Orlacchio A - Search Results

1

Choreoathetosis, Dystonia, and Myoclonus in 3 Siblings With Autosomal Recessive Spinocerebellar Ataxia Type 16.

Kawarai T, Miyamoto R, Shimatani Y, Orlacchio A, Kaji R. Kawarai T, et al. Among authors: orlacchio a. JAMA Neurol. 2016 Jul 1;73(7):888-90. doi: 10.1001/jamaneurol.2016.0647. JAMA Neurol. 2016. PMID: 27182963 No abstract available.

2

Association study of the 5-hydroxytryptamine(6) receptor gene in Alzheimer's disease.

Orlacchio A, Kawarai T, Paciotti E, Stefani A, Orlacchio A, Sorbi S, St George-Hyslop PH, Bernardi G. Orlacchio A, et al. Neurosci Lett. 2002 May 31;325(1):13-6. doi: 10.1016/s0304-3940(02)00221-5. Neurosci Lett. 2002. PMID: 12023056

3

Association analysis between Alzheimer's disease and the Nicastrin gene polymorphisms.

Orlacchio A, Kawarai T, Polidoro M, Stefani A, Orlacchio A, St George-Hyslop PH, Bernardi G. Orlacchio A, et al. Neurosci Lett. 2002 Nov 22;333(2):115-8. doi: 10.1016/s0304-3940(02)01022-4. Neurosci Lett. 2002. PMID: 12419494

4

Lack of association between Alzheimer's disease and the promoter region polymorphisms of the nicastrin gene.

Orlacchio A, Kawarai T, Polidoro M, Paterson AD, Rogaeva E, Orlacchio A, St George-Hyslop PH, Bernardi G. Orlacchio A, et al. Neurosci Lett. 2004 Jun 3;363(1):49-53. doi: 10.1016/j.neulet.2004.03.044. Neurosci Lett. 2004. PMID: 15157994

5

Hereditary spastic paraplegia: clinical genetic study of 15 families.

Orlacchio A, Kawarai T, Totaro A, Errico A, St George-Hyslop PH, Rugarli EI, Bernardi G. Orlacchio A, et al. Arch Neurol. 2004 Jun;61(6):849-55. doi: 10.1001/archneur.61.6.849. Arch Neurol. 2004. PMID: 15210521

6

Clinical and genetic study of a large SPG4 Italian family.

Orlacchio A, Kawarai T, Gaudiello F, Totaro A, Schillaci O, Stefani A, Floris R, St George-Hyslop PH, Sorbi S, Bernardi G. Orlacchio A, et al. Mov Disord. 2005 Aug;20(8):1055-9. doi: 10.1002/mds.20494. Mov Disord. 2005. PMID: 15858810

7

New locus for hereditary spastic paraplegia maps to chromosome 1p31.1-1p21.1.

Orlacchio A, Kawarai T, Gaudiello F, St George-Hyslop PH, Floris R, Bernardi G. Orlacchio A, et al. Ann Neurol. 2005 Sep;58(3):423-9. doi: 10.1002/ana.20590. Ann Neurol. 2005. PMID: 16130112

8

Novel SPG6 mutation p.A100T in a Japanese family with autosomal dominant form of hereditary spastic paraplegia.

Kaneko S, Kawarai T, Yip E, Salehi-Rad S, Sato C, Orlacchio A, Bernardi G, Liang Y, Hasegawa H, Rogaeva E, St George-Hyslop P. Kaneko S, et al. Among authors: orlacchio a. Mov Disord. 2006 Sep;21(9):1531-3. doi: 10.1002/mds.21005. Mov Disord. 2006. PMID: 16795073

9

Neuroacanthocytosis associated with a defect of the 4.1R membrane protein.

Orlacchio A, Calabresi P, Rum A, Tarzia A, Salvati AM, Kawarai T, Stefani A, Pisani A, Bernardi G, Cianciulli P, Caprari P. Orlacchio A, et al. BMC Neurol. 2007 Feb 13;7:4. doi: 10.1186/1471-2377-7-4. BMC Neurol. 2007. PMID: 17298666 Free PMC article.

10

A novel mutation in the SPG3A gene (atlastin) in hereditary spastic paraplegia.

Matsui M, Kawarai T, Hase Y, Tomimoto H, Iseki K, Rogaeva E, Orlacchio A, Bernardi G, St George-Hyslop P, Takahashi R, Matsui M. Matsui M, et al. Among authors: orlacchio a. J Neurol. 2007 Jul;254(7):972-4. doi: 10.1007/s00415-006-0446-y. Epub 2007 Mar 22. J Neurol. 2007. PMID: 17380240 No abstract available.

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