Garavaglia B - Search Results

1

ANO3 as a Cause of Early-Onset Chorea Combined with Dystonia: Illustration of Phenotypic Evolution.

Romito LM, Leta V, Garavaglia B, Panteghini C, Zorzi G, Elia AE, Colucci F, Carecchio M, Eleopra R. Romito LM, et al. Among authors: garavaglia b. Mov Disord. 2024 Jan;39(1):220-221. doi: 10.1002/mds.29672. Epub 2023 Dec 10. Mov Disord. 2024. PMID: 38073131 No abstract available.

2

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: garavaglia b. Mov Disord. 2002 Mar;17(2):407-8. doi: 10.1002/mds.10045. Mov Disord. 2002. PMID: 11921134

3

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

4

Analysis of the epsilon-sarcoglycan gene in familial and sporadic myoclonus-dystonia: evidence for genetic heterogeneity.

Valente EM, Misbahuddin A, Brancati F, Placzek MR, Garavaglia B, Salvi S, Nemeth A, Shaw-Smith C, Nardocci N, Bentivoglio AR, Berardelli A, Eleopra R, Dallapiccola B, Warner TT. Valente EM, et al. Among authors: garavaglia b. Mov Disord. 2003 Sep;18(9):1047-51. doi: 10.1002/mds.10476. Mov Disord. 2003. PMID: 14502674

5

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. J Inherit Metab Dis. 2004;27(4):455-63. doi: 10.1023/B:BOLI.0000037349.08483.96. J Inherit Metab Dis. 2004. PMID: 15303002

6

High frequency stimulation of the subthalamic nucleus is efficacious in Parkin disease.

Romito LM, Contarino MF, Ghezzi D, Franzini A, Garavaglia B, Albanese A. Romito LM, et al. Among authors: garavaglia b. J Neurol. 2005 Feb;252(2):208-11. doi: 10.1007/s00415-005-0638-x. J Neurol. 2005. PMID: 15729528 Clinical Trial.

7

Frequency and phenotypes of LRRK2 G2019S mutation in Italian patients with Parkinson's disease.

Marongiu R, Ghezzi D, Ialongo T, Soleti F, Elia A, Cavone S, Albanese A, Altavista MC, Barone P, Brusa L, Cortelli P, Petrozzi L, Scaglione C, Stanzione P, Tinazzi M, Zeviani M, Dallapiccola B, Bentivoglio AR, Valente EM, Garavaglia B; Italian PD Study Group. Marongiu R, et al. Among authors: garavaglia b. Mov Disord. 2006 Aug;21(8):1232-5. doi: 10.1002/mds.20890. Mov Disord. 2006. PMID: 16622859

8

Normal cardiovascular reflex testing in patients with parkin disease.

Del Sorbo F, Elia AE, De Joanna G, Romito LM, Garavaglia B, Albanese A. Del Sorbo F, et al. Among authors: garavaglia b. Mov Disord. 2007 Mar 15;22(4):528-32. doi: 10.1002/mds.21307. Mov Disord. 2007. PMID: 17230469

9

Myoclonus-dystonia syndrome: clinical presentation, disease course, and genetic features in 11 families.

Nardocci N, Zorzi G, Barzaghi C, Zibordi F, Ciano C, Ghezzi D, Garavaglia B. Nardocci N, et al. Among authors: garavaglia b. Mov Disord. 2008 Jan;23(1):28-34. doi: 10.1002/mds.21715. Mov Disord. 2008. PMID: 17853490 Free article.

10

A neurophysiological study of myoclonus in patients with DYT11 myoclonus-dystonia syndrome.

Marelli C, Canafoglia L, Zibordi F, Ciano C, Visani E, Zorzi G, Garavaglia B, Barzaghi C, Albanese A, Soliveri P, Leone M, Panzica F, Scaioli V, Pincherle A, Nardocci N, Franceschetti S. Marelli C, et al. Among authors: garavaglia b. Mov Disord. 2008 Oct 30;23(14):2041-8. doi: 10.1002/mds.22256. Mov Disord. 2008. PMID: 18759336

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