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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

231 related items for PubMed ID: 12963686

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2. Early diagnosis and management of patients with familial ATTR amyloidosis receiving livers from asymptomatic variant TTR carriers.
    Munar-Qués M, Viader-Farré C, Zabay-Becerril JM, Mulet-Ferrer JM.
    Amyloid; 2011 Sep; 18(3):172-3. PubMed ID: 21774739
    [Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4. [Hereditary amyloidoses associated with transthyretin mutations].
    Hund E, Singer R, Linke RP, Willig F, Grau A.
    Nervenarzt; 2002 Oct; 73(10):930-6. PubMed ID: 12376880
    [Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6. [Pathogenesis and therapy for transthyretin related amyloidosis].
    Ando Y, Jono H.
    Rinsho Byori; 2008 Feb; 56(2):114-20. PubMed ID: 18402051
    [Abstract] [Full Text] [Related]

  • 7. Periorbital ecchymoses are not pathognomonic of the light-chain type of amyloidosis.
    Outteryck O, Stojkovic T, Launay D, Meignie-Ramon B, Vermersch P.
    Acta Derm Venereol; 2007 Feb; 87(6):544-5. PubMed ID: 17989898
    [No Abstract] [Full Text] [Related]

  • 8. Images in cardiovascular medicine. Restrictive cardiomyopathy in familial amyloidosis TTR-Arg-50.
    Singer R, Schnabel A, Strasser RH.
    Circulation; 2003 Feb 04; 107(4):643-4. PubMed ID: 12566380
    [No Abstract] [Full Text] [Related]

  • 9. 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 04; 259(10):2226-8. PubMed ID: 22580845
    [No Abstract] [Full Text] [Related]

  • 10. [Clinical diversity, diagnosis and treatment of hereditary amyloid neuropathy].
    Sekijima Y.
    Rinsho Shinkeigaku; 2014 Oct 04; 54(12):953-6. PubMed ID: 25672679
    [Abstract] [Full Text] [Related]

  • 11. Heart failure and cardiac involvement as isolated manifestation of familial form of transthyretin amyloidosis resulting from Val30Met mutation with no clinical signs of polyneuropathy.
    Christoph DC, Boese D, Johnson KT, Schlosser TW, Hunold P, Baba HA, Erbel R, Philipp S.
    Circ Heart Fail; 2009 Sep 04; 2(5):512-5. PubMed ID: 19808383
    [No Abstract] [Full Text] [Related]

  • 12. Amyloid heart disease mimicking hypertrophic cardiomyopathy.
    Mörner S, Hellman U, Suhr OB, Kazzam E, Waldenström A.
    J Intern Med; 2005 Sep 04; 258(3):225-30. PubMed ID: 16115295
    [Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14. Novel methods for detecting amyloidogenic proteins in transthyretin related amyloidosis.
    Ando Y, Ueda M.
    Front Biosci; 2008 May 01; 13():5548-58. PubMed ID: 18508604
    [Abstract] [Full Text] [Related]

  • 15. [Familial approach in hereditary transthyretin cardiac amyloidosis].
    García-Pavía P, Avellana P, Bornstein B, Heine-Suñer D, Cobo-Marcos M, Gómez-Bueno M, Segovia J, Alonso-Pulpón LA.
    Rev Esp Cardiol; 2011 Jun 01; 64(6):523-6. PubMed ID: 21439703
    [Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19. Long-term treatment of anemia with recombinant human erythropoietin in familial amyloidosis TTR V30M.
    Beirão I, Lobato L, Moreira L, Mp Costa P, Fonseca I, Cabrita A, Porto G.
    Amyloid; 2008 Sep 01; 15(3):205-9. PubMed ID: 18925459
    [Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 12.