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Mostrati risultati da 1 a 20 di 74
Titolo Data di pubblicazione Autore(i) File
[Acute urinary retention in a child with acute disseminatedencephalomyelitis] 1-gen-2006 Doria Lamba, L; DE GRANDIS, Elisa; De Negri, E; Montaldi, L; Grosso, P; Marazzi, MARIA GRAZIA; Rossi, A; Tuo, P.
Efficacious vitamin E treatment in a child with ataxia with isolatedvitamin E deficiency 1-gen-2006 Doria Lamba, L; DE GRANDIS, Elisa; Cristiani, E; Fiocchi, I; Montaldi, L; Grosso, P; Gellera, C.
Opsoclonus-myoclonus-atassia syndrome: Neuropsychological and neuroradiological series 1-gen-2007 DE GRANDIS, Elisa; Conte, M; Battaglia, Mf; Pessagno, A; Angelini, P; Liberati, P; Gandolfo, C; Morana, G; Mancardi, M; De Bernardi, B; Garaventa, A; Veneselli, EDVIGE MARIA
A case of major form familial hyperekplexia: prenatal diagnosis and effective treatment with clonazepam. 1-gen-2007 DORIA LAMBA, L; Giribaldi, G; DE NEGRI, E; Follo, R; DE GRANDIS, Elisa; Pintaudi, M; Veneselli, EDVIGE MARIA
Paroxysmal dyskinesiawith interictal myoclonus and dystonia: a report of two cases. 1-gen-2008 DE GRANDIS, Elisa; Mir, P; Edwards, Mj; Quinn, Np; Bhatia, K. P.
Childhood thalidomide neuropathy: a clinical and neurophysiologic study. 1-gen-2008 Priolo, T; DORIA LAMBA, L; Giribaldi, G; DE NEGRI, E; Grosso, P; DE GRANDIS, Elisa; Veneselli, EDVIGE MARIA; Buoncompagni, A; Viola, S; Alpigiani, Mg; Gandullia, P; Calevo, Mg
Immunological mechanisms inopsoclonus-myoclonus associated neuroblastoma 1-gen-2008 Raffaghello, L; Conte, M; DE GRANDIS, Elisa; Pistoia, V.
Restless legs may be associatedwith the post-polio syndrome. 1-gen-2009 DE GRANDIS, Elisa; Mir, P; Edwards, Mj; Bhatia, K. P.
Molecular study and response to levodopa therapy in eight children with tyrosine hydroxylase deficiency 1-gen-2009 Perez Duenas, B; Serrano, M; Garcia Cazorla, A; Ormazabal, A; Montero, R; DE GRANDIS, Elisa; Pineda, M; Fernandez Alvarez, E; Pons, R; Artuch, R.
Secondary dopamine and serotonine deficiencies in children with movement disorders 1-gen-2009 DE GRANDIS, Elisa; Perez Duenas, B; Serrano, M; Ormazabal, A; Montero, R; Veneselli, EDVIGE MARIA; Artuch, R; Garcia Cazorla, A.
MR imaging findings in 2 cases of late infantile GM1 gangliosidosis. 1-gen-2009 DE GRANDIS, Elisa; M., DI ROCCO; A., Pessagno; Veneselli, EDVIGE MARIA; A., Rossi
Long-term follow-up of neuroblastoma-associated opsoclonus-myoclonus-ataxia syndrome 1-gen-2009 De Grandis, E.; Parodi, S.; Conte, M.; Angelini, P.; Battaglia, F.; Gandolfo, C.; Pessagno, A.; Pistoia, V.; Mitchell, W. G.; Pike, M.; Haupt, R.; Veneselli, E.
Cerebrospinal fluid alterations of the serotonin product, 5-hydroxyindolacetic acid, in neurological disorders. 1-gen-2010 DE GRANDIS, Elisa; Serrano, M; Pérez Dueñas, B; Ormazábal, A; Montero, R; Veneselli, EDVIGE MARIA; Pineda, M; González, V; Sanmartí, F; Fons, C; Sans, A; Cormand, B; Puelles, L; Alonso, A; Campistol, J; Artuch, R; García Cazorla, A.
Synchronization and continuation: Analysis of repetitive finger movements in patients with Tourette syndrome 1-gen-2010 Avanzino, Laura; Tachino, A; Bove, Marco; Martino, D; DE GRANDIS, Elisa; Mirabelli, M; Pelosin, Elisa; Veneselli, EDVIGE MARIA; Abbruzzese, Giovanni
USE OF RITUXIMAB IN THE TREATMENT OF THE SYNDROME OPSOMIOCLONIC. EXPERIENCE IN THE G. GASLINI INSTITUTE 1-gen-2010 Battaglia, T; DE GRANDIS, Elisa; Sorrentino, S; Mirabelli, M; Morcaldi, G; Garaventa, A; Conte, M.
CEREBRAL FOLATE DEFICIENCY AND DISEASES OF THE CENTRAL NERVOUS SYSTEM IN CHILDHOOD 1-gen-2010 Perez Duenas, B; Ormazabal, A; Toma, C; Torrico, B; Cormand, B; Serrano, M; Sierra, C; DE GRANDIS, Elisa; Pineda, M; Campistol, J; Garcia Cazorla, A; Artuch, R.
Pediatric Neuroblastoma-Associated Opsoclonus-Myoclonus-Ataxia Syndrome: Early Diagnosis 1-gen-2011 DE GRANDIS, Elisa
Movement lateralization and bimanual coordination in children with Tourette syndrome. 1-gen-2011 Avanzino, Laura; D., Martino; Bove, Marco; DE GRANDIS, Elisa; A., Tacchino; Pelosin, Elisa; MIRABELLI BADENIER, MARISOL ELENA; Veneselli, EDVIGE MARIA; Abbruzzese, Giovanni
Cerebral folate deficiency syndromes in childhood: clinical, analytical, and etiologic aspects. 1-gen-2011 Pérez Dueñas, B; Ormazábal, A; Toma, C; Torrico, B; Cormand, B; Serrano, M; Sierra, C; DE GRANDIS, Elisa; Marfa, Mp; García Cazorla, A; Campistol, J; Pascual, Jm; Artuch, R.
De novo mutations in ATP1A3 cause alternating hemiplegia of childhood 1-gen-2012 Heinzen, El; Swoboda, Kj; Hitomi, Y; Gurrieri, F; De Vries, B; Tiziano, Fd; Fontaine, B; Walley, Nm; Heavin, S; Panagiotakaki, El; Fiori, S; Abiusi, E; Di Pietro, L; Sweney, Mt; Newcomb, Tm; Viollet, L; Huff, C; Jorde, Lb; Reyna, Sp; Murphy, K; Shianna, Kv; Gumbs, Ce; Little, L; Silver, K; Ptáček, Lj; Haan, J; Ferrari, Md; Bye, Am; Herkes, Gk; Whitelaw, Cm; Webb, D; Lynch, Bj; Uldall, P; King, Md; Scheffer, Ie; Neri, G; Arzimanoglou, A; Van Den Maagdenberg, A; Sisodiya, Sm; Mikati, Ma; Goldstein, Db; Koelewijn, S; Kamphorst, J; Geilenkirchen, M; Pelzer, N; Ferrari, M; Van Den Maagdenberg, A; Zucca, C; Franchini, F; Vavassori, R; Giannotta, M; Gobbi, G; Granata, T; Nardocci, N; De Grandis, E; Veneselli, E; Stagnaro, M; Vigevano, F; Oechsler, C; Nicole, S; Ninan, M; Neville, B; Ebinger, F; Fons, C; Campistol, J; Kemlink, D; Nevsimalova, S; Laan, L; Peetersscholte, C; Casaer, P; Casari, G; Sange, G; Spiel, G; Boneschi, Fm; Bassi, M; Schyns, T; Crawley, F; Poncelin, D.
Mostrati risultati da 1 a 20 di 74
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