Zorzi G - Search Results

1

A PDE10A de novo mutation causes childhood-onset chorea with diurnal fluctuations.

Esposito S, Carecchio M, Tonduti D, Saletti V, Panteghini C, Chiapparini L, Zorzi G, Pantaleoni C, Garavaglia B, Krainc D, Lubbe SJ, Nardocci N, Mencacci NE. Esposito S, et al. Among authors: zorzi g. Mov Disord. 2017 Nov;32(11):1646-1647. doi: 10.1002/mds.27175. Epub 2017 Sep 26. Mov Disord. 2017. PMID: 28949041 No abstract available.

2

Neuronal ceroid-lipofuscinosis: a clinical and morphological study of 19 patients.

Nardocci N, Verga ML, Binelli S, Zorzi G, Angelini L, Bugiani O. Nardocci N, et al. Among authors: zorzi g. Am J Med Genet. 1995 Jun 5;57(2):137-41. doi: 10.1002/ajmg.1320570205. Am J Med Genet. 1995. PMID: 7668317

3

Paroxysmal dystonia and paroxysmal tremor in a young patient with multiple sclerosis.

Nardocci N, Zorzi G, Savoldelli M, Rumi V, Angelini L. Nardocci N, et al. Among authors: zorzi g. Ital J Neurol Sci. 1995 Jun;16(5):315-9. doi: 10.1007/BF02249107. Ital J Neurol Sci. 1995. PMID: 8537220

4

Neurological disorders, other than stroke, associated with antiphospholipid antibodies in childhood.

Angelini L, Zibordi F, Zorzi G, Nardocci N, Caporali R, Ravelli A, Martini A. Angelini L, et al. Among authors: zorzi g. Neuropediatrics. 1996 Jun;27(3):149-53. doi: 10.1055/s-2007-973766. Neuropediatrics. 1996. PMID: 8837075

5

Acquired hemidystonia in childhood: a clinical and neuroradiological study of thirteen patients.

Nardocci N, Zorzi G, Grisoli M, Rumi V, Broggi G, Angelini L. Nardocci N, et al. Among authors: zorzi g. Pediatr Neurol. 1996 Sep;15(2):108-13. doi: 10.1016/0887-8994(96)00152-x. Pediatr Neurol. 1996. PMID: 8888043

6

Infantile neuroaxonal dystrophy: clinical spectrum and diagnostic criteria.

Nardocci N, Zorzi G, Farina L, Binelli S, Scaioli W, Ciano C, Verga L, Angelini L, Savoiardo M, Bugiani O. Nardocci N, et al. Among authors: zorzi g. Neurology. 1999 Apr 22;52(7):1472-8. doi: 10.1212/wnl.52.7.1472. Neurology. 1999. PMID: 10227637

7

Infantile neuroaxonal dystrophy: neuroradiological studies in 11 patients.

Farina L, Nardocci N, Bruzzone MG, D'Incerti L, Zorzi G, Verga L, Morbin M, Savoiardo M. Farina L, et al. Among authors: zorzi g. Neuroradiology. 1999 May;41(5):376-80. doi: 10.1007/s002340050768. Neuroradiology. 1999. PMID: 10379598

8

Frequency of DYT1 mutation in early onset primary dystonia in Italian patients.

Zorzi G, Garavaglia B, Invernizzi F, Girotti F, Soliveri P, Zeviani M, Angelini L, Nardocci N. Zorzi G, et al. Mov Disord. 2002 Mar;17(2):407-8. doi: 10.1002/mds.10045. Mov Disord. 2002. PMID: 11921134

9

Neonatal dopa-responsive extrapyramidal syndrome in twins with recessive GTPCH deficiency.

Nardocci N, Zorzi G, Blau N, Fernandez Alvarez E, Sesta M, Angelini L, Pannacci M, Invernizzi F, Garavaglia B. Nardocci N, et al. Among authors: zorzi g. Neurology. 2003 Jan 28;60(2):335-7. doi: 10.1212/01.wnl.0000044049.99690.ad. Neurology. 2003. PMID: 12552057

10

Paroxysmal dyskinesias in childhood.

Zorzi G, Conti C, Erba A, Granata T, Angelini L, Nardocci N. Zorzi G, et al. Pediatr Neurol. 2003 Mar;28(3):168-72. doi: 10.1016/s0887-8994(02)00512-x. Pediatr Neurol. 2003. PMID: 12770667

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