Perlman SL - Search Results

1

The Cerebellar Cognitive Affective/Schmahmann Syndrome Scale in Spinocerebellar Ataxias.

Selvadurai LP, Perlman SL, Ashizawa T, Wilmot GR, Onyike CU, Rosenthal LS, Shakkottai VG, Paulson HL, Subramony SH, Bushara KO, Kuo SH, Dietiker C, Geschwind MD, Nelson AB, Gomez CM, Opal P, Zesiewicz TA, Hawkins T, Yacoubian TA, Nopoulos PC, Sha SJ, Morrison PE, Figueroa KP, Pulst SM, Schmahmann JD. Selvadurai LP, et al. Among authors: perlman sl. Cerebellum. 2024 Aug;23(4):1411-1425. doi: 10.1007/s12311-023-01651-0. Epub 2024 Jan 2. Cerebellum. 2024. PMID: 38165578 Free PMC article.

2

Spinocerebellar ataxia type 1 and Machado-Joseph disease: incidence of CAG expansions among adult-onset ataxia patients from 311 families with dominant, recessive, or sporadic ataxia.

Ranum LP, Lundgren JK, Schut LJ, Ahrens MJ, Perlman S, Aita J, Bird TD, Gomez C, Orr HT. Ranum LP, et al. Am J Hum Genet. 1995 Sep;57(3):603-8. Am J Hum Genet. 1995. PMID: 7668288 Free PMC article.

3

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. Am J Hum Genet. 1997 Apr;60(4):842-50. Am J Hum Genet. 1997. PMID: 9106530 Free PMC article.

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. Neurology. 1997 Nov;49(5):1247-51. doi: 10.1212/wnl.49.5.1247. Neurology. 1997. PMID: 9371902

5

Spinocerebellar ataxia type 6: gaze-evoked and vertical nystagmus, Purkinje cell degeneration, and variable age of onset.

Gomez CM, Thompson RM, Gammack JT, Perlman SL, Dobyns WB, Truwit CL, Zee DS, Clark HB, Anderson JH. Gomez CM, et al. Among authors: perlman sl. Ann Neurol. 1997 Dec;42(6):933-50. doi: 10.1002/ana.410420616. Ann Neurol. 1997. PMID: 9403487

6

Analysis of the dynamic mutation in the SCA7 gene shows marked parental effects on CAG repeat transmission.

Gouw LG, Castañeda MA, McKenna CK, Digre KB, Pulst SM, Perlman S, Lee MS, Gomez C, Fischbeck K, Gagnon D, Storey E, Bird T, Jeri FR, Ptácek LJ. Gouw LG, et al. Hum Mol Genet. 1998 Mar;7(3):525-32. doi: 10.1093/hmg/7.3.525. Hum Mol Genet. 1998. PMID: 9467013

7

Oculomotor phenotypes in autosomal dominant ataxias.

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

8

SCA8 repeat expansions in ataxia: a controversial association.

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

9

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

10

The SCA12 mutation as a rare cause of spinocerebellar ataxia.

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

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

168 results

Search Page

Filters