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Volumn 78, Issue 3, 2007, Pages 321-323

Familial prion disease in a Hungarian family with a novel 144-base pair insertion in the prion protein gene

Author keywords

[No Author keywords available]

Indexed keywords

FLUORODEOXYGLUCOSE F 18; PRION PROTEIN; PRNP PROTEIN, HUMAN; UNCLASSIFIED DRUG;

EID: 33847721426     PISSN: 00223050     EISSN: 1468330X     Source Type: Journal    
DOI: 10.1136/jnnp.2006.104372     Document Type: Article
Times cited : (7)

References (11)
  • 1
    • 0034916581 scopus 로고    scopus 로고
    • Prion diseases of humans and animals: Their causes and molecular basis
    • Collinge J. Prion diseases of humans and animals: their causes and molecular basis. Annu Rev Neurosci 2001;24:519-50.
    • (2001) Annu Rev Neurosci , vol.24 , pp. 519-550
    • Collinge, J.1
  • 2
    • 21344445937 scopus 로고    scopus 로고
    • Molecular neurology of prion disease
    • Collinge J. Molecular neurology of prion disease. J Neurol Neurosurg Psychiatry 2005;76:906-19.
    • (2005) J Neurol Neurosurg Psychiatry , vol.76 , pp. 906-919
    • Collinge, J.1
  • 3
    • 0037385558 scopus 로고    scopus 로고
    • Phenotypic variability in the brains of a family with a prion disease chracterized by a 144-base pair insertion in the prion protein gene
    • King A, Doey L, Rossor M, et al. Phenotypic variability in the brains of a family with a prion disease chracterized by a 144-base pair insertion in the prion protein gene. Neuropathol Appl Neurobiol 2003;29:98-105.
    • (2003) Neuropathol Appl Neurobiol , vol.29 , pp. 98-105
    • King, A.1    Doey, L.2    Rossor, M.3
  • 4
    • 15444352327 scopus 로고    scopus 로고
    • Prion encephalopathy with insertion of octapeptide repeats: The number of repeats determines the type of cerebellar deposits
    • Vital C, Gray F, Vital A, et al. Prion encephalopathy with insertion of octapeptide repeats: the number of repeats determines the type of cerebellar deposits. Neuropathol Appl Neurobiol 1998;24:125-30.
    • (1998) Neuropathol Appl Neurobiol , vol.24 , pp. 125-130
    • Vital, C.1    Gray, F.2    Vital, A.3
  • 5
    • 0035943060 scopus 로고    scopus 로고
    • Two-octapeptide repeat deletion of prion protein associated with rapidly progressive dementia
    • Beck JA, Mead S, Campbell TA, et al. Two-octapeptide repeat deletion of prion protein associated with rapidly progressive dementia. Neurology 2001;57:354-6.
    • (2001) Neurology , vol.57 , pp. 354-356
    • Beck, J.A.1    Mead, S.2    Campbell, T.A.3
  • 6
    • 0026636605 scopus 로고
    • Inherited prion disease with 144 base pair gene insertion. 1. Genealogical and molecular studies
    • Poulter M, Baker FM, Frith CD, et al. Inherited prion disease with 144 base pair gene insertion. 1. Genealogical and molecular studies. Brain 1992;115:675-85.
    • (1992) Brain , vol.115 , pp. 675-685
    • Poulter, M.1    Baker, F.M.2    Frith, C.D.3
  • 7
    • 0026650443 scopus 로고
    • Inherited prion disease with 144 base pair gene insertion. 2. Clinical and pathological features
    • Collinge J, Brown J, Hardy J, et al. Inherited prion disease with 144 base pair gene insertion. 2. Clinical and pathological features. Brain 1992;115:687-710.
    • (1992) Brain , vol.115 , pp. 687-710
    • Collinge, J.1    Brown, J.2    Hardy, J.3
  • 8
    • 0028946529 scopus 로고
    • Inherited Creutzfeldt-Jakob disease in a British family associated with novel 144 base pair insertion of the prion protein gene
    • Nicholl D, Windl O, de Silva R, et al. Inherited Creutzfeldt-Jakob disease in a British family associated with novel 144 base pair insertion of the prion protein gene. J Neurol Neurosurg Psychiatry 1995;58:65-9.
    • (1995) J Neurol Neurosurg Psychiatry , vol.58 , pp. 65-69
    • Nicholl, D.1    Windl, O.2    de Silva, R.3
  • 9
    • 0029004216 scopus 로고
    • Prion disease with 144 base pair insertion in a Japanese family line
    • Oda T, Kitamoto T, Tateishi J, et al. Prion disease with 144 base pair insertion in a Japanese family line. Acta Neuropathol 1995;90:80-6.
    • (1995) Acta Neuropathol , vol.90 , pp. 80-86
    • Oda, T.1    Kitamoto, T.2    Tateishi, J.3
  • 10
    • 0030756021 scopus 로고    scopus 로고
    • Familial prion disease with a novel 144-bp insertion in the prion protein gene in a Basque family
    • Capellari S, Vital C, Parchi P, et al. Familial prion disease with a novel 144-bp insertion in the prion protein gene in a Basque family. Neurology 1997;49:133-41.
    • (1997) Neurology , vol.49 , pp. 133-141
    • Capellari, S.1    Vital, C.2    Parchi, P.3
  • 11
    • 0037456356 scopus 로고    scopus 로고
    • Detection of pathologic prion protein in the olfactory epithelium in sporadic Creutzfeldt-Jakob disease
    • Zanusso G, Ferrari S, Cardone F, et al. Detection of pathologic prion protein in the olfactory epithelium in sporadic Creutzfeldt-Jakob disease. N Engl J Med 2003;348:711-19.
    • (2003) N Engl J Med , vol.348 , pp. 711-719
    • Zanusso, G.1    Ferrari, S.2    Cardone, F.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.