187 related articles for article (PubMed ID: 8684395)
1. Ataxia without telangiectasia masquerading as benign hereditary chorea.
Klein C; Wenning GK; Quinn NP; Marsden CD
Mov Disord; 1996 Mar; 11(2):217-20. PubMed ID: 8684395
[TBL] [Abstract][Full Text] [Related]
2. [Clinico-genetic diagnosis of ataxia telangiectatica (Louis-Bar syndrome)].
Fuhrmann E; Pfeiffer L; Zschenderlein R; Leonhardt T; Melster U; Kölmel HW
Nervenarzt; 1993 Feb; 64(2):140-2. PubMed ID: 8450897
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Choreas, hereditary and other ataxias, tics, myoclonus, and other movement disorders.
Tolosa E; Berciano J
Curr Opin Neurol Neurosurg; 1993 Jun; 6(3):358-68. PubMed ID: 8507906
[TBL] [Abstract][Full Text] [Related]
5. Ataxia without telangiectasia revisited: update on genetic findings in two brothers with an ataxia-telangiectasia-like disorder.
Klein C; Stewart GS; Quinn NP; Taylor AM
Mov Disord; 2001 Jul; 16(4):788-9. PubMed ID: 11481721
[No Abstract] [Full Text] [Related]
6. [A case of adult-onset Huntington disease presenting with spasticity and cerebellar ataxia, mimicking spinocerebellar degeneration].
Kageyama Y; Yamamoto S; Ueno M; Ichikawa K
Rinsho Shinkeigaku; 2003; 43(1-2):16-9. PubMed ID: 12820545
[TBL] [Abstract][Full Text] [Related]
7. Ataxia with oculomotor apraxia type 1 (AOA1): clinical and neuropsychological features in 2 new patients and differential diagnosis.
D'Arrigo S; Riva D; Bulgheroni S; Chiapparini L; Castellotti B; Gellera C; Pantaleoni C
J Child Neurol; 2008 Aug; 23(8):895-900. PubMed ID: 18403580
[TBL] [Abstract][Full Text] [Related]
8. [Ataxia telangiectasia: a model of investigation of chromosomal translocations].
Stern MH
Pathol Biol (Paris); 1990 Sep; 38(7):675-7. PubMed ID: 2235081
[No Abstract] [Full Text] [Related]
9. Spinocerebellar ataxia type 17 repeat in patients with Huntington's disease-like and ataxia.
Cellini E; Forleo P; Nacmias B; Tedde A; Bagnoli S; Piacentini S; Sorbi S
Ann Neurol; 2004 Jul; 56(1):163; author reply 163-4. PubMed ID: 15236416
[No Abstract] [Full Text] [Related]
10. 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]
11. [Huntington chorea in childhood].
Dralle D; Schock G; Neuhäuser G
Klin Padiatr; 1985; 197(2):90-3. PubMed ID: 3157827
[TBL] [Abstract][Full Text] [Related]
12. The differential diagnosis of chorea.
Wild EJ; Tabrizi SJ
Pract Neurol; 2007 Nov; 7(6):360-73. PubMed ID: 18024776
[TBL] [Abstract][Full Text] [Related]
13. [Clinico-genetic study of type I spinocerebelllar ataxia].
Svetel M; Culjković B; Sternić N; Dragasević B; Stojković I; Romac S; Kostić VS
Srp Arh Celok Lek; 1999; 127(5-6):157-62. PubMed ID: 10500422
[TBL] [Abstract][Full Text] [Related]
14. Complete deletion of the aprataxin gene: ataxia with oculomotor apraxia type 1 with severe phenotype and cognitive deficit.
Yoon G; Westmacott R; MacMillan L; Quercia N; Koutsou P; Georghiou A; Christodoulou K; Banwell B
J Neurol Neurosurg Psychiatry; 2008 Feb; 79(2):234-6. PubMed ID: 18202221
[No Abstract] [Full Text] [Related]
15. Cerebellar ataxia with oculomotor apraxia type 1: clinical and genetic studies.
Le Ber I; Moreira MC; Rivaud-Péchoux S; Chamayou C; Ochsner F; Kuntzer T; Tardieu M; Saïd G; Habert MO; Demarquay G; Tannier C; Beis JM; Brice A; Koenig M; Dürr A
Brain; 2003 Dec; 126(Pt 12):2761-72. PubMed ID: 14506070
[TBL] [Abstract][Full Text] [Related]
16. [Description of an endogamous, multigenerational and extensive family with benign hereditary chorea from the Paisa community].
Pérez-Póveda JC; Palacio LG; Arcos-Burgos M
Rev Neurol; 2005 Jul 16-31; 41(2):95-8. PubMed ID: 16028188
[TBL] [Abstract][Full Text] [Related]
17. [Molecular genetics of hereditary spinocerebellar ataxia].
Tsuji S
No To Shinkei; 1995 Oct; 47(10):955-61. PubMed ID: 7577140
[No Abstract] [Full Text] [Related]
18. Focal dystonia as a presenting sign of spinocerebellar ataxia 17.
Hagenah JM; Zühlke C; Hellenbroich Y; Heide W; Klein C
Mov Disord; 2004 Feb; 19(2):217-20. PubMed ID: 14978680
[TBL] [Abstract][Full Text] [Related]
19. Prevalence of hereditary ataxia and spastic paraplegia in southeast Norway: a population-based study.
Erichsen AK; Koht J; Stray-Pedersen A; Abdelnoor M; Tallaksen CM
Brain; 2009 Jun; 132(Pt 6):1577-88. PubMed ID: 19339254
[TBL] [Abstract][Full Text] [Related]
20. Problems and possibilities in the differential diagnosis of Syndrome Spinocerebellar Ataxia.
Zumrová A
Neuro Endocrinol Lett; 2005 Apr; 26(2):98-108. PubMed ID: 15855879
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
