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CT and MRI in maple syrup urine diseaseUZIEL, G; SAVOIARDO, M; NARDOCCI, N et al.Neurology. 1988, Vol 38, Num 3, pp 486-488, issn 0028-3878Article

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Progressive dystonia symptomatic of juvenile GM2 gangliosidosisNARDOCCI, N; BERTAGNOLIO, B; RUMI, V et al.Movement disorders. 1992, Vol 7, Num 1, pp 64-67, issn 0885-3185Article

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PAROXYSMAL MOVEMENT DISORDERS IN GLUT1 DEFICIENCY SYNDROMEZORZI, G; CASTELLOTTI, B; ZIBORDI, F et al.Neurology. 2008, Vol 71, Num 2, pp 146-148, issn 0028-3878, 3 p.Article

Neurological disorders, other than stroke, associated with antiphospholipid antibodies in childhoodANGELINI, L; ZIBORDI, F; ZORZI, G et al.Neuropediatrics. 1996, Vol 27, Num 3, pp 149-153, issn 0174-304XArticle

Acquired hemidystonia in childhood : A clinical and neuroradiological study of thirteen patientsNARDOCCI, N; ZORZI, G; GRISOLI, M et al.Pediatric neurology. 1996, Vol 15, Num 2, pp 108-113, issn 0887-8994Article

Hallervorden-Spatz disease : clinical and MRI study of 11 cases diagnosed in lifeANGELINI, L; NARDOCCI, N; RUMI, V et al.Journal of neurology. 1992, Vol 239, Num 8, pp 417-425, issn 0340-5354Article

High prevalence of antiphospholipid antibodies in children with idiopathic cerebral ischemiaANGELINI, L; RAVELLI, A; CAPORALI, R et al.Pediatrics (Evanston). 1994, Vol 94, Num 4, pp 500-503, issn 0031-4005, 1Article

Progressive myoclonus epilepsies : an electroclinical, biochemical, morphological and molecular genetic study of 17 casesFRANCESCHETTI, S; ANTOZZI, C; BINELLI, S et al.Acta neurologica scandinavica. 1993, Vol 87, Num 3, pp 219-223, issn 0001-6314Article

Autosomal recessive Rolandic epilepsy with paroxysmal exercise-induced dystonia and writer's cramp : Delineation of the syndrome and gene mapping to chromosome 16p12-11.2GUERRINI, R; BONANNI, P; NARDOCCI, N et al.Annals of neurology. 1999, Vol 45, Num 3, pp 344-352, issn 0364-5134Article

Hallervorden-Spatz disease : MR and pathologic findingsSAVOIARDO, M; HALLIDAY, W. C; NARDOCCI, N et al.American journal of neuroradiology. 1993, Vol 14, Num 1, pp 155-162, issn 0195-6108Article

GTP-cyclohydrolase I gene mutations in patients with autosomal dominant and recessive GTP-CH1 deficiency: Identification and functional characterization of four novel mutationsGARAVAGLIA, B; INVERNIZZI, F; AGOSTONI CARBONE, M. L et al.Journal of inherited metabolic disease. 2004, Vol 27, Num 4, pp 455-463, issn 0141-8955, 9 p.Article

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Infantile neuroaxonal dystrophy : Clinical spectrum and diagnostic criteriaNARDOCCI, N; ZORZI, G; FARINA, L et al.Neurology. 1999, Vol 52, Num 7, pp 1472-1478, issn 0028-3878Article

Infantile neuroaxonal dystrophy : neuroradiological studies in 11 patientsFARINA, L; NARDOCCI, N; BRUZZONE, M. G et al.Neuroradiology (Berlin. Print). 1999, Vol 41, Num 5, pp 376-380, issn 0028-3940Article

Hemidystonia symptomatic of primary antiphospholipid syndrome in childhoodANGELINI, L; RUMI, V; NARDOCCI, N et al.Movement disorders. 1993, Vol 8, Num 3, pp 383-386, issn 0885-3185Conference Paper

Revelation of a novel CLN5 mutation in early juvenile neuronal ceroid lipofuscinosisCANNELLI, N; NARDOCCI, N; BERTINI, E et al.Neuropediatrics. 2007, Vol 38, Num 1, pp 46-49, issn 0174-304X, 4 p.Article

Homozygosity mapping of Hallervorden-Spatz syndrome to chromosome 20p12.3-p13TAYLOR, T. D; LITT, M; CILIO, M. R et al.Nature genetics. 1996, Vol 14, Num 4, pp 479-481, issn 1061-4036Article