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 *

81 related articles for article (PubMed ID: 3789669)

  • 41. Gerstmann-Sträussler-Scheinker disease with the Q217R mutation mimicking frontotemporal dementia.
    Woulfe J; Kertesz A; Frohn I; Bauer S; George-Hyslop PS; Bergeron C
    Acta Neuropathol; 2005 Sep; 110(3):317-9. PubMed ID: 16025285
    [No Abstract]   [Full Text] [Related]  

  • 42. Atypical Gerstmann-Straüssler syndrome or familial spinocerebellar ataxia and Alzheimer's disease?
    de Courten-Myers G; Mandybur TI
    Neurology; 1987 Feb; 37(2):269-75. PubMed ID: 3808307
    [TBL] [Abstract][Full Text] [Related]  

  • 43. [Familial atrophic form of spinocerebellar ataxia].
    Gaj T; Grendus-Tota B
    Neurol Neurochir Pol; 1973; 7(5):679-83. PubMed ID: 4763007
    [No Abstract]   [Full Text] [Related]  

  • 44. A case of Gerstmann-Sträussler-Scheinker syndrome with the P105L prion protein gene mutation presenting with ataxia and extrapyramidal signs without spastic paraparesis.
    Iwasaki Y; Kizawa M; Hori N; Kitamoto T; Sobue G
    Clin Neurol Neurosurg; 2009 Sep; 111(7):606-9. PubMed ID: 19443103
    [TBL] [Abstract][Full Text] [Related]  

  • 45. 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]  

  • 46. Syndrome of bilateral ophthalmoplegia and ataxia (a varient of Fisher's syndrome) (case report).
    Bomb BS; Bedi HK; Saifee AA
    J Assoc Physicians India; 1979 Feb; 27(2):175-7. PubMed ID: 511838
    [No Abstract]   [Full Text] [Related]  

  • 47. Spino-cerebello-cerebral degeneration with amyloid plaques (Gerstmann, Sträussler, Scheinker syndrome).
    Dolman CL; Daly LL
    Can J Neurol Sci; 1982 Nov; 9(4):439-42. PubMed ID: 7151028
    [No Abstract]   [Full Text] [Related]  

  • 48. Clinical phenotype and neuroimaging findings in a French family with hereditary ferritinopathy (FTL498-499InsTC).
    Ory-Magne F; Brefel-Courbon C; Payoux P; Debruxelles S; Sibon I; Goizet C; Labauge P; Menegon P; Uro-Coste E; Ghetti B; Delisle MB; Vidal R; Rascol O
    Mov Disord; 2009 Aug; 24(11):1676-83. PubMed ID: 19514068
    [TBL] [Abstract][Full Text] [Related]  

  • 49. A newly formed amyloidogenic fragment due to a stop codon mutation causes familial British dementia.
    Ghiso J; Vidal R; Rostagno A; Mead S; Révész T; Plant G; Frangione B
    Ann N Y Acad Sci; 2000 Apr; 903():129-37. PubMed ID: 10818498
    [TBL] [Abstract][Full Text] [Related]  

  • 50. A Novel ITM2B Mutation Associated with Familial Chinese Dementia.
    Liu X; Chen KL; Wang Y; Huang YY; Chen SD; Dong Q; Cui M; Yu JT
    J Alzheimers Dis; 2021; 81(2):499-505. PubMed ID: 33814452
    [TBL] [Abstract][Full Text] [Related]  

  • 51. [An autopsy case of Crow-Fukase syndrome with massive appearance of amyloid bodies in the central nervous systems].
    Tomi H; Mukoyama M; Kamei N; Sunohara N; Satoyoshi E
    Rinsho Shinkeigaku; 1988 Aug; 28(8):887-90. PubMed ID: 3240625
    [No Abstract]   [Full Text] [Related]  

  • 52. Gerstmann-Sträussler-Scheinker disease. I. Extending the clinical spectrum.
    Farlow MR; Yee RD; Dlouhy SR; Conneally PM; Azzarelli B; Ghetti B
    Neurology; 1989 Nov; 39(11):1446-52. PubMed ID: 2812321
    [TBL] [Abstract][Full Text] [Related]  

  • 53. [Gerstmann-Straussler-Scheinker disease].
    Renard JL
    Soins; 1990 Jan; (532):47-8. PubMed ID: 2326674
    [No Abstract]   [Full Text] [Related]  

  • 54. [A novel variation in ATP1A3 gene in a child with CAPOS syndrome].
    Zhang F; Wang J; Zou LP; Zhang MN; Dun S; Yang G
    Zhonghua Er Ke Za Zhi; 2020 Mar; 58(3):233-235. PubMed ID: 32135597
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Clinical presentation of rapidly progressive familial Danish dementia.
    Zhou Z; Ainger TJ; Han DY
    Neurocase; 2018; 24(5-6):287-289. PubMed ID: 30843473
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome: a histopathologic case report.
    Szmulewicz DJ; Merchant SN; Halmagyi GM
    Otol Neurotol; 2011 Oct; 32(8):e63-5. PubMed ID: 21451431
    [No Abstract]   [Full Text] [Related]  

  • 57. Cataract, deafness, cerebellar ataxia, psychosis and dementia--a new syndrome.
    Strömgren E; Dalby A; Dalby MA; Ranheim B
    Acta Neurol Scand; 1970; 46(S43):261-2. PubMed ID: 5457846
    [No Abstract]   [Full Text] [Related]  

  • 58. Miniplaques and shapeless cerebral amyloid deposits in a case of Gerstmann-Sträussler-Scheinker's syndrome.
    Boellaard JW; Doerr-Schott J; Schlote W
    Acta Neuropathol; 1993; 86(5):532-5. PubMed ID: 8310806
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Rapidly progressive dementia caused by spongiform encephalopathy.
    Enos BE; Vinters HV
    West J Med; 1988 Mar; 148(3):313-9. PubMed ID: 3284205
    [No Abstract]   [Full Text] [Related]  

  • 60. Early-onset dementia and extrapyramidal disease: clinicopathological variant of Gerstmann-Straussler-Scheinker or Alzheimer's disease?
    Hart J; Gordon B
    J Neurol Neurosurg Psychiatry; 1990 Nov; 53(11):932-4. PubMed ID: 2283522
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.