121 related articles for article (PubMed ID: 12020276)
1. Ocular apraxia in recessive ataxia.
Koeppen AH
Arch Neurol; 2002 May; 59(5):874; author reply 874. PubMed ID: 12020276
[No Abstract] [Full Text] [Related]
2. [Friedreich ataxia--diagnosis after a decade. Differential diagnosis of inherited spinocerebellar ataxias].
Vitaszil E; Jelencsik I; Szirmai I
Ideggyogy Sz; 2002 Nov; 55(11-12):382-93. PubMed ID: 12632799
[TBL] [Abstract][Full Text] [Related]
3. Ocular motor paresis versus apraxia.
Sharpe JA; Johnston JL
Ann Neurol; 1989 Feb; 25(2):209-10. PubMed ID: 2919873
[No Abstract] [Full Text] [Related]
4. Spinocerebellar ataxia with ocular motor apraxia and DNA repair.
Onodera O
Neuropathology; 2006 Aug; 26(4):361-7. PubMed ID: 16961074
[TBL] [Abstract][Full Text] [Related]
5. Mitochondrial recessive ataxia syndrome: A neurological rarity not to be missed.
Mignarri A; Cenciarelli S; Da Pozzo P; Cardaioli E; Malandrini A; Federico A; Dotti MT
J Neurol Sci; 2015 Feb; 349(1-2):254-5. PubMed ID: 25586537
[No Abstract] [Full Text] [Related]
6. Ocular and oculomotor signs in Joubert syndrome.
Tusa RJ; Hove MT
J Child Neurol; 1999 Oct; 14(10):621-7. PubMed ID: 10511333
[TBL] [Abstract][Full Text] [Related]
7. 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. PubMed ID: 11176957
[TBL] [Abstract][Full Text] [Related]
8. Progressive cerebellar atrophy: hereditary ataxias and disorders with spinocerebellar degeneration.
Wolf NI; Koenig M
Handb Clin Neurol; 2013; 113():1869-78. PubMed ID: 23622410
[TBL] [Abstract][Full Text] [Related]
9. Exome sequencing reveals a novel ANO10 mutation in a Japanese patient with autosomal recessive spinocerebellar ataxia.
Maruyama H; Morino H; Miyamoto R; Murakami N; Hamano T; Kawakami H
Clin Genet; 2014 Mar; 85(3):296-7. PubMed ID: 23551081
[No Abstract] [Full Text] [Related]
10. [Clinical features and diagnosis of spinocerebellar ataxia].
Klivényi P; Horváth Z; Vécsei L
Ideggyogy Sz; 2004 Jan; 57(1-2):11-22. PubMed ID: 15042864
[TBL] [Abstract][Full Text] [Related]
11. Early-Onset Friedreich's Ataxia With Oculomotor Apraxia.
Saghazadeh A; Hafizi S; Hosseini F; Ashrafi MR; Rezaei N
Acta Med Iran; 2017 Feb; 55(2):128-130. PubMed ID: 28282710
[TBL] [Abstract][Full Text] [Related]
12. Ataxia-ocular motor apraxia: a syndrome mimicking ataxia-telangiectasia.
Aicardi J; Barbosa C; Andermann E; Andermann F; Morcos R; Ghanem Q; Fukuyama Y; Awaya Y; Moe P
Ann Neurol; 1988 Oct; 24(4):497-502. PubMed ID: 3239952
[TBL] [Abstract][Full Text] [Related]
13. Hereditary spastic paraplegia or spinocerebellar ataxia? Not always as easy as it seems.
Hedera P
Eur J Neurol; 2009 Aug; 16(8):887-8. PubMed ID: 19453405
[No Abstract] [Full Text] [Related]
14. Ataxia-oculomotor apraxia syndrome.
Gascon GG; Abdo N; Sigut D; Hemidan A; Hannan MA
J Child Neurol; 1995 Mar; 10(2):118-22. PubMed ID: 7782601
[TBL] [Abstract][Full Text] [Related]
15. Mitochondrial recessive ataxia syndrome mimicking dominant spinocerebellar ataxia.
Palin EJ; Hakonen AH; Korpela M; Paetau A; Suomalainen A
J Neurol Sci; 2012 Apr; 315(1-2):160-3. PubMed ID: 22166854
[TBL] [Abstract][Full Text] [Related]
16. Extrapyramidal signs are a common feature of spinocerebellar ataxia type 17.
Lee WW; Kim SY; Kim JY; Kim HJ; Park SS; Jeon BS
Neurology; 2009 Nov; 73(20):1708-9. PubMed ID: 19917997
[No Abstract] [Full Text] [Related]
17. Difficulty identifying spinocerebellar ataxia 17 from preceding psychiatric symptoms.
Ohi K; Hashimoto R; Sugai F; Yasuda Y; Tagami S; Takamura H; Morihara T; Okochi M; Tanaka T; Kudo T; Sakoda S; Takeda M
Psychiatry Clin Neurosci; 2008 Oct; 62(5):625. PubMed ID: 18950389
[No Abstract] [Full Text] [Related]
18. Re: clinical feature profile of spinocerebellar ataxia type 1-8 predicts genetically defined subtypes.
Friedman J
Mov Disord; 2007 Apr; 22(5):753; author reply 753-4. PubMed ID: 17115400
[No Abstract] [Full Text] [Related]
19. Premutation alleles and fragile X-associated tremor/ataxia syndrome.
Toft M; Farrer M
JAMA; 2005 Jan; 293(3):296; author reply 296-7. PubMed ID: 15657320
[No Abstract] [Full Text] [Related]
20. Autosomal recessive ataxias: 20 types, and counting.
Embiruçu EK; Martyn ML; Schlesinger D; Kok F
Arq Neuropsiquiatr; 2009 Dec; 67(4):1143-56. PubMed ID: 20069237
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
