourenne, C, Messer, J, Philippi, H, Tzeli, Sk, Halldorsson, S, Johannsdottir, J, Ludvigsson, P, Magee, A, Stuart, B, Lev, D, Michelson, M, Ben Zeev, B, Fischetto, R, Gentile, M, Battaglia, Giordano, L, Boccone, L, Ruggieri, M, Bigoni, S, Ferlini, A, Donati, Ma, Procopio, E, Lapi, E, Genuardi, M, Caridi, G, Faravelli, F, Ghiggeri, G, Briuglia, Silvana, Tortorella, Gaetano, Rigoli, Luciana Concetta, SALPIETRO DAMIANO, Carmelo, D’Arrigo, S, Pantaleoni, C, Riva, D, Uziel, G, Laverda, Am, Permunian, A, Bova, S, Fazz, Ei, Sabrina, S, Battini, R, Bertini, E, Dallapiccola, B, Cilio, Mr, Di Sabato, M, Emma, F, Leuzzi, V, Parisi, P, Simonati, A, Al Tawari AA, Bastaki, L, Ahmad Aqueel, A, Jong, Mm, Koul, R, Rajab, A, Sztriha, L, Azam, M, Barbot, C, Rodriguez, B, Pascual Castroviejo, I, Eugen Boltshauser, E, Hulya, H, Comu, S, Akcakus, M, Sahin, Y, Phadke, Sr, Melick, N, Mikati, M, Nicholl, D, Hurst, J, Hennekam, Rcm, Bernes, S, Sanchez, H, Clark, Ae, Wynshaw Boris, A, Donahue, C, Sherr, Eh, Barkovich, Aj, Hahn, D., Sanger, Td, Gallager, Te, Daugherty, C, Krishnamoorthy, Ks, Sarco, D, Walsh CA, Soul, Jmckanna, T, Joanne Milisa, J, Chung, Wk, De Vivo DC, Raynes, H, Schubert, R, Seward, A, Brooks, Dg, Amy Goldstein, A, Caldwell, J, Finsecke, E, Maria, Bl, Cruse, Rp, Lotzete, Swoboda, Kj, Viskochil, Dh, Valente, Em, Woods, Cg, Gleeson, Jg
Joubert syndrome (JS) and related disorders are a group of autosomal-recessive conditions sharing the “molar tooth sign” on axial brain MRI, together with cerebellar vermis hypoplasia, ataxia, and psychomotor delay. JS is suggested to be a disord
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f67997970c24a4b253fb5a24caa916b
http://hdl.handle.net/11386/3949698
http://hdl.handle.net/11386/3949698