Perlman S - Search Results

1

Prevalence of spinocerebellar ataxia 36 in a US population.

Valera JM, Diaz T, Petty LE, Quintáns B, Yáñez Z, Boerwinkle E, Muzny D, Akhmedov D, Berdeaux R, Sobrido MJ, Gibbs R, Lupski JR, Geschwind DH, Perlman S, Below JE, Fogel BL. Valera JM, et al. Among authors: perlman s. Neurol Genet. 2017 Jul 18;3(4):e174. doi: 10.1212/NXG.0000000000000174. eCollection 2017 Aug. Neurol Genet. 2017. PMID: 28761930 Free PMC article.

2

The prevalence and wide clinical spectrum of the spinocerebellar ataxia type 2 trinucleotide repeat in patients with autosomal dominant cerebellar ataxia.

Geschwind DH, Perlman S, Figueroa CP, Treiman LJ, Pulst SM. Geschwind DH, et al. Among authors: perlman s. Am J Hum Genet. 1997 Apr;60(4):842-50. Am J Hum Genet. 1997. PMID: 9106530 Free PMC article.

3

Friedreich's ataxia GAA repeat expansion in patients with recessive or sporadic ataxia.

Geschwind DH, Perlman S, Grody WW, Telatar M, Montermini L, Pandolfo M, Gatti RA. Geschwind DH, et al. Among authors: perlman s. Neurology. 1997 Oct;49(4):1004-9. doi: 10.1212/wnl.49.4.1004. Neurology. 1997. PMID: 9339680

4

Spinocerebellar ataxia type 6. Frequency of the mutation and genotype-phenotype correlations.

Geschwind DH, Perlman S, Figueroa KP, Karrim J, Baloh RW, Pulst SM. Geschwind DH, et al. Among authors: perlman s. Neurology. 1997 Nov;49(5):1247-51. doi: 10.1212/wnl.49.5.1247. Neurology. 1997. PMID: 9371902

5

Oculomotor phenotypes in autosomal dominant ataxias.

Buttner N, Geschwind D, Jen JC, Perlman S, Pulst SM, Baloh RW. Buttner N, et al. Among authors: perlman s. Arch Neurol. 1998 Oct;55(10):1353-7. doi: 10.1001/archneur.55.10.1353. Arch Neurol. 1998. PMID: 9779665

6

SCA8 repeat expansions in ataxia: a controversial association.

Sobrido MJ, Cholfin JA, Perlman S, Pulst SM, Geschwind DH. Sobrido MJ, et al. Among authors: perlman s. Neurology. 2001 Oct 9;57(7):1310-2. doi: 10.1212/wnl.57.7.1310. Neurology. 2001. PMID: 11591855

7

Association of moderate polyglutamine tract expansions in the slow calcium-activated potassium channel type 3 with ataxia.

Figueroa KP, Chan P, Schöls L, Tanner C, Riess O, Perlman SL, Geschwind DH, Pulst SM. Figueroa KP, et al. Among authors: perlman sl. Arch Neurol. 2001 Oct;58(10):1649-53. doi: 10.1001/archneur.58.10.1649. Arch Neurol. 2001. PMID: 11594924

8

The SCA12 mutation as a rare cause of spinocerebellar ataxia.

Cholfin JA, Sobrido MJ, Perlman S, Pulst SM, Geschwind DH. Cholfin JA, et al. Among authors: perlman s. Arch Neurol. 2001 Nov;58(11):1833-5. doi: 10.1001/archneur.58.11.1833. Arch Neurol. 2001. PMID: 11708992

9

Late-onset Friedreich ataxia: phenotypic analysis, magnetic resonance imaging findings, and review of the literature.

Bhidayasiri R, Perlman SL, Pulst SM, Geschwind DH. Bhidayasiri R, et al. Arch Neurol. 2005 Dec;62(12):1865-9. doi: 10.1001/archneur.62.12.1865. Arch Neurol. 2005. PMID: 16344344

10

An approach to the patient with late-onset cerebellar ataxia.

Fogel BL, Perlman S. Fogel BL, et al. Among authors: perlman s. Nat Clin Pract Neurol. 2006 Nov;2(11):629-35; quiz 1 p following 635. doi: 10.1038/ncpneuro0319. Nat Clin Pract Neurol. 2006. PMID: 17057750

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