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N Nardocci

Showing results (31-40 of 49) with videos related to

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Neuropediatrics|March 19, 2005
Persistent fixed torticollis due to Atlanto-axial rotatory fixation: report of 4 pediatric casesL Chiapparini, G Zorzi, T De Simone, et al.
Child Neuropsychology : a Journal on Normal and Abnormal Development in Childhood and Adolescence|March 1, 2021
Automatic imitation in youngsters with Gilles de la Tourette syndrome: A behavioral studyE Quadrelli, B Bartoli, N Bolognini, et al.
Neuroradiology|June 24, 1999
Infantile neuroaxonal dystrophy: neuroradiological studies in 11 patientsL Farina, N Nardocci, M G Bruzzone, et al.
AJNR. American Journal of Neuroradiology|January 1, 1993
Hallervorden-Spatz disease: MR and pathologic findingsM Savoiardo, W C Halliday, N Nardocci, et al.
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.
Neuropediatrics|August 31, 2011
The "eye-of-the-tiger" sign may be absent in the early stages of classic pantothenate kinase associated neurodegenerationL Chiapparini, M Savoiardo, S D'Arrigo, et al.
Annals of Neurology|March 11, 1999
Autosomal recessive rolandic epilepsy with paroxysmal exercise-induced dystonia and writer's cramp: delineation of the syndrome and gene mapping to chromosome 16p12-11.2R Guerrini, P Bonanni, N Nardocci, et al.
Pageof 5

Showing results (31-40 of 49) with videos related to

Sort By:
Pageof 5
Neuropediatrics|March 19, 2005
Persistent fixed torticollis due to Atlanto-axial rotatory fixation: report of 4 pediatric casesL Chiapparini, G Zorzi, T De Simone, et al.
Child Neuropsychology : a Journal on Normal and Abnormal Development in Childhood and Adolescence|March 1, 2021
Automatic imitation in youngsters with Gilles de la Tourette syndrome: A behavioral studyE Quadrelli, B Bartoli, N Bolognini, et al.
Neuroradiology|June 24, 1999
Infantile neuroaxonal dystrophy: neuroradiological studies in 11 patientsL Farina, N Nardocci, M G Bruzzone, et al.
AJNR. American Journal of Neuroradiology|January 1, 1993
Hallervorden-Spatz disease: MR and pathologic findingsM Savoiardo, W C Halliday, N Nardocci, et al.
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.
Neuropediatrics|August 31, 2011
The "eye-of-the-tiger" sign may be absent in the early stages of classic pantothenate kinase associated neurodegenerationL Chiapparini, M Savoiardo, S D'Arrigo, et al.
Annals of Neurology|March 11, 1999
Autosomal recessive rolandic epilepsy with paroxysmal exercise-induced dystonia and writer's cramp: delineation of the syndrome and gene mapping to chromosome 16p12-11.2R Guerrini, P Bonanni, N Nardocci, et al.
Pageof 5