These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

187 related articles for article (PubMed ID: 10198907)

  • 21. Neuropathological and molecular studies of spinocerebellar ataxia type 6 (SCA6).
    Sasaki H; Kojima H; Yabe I; Tashiro K; Hamada T; Sawa H; Hiraga H; Nagashima K
    Acta Neuropathol; 1998 Feb; 95(2):199-204. PubMed ID: 9498057
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [A sporadic case of dentatorubral-pallidoluysian atrophy (DRPLA) having an elderly age of onset].
    Horikawa H; Futamura N; Uetakagaito M
    Rinsho Shinkeigaku; 1996 Apr; 36(4):584-6. PubMed ID: 8810854
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Hereditary paroxysmal ataxia with mental retardation: a clinicopathological study in relation to episodic ataxia type 2.
    Mochizuki Y; Kawata A; Mizutani T; Takamoto K; Hayashi H; Taki K; Morimatsu Y
    Acta Neuropathol; 2004 Oct; 108(4):345-9. PubMed ID: 15300451
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Spinocerebellar ataxia type 6: genotype and phenotype in German kindreds.
    Schöls L; Krüger R; Amoiridis G; Przuntek H; Epplen JT; Riess O
    J Neurol Neurosurg Psychiatry; 1998 Jan; 64(1):67-73. PubMed ID: 9436730
    [TBL] [Abstract][Full Text] [Related]  

  • 25. SCA6 is caused by moderate CAG expansion in the alpha1A-voltage-dependent calcium channel gene.
    Riess O; Schöls L; Bottger H; Nolte D; Vieira-Saecker AM; Schimming C; Kreuz F; Macek M; Krebsová A; Macek M Sen ; Klockgether T; Zühlke C; Laccone FA
    Hum Mol Genet; 1997 Aug; 6(8):1289-93. PubMed ID: 9259275
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Clinical features and neuropathology of autosomal dominant spinocerebellar ataxia (SCA17).
    Rolfs A; Koeppen AH; Bauer I; Bauer P; Buhlmann S; Topka H; Schöls L; Riess O
    Ann Neurol; 2003 Sep; 54(3):367-75. PubMed ID: 12953269
    [TBL] [Abstract][Full Text] [Related]  

  • 27. A Japanese family with spinocerebellar ataxia type 6 which includes three individuals homozygous for an expanded CAG repeat in the SCA6/CACNL1A4 gene.
    Takiyama Y; Sakoe K; Namekawa M; Soutome M; Esumi E; Ogawa T; Ishikawa K; Mizusawa H; Nakano I; Nishizawa M
    J Neurol Sci; 1998 Jun; 158(2):141-7. PubMed ID: 9702684
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [An autopsy case of dentatorubropallidoluysian atrophy showing marked atrophy of the brain stem].
    Morioka E; Nakatsu T; Kuroda S; Yamamoto M; Hosokawa K; Otsuki S
    No To Shinkei; 1987 Aug; 39(8):769-73. PubMed ID: 2962593
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Case control analysis of repeat expansion size in ataxia.
    Majounie E; Wardle M; Muzaimi M; Cross WC; Robertson NP; Williams NM; Morris HR
    Neurosci Lett; 2007 Dec; 429(1):28-32. PubMed ID: 17961920
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Spinocerebellar ataxia type 26 maps to chromosome 19p13.3 adjacent to SCA6.
    Yu GY; Howell MJ; Roller MJ; Xie TD; Gomez CM
    Ann Neurol; 2005 Mar; 57(3):349-54. PubMed ID: 15732118
    [TBL] [Abstract][Full Text] [Related]  

  • 31. An untranslated CTG expansion causes a novel form of spinocerebellar ataxia (SCA8).
    Koob MD; Moseley ML; Schut LJ; Benzow KA; Bird TD; Day JW; Ranum LP
    Nat Genet; 1999 Apr; 21(4):379-84. PubMed ID: 10192387
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [CAG trinucleotide mutation detection in patients with hereditary spinocerebellar ataxia].
    Tang B; Xia J; Wang D; Tang X; Shen L; Liu C; Dai H; Yan X; Pan Q; Xiao J; Zhang B; Ou Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1999 Oct; 16(5):281-4. PubMed ID: 10514531
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Clinical and molecular genetic study in seven Japanese families with spinocerebellar ataxia type 6.
    Nagai Y; Azuma T; Funauchi M; Fujita M; Umi M; Hirano M; Matsubara T; Ueno S
    J Neurol Sci; 1998 Apr; 157(1):52-9. PubMed ID: 9600677
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Episodic ataxia type 2 (EA2) and spinocerebellar ataxia type 6 (SCA6) due to CAG repeat expansion in the CACNA1A gene on chromosome 19p.
    Jodice C; Mantuano E; Veneziano L; Trettel F; Sabbadini G; Calandriello L; Francia A; Spadaro M; Pierelli F; Salvi F; Ophoff RA; Frants RR; Frontali M
    Hum Mol Genet; 1997 Oct; 6(11):1973-8. PubMed ID: 9302278
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Spinocerebellar ataxia associated with a mutation in the fibroblast growth factor 14 gene (SCA27): A new phenotype.
    Brusse E; de Koning I; Maat-Kievit A; Oostra BA; Heutink P; van Swieten JC
    Mov Disord; 2006 Mar; 21(3):396-401. PubMed ID: 16211615
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [An MRI study of hereditary spinocerebellar degenerations].
    Konagaya M; Konagaya Y; Morishita S; Nakamuro T
    Rinsho Shinkeigaku; 1990 Jun; 30(6):610-6. PubMed ID: 2225653
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [A case of spinocerebellar ataxia type 6 with its initial symptom of episodic ataxia-like phenotype].
    Shimazaki H; Nakao K; Ishikawa K; Takiyama Y; Nakano I
    No To Shinkei; 2006 Jan; 58(1):63-7. PubMed ID: 16482924
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [A sporadic dentatorubral-pallidoluysian atrophy (DRPLA) diagnosed by gene analysis].
    Yoshimoto H; Sahara M; Tanaka K; Ikeuchi T; Koide R; Tsuji S
    Rinsho Shinkeigaku; 1995 Feb; 35(2):201-3. PubMed ID: 7781240
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Japanese families with autosomal dominant pure cerebellar ataxia map to chromosome 19p13.1-p13.2 and are strongly associated with mild CAG expansions in the spinocerebellar ataxia type 6 gene in chromosome 19p13.1.
    Ishikawa K; Tanaka H; Saito M; Ohkoshi N; Fujita T; Yoshizawa K; Ikeuchi T; Watanabe M; Hayashi A; Takiyama Y; Nishizawa M; Nakano I; Matsubayashi K; Miwa M; Shoji S; Kanazawa I; Tsuji S; Mizusawa H
    Am J Hum Genet; 1997 Aug; 61(2):336-46. PubMed ID: 9311738
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [An autopsied case of dentato-rubro-pallido-luysian atrophy with atypical pathological lesions].
    Konagaya M; Sakai M; Kato T; Kuru S; Matsuoka Y; Sobue G; Hashizume Y; Yoshida M
    No To Shinkei; 2002 Jun; 54(6):513-20. PubMed ID: 12166103
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.