Raskin S - Search Results

1

Repeat interruptions in spinocerebellar ataxia type 10 expansions are strongly associated with epileptic seizures.

McFarland KN, Liu J, Landrian I, Zeng D, Raskin S, Moscovich M, Gatto EM, Ochoa A, Teive HA, Rasmussen A, Ashizawa T. McFarland KN, et al. Among authors: raskin s. Neurogenetics. 2014 Mar;15(1):59-64. doi: 10.1007/s10048-013-0385-6. Epub 2013 Dec 7. Neurogenetics. 2014. PMID: 24318420 Free PMC article.

2

Huntington disease: DNA analysis in Brazilian population.

Raskin S, Allan N, Teive HA, Cardoso F, Haddad MS, Levi G, Boy R, Lerena Junior J, Sotomaior VS, Janzen-Dück M, Jardim LB, Fellander FR, Andrade LA. Raskin S, et al. Arq Neuropsiquiatr. 2000 Dec;58(4):977-85. doi: 10.1590/s0004-282x2000000600001. Arq Neuropsiquiatr. 2000. PMID: 11105061 Free article.

3

Clinical phenotype of Brazilian families with spinocerebellar ataxia 10.

Teive HA, Roa BB, Raskin S, Fang P, Arruda WO, Neto YC, Gao R, Werneck LC, Ashizawa T. Teive HA, et al. Among authors: raskin s. Neurology. 2004 Oct 26;63(8):1509-12. doi: 10.1212/01.wnl.0000142109.62056.57. Neurology. 2004. PMID: 15505178

4

Kennedy's disease phenotype with positive genetic study for Kugelberg-Welander's disease: case report.

Trentin AP, Scola RH, Teive HA, Raskin S, Germiniani FM, Werneck LC. Trentin AP, et al. Among authors: raskin s. Arq Neuropsiquiatr. 2005 Jun;63(2A):330-1. doi: 10.1590/s0004-282x2005000200025. Arq Neuropsiquiatr. 2005. PMID: 16100985 Free article.

5

Clinical and genetic study of a Brazilian family with spastic paraplegia (SPG6 locus).

Munhoz RP, Kawarai T, Teive HA, Raskin S, Sato C, Liang Y, St George-Hyslop PH, Rogaeva E. Munhoz RP, et al. Among authors: raskin s. Mov Disord. 2006 Feb;21(2):279-81. doi: 10.1002/mds.20775. Mov Disord. 2006. PMID: 16267846

6

Reduced penetrance in a Brazilian family with spinocerebellar ataxia type 10.

Raskin S, Ashizawa T, Teive HA, Arruda WO, Fang P, Gao R, White MC, Werneck LC, Roa B. Raskin S, et al. Arch Neurol. 2007 Apr;64(4):591-4. doi: 10.1001/archneur.64.4.591. Arch Neurol. 2007. PMID: 17420323

7

Non-choreic movement disorders as initial manifestations of Huntington's disease.

Becker N, Munhoz RP, Raskin S, Werneck LC, Teive HA. Becker N, et al. Among authors: raskin s. Arq Neuropsiquiatr. 2007 Jun;65(2B):402-5. doi: 10.1590/s0004-282x2007000300007. Arq Neuropsiquiatr. 2007. PMID: 17665004 Free article.

8

The G2019S LRRK2 mutation in Brazilian patients with Parkinson's disease: phenotype in monozygotic twins.

Munhoz RP, Wakutani Y, Marras C, Teive HA, Raskin S, Werneck LC, Moreno D, Sato C, Lang AE, Rogaeva E. Munhoz RP, et al. Among authors: raskin s. Mov Disord. 2008 Jan 30;23(2):290-4. doi: 10.1002/mds.21832. Mov Disord. 2008. PMID: 17999435

9

The history of spinocerebellar ataxia type 10 in Brazil: travels of a gene.

Teive HA, Arruda WO, Raskin S, Ashizawa T, Werneck LC. Teive HA, et al. Among authors: raskin s. Arq Neuropsiquiatr. 2007 Dec;65(4A):965-8. doi: 10.1590/s0004-282x2007000600008. Arq Neuropsiquiatr. 2007. PMID: 18094855 Free article.

10

Cerebellar ataxia, myoclonus, cervical lipomas, and MERRF syndrome. Case report.

Teive HA, Munhoz RP, Muzzio JA, Scola RH, Kay CK, Raskin S, Werneck LC, Bruhn H. Teive HA, et al. Among authors: raskin s. Mov Disord. 2008 Jun 15;23(8):1191-2. doi: 10.1002/mds.21990. Mov Disord. 2008. PMID: 18412280 No abstract available.

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