Nardocci N - Search Results

1

Loss-of-Function Variants in HOPS Complex Genes VPS16 and VPS41 Cause Early Onset Dystonia Associated with Lysosomal Abnormalities.

Steel D, Zech M, Zhao C, Barwick KES, Burke D, Demailly D, Kumar KR, Zorzi G, Nardocci N, Kaiyrzhanov R, Wagner M, Iuso A, Berutti R, Škorvánek M, Necpál J, Davis R, Wiethoff S, Mankad K, Sudhakar S, Ferrini A, Sharma S, Kamsteeg EJ, Tijssen MA, Verschuuren C, van Egmond ME, Flowers JM, McEntagart M, Tucci A, Coubes P, Bustos BI, Gonzalez-Latapi P, Tisch S, Darveniza P, Gorman KM, Peall KJ, Bötzel K, Koch JC, Kmieć T, Plecko B, Boesch S, Haslinger B, Jech R, Garavaglia B, Wood N, Houlden H, Gissen P, Lubbe SJ, Sue CM, Cif L, Mencacci NE, Anderson G, Kurian MA, Winkelmann J; Genomics England Research Consortium. Steel D, et al. Among authors: nardocci n. Ann Neurol. 2020 Nov;88(5):867-877. doi: 10.1002/ana.25879. Epub 2020 Sep 21. Ann Neurol. 2020. PMID: 32808683

2

Hallervorden-Spatz disease: clinical and MRI study of 11 cases diagnosed in life.

Angelini L, Nardocci N, Rumi V, Zorzi C, Strada L, Savoiardo M. Angelini L, et al. Among authors: nardocci n. J Neurol. 1992 Oct;239(8):417-25. doi: 10.1007/BF00856805. J Neurol. 1992. PMID: 1447570

3

Idiopathic dystonia with onset in childhood.

Angelini L, Nardocci N, Rumi V, Lamperti E. Angelini L, et al. Among authors: nardocci n. J Neurol. 1989 Sep;236(6):319-21. doi: 10.1007/BF00314372. J Neurol. 1989. PMID: 2795098

4

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. Am J Med Genet. 1995 Jun 5;57(2):137-41. doi: 10.1002/ajmg.1320570205. Am J Med Genet. 1995. PMID: 7668317

5

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: nardocci n. Ital J Neurol Sci. 1996 Apr;17(2):157-9. doi: 10.1007/BF02000848. Ital J Neurol Sci. 1996. PMID: 8797071

6

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. Pediatr Neurol. 1996 Sep;15(2):108-13. doi: 10.1016/0887-8994(96)00152-x. Pediatr Neurol. 1996. PMID: 8888043

7

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. Neurology. 1999 Apr 22;52(7):1472-8. doi: 10.1212/wnl.52.7.1472. Neurology. 1999. PMID: 10227637

8

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: nardocci n. Neuroradiology. 1999 May;41(5):376-80. doi: 10.1007/s002340050768. Neuroradiology. 1999. PMID: 10379598

9

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. Among authors: nardocci n. Mov Disord. 2002 Mar;17(2):407-8. doi: 10.1002/mds.10045. Mov Disord. 2002. PMID: 11921134

10

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. Neurology. 2003 Jan 28;60(2):335-7. doi: 10.1212/01.wnl.0000044049.99690.ad. Neurology. 2003. PMID: 12552057

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

181 results

Search Page