Albanese A - Search Results

1

Progressive supranuclear palsy and Parkinson's disease in a family with a new mutation in the tau gene.

Rossi G, Gasparoli E, Pasquali C, Di Fede G, Testa D, Albanese A, Bracco F, Tagliavini F. Rossi G, et al. Among authors: albanese a. Ann Neurol. 2004 Mar;55(3):448. doi: 10.1002/ana.20006. Ann Neurol. 2004. PMID: 14991829 No abstract available.

2

A case of dementia parkinsonism resembling progressive supranuclear palsy due to mutation in the tau protein gene.

Soliveri P, Rossi G, Monza D, Tagliavini F, Piacentini S, Albanese A, Bugiani O, Girotti F. Soliveri P, et al. Among authors: albanese a. Arch Neurol. 2003 Oct;60(10):1454-6. doi: 10.1001/archneur.60.10.1454. Arch Neurol. 2003. PMID: 14568818

3

The PINK1 phenotype can be indistinguishable from idiopathic Parkinson disease.

Albanese A, Valente EM, Romito LM, Bellacchio E, Elia AE, Dallapiccola B. Albanese A, et al. Neurology. 2005 Jun 14;64(11):1958-60. doi: 10.1212/01.WNL.0000163999.72864.FD. Neurology. 2005. PMID: 15955954

4

Safety and efficacy of tilavonemab in progressive supranuclear palsy: a phase 2, randomised, placebo-controlled trial.

Höglinger GU, Litvan I, Mendonca N, Wang D, Zheng H, Rendenbach-Mueller B, Lon HK, Jin Z, Fisseha N, Budur K, Gold M, Ryman D, Florian H; Arise Investigators. Höglinger GU, et al. Lancet Neurol. 2021 Mar;20(3):182-192. doi: 10.1016/S1474-4422(20)30489-0. Lancet Neurol. 2021. PMID: 33609476 Clinical Trial.

5

Non-motor symptoms in atypical and secondary parkinsonism: the PRIAMO study.

Colosimo C, Morgante L, Antonini A, Barone P, Avarello TP, Bottacchi E, Cannas A, Ceravolo MG, Ceravolo R, Cicarelli G, Gaglio RM, Giglia L, Iemolo F, Manfredi M, Meco G, Nicoletti A, Pederzoli M, Petrone A, Pisani A, Pontieri FE, Quatrale R, Ramat S, Scala R, Volpe G, Zappulla S, Bentivoglio AR, Stocchi F, Trianni G, Del Dotto P, Simoni L, Marconi R; PRIAMO STUDY GROUP. Colosimo C, et al. J Neurol. 2010 Jan;257(1):5-14. doi: 10.1007/s00415-009-5255-7. Epub 2009 Aug 9. J Neurol. 2010. PMID: 19669613

6

A 52-Year-Old Man with Myoclonic Jerks.

Giaccone G, Carella F, Parravicini C, Longhi E, Chiapparini L, Savoiardo M, Montano N, Morbin M, Albanese A, Tagliavini F. Giaccone G, et al. Among authors: albanese a. Brain Pathol. 2016 Mar;26(2):291-2. doi: 10.1111/bpa.12359. Brain Pathol. 2016. PMID: 27000489 Free PMC article. No abstract available.

7

Using global team science to identify genetic parkinson's disease worldwide.

Vollstedt EJ, Kasten M, Klein C; MJFF Global Genetic Parkinson's Disease Study Group. Vollstedt EJ, et al. Ann Neurol. 2019 Aug;86(2):153-157. doi: 10.1002/ana.25514. Epub 2019 Jun 26. Ann Neurol. 2019. PMID: 31155756 Free PMC article. No abstract available.

8

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: albanese a. J Neurol. 2005 Feb;252(2):208-11. doi: 10.1007/s00415-005-0638-x. J Neurol. 2005. PMID: 15729528 Clinical Trial.

9

Some specific clinical features differentiate multiple system atrophy (striatonigral variety) from Parkinson's disease.

Colosimo C, Albanese A, Hughes AJ, de Bruin VM, Lees AJ. Colosimo C, et al. Among authors: albanese a. Arch Neurol. 1995 Mar;52(3):294-8. doi: 10.1001/archneur.1995.00540270090024. Arch Neurol. 1995. PMID: 7872884

10

Clinical genetic study of familial Parkinson's disease in Italy.

Rossi P, Albanese A, Moro E, Genvardi M, Tonali P. Rossi P, et al. Among authors: albanese a. Adv Neurol. 1999;80:181-6. Adv Neurol. 1999. PMID: 10410719 No abstract available.

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