BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

173 related articles for article (PubMed ID: 3032328)

  • 1. Hereditary generalized amyloidosis with polyneuropathy. Clinicopathological study of 65 Japanese patients.
    Ikeda S; Hanyu N; Hongo M; Yoshioka J; Oguchi H; Yanagisawa N; Kobayashi T; Tsukagoshi H; Ito N; Yokota T
    Brain; 1987 Apr; 110 ( Pt 2)():315-37. PubMed ID: 3032328
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Diagnosis by recombinant DNA techniques and clinical features of familial amyloid polyneuropathy].
    Harada T
    No To Shinkei; 1988 Jul; 40(7):617-21. PubMed ID: 2852018
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Familial amyloid polyneuropathy associated with the transthyretin Cys114 gene in a Japanese kindred.
    Ueno S; Fujimura H; Yorifuji S; Nakamura Y; Takahashi M; Tarui S; Yanagihara T
    Brain; 1992 Oct; 115 ( Pt 5)():1275-89. PubMed ID: 1330202
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Diagnosis of familial amyloid polyneuropathy--gene analysis with primer-directed enzymatic amplification of DNA, isolation of plasma variant prealbumin and immunohistochemical identification of tissue amyloid protein].
    Ikeda S; Nakano T; Yanagisawa N; Hanyu N; Suzuki T; Sakaki Y
    Rinsho Shinkeigaku; 1991 Apr; 31(4):363-71. PubMed ID: 1655325
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Clinical features and diagnosis by recombinant DNA techniques of familial amyloid polyneuropathy in Japan.
    Harada T; Kito S; Ishizaki F; Matsubayashi H; Katayama S; Sasaki H; Furuya H; Sakaki Y
    Res Commun Chem Pathol Pharmacol; 1989 Aug; 65(2):237-44. PubMed ID: 2587841
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Hereditary amyloidosis: description of a new American kindred with late onset cardiomyopathy. Appalachian amyloid.
    Benson MD; Wallace MR; Tejada E; Baumann H; Page B
    Arthritis Rheum; 1987 Feb; 30(2):195-200. PubMed ID: 3030336
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genetic and clinical studies of Japanese patients with familial amyloid polyneuropathy.
    Harada T; Kito S; Shimoyama M; Katayama S; Sasaki H; Furuya H; Yoshioka K; Sakaki Y
    Eur Neurol; 1989; 29(1):48-52. PubMed ID: 2707291
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Late-onset familial amyloid polyneuropathy type I (transthyretin Met30-associated familial amyloid polyneuropathy) unrelated to endemic focus in Japan. Clinicopathological and genetic features.
    Misu Ki; Hattori N; Nagamatsu M; Ikeda Si; Ando Y; Nakazato M; Takei Yi; Hanyu N; Usui Y; Tanaka F; Harada T; Inukai A; Hashizume Y; Sobue G
    Brain; 1999 Oct; 122 ( Pt 10)():1951-62. PubMed ID: 10506096
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Familial amyloid polyneuropathy: report of a family.
    Giangaspero F; Salvi F; Ceccarelli C; Ambrosetto G; Govoni E; Tassinari CA
    Clin Neuropathol; 1985; 4(3):105-10. PubMed ID: 2990786
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Biochemical characterization of familial amyloidotic polyneuropathy in various districts of Japan.
    Tanaka M; Nakazato M; Kurihara T; Matsukura S; Kangawa K; Matsuo H
    Jpn J Med; 1987 May; 26(2):189-93. PubMed ID: 3041083
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Vagus nerve and celiac ganglion lesions in generalized amyloidosis. A correlative study of familial amyloid polyneuropathy and AL-amyloidosis.
    Ikeda S; Yanagisawa N; Hongo M; Ito N
    J Neurol Sci; 1987 Jun; 79(1-2):129-39. PubMed ID: 3039063
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Portuguese-type amyloidosis (transthyretin amyloidosis, ATTR V30M).
    Lobato L
    J Nephrol; 2003; 16(3):438-42. PubMed ID: 12832749
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Type I familial amyloidotic polyneuropathy (Japanese type).
    Araki S
    Brain Dev; 1984; 6(2):128-33. PubMed ID: 6087691
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Onset in the seventh decade and lack of symptoms in heterozygotes for the TTRMet30 mutation in hereditary amyloid neuropathy-type I (Portuguese, Andrade).
    Sequeiros J; Saraiva MJ
    Am J Med Genet; 1987 Jun; 27(2):345-57. PubMed ID: 3037905
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Familial amyloid polyneuropathy with marked hypertrophy of the peripheral nerves.
    Sumino S; Nagashima K; Shimamine T; Abe T; Tsuneyoshi H; Murao S
    Acta Pathol Jpn; 1983 May; 33(3):629-43. PubMed ID: 6312734
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genetic analysis of familial amyloidotic polyneuropathy, an autosomal dominant disease.
    Sakaki Y; Sasaki H; Yoshioka K; Furuya H
    Clin Chim Acta; 1989 Dec; 185(3):291-7. PubMed ID: 2559819
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Coexistence of familial transthyretin amyloidosis ATTR Val30Met and spinocerebellar ataxia type 1 in a Japanese family--a follow-up autopsy report.
    Oide T; Arima K; Yamazaki M; Hanyu N; Ikeda S
    Amyloid; 2004 Sep; 11(3):191-9. PubMed ID: 15523922
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Family studies of the genetic abnormality in transthyretin (prealbumin) in Portuguese patients with familial amyloidotic polyneuropathy.
    Saraiva MJ; Birken S; Costa PP; Goodman DS
    Ann N Y Acad Sci; 1984; 435():86-100. PubMed ID: 6099706
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A novel variant of transthyretin, 59Thr-->Lys, associated with autosomal dominant cardiac amyloidosis in an Italian family.
    Booth DR; Tan SY; Hawkins PN; Pepys MB; Frustaci A
    Circulation; 1995 Feb; 91(4):962-7. PubMed ID: 7850982
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Familial amyloid polyneuropathy. Demonstration of prealbumin in a kinship of German/English ancestry with onset in the seventh decade.
    Libbey CA; Rubinow A; Shirahama T; Deal C; Cohen AS
    Am J Med; 1984 Jan; 76(1):18-24. PubMed ID: 6691355
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.