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Acta Neurochirurgica|October 14, 2020
Globus pallidus internus activity during simultaneous bilateral microelectrode recordings in status dystonicusVincenzo Levi, A Franzini, S Rinaldo, et al.Neurology|January 29, 2003
Neonatal dopa-responsive extrapyramidal syndrome in twins with recessive GTPCH deficiencyN Nardocci, G Zorzi, N Blau, et al.Journal of Inherited Metabolic Disease|August 11, 2004
GTP-cyclohydrolase I gene mutations in patients with autosomal dominant and recessive GTP-CH1 deficiency: identification and functional characterization of four novel mutationsB Garavaglia, F Invernizzi, M L Agostoni Carbone, et al.Neurology|May 5, 1999
Infantile neuroaxonal dystrophy: clinical spectrum and diagnostic criteriaN Nardocci, G Zorzi, L Farina, et al.Neurology|February 13, 2003
Rasmussen's encephalitis: early characteristics allow diagnosisT Granata, G Gobbi, R Spreafico, et al.Neuroradiology|April 10, 2003
Diagnostic imaging in 13 cases of Rasmussen's encephalitis: can early MRI suggest the diagnosis?L Chiapparini, T Granata, L Farina, et al.Brain & Development|October 25, 2018
Restless Legs Syndrome in NKX2-1-related chorea: An expansion of the disease spectrumA Iodice, M Carecchio, G Zorzi, et al.Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|August 10, 2004
Ataxia with isolated vitamin E deficiency: neurological phenotype, clinical follow-up and novel mutations in TTPA gene in Italian familiesC Mariotti, C Gellera, M Rimoldi, et al.Journal of Neurology|December 6, 2012
Extragenetic factors and clinical penetrance of DYT1 dystonia: an exploratory studyD Martino, A Gajos, V Gallo, et al.Neurology|September 19, 2008
Neurodegeneration associated with genetic defects in phospholipase A(2)A Gregory, S K Westaway, I E Holm, et al.Pageof 7