Zorzi G - Search Results

1

Spontaneous MRI improvement and absence of cerebral calcification in Aicardi-Goutières syndrome: Diagnostic and disease-monitoring implications.

Tonduti D, Izzo G, D'Arrigo S, Riva D, Moroni I, Zorzi G, Cavallera V, Pichiecchio A, Uggetti C, Veggiotti P, Orcesi S, Chiapparini L, Parazzini C. Tonduti D, et al. Among authors: zorzi g. Mol Genet Metab. 2019 Apr;126(4):489-494. doi: 10.1016/j.ymgme.2019.02.006. Epub 2019 Feb 25. Mol Genet Metab. 2019. PMID: 30826161

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

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

4

Stimulation of the globus pallidus internus for childhood-onset dystonia.

Zorzi G, Marras C, Nardocci N, Franzini A, Chiapparini L, Maccagnano E, Angelini L, Caldiroli D, Broggi G. Zorzi G, et al. Mov Disord. 2005 Sep;20(9):1194-200. doi: 10.1002/mds.20510. Mov Disord. 2005. PMID: 15895426

5

Glucose transporter type 1 deficiency: ketogenic diet in three patients with atypical phenotype.

Veggiotti P, Teutonico F, Alfei E, Nardocci N, Zorzi G, Tagliabue A, De Giorgis V, Balottin U. Veggiotti P, et al. Among authors: zorzi g. Brain Dev. 2010 May;32(5):404-8. doi: 10.1016/j.braindev.2009.04.013. Epub 2009 Jun 9. Brain Dev. 2010. PMID: 19515520

6

Ataxia with oculomotor apraxia type1 (AOA1): novel and recurrent aprataxin mutations, coenzyme Q10 analyses, and clinical findings in Italian patients.

Castellotti B, Mariotti C, Rimoldi M, Fancellu R, Plumari M, Caimi S, Uziel G, Nardocci N, Moroni I, Zorzi G, Pareyson D, Di Bella D, Di Donato S, Taroni F, Gellera C. Castellotti B, et al. Among authors: zorzi g. Neurogenetics. 2011 Aug;12(3):193-201. doi: 10.1007/s10048-011-0281-x. Epub 2011 Apr 5. Neurogenetics. 2011. PMID: 21465257

7

Zorzi G, Zibordi F, Chiapparini L, Bertini E, Russo L, Piga A, Longo F, Garavaglia B, Aquino D, Savoiardo M, Solari A, Nardocci N. Zorzi G, et al. Mov Disord. 2011 Aug 1;26(9):1756-9. doi: 10.1002/mds.23751. Epub 2011 May 6. Mov Disord. 2011. PMID: 21557313 Clinical Trial.

8

The "eye-of-the-tiger" sign may be absent in the early stages of classic pantothenate kinase associated neurodegeneration.

Chiapparini L, Savoiardo M, D'Arrigo S, Reale C, Zorzi G, Zibordi F, Cordelli DM, Franzoni E, Garavaglia B, Nardocci N. Chiapparini L, et al. Among authors: zorzi g. Neuropediatrics. 2011 Aug;42(4):159-62. doi: 10.1055/s-0031-1285925. Epub 2011 Aug 29. Neuropediatrics. 2011. PMID: 21877312

9

Metabolic consequences of mitochondrial coenzyme A deficiency in patients with PANK2 mutations.

Leoni V, Strittmatter L, Zorzi G, Zibordi F, Dusi S, Garavaglia B, Venco P, Caccia C, Souza AL, Deik A, Clish CB, Rimoldi M, Ciusani E, Bertini E, Nardocci N, Mootha VK, Tiranti V. Leoni V, et al. Among authors: zorzi g. Mol Genet Metab. 2012 Mar;105(3):463-71. doi: 10.1016/j.ymgme.2011.12.005. Epub 2011 Dec 14. Mol Genet Metab. 2012. PMID: 22221393 Free PMC article.

10

Phenomenology of psychogenic movement disorders in children.

Canavese C, Ciano C, Zibordi F, Zorzi G, Cavallera V, Nardocci N. Canavese C, et al. Among authors: zorzi g. Mov Disord. 2012 Aug;27(9):1153-7. doi: 10.1002/mds.24947. Epub 2012 Mar 7. Mov Disord. 2012. PMID: 22407521

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