Perlman S - Search Results

1

Comprehensive systematic review summary: Treatment of cerebellar motor dysfunction and ataxia: Report of the Guideline Development, Dissemination, and Implementation Subcommittee of the American Academy of Neurology.

Zesiewicz TA, Wilmot G, Kuo SH, Perlman S, Greenstein PE, Ying SH, Ashizawa T, Subramony SH, Schmahmann JD, Figueroa KP, Mizusawa H, Schöls L, Shaw JD, Dubinsky RM, Armstrong MJ, Gronseth GS, Sullivan KL. Zesiewicz TA, et al. Among authors: perlman s. Neurology. 2018 Mar 6;90(10):464-471. doi: 10.1212/WNL.0000000000005055. Epub 2018 Feb 9. Neurology. 2018. PMID: 29440566 Free PMC article.

2

Idiopathic central diabetes insipidus followed by progressive spastic cerebral ataxia. Report of four cases.

Birnbaum DC, Shields D, Lippe B, Perlman S, Phillipart M. Birnbaum DC, et al. Among authors: perlman s. Arch Neurol. 1989 Sep;46(9):1001-3. doi: 10.1001/archneur.1989.00520450071022. Arch Neurol. 1989. PMID: 2775003

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

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

6

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

7

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

8

Ataxia-telangiectasia: diagnosis and treatment.

Perlman S, Becker-Catania S, Gatti RA. Perlman S, et al. Semin Pediatr Neurol. 2003 Sep;10(3):173-82. doi: 10.1016/s1071-9091(03)00026-3. Semin Pediatr Neurol. 2003. PMID: 14653405 Review.

9

Relative atrophy of the flocculus and ocular motor dysfunction in SCA2 and SCA6.

Ying SH, Choi SI, Lee M, Perlman SL, Baloh RW, Toga AW, Zee DS. Ying SH, et al. Among authors: perlman sl. Ann N Y Acad Sci. 2005 Apr;1039:430-5. doi: 10.1196/annals.1325.040. Ann N Y Acad Sci. 2005. PMID: 15826995

10

Clinical feature profile of spinocerebellar ataxia type 1-8 predicts genetically defined subtypes.

Maschke M, Oehlert G, Xie TD, Perlman S, Subramony SH, Kumar N, Ptacek LJ, Gomez CM. Maschke M, et al. Among authors: perlman s. Mov Disord. 2005 Nov;20(11):1405-12. doi: 10.1002/mds.20533. Mov Disord. 2005. PMID: 16037936

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