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 *

170 related articles for article (PubMed ID: 27784877)

  • 1. [An autopsy case of leptomeningeal amyloidosis associated with transthyretin Gly47Arg mutation].
    Uehara T; Kakuda K; Sumi-Akamaru H; Yamauchi A; Mochizuki H; Naka T
    Rinsho Shinkeigaku; 2016 Nov; 56(11):777-780. PubMed ID: 27784877
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Oculoleptomeningeal Amyloidosis Secondary to the Rare Transthyretin c.381T>G (p.Ile127Met) Mutation.
    Mathieu F; Morgan E; So J; Munoz DG; Mason W; Kongkham P
    World Neurosurg; 2018 Mar; 111():190-193. PubMed ID: 29277593
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Postmortem findings in a familial amyloid polyneuropathy patient with homozygosity of the mutant Val30Met transthyretin gene.
    Yoshinaga T; Takei Y; Katayanagi K; Ikeda S
    Amyloid; 2004 Mar; 11(1):56-60. PubMed ID: 15185500
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Clinical and pathological findings in familial amyloid polyneuropathy caused by a transthyretin E61K mutation.
    Murakami T; Nishimura H; Nagai T; Hemmi S; Kutoku Y; Ohsawa Y; Sunada Y
    J Neurol Sci; 2017 Oct; 381():55-58. PubMed ID: 28991715
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Distinct characteristics of amyloid deposits in early- and late-onset transthyretin Val30Met familial amyloid polyneuropathy.
    Koike H; Ando Y; Ueda M; Kawagashira Y; Iijima M; Fujitake J; Hayashi M; Yamamoto M; Mukai E; Nakamura T; Katsuno M; Hattori N; Sobue G
    J Neurol Sci; 2009 Dec; 287(1-2):178-84. PubMed ID: 19709674
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Evidence that glial cells attenuate G47R transthyretin accumulation in the central nervous system.
    Sumi-Akamaru H; Eto M; Yamauchi A; Uehara T; Kakuda K; Obayashi K; Kato S; Naka T; Mochizuki H
    Neuropathology; 2018 Feb; 38(1):11-21. PubMed ID: 28960480
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Familial amyloid polyneuropathy: a clinico-pathologic study.
    Said G; Planté-Bordeneuve V
    J Neurol Sci; 2009 Sep; 284(1-2):149-54. PubMed ID: 19467548
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Case of hereditary Y69H (p.Y89H) transthyretin variant leptomeningeal amyloidosis presenting with drop attacks and recurrent transient language disorder].
    Saito N; Kuroha Y; Hasegawa A; Tada M; Kakita A; Watanabe K; Takahashi T
    Rinsho Shinkeigaku; 2023 Oct; 63(10):650-655. PubMed ID: 37779024
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A woman with a rare p.Glu74Gly transthyretin mutation presenting exclusively with a rapidly progressive neuropathy: a case report.
    Schänzer A; Kimmich C; Röcken C; Haverkamp T; Weidner I; Acker T; Krämer HH
    J Med Case Rep; 2014 Dec; 8():403. PubMed ID: 25471118
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Clinical and histopathological features of progressive-type familial amyloidotic polyneuropathy with TTR Lys54.
    Nagasaka T; Togashi S; Watanabe H; Iida H; Nagasaka K; Nakamura Y; Miwa M; Kobayashi F; Shindo K; Shiozawa Z
    J Neurol Sci; 2009 Jan; 276(1-2):88-94. PubMed ID: 18930252
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Familial amyloidotic polyneuropathy and transthyretin.
    Nagasaka T
    Subcell Biochem; 2012; 65():565-607. PubMed ID: 23225017
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Phenotypic heterogeneity in a family with FAP due to a TTR Leu58Arg mutation: a clinicopathologic study.
    Motozaki Y; Sugiyama Y; Ishida C; Komai K; Matsubara S; Yamada M
    J Neurol Sci; 2007 Sep; 260(1-2):236-9. PubMed ID: 17466336
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The pathologic spectrum of oculoleptomeningeal amyloidosis with Val30Gly transthyretin gene mutation in a postmortem case.
    Martin SE; Benson MD; Hattab EM
    Hum Pathol; 2014 May; 45(5):1105-8. PubMed ID: 24613567
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Case report of a young patient with transthyretin amyloidosis associated with Gly67Ala mutation.
    Salihoglu A; Yildirim S; Ar MC; Hancer VS; Bozcan S; Yilmaz U; Serin N; Tuzuner N; Celik AF
    Amyloid; 2019; 26(sup1):75-76. PubMed ID: 31343303
    [No Abstract]   [Full Text] [Related]  

  • 15. Oculoleptomeningeal amyloidosis in a patient with a TTR Val30Gly mutation in the transthyretin gene.
    Roe RH; Fisher Y; Eagle RC; Fine HF; Cunningham ET
    Ophthalmology; 2007 Nov; 114(11):e33-7. PubMed ID: 17980738
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Cutaneous nerve biomarkers in transthyretin familial amyloid polyneuropathy.
    Ebenezer GJ; Liu Y; Judge DP; Cunningham K; Truelove S; Carter ND; Sebastian B; Byrnes K; Polydefkis M
    Ann Neurol; 2017 Jul; 82(1):44-56. PubMed ID: 28598015
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Novel transthyretin gene mutation in familial amyloid neuropathy in India: Case.
    Rohatgi S; Nirhale S; Manohar P; Rao P; Naphade P; Khan FMA; Dave D; Sravya Kotaru VV; Gupta S; Gitay A; Dubey P
    Ann Afr Med; 2022; 21(3):296-298. PubMed ID: 36204920
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Three Turkish families with different transthyretin mutations.
    Bekircan-Kurt CE; Güneş N; Yılmaz A; Erdem-Özdamar S; Tan E
    Neuromuscul Disord; 2015 Sep; 25(9):686-92. PubMed ID: 26115788
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Late-onset familial amyloid polyneuropathy: an autopsy study of two Japanese brothers.
    Fujitake J; Mizuta H; Fujii H; Ishikawa Y; Katsuyama E; Takasu K; Saida K; Tatsuoka Y
    Amyloid; 2003 Sep; 10(3):198-205. PubMed ID: 14640033
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Familial amyloid polyneuropathy associated with the novel transthyretin variant Arg34Gly.
    Levy J; Hawkins PN; Rowczenio D; Godfrey T; Stawell R; Zamir E
    Amyloid; 2012 Dec; 19(4):201-3. PubMed ID: 22973891
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.