Zorzi G - Search Results

1

Molecular Genetics and Interferon Signature in the Italian Aicardi Goutières Syndrome Cohort: Report of 12 New Cases and Literature Review.

Garau J, Cavallera V, Valente M, Tonduti D, Sproviero D, Zucca S, Battaglia D, Battini R, Bertini E, Cappanera S, Chiapparini L, Crasà C, Crichiutti G, Dalla Giustina E, D'Arrigo S, De Giorgis V, De Simone M, Galli J, La Piana R, Messana T, Moroni I, Nardocci N, Panteghini C, Parazzini C, Pichiecchio A, Pini A, Ricci F, Saletti V, Salvatici E, Santorelli FM, Sartori S, Tinelli F, Uggetti C, Veneselli E, Zorzi G, Garavaglia B, Fazzi E, Orcesi S, Cereda C. Garau J, et al. Among authors: zorzi g. J Clin Med. 2019 May 26;8(5):750. doi: 10.3390/jcm8050750. J Clin Med. 2019. PMID: 31130681 Free PMC article.

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

Transient paroxysmal dystonia in an infant possibly induced by cisapride.

Angelini L, Zorzi G, Rumi V, Nardocci N, Mennini T. Angelini L, et al. Among authors: zorzi g. Ital J Neurol Sci. 1996 Apr;17(2):157-9. doi: 10.1007/BF02000848. Ital J Neurol Sci. 1996. PMID: 8797071

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

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

7

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

8

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

9

GTP-cyclohydrolase I gene mutations in patients with autosomal dominant and recessive GTP-CH1 deficiency: identification and functional characterization of four novel mutations.

Garavaglia B, Invernizzi F, Carbone ML, Viscardi V, Saracino F, Ghezzi D, Zeviani M, Zorzi G, Nardocci N. Garavaglia B, et al. Among authors: zorzi g. J Inherit Metab Dis. 2004;27(4):455-63. doi: 10.1023/B:BOLI.0000037349.08483.96. J Inherit Metab Dis. 2004. PMID: 15303002

10

Persistent fixed torticollis due to Atlanto-axial rotatory fixation: report of 4 pediatric cases.

Chiapparini L, Zorzi G, De Simone T, Maccagnano C, Seaman B, Savoiardo M, Corona C, Nardocci N. Chiapparini L, et al. Among authors: zorzi g. Neuropediatrics. 2005 Feb;36(1):45-9. doi: 10.1055/s-2004-830533. Neuropediatrics. 2005. PMID: 15776322

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