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 *

177 related articles for article (PubMed ID: 17405764)

  • 1. Novel locus for benign hereditary chorea with adult onset maps to chromosome 8q21.3 q23.3.
    Shimohata T; Hara K; Sanpei K; Nunomura J; Maeda T; Kawachi I; Kanazawa M; Kasuga K; Miyashita A; Kuwano R; Hirota K; Tsuji S; Onodera O; Nishizawa M; Honma Y
    Brain; 2007 Sep; 130(Pt 9):2302-9. PubMed ID: 17405764
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Differential diagnosis of chorea].
    Shimohata T; Nishizawa M
    Brain Nerve; 2009 Aug; 61(8):963-71. PubMed ID: 19697886
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Huntington disease and Huntington disease-like in a case series from Brazil.
    Castilhos RM; Souza AF; Furtado GV; Gheno TC; Silva AL; Vargas FR; Lima MA; Barsottini O; Pedroso JL; Godeiro C; Salarini D; Pereira ET; Lin K; Toralles MB; Saute JA; Rieder CR; Quintas M; Sequeiros J; Alonso I; Saraiva-Pereira ML; Jardim LB
    Clin Genet; 2014 Oct; 86(4):373-7. PubMed ID: 24102565
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Benign hereditary chorea of early onset maps to chromosome 14q.
    de Vries BB; Arts WF; Breedveld GJ; Hoogeboom JJ; Niermeijer MF; Heutink P
    Am J Hum Genet; 2000 Jan; 66(1):136-42. PubMed ID: 10631144
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A novel autosomal dominant spinocerebellar ataxia (SCA22) linked to chromosome 1p21-q23.
    Chung MY; Lu YC; Cheng NC; Soong BW
    Brain; 2003 Jun; 126(Pt 6):1293-9. PubMed ID: 12764052
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Clinical and genetic heterogeneity in benign hereditary chorea.
    Breedveld GJ; Percy AK; MacDonald ME; de Vries BB; Yapijakis C; Dure LS; Ippel EF; Sandkuijl LA; Heutink P; Arts WF
    Neurology; 2002 Aug; 59(4):579-84. PubMed ID: 12196653
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Benign hereditary chorea 2: pathological findings in an autopsy case.
    Yoshida Y; Nunomura J; Shimohata T; Nanjo H; Miyata H
    Neuropathology; 2012 Oct; 32(5):557-65. PubMed ID: 22239265
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Benign hereditary chorea: clinical, genetic, and pathological findings.
    Kleiner-Fisman G; Rogaeva E; Halliday W; Houle S; Kawarai T; Sato C; Medeiros H; St George-Hyslop PH; Lang AE
    Ann Neurol; 2003 Aug; 54(2):244-7. PubMed ID: 12891678
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Gene diagnosis of patients with chorea].
    Shimohata T; Onodera O; Honma Y; Hirota K; Nunomura Y; Kimura T; Kawachi I; Sanpei K; Nishizawa M; Tsuji S
    Rinsho Shinkeigaku; 2004 Mar; 44(3):149-53. PubMed ID: 15233265
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A novel autosomal dominant spinocerebellar ataxia (SCA16) linked to chromosome 8q22.1-24.1.
    Miyoshi Y; Yamada T; Tanimura M; Taniwaki T; Arakawa K; Ohyagi Y; Furuya H; Yamamoto K; Sakai K; Sasazuki T; Kira J
    Neurology; 2001 Jul; 57(1):96-100. PubMed ID: 11445634
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Early onset autosomal dominant dementia with ataxia, extrapyramidal features, and epilepsy.
    Filla A; De Michele G; Cocozza S; Patrignani A; Volpe G; Castaldo I; Ruggiero G; Bonavita V; Masters C; Casari G; Bruni A
    Neurology; 2002 Mar; 58(6):922-8. PubMed ID: 11914409
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Benign hereditary chorea: clinical, neuroimaging, and genetic findings.
    Mahajnah M; Inbar D; Steinmetz A; Heutink P; Breedveld GJ; Straussberg R
    J Child Neurol; 2007 Oct; 22(10):1231-4. PubMed ID: 17940252
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Hereditary benign chorea: clinical and genetic features of a distinct disease.
    Fernandez M; Raskind W; Matsushita M; Wolff J; Lipe H; Bird T
    Neurology; 2001 Jul; 57(1):106-10. PubMed ID: 11445636
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mutations in TITF-1 are associated with benign hereditary chorea.
    Breedveld GJ; van Dongen JW; Danesino C; Guala A; Percy AK; Dure LS; Harper P; Lazarou LP; van der Linde H; Joosse M; Grüters A; MacDonald ME; de Vries BB; Arts WF; Oostra BA; Krude H; Heutink P
    Hum Mol Genet; 2002 Apr; 11(8):971-9. PubMed ID: 11971878
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A novel de novo mutation of the TITF1/NKX2-1 gene causing ataxia, benign hereditary chorea, hypothyroidism and a pituitary mass in a UK family and review of the literature.
    Veneziano L; Parkinson MH; Mantuano E; Frontali M; Bhatia KP; Giunti P
    Cerebellum; 2014 Oct; 13(5):588-95. PubMed ID: 24930029
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Exclusion mapping of the hereditary dentatorubropallidoluysian atrophy gene from the Huntington's disease locus.
    Kondo I; Ohta H; Yazaki M; Ikeda JE; Gusella JF; Kanazawa I
    J Med Genet; 1990 Feb; 27(2):105-8. PubMed ID: 1969487
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Chorea-acanthocytosis: genetic linkage to chromosome 9q21.
    Rubio JP; Danek A; Stone C; Chalmers R; Wood N; Verellen C; Ferrer X; Malandrini A; Fabrizi GM; Manfredi M; Vance J; Pericak-Vance M; Brown R; Rudolf G; Picard F; Alonso E; Brin M; Németh AH; Farrall M; Monaco AP
    Am J Hum Genet; 1997 Oct; 61(4):899-908. PubMed ID: 9382101
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Molecular and clinical findings in a family with dentatorubral-pallidoluysian atrophy.
    Potter NT; Meyer MA; Zimmerman AW; Eisenstadt ML; Anderson IJ
    Ann Neurol; 1995 Feb; 37(2):273-7. PubMed ID: 7847869
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Autosomal dominant sensory/motor neuropathy with Ataxia (SMNA): Linkage to chromosome 7q22-q32.
    Brkanac Z; Fernandez M; Matsushita M; Lipe H; Wolff J; Bird TD; Raskind WH
    Am J Med Genet; 2002 May; 114(4):450-7. PubMed ID: 11992570
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Case of benign familial chorea].
    Amore M; Ambrosetto G; De Maria R
    Riv Patol Nerv Ment; 1983; 104(1):9-14. PubMed ID: 6678482
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.