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Volumn 51, Issue 5, 1998, Pages 1462-1464

Transthyretin amyloidosis (serine 44) with headache, hearing loss, and peripheral neuropathy

Author keywords

[No Author keywords available]

Indexed keywords

AMYLOID; ANTIINFLAMMATORY AGENT; DIHYDROERGOTAMINE; DNA; NARCOTIC AGENT; PHENYLALANINE; PREALBUMIN; SERINE;

EID: 0031774375     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/WNL.51.5.1462     Document Type: Article
Times cited : (23)

References (10)
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    • Meningocerebrovascular amyloidosis associated with a novel transthyretin mis-sense mutation at codon 18 (TTRD18G)
    • Vidai R, Garzuly F, Budka H, et al. Meningocerebrovascular amyloidosis associated with a novel transthyretin mis-sense mutation at codon 18 (TTRD18G). Am J Pathol 1996;148:361-366.
    • (1996) Am J Pathol , vol.148 , pp. 361-366
    • Vidai, R.1    Garzuly, F.2    Budka, H.3
  • 3
    • 0031055128 scopus 로고    scopus 로고
    • Transthyretin amyloidosis: A new mutation associated with dementia
    • Petersen RB, Goren H, Cohen M, et al. Transthyretin amyloidosis: a new mutation associated with dementia. Ann Neurol 1997;41:307-313.
    • (1997) Ann Neurol , vol.41 , pp. 307-313
    • Petersen, R.B.1    Goren, H.2    Cohen, M.3
  • 4
    • 0018952424 scopus 로고
    • Familial oculoleptomeningeal amyloidosis
    • Goren J, Steinberg M, Farboody G. Familial oculoleptomeningeal amyloidosis. Brain 1980;103:473-495.
    • (1980) Brain , vol.103 , pp. 473-495
    • Goren, J.1    Steinberg, M.2    Farboody, G.3
  • 5
    • 0029730803 scopus 로고    scopus 로고
    • Familial meningocerebrovascular amyloidosis, Hungarian type, with mutant transthyretin (TTR Asp18Gly)
    • Garzuly F, Wisniewksi MD, Brittig, Budka H. Familial meningocerebrovascular amyloidosis, Hungarian type, with mutant transthyretin (TTR Asp18Gly). Neurology 1996;47:1562-1567.
    • (1996) Neurology , vol.47 , pp. 1562-1567
    • Garzuly, F.1    Wisniewksi, M.D.2    Brittig3    Budka, H.4
  • 6
    • 0024756969 scopus 로고
    • Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction
    • Orita M, Suzuki Y, Sekiya T, Hayashi K. Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction. Genomics 1989;5:874-879.
    • (1989) Genomics , vol.5 , pp. 874-879
    • Orita, M.1    Suzuki, Y.2    Sekiya, T.3    Hayashi, K.4
  • 7
    • 0025174736 scopus 로고
    • Hereditary amyloidosis: Detection of variant prealbumin genes by restriction enzyme analysis of amplified genomic DNA sequences
    • Nichols WC, Benson MD. Hereditary amyloidosis: detection of variant prealbumin genes by restriction enzyme analysis of amplified genomic DNA sequences. Clin Genet 1990;37:44-53.
    • (1990) Clin Genet , vol.37 , pp. 44-53
    • Nichols, W.C.1    Benson, M.D.2
  • 8
    • 0026612659 scopus 로고
    • Transthyretin Pro 55, a variant associated with early onset, aggressive diffuse amyloidosis with cardiac and neurologic involvement
    • Jacobson DR, McFarlin DE, Kane I, Buxbaum JN. Transthyretin Pro 55, a variant associated with early onset, aggressive diffuse amyloidosis with cardiac and neurologic involvement. Hum Genet 1992;89:353-356.
    • (1992) Hum Genet , vol.89 , pp. 353-356
    • Jacobson, D.R.1    McFarlin, D.E.2    Kane, I.3    Buxbaum, J.N.4
  • 10
    • 0028838359 scopus 로고
    • Occupational and other risk factors for clinically overt familial amyloid polyneuropathy
    • Hardell L, Holmgren G, Steen L, Fredrikson M, Axelson O. Occupational and other risk factors for clinically overt familial amyloid polyneuropathy. Epidemiology 1995;6:598-600.
    • (1995) Epidemiology , vol.6 , pp. 598-600
    • Hardell, L.1    Holmgren, G.2    Steen, L.3    Fredrikson, M.4    Axelson, O.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.