Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 78

1.

New-onset psychosis in a patient with spinocerebellar ataxia type 10.

Wexler E, Fogel BL.

Am J Psychiatry. 2011 Dec;168(12):1339-40. doi: 10.1176/appi.ajp.2011.11050737. No abstract available.

PMID:
22193677
2.

Schizophrenia in a patient with spinocerebellar ataxia 2: coincidence of two disorders or a neurodegenerative disease presenting with psychosis?

Rottnek M, Riggio S, Byne W, Sano M, Margolis RL, Walker RH.

Am J Psychiatry. 2008 Aug;165(8):964-7. doi: 10.1176/appi.ajp.2008.08020285. No abstract available.

PMID:
18676601
3.

Sporadic case of spinocerebellar ataxia type 17: treatment observations for managing urinary and psychotic symptoms.

Kanai K, Sakakibara R, Uchiyama T, Liu Z, Yamamoto T, Ito T, Hirano S, Asahina M, Kuwabara S, Hattori T, Fukami G, Arai K, Yamaguchi C, Nomura F.

Mov Disord. 2007 Feb 15;22(3):441-3. No abstract available.

PMID:
17216650
4.

[Clinical features and MRI findings in spinocerebellar ataxia type 31 (SCA31) comparing with spinocerebellar ataxia type 6 (SCA6)].

Sakakibara S, Aiba I, Saito Y, Inukai A, Ishikawa K, Mizusawa H.

Rinsho Shinkeigaku. 2014;54(6):473-9. Japanese.

PMID:
24990830
5.

Fatigue is frequent and severe in spinocerebellar ataxia type 1.

Martins CR Jr, Martinez AR, D'Abreu A, Lopes-Cendes I, França MC Jr.

Parkinsonism Relat Disord. 2015 Jul;21(7):821-2. doi: 10.1016/j.parkreldis.2015.04.015. Epub 2015 Apr 23. No abstract available.

PMID:
25943530
6.

Dystonia in spinocerebellar ataxia type 6.

Sethi KD, Jankovic J.

Mov Disord. 2002 Jan;17(1):150-3.

PMID:
11835453
7.

Spinocerebellar Ataxia (SCA) type 2 presenting with chorea.

Bhalsing KS, Sowmya V, Netravathi M, Jain S, Pal PK.

Parkinsonism Relat Disord. 2013 Dec;19(12):1171-2. doi: 10.1016/j.parkreldis.2013.08.004. Epub 2013 Aug 22. No abstract available.

PMID:
24012020
8.

[Writer's cramp secondary to spinocerebellar ataxia type 7].

Gaillard N, Castelnovo G, Brice A, Labauge P.

Rev Neurol (Paris). 2007 May;163(5):589-91. French.

PMID:
17571027
9.

Ocular motor characteristics of different subtypes of spinocerebellar ataxia: distinguishing features.

Kim JS, Kim JS, Youn J, Seo DW, Jeong Y, Kang JH, Park JH, Cho JW.

Mov Disord. 2013 Aug;28(9):1271-7. doi: 10.1002/mds.25464. Epub 2013 Apr 22.

PMID:
23609488
10.

Positional vertigo and macroscopic downbeat positioning nystagmus in spinocerebellar ataxia type 6 (SCA6).

Yabe I, Sasaki H, Takeichi N, Takei A, Hamada T, Fukushima K, Tashiro K.

J Neurol. 2003 Apr;250(4):440-3.

PMID:
12700909
11.

A case of nocturnal frontal lobe epilepsy in a patient with spinocerebellar ataxia type 17.

Belluzzo M, Musho-Ilbeh S, Monti F, Pizzolato G.

Seizure. 2012 Dec;21(10):805-6. doi: 10.1016/j.seizure.2012.08.006. Epub 2012 Sep 19. No abstract available.

12.

The prevalence of familial hemiplegic migraine with cerebellar ataxia and spinocerebellar ataxia type 6 in Portugal.

Barros J, Ruano L, Domingos J, Tuna A, Damásio J, Alonso I, Silveira I, Sequeiros J, Coutinho P.

Headache. 2014 May;54(5):911-5. doi: 10.1111/head.12260. Epub 2013 Oct 30.

PMID:
24898624
13.

Spastic paraparesis as the onset manifestation of spinocerebellar ataxia type 7.

Linhares Sda C, Horta WG, Cunha FM, Castro JD, Santos AC, Marques W Jr.

Arq Neuropsiquiatr. 2008 Jun;66(2A):246-8. No abstract available.

14.

Early onset autosomal dominant spinocerebellar ataxia with miosis: four cases.

Timby N, Stattin EL, Kristiansen I, Eriksson U, Erikson A.

Eur J Paediatr Neurol. 2008 Jan;12(1):38-40. Epub 2007 Jun 20.

PMID:
17584505
15.

Differences in saccade dynamics between spinocerebellar ataxia 2 and late-onset cerebellar ataxias.

Federighi P, Cevenini G, Dotti MT, Rosini F, Pretegiani E, Federico A, Rufa A.

Brain. 2011 Mar;134(Pt 3):879-91. doi: 10.1093/brain/awr009.

PMID:
21354979
16.

[Type 7 spinocerebellar ataxia (SCA) dignosed by the appearance of the fundus].

Jaja Z, Laghmari A.

Pan Afr Med J. 2014 Feb 14;17:110. doi: 10.11604/pamj.2014.17.110.3961. eCollection 2014. French. No abstract available.

17.

Cognitive changes in spinocerebellar ataxia type 2.

Valis M, Masopust J, Bažant J, Ríhová Z, Kalnická D, Urban A, Zumrová A, Hort J.

Neuro Endocrinol Lett. 2011;32(3):354-9.

PMID:
21712788
18.

Spinocerebellar ataxia: perceptual and acoustic analysis of speech in three cases.

Barreto Sdos S, Nagaoka JM, Martins FC, Ortiz KZ.

Pro Fono. 2009 Apr-Jun;21(2):167-70.

19.

[A case of 77-year-old male with spinocerebellar ataxia type 31 with left dominant dystonia].

Saito R, Kanzaki M, Uesaka Y.

Rinsho Shinkeigaku. 2015;55(6):434. doi: 10.5692/clinicalneurol.cn-000677. Japanese. No abstract available.

PMID:
26103820
20.

Genotype-specific patterns of atrophy progression are more sensitive than clinical decline in SCA1, SCA3 and SCA6.

Reetz K, Costa AS, Mirzazade S, Lehmann A, Juzek A, Rakowicz M, Boguslawska R, Schöls L, Linnemann C, Mariotti C, Grisoli M, Dürr A, van de Warrenburg BP, Timmann D, Pandolfo M, Bauer P, Jacobi H, Hauser TK, Klockgether T, Schulz JB; axia Study Group Investigators.

Brain. 2013 Mar;136(Pt 3):905-17. doi: 10.1093/brain/aws369. Epub 2013 Feb 18.

PMID:
23423669

Supplemental Content

Support Center