Salehi-Rad S - Search Results

1

Analysis of the glucocerebrosidase gene in Parkinson's disease.

Sato C, Morgan A, Lang AE, Salehi-Rad S, Kawarai T, Meng Y, Ray PN, Farrer LA, St George-Hyslop P, Rogaeva E. Sato C, et al. Mov Disord. 2005 Mar;20(3):367-70. doi: 10.1002/mds.20319. Mov Disord. 2005. PMID: 15517592

2

Genetic association study of PINK1 coding polymorphisms in Parkinson's disease.

Groen JL, Kawarai T, Toulina A, Rivoiro C, Salehi-Rad S, Sato C, Morgan A, Liang Y, Postuma RB, St George-Hyslop P, Lang AE, Rogaeva E. Groen JL, et al. Neurosci Lett. 2004 Dec 6;372(3):226-9. doi: 10.1016/j.neulet.2004.09.043. Neurosci Lett. 2004. PMID: 15542245

3

Analysis of the PINK1 gene in a large cohort of cases with Parkinson disease.

Rogaeva E, Johnson J, Lang AE, Gulick C, Gwinn-Hardy K, Kawarai T, Sato C, Morgan A, Werner J, Nussbaum R, Petit A, Okun MS, McInerney A, Mandel R, Groen JL, Fernandez HH, Postuma R, Foote KD, Salehi-Rad S, Liang Y, Reimsnider S, Tandon A, Hardy J, St George-Hyslop P, Singleton AB. Rogaeva E, et al. Arch Neurol. 2004 Dec;61(12):1898-904. doi: 10.1001/archneur.61.12.1898. Arch Neurol. 2004. PMID: 15596610

4

Homozygous and heterozygous PINK1 mutations: considerations for diagnosis and care of Parkinson's disease patients.

Zadikoff C, Rogaeva E, Djarmati A, Sato C, Salehi-Rad S, St George-Hyslop P, Klein C, Lang AE. Zadikoff C, et al. Among authors: salehi rad s. Mov Disord. 2006 Jun;21(6):875-9. doi: 10.1002/mds.20854. Mov Disord. 2006. PMID: 16547921

5

Childhood onset in familial prion disease with a novel mutation in the PRNP gene.

Rogaeva E, Zadikoff C, Ponesse J, Schmitt-Ulms G, Kawarai T, Sato C, Salehi-Rad S, St George-Hyslop P, Lang AE. Rogaeva E, et al. Among authors: salehi rad s. Arch Neurol. 2006 Jul;63(7):1016-21. doi: 10.1001/archneur.63.7.1016. Arch Neurol. 2006. PMID: 16831973

6

LRRK2 gene in Parkinson disease: mutation analysis and case control association study.

Paisán-Ruíz C, Lang AE, Kawarai T, Sato C, Salehi-Rad S, Fisman GK, Al-Khairallah T, St George-Hyslop P, Singleton A, Rogaeva E. Paisán-Ruíz C, et al. Among authors: salehi rad s. Neurology. 2005 Sep 13;65(5):696-700. doi: 10.1212/01.wnl.0000167552.79769.b3. Neurology. 2005. PMID: 16157901

7

Clinical findings in a large family with a parkin ex3delta40 mutation.

Munhoz RP, Sa DS, Rogaeva E, Salehi-Rad S, Sato C, Medeiros H, Farrer M, Lang AE. Munhoz RP, et al. Arch Neurol. 2004 May;61(5):701-4. doi: 10.1001/archneur.61.5.701. Arch Neurol. 2004. PMID: 15148147

8

Wild-type PINK1 prevents basal and induced neuronal apoptosis, a protective effect abrogated by Parkinson disease-related mutations.

Petit A, Kawarai T, Paitel E, Sanjo N, Maj M, Scheid M, Chen F, Gu Y, Hasegawa H, Salehi-Rad S, Wang L, Rogaeva E, Fraser P, Robinson B, St George-Hyslop P, Tandon A. Petit A, et al. J Biol Chem. 2005 Oct 7;280(40):34025-32. doi: 10.1074/jbc.M505143200. Epub 2005 Aug 2. J Biol Chem. 2005. PMID: 16079129 Free article.

9

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: salehi rad s. Mov Disord. 2006 Sep;21(9):1531-3. doi: 10.1002/mds.21005. Mov Disord. 2006. PMID: 16795073

10

Novel PS1 mutation in a Bavarian kindred with familial Alzheimer disease.

Klünemann HH, Rogaeva E, Neumann M, Kretzschmar HA, Kandel M, Toulina A, Sato C, Salehi-Rad S, Pfister K, Klein HE, St George-Hyslop PH. Klünemann HH, et al. Alzheimer Dis Assoc Disord. 2004 Oct-Dec;18(4):256-8. Alzheimer Dis Assoc Disord. 2004. PMID: 15592140

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