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Items: 1 to 20 of 335

1.

Spinocerebellar ataxias: genotype-phenotype correlations in 104 Brazilian families.

Teive HA, Munhoz RP, Arruda WO, Lopes-Cendes I, Raskin S, Werneck LC, Ashizawa T.

Clinics (Sao Paulo). 2012;67(5):443-9.

2.

Clinical features of hereditary spinocerebellar ataxia diagnosed by molecular genetic analysis.

Lau KK, Lam K, Shiu KL, Au KM, Tsoi TH, Chan AY, Li HL, Sheng B.

Hong Kong Med J. 2004 Aug;10(4):255-9.

3.

Phenotype variability and early onset ataxia symptoms in spinocerebellar ataxia type 7: comparison and correlation with other spinocerebellar ataxias.

Albuquerque MV, Pedroso JL, Braga Neto P, Barsottini OG.

Arq Neuropsiquiatr. 2015 Jan;73(1):18-21. doi: 10.1590/0004-282X20140192. Epub 2015 Jan 1.

4.

Molecular and clinical correlations in spinocerebellar ataxia type 3 and Machado-Joseph disease.

Matilla T, McCall A, Subramony SH, Zoghbi HY.

Ann Neurol. 1995 Jul;38(1):68-72.

PMID:
7611728
5.

Clinical Characteristics, Radiological Features and Gene Mutation in 10 Chinese Families with Spinocerebellar Ataxias.

Chen JW, Zhao L, Zhang F, Li L, Gu YH, Zhou JY, Zhang H, Meng M, Zhang KH, Le WD, Dong CB.

Chin Med J (Engl). 2015 Jul 5;128(13):1714-23. doi: 10.4103/0366-6999.159340.

6.

Spinocerebellar ataxia types 2 and 3 segregating simultaneously in a single family.

França MC Jr, Calcagnotto ME, da Costa JC, Lopes-Cendes I.

Mov Disord. 2006 Jul;21(7):1051-3.

PMID:
16628604
7.

Clinical and molecular correlations in spinocerebellar ataxia type 6: a study of 24 Dutch families.

Sinke RJ, Ippel EF, Diepstraten CM, Beemer FA, Wokke JH, van Hilten BJ, Knoers NV, van Amstel HK, Kremer HP.

Arch Neurol. 2001 Nov;58(11):1839-44.

PMID:
11708993
8.
9.

Machado-Joseph disease and other rare spinocerebellar ataxias.

Matilla-Dueñas A.

Adv Exp Med Biol. 2012;724:172-88. doi: 10.1007/978-1-4614-0653-2_14. Review.

PMID:
22411243
11.

Structural and functional MRI abnormalities of cerebellar cortex and nuclei in SCA3, SCA6 and Friedreich's ataxia.

Stefanescu MR, Dohnalek M, Maderwald S, Thürling M, Minnerop M, Beck A, Schlamann M, Diedrichsen J, Ladd ME, Timmann D.

Brain. 2015 May;138(Pt 5):1182-97. doi: 10.1093/brain/awv064. Epub 2015 Mar 28.

PMID:
25818870
12.

Clinical neurogenetics: autosomal dominant spinocerebellar ataxia.

Shakkottai VG, Fogel BL.

Neurol Clin. 2013 Nov;31(4):987-1007. doi: 10.1016/j.ncl.2013.04.006. Epub 2013 Jul 30. Review.

13.

Masseter reflex in the study of spinocerebellar ataxia type 2 and type 3.

García A, Alvarez S, Infante J, Berciano J.

Muscle Nerve. 2009 Oct;40(4):640-2. doi: 10.1002/mus.21334.

PMID:
19618433
14.

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.

Neurology. 2004 Oct 26;63(8):1509-12.

PMID:
15505178
15.

Possible reduced penetrance of expansion of 44 to 47 CAG/CAA repeats in the TATA-binding protein gene in spinocerebellar ataxia type 17.

Oda M, Maruyama H, Komure O, Morino H, Terasawa H, Izumi Y, Imamura T, Yasuda M, Ichikawa K, Ogawa M, Matsumoto M, Kawakami H.

Arch Neurol. 2004 Feb;61(2):209-12.

PMID:
14967767
16.

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
17.

Cerebellar ataxia with spasmodic cough: a new form of dominant ataxia.

Coutinho P, Cruz VT, Tuna A, Silva SE, Guimarães J.

Arch Neurol. 2006 Apr;63(4):553-5.

PMID:
16606768
18.

Frequency of spinocerebellar ataxia types 1,2,3,6,7 and dentatorubral pallidoluysian atrophy mutations in Korean patients with spinocerebellar ataxia.

Jin DK, Oh MR, Song SM, Koh SW, Lee M, Kim GM, Lee WY, Chung CS, Lee KH, Im JH, Lee MJ, Kim JW, Lee MS.

J Neurol. 1999 Mar;246(3):207-10.

PMID:
10323319
19.

[Clinical features and diagnosis of spinocerebellar ataxia].

Klivényi P, Horváth Z, Vécsei L.

Ideggyogy Sz. 2004 Jan 20;57(1-2):11-22. Review. Hungarian.

PMID:
15042864
20.

Adult onset spinocerebellar ataxia in a Canadian movement disorders clinic.

Kraft S, Furtado S, Ranawaya R, Parboosingh J, Bleoo S, McElligott K, Bridge P, Spacey S, Das S, Suchowersky O.

Can J Neurol Sci. 2005 Nov;32(4):450-8.

PMID:
16408574

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