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Results: 1 to 20 of 238

1.

Familial spinocerebellar ataxia with cerebellar atrophy, peripheral neuropathy, and elevated level of serum creatine kinase, gamma-globulin, and alpha-fetoprotein.

Watanabe M, Sugai Y, Concannon P, Koenig M, Schmitt M, Sato M, Shizuka M, Mizushima K, Ikeda Y, Tomidokoro Y, Okamoto K, Shoji M.

Ann Neurol. 1998 Aug;44(2):265-9.

PMID:
9708552
[PubMed - indexed for MEDLINE]
2.

Autosomal recessive spinocerebellar ataxia and peripheral neuropathy with raised alpha-fetoprotein.

Izatt L, Németh AH, Meesaq A, Mills KR, Taylor AM, Shaw CE.

J Neurol. 2004 Jul;251(7):805-12.

PMID:
15258781
[PubMed - indexed for MEDLINE]
3.

Early-onset ataxia with ocular motor apraxia and hypoalbuminemia: the aprataxin gene mutations.

Shimazaki H, Takiyama Y, Sakoe K, Ikeguchi K, Niijima K, Kaneko J, Namekawa M, Ogawa T, Date H, Tsuji S, Nakano I, Nishizawa M.

Neurology. 2002 Aug 27;59(4):590-5.

PMID:
12196655
[PubMed - indexed for MEDLINE]
4.

[Familial cerebellar ataxia: clinical, radiological and electrophysiological findings].

Gajkowski K, Rysz A, Walecki J, Bojakowski J.

Neurol Neurochir Pol. 1988 Jan-Feb;22(1):22-7. Polish.

PMID:
3164096
[PubMed - indexed for MEDLINE]
5.

Linkage to chromosome 13q11-12 of an autosomal recessive cerebellar ataxia in a Tunisian family.

Mrissa N, Belal S, Hamida CB, Amouri R, Turki I, Mrissa R, Hamida MB, Hentati F.

Neurology. 2000 Apr 11;54(7):1408-14.

PMID:
10751248
[PubMed - indexed for MEDLINE]
6.

Isolated vitamin E deficiency with demyelinating neuropathy.

Puri V, Chaudhry N, Tatke M, Prakash V.

Muscle Nerve. 2005 Aug;32(2):230-5.

PMID:
15803482
[PubMed - indexed for MEDLINE]
7.

A Japanese family with early-onset ataxia with motor and sensory neuropathy.

Kobayashi S, Takuma H, Murayama S, Sakurai M, Kanazawa I.

J Neurol Sci. 2007 Mar 15;254(1-2):44-8. Epub 2007 Jan 29.

PMID:
17258771
[PubMed - indexed for MEDLINE]
8.

[Familial idiopathic vitamin E deficiency associated with cerebellar atrophy].

Aoki K, Washimi Y, Fujimori N, Maruyama K, Yanagisawa N.

Rinsho Shinkeigaku. 1990 Sep;30(9):966-71. Japanese.

PMID:
2265507
[PubMed - indexed for MEDLINE]
9.
10.

CAG repeat expansion in an italian family with spinocerebellar ataxia type 2 (SCA2): a clinical and genetic study.

Malandrini A, Galli L, Villanova M, Palmeri S, Parrotta E, DeFalco D, Cappelli M, Grieco GS, Renieri A, Guazzi G.

Eur Neurol. 1998 Oct;40(3):164-8.

PMID:
9748675
[PubMed - indexed for MEDLINE]
11.

Electrophysiology and nerve biopsy: comparative study in Friedreich's ataxia and Friedreich's ataxia phenotype with vitamin E deficiency.

Zouari M, Feki M, Ben Hamida C, Larnaout A, Turki I, Belal S, Mebazaa A, Ben Hamida M, Hentati F.

Neuromuscul Disord. 1998 Aug;8(6):416-25.

PMID:
9713861
[PubMed - indexed for MEDLINE]
12.

Homozygosity mapping of spinocerebellar ataxia with cerebellar atrophy and peripheral neuropathy to 9q33-34, and with hearing impairment and optic atrophy to 6p21-23.

Bomont P, Watanabe M, Gershoni-Barush R, Shizuka M, Tanaka M, Sugano J, Guiraud-Chaumeil C, Koenig M.

Eur J Hum Genet. 2000 Dec;8(12):986-90.

PMID:
11175288
[PubMed - indexed for MEDLINE]
Free Article
13.

A spinocerebellar degeneration with X-linked inheritance.

Spira PJ, McLeod JG, Evans WA.

Brain. 1979 Mar;102(1):27-41.

PMID:
427531
[PubMed - indexed for MEDLINE]
14.

Recessive ataxia with ocular apraxia: review of 22 Portuguese patients.

Barbot C, Coutinho P, Chorão R, Ferreira C, Barros J, Fineza I, Dias K, Monteiro J, Guimarães A, Mendonça P, do Céu Moreira M, Sequeiros J.

Arch Neurol. 2001 Feb;58(2):201-5.

PMID:
11176957
[PubMed - indexed for MEDLINE]
15.

Clinical and genetic studies of spinocerebellar ataxia type 2 in Japanese kindreds.

Ueyama H, Kumamoto T, Nagao S, Mita S, Uchino M, Tsuda T.

Acta Neurol Scand. 1998 Dec;98(6):427-32.

PMID:
9875622
[PubMed - indexed for MEDLINE]
16.

Autosomal recessive ataxia with peripheral neuropathy and elevated AFP: novel mutations in SETX.

Asaka T, Yokoji H, Ito J, Yamaguchi K, Matsushima A.

Neurology. 2006 May 23;66(10):1580-1.

PMID:
16717225
[PubMed - indexed for MEDLINE]
17.

Spinocerebellar degenerations.

Perlman SL.

Handb Clin Neurol. 2011;100:113-40. doi: 10.1016/B978-0-444-52014-2.00006-9. Review.

PMID:
21496573
[PubMed - indexed for MEDLINE]
18.

Adult-onset familial laryngeal abductor paralysis, cerebellar ataxia, and pure motor neuropathy.

Barbieri F, Pellecchia MT, Esposito E, Di Stasio E, Castaldo I, Santorelli F, Perretti A, Santoro L, De Michele G.

Neurology. 2001 May 22;56(10):1412-4.

PMID:
11376202
[PubMed - indexed for MEDLINE]
19.

[A 60-year-old man with intention tremor as an initial symptom followed by cerebellar ataxia, peripheral neuropathy and dementia].

Machida Y, Lijima M, Nakamura K, Ota S, Hattori N, Mizuno Y.

No To Shinkei. 2005 Aug;57(8):710-9. Japanese.

PMID:
16146216
[PubMed - indexed for MEDLINE]
20.

Motor evoked potentials by magnetic stimulation in hereditary and sporadic ataxia.

Mondelli M, Rossi A, Scarpini C, Guazzi GC.

Electromyogr Clin Neurophysiol. 1995 Nov;35(7):415-24.

PMID:
8549432
[PubMed - indexed for MEDLINE]

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