188 related articles for article (PubMed ID: 10198907)
1. [A sporadic case of spinocerebellar ataxia 6 (SCA 6) with large CAG expansion of the CACNL1A4 gene].
Izumi Y; Sawada H; Matsuyama Z; Kawakami H; Udaka F; Nakamura S; Kameyama M
No To Shinkei; 1999 Feb; 51(2):167-70. PubMed ID: 10198907
[TBL] [Abstract][Full Text] [Related]
2. [An apparently sporadic case with spinocerebellar ataxia type 1 (SCA1)].
Futamura N; Matsumura R; Murata K; Suzumura A; Takayanagi T
Rinsho Shinkeigaku; 1997 Aug; 37(8):708-10. PubMed ID: 9404150
[TBL] [Abstract][Full Text] [Related]
3. An autopsy case of spinocerebellar ataxia type 6 with mental symptoms of schizophrenia and dementia.
Tashiro H; Suzuki SO; Hitotsumatsu T; Iwaki T
Clin Neuropathol; 1999; 18(4):198-204. PubMed ID: 10442462
[TBL] [Abstract][Full Text] [Related]
4. [Siblings with spinocerebellar ataxia type 1 (SCA 1)--diagnosis by detecting the expansion of CAG repeat on chromosome 6p].
Hanihara T; Takahashi T; Inoue K; Yamada Y; Iwabuchi K
Rinsho Shinkeigaku; 1994 May; 34(5):508-10. PubMed ID: 7924069
[TBL] [Abstract][Full Text] [Related]
5. 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. PubMed ID: 14967767
[TBL] [Abstract][Full Text] [Related]
6. [A case of spinocerebellar ataxia type 6 with hypochondriasis and severe parkinsonism].
Kohira I; Ujike H; Katsu T; Ninomiya Y; Ohashi K
No To Shinkei; 2001 Dec; 53(12):1119-22. PubMed ID: 11806119
[TBL] [Abstract][Full Text] [Related]
7. Spinocerebellar ataxia type 2 (SCA 2) in an infant with extreme CAG repeat expansion.
Babovic-Vuksanovic D; Snow K; Patterson MC; Michels VV
Am J Med Genet; 1998 Oct; 79(5):383-7. PubMed ID: 9779806
[TBL] [Abstract][Full Text] [Related]
8. [A case of spinocerebellar ataxia 6 accompanied with schizophrenia].
Nakanishi I; Miwa H; Hayata T; Kawada A; Kondo T
No To Shinkei; 2004 Jan; 56(1):49-52. PubMed ID: 15024829
[TBL] [Abstract][Full Text] [Related]
9. [A familial case of spinocerebellar ataxia type 8 (SCA 8)--its clinical findings and an issue about the genetic basis].
Hokezu Y; Takiyama Y; Sakoe K; Nagamatsu K
Rinsho Shinkeigaku; 2000 Nov; 40(11):1116-21. PubMed ID: 11332193
[TBL] [Abstract][Full Text] [Related]
10. Genetics of the SCA6 gene in a large family segregating an autosomal dominant "pure" cerebellar ataxia.
García-Planells J; Cuesta A; Vilchez JJ; Martínez F; Prieto F; Palau F
J Med Genet; 1999 Feb; 36(2):148-51. PubMed ID: 10051016
[TBL] [Abstract][Full Text] [Related]
11. [Initial symptoms and mode of neurological progression in spinocerebellar ataxia type 6 (SCA6)].
Yabe I; Sasaki H; Yamashita I; Takei A; Fukazawa T; Hamada T; Tashiro K
Rinsho Shinkeigaku; 1998 Jun; 38(6):489-94. PubMed ID: 9847664
[TBL] [Abstract][Full Text] [Related]
12. Meiotic CAG repeat instability in spinocerebellar ataxia type 6: maternally transmitted elongation in a presumed sporadic case.
Lindquist SG; Nørremølle A; Hjermind LE; Hasholt L; Nielsen JE
J Neurol Sci; 2006 Feb; 241(1-2):95-8. PubMed ID: 16310805
[TBL] [Abstract][Full Text] [Related]
13. The effect of CAT trinucleotide interruptions on the age at onset of spinocerebellar ataxia type 1 (SCA1).
Matsuyama Z; Izumi Y; Kameyama M; Kawakami H; Nakamura S
J Med Genet; 1999 Jul; 36(7):546-8. PubMed ID: 10424816
[TBL] [Abstract][Full Text] [Related]
14. Spinocerebellar ataxia type 6: gaze-evoked and vertical nystagmus, Purkinje cell degeneration, and variable age of onset.
Gomez CM; Thompson RM; Gammack JT; Perlman SL; Dobyns WB; Truwit CL; Zee DS; Clark HB; Anderson JH
Ann Neurol; 1997 Dec; 42(6):933-50. PubMed ID: 9403487
[TBL] [Abstract][Full Text] [Related]
15. [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]
16. Spinocerebellar degeneration and cerebral hypomyelination in a family.
Chatkupt S; Wolansky LJ; Jotkowitz A; Shih LY; Cook SD
Am J Med Genet; 1995 Jun; 60(3):188-91. PubMed ID: 7573169
[TBL] [Abstract][Full Text] [Related]
17. [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]
18. [Spinocerebellar ataxia 7. Clinical and genetic investigation in an Argentine family].
Rojas JI; Romano M; Patrucco L; Zurru MC; Igarreta P; Cristiano E
Medicina (B Aires); 2007; 67(2):147-50. PubMed ID: 17593599
[TBL] [Abstract][Full Text] [Related]
19. Evidence for a new spinocerebellar ataxia locus.
Higgins JJ; Pho LT; Ide SE; Nee LE; Polymeropoulos MH
Mov Disord; 1997 May; 12(3):412-7. PubMed ID: 9159738
[TBL] [Abstract][Full Text] [Related]
20. [Spinocerebellar ataxia 1--clinical study of 17 patients in a large pedigree].
Sasaki H; Wakisaka A; Koyama T; Hamada T; Shima K; Tashiro K; Hashimoto K; Miyagishi T
No To Shinkei; 1993 Jun; 45(6):502-8. PubMed ID: 8363844
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
