BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

301 related articles for article (PubMed ID: 23317988)

  • 1. Delayed diagnosis of transthyretin amyloidosis with a novel mutation (c.210T>A) in the transthyretin gene.
    Dekmezian MS; Tschen JA; Cho-Vega JH
    J Am Acad Dermatol; 2013 Feb; 68(2):e49-51. PubMed ID: 23317988
    [No Abstract]   [Full Text] [Related]  

  • 2. Vitreal deposits in Val71Ala transthyretin amyloidosis.
    Suan D; Booth DR; Kennedy IH; Downie J; Earls P; Gottlieb D; Stewart GJ; Lin MW
    Intern Med J; 2012 Jan; 42(1):106-8. PubMed ID: 22276564
    [No Abstract]   [Full Text] [Related]  

  • 3. Clinical variant of familial amyloid polyneuropathy.
    Quan D; Cohen JA
    Muscle Nerve; 2002 Sep; 26(3):417-20. PubMed ID: 12210373
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Chinese familial transthyretin amyloidosis with vitreous involvement is associated with the transthyretin mutation Gly83Arg: a case report and literature review.
    Yin J; Xia X; Shi Y; Lu Y; Zhao C; Huang Z; Tian N
    Amyloid; 2014 Jun; 21(2):140-2. PubMed ID: 24601824
    [No Abstract]   [Full Text] [Related]  

  • 6. Myopathic phenotype of familial amyloid polyneuropathy with a rare transthyretin variant: ATTR Ala45Asp.
    Misumi Y; Doki T; Ueda M; Obayashi K; Tasaki M; Tamura A; Ando Y
    Amyloid; 2014 Sep; 21(3):216-7. PubMed ID: 24953234
    [No Abstract]   [Full Text] [Related]  

  • 7. Rapid detection of wild-type and mutated transthyretins.
    Tasaki M; Ueda M; Obayashi K; Motokawa H; Kinoshita Y; Suenaga G; Yanagisawa A; Toyoshima R; Misumi Y; Masuda T; Yamashita T; Ando Y
    Ann Clin Biochem; 2016 Jul; 53(Pt 4):508-10. PubMed ID: 26342004
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Diagnostic pitfalls in sporadic transthyretin familial amyloid polyneuropathy (TTR-FAP).
    Ikeda K; Kano O; Ito H; Kawase Y; Iwamoto K; Sato R; Sekine T; Nagata R; Nakamura Y; Hirayama T; Iwasaki Y
    Neurology; 2008 Apr; 70(17):1576; author reply 1576-7. PubMed ID: 18427077
    [No Abstract]   [Full Text] [Related]  

  • 9. First report of a rare mutation in a Polish patient with painful late-onset transthyretin amyloidosis.
    Hagenacker T; Brenck J; Kastrup O
    J Neurol Sci; 2014 Nov; 346(1-2):331-2. PubMed ID: 25130926
    [No Abstract]   [Full Text] [Related]  

  • 10. [A sporadic case of late-onset familial amyloid polyneuropathy type I (transthyretin Met 30-associated familial amyloid polyneuropathy) inborn habitant of Ehime prefecture].
    Harada T; Ishizaki F; Togo M; Yamashita H; Nitta K; Date Y; Nakazato M; Yamamura Y; Nakamura S
    No To Shinkei; 2002 Jul; 54(7):615-9. PubMed ID: 12187722
    [TBL] [Abstract][Full Text] [Related]  

  • 11. TTR-familial amyloid polyneuropathy--neurological aspects.
    Said G; Planté-Bordeneuve V
    Amyloid; 2012 Jun; 19 Suppl 1():25-7. PubMed ID: 22620963
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Patients with transthyretin amyloidosis enrolled in THAOS between 2018 and 2021 continue to experience substantial diagnostic delay.
    Coelho T; Dispenzieri A; Grogan M; Conceição I; Waddington-Cruz M; Kristen AV; Wixner J; Diemberger I; Gonzalez-Moreno J; Maurer MS; Planté-Bordeneuve V; Garcia-Pavia P; Tournev I; Gonzalez-Costello J; Cariou E; González-Duarte A; Glass O; Chapman D; Amass L;
    Amyloid; 2023 Dec; 30(4):445-448. PubMed ID: 37459334
    [No Abstract]   [Full Text] [Related]  

  • 13. Carpal tunnel syndrome as an initial manifestation in a case of transthyretin-related familial amyloid polyneuropathy with a novel A120T mutation.
    Koyama S; Kawanami T; Kurokawa K; Tanji H; Iseki C; Arawaka S; Wada M; Kato T
    Clin Neurol Neurosurg; 2012 Jul; 114(6):707-9. PubMed ID: 22209138
    [No Abstract]   [Full Text] [Related]  

  • 14. Upper limb neuropathy such as carpal tunnel syndrome as an initial manifestation of ATTR Val30Met familial amyloid polyneuropathy.
    Tojo K; Tsuchiya-Suzuki A; Sekijima Y; Morita H; Sumita N; Ikeda S
    Amyloid; 2010 Mar; 17(1):32-5. PubMed ID: 20132088
    [TBL] [Abstract][Full Text] [Related]  

  • 15. From hypertrophic cardiomyopathy to transthyretin amyloidosis: an unusual case and challenging diagnosis.
    Petkow-Dimitrow P; Rajtar-Salwa R; Holcman K; Kostkiewicz M; Rubiś P
    Pol Arch Intern Med; 2020 Feb; 130(2):153-154. PubMed ID: 31933485
    [No Abstract]   [Full Text] [Related]  

  • 16. Poor outcome after liver transplantation for transthyretin amyloid neuropathy in a family with an Ala36Pro transthyretin mutation: case report.
    Muller KR; Padbury R; Jeffrey GP; Poplawski NK; Thompson P; Tonkin A; Harley HA
    Liver Transpl; 2010 Apr; 16(4):470-3. PubMed ID: 20373457
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Sporadic transthyretin amyloidosis with a novel TTR gene mutation misdiagnosed as primary amyloidosis.
    Briani C; Cavallaro T; Ferrari S; Taioli F; Calamelli S; Verga L; Adami F; Fabrizi GM
    J Neurol; 2012 Oct; 259(10):2226-8. PubMed ID: 22580845
    [No Abstract]   [Full Text] [Related]  

  • 18. Transthyretin-related familial amyloidotic polyneuropathy.
    Ando Y; Nakamura M; Araki S
    Arch Neurol; 2005 Jul; 62(7):1057-62. PubMed ID: 16009758
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Gene therapy: lessons learned from liver transplantation for transthyretin-amyloidosis.
    Suhr OB; Holmgren G; Lundgren E
    Liver Transpl; 2004 Dec; 10(12):1551-3. PubMed ID: 15558840
    [No Abstract]   [Full Text] [Related]  

  • 20. Dominant cardiac type of familial amyloidotic polyneuropathy associated with a novel transthyretin variant Thr59Arg.
    Obayashi K; Misumi Y; Watanabe T; Ando T; Akagami T; Tasaki M; Shinriki S; Ueda M; Yamashita T; Hirotani S; Ando Y
    Muscle Nerve; 2013 Nov; 48(5):839-41. PubMed ID: 23836350
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 16.