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Journal Abstract Search

245 related items for PubMed ID: 28395866

  • 21. 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
    [Abstract] [Full Text] [Related]

  • 22. A transthyretin variant, Asp18Asn, associated with amyloid cardiomyopathy: a new African-American variant?
    Quarta CC, Falk RH.
    Amyloid; 2012 Dec; 19(4):204-7. PubMed ID: 23126592
    [Abstract] [Full Text] [Related]

  • 23. Molecular diagnosis of the transthyretin (TTR) Met111 mutation in familial amyloid cardiomyopathy of Danish origin.
    Nordvåg BY, Husby G, Ranløv I, el-Gewely MR.
    Hum Genet; 1992 Jun; 89(4):459-61. PubMed ID: 1618497
    [Abstract] [Full Text] [Related]

  • 24. Pressure-volume relationships in patients with transthyretin (ATTR) cardiac amyloidosis secondary to V122I mutations and wild-type transthyretin: Transthyretin Cardiac Amyloid Study (TRACS).
    Bhuiyan T, Helmke S, Patel AR, Ruberg FL, Packman J, Cheung K, Grogan D, Maurer MS.
    Circ Heart Fail; 2011 Mar; 4(2):121-8. PubMed ID: 21191093
    [Abstract] [Full Text] [Related]

  • 25. Cardiac involvement in hereditary-transthyretin related amyloidosis.
    Rapezzi C, Longhi S, Milandri A, Lorenzini M, Gagliardi C, Gallelli I, Leone O, Quarta CC.
    Amyloid; 2012 Jun; 19 Suppl 1():16-21. PubMed ID: 22494034
    [Abstract] [Full Text] [Related]

  • 26. Transthyretin VAL107, a new variant associated with familial cardiac and neuropathic amyloidosis.
    Jacobson DR, Gertz MA, Buxbaum JN.
    Hum Mutat; 1994 Jun; 3(4):399-401. PubMed ID: 8081397
    [No Abstract] [Full Text] [Related]

  • 27. Transthyretin-related amyloidoses and the heart: a clinical overview.
    Rapezzi C, Quarta CC, Riva L, Longhi S, Gallelli I, Lorenzini M, Ciliberti P, Biagini E, Salvi F, Branzi A.
    Nat Rev Cardiol; 2010 Jul; 7(7):398-408. PubMed ID: 20479782
    [Abstract] [Full Text] [Related]

  • 28. [Fibril-forming proteins: the amyloidosis. New hopes for a disease that cardiologists must know].
    Arbustini E, Gavazzi A, Merlini G.
    Ital Heart J Suppl; 2002 Jun; 3(6):590-7. PubMed ID: 12116807
    [Abstract] [Full Text] [Related]

  • 29. Cardiac phenotype and clinical outcome of familial amyloid polyneuropathy associated with transthyretin alanine 60 variant.
    Sattianayagam PT, Hahn AF, Whelan CJ, Gibbs SD, Pinney JH, Stangou AJ, Rowczenio D, Pflugfelder PW, Fox Z, Lachmann HJ, Wechalekar AD, Hawkins PN, Gillmore JD.
    Eur Heart J; 2012 May; 33(9):1120-7. PubMed ID: 21992998
    [Abstract] [Full Text] [Related]

  • 30. Two transthyretin variants (TTR Ala-49 and TTR Gln-89) in two Sicilian kindreds with hereditary amyloidosis.
    Almeida MR, Ferlini A, Forabosco A, Gawinowicz M, Costa PP, Salvi F, Plasmati R, Tassinari CA, Altland K, Saraiva MJ.
    Hum Mutat; 1992 May; 1(3):211-5. PubMed ID: 1301926
    [Abstract] [Full Text] [Related]

  • 31. Cardiac amyloidosis: report of a patient heterozygous for the transthyretin isoleucine 122 variant.
    Saraiva MJ, Sherman W, Marboe C, Figueira A, Costa P, de Freitas AF, Gawinowicz MA.
    Scand J Immunol; 1990 Oct; 32(4):341-6. PubMed ID: 2237288
    [Abstract] [Full Text] [Related]

  • 32. Cardiac amyloidosis, a monoclonal gammopathy and a potentially misleading mutation.
    Wechalekar AD, Offer M, Gillmore JD, Hawkins PN, Lachmann HJ.
    Nat Clin Pract Cardiovasc Med; 2009 Feb; 6(2):128-33. PubMed ID: 19079367
    [Abstract] [Full Text] [Related]

  • 33. [Hereditary amyloid cardiomyopathy related to a mutation at transthyretin protein number 111. A clinical, genetic and echocardiographic study of an affected Danish family].
    Svendsen IH, Steensgaard-Hansen F, Nordvåg BY.
    Ugeskr Laeger; 1999 Sep 06; 161(36):4995-9. PubMed ID: 10489791
    [Abstract] [Full Text] [Related]

  • 34. A new mutation (TTR Ala-47) in the transthyretin gene associated with hereditary amyloidosis.
    Ferlini A, Patrosso MC, Repetto M, Frattini A, Villa A, Fini S, Salvi F, Vezzoni P, Forabosco A.
    Hum Mutat; 1994 Sep 06; 4(1):61-4. PubMed ID: 7951260
    [No Abstract] [Full Text] [Related]

  • 35. Cardiomyopathy in Swedish patients with the Gly53Glu and His88Arg transthyretin variants.
    Holmgren G, Hellman U, Anan I, Lundgren HE, Jonasson J, Stafberg C, Fahoum S, Suhr OB.
    Amyloid; 2005 Sep 06; 12(3):184-8. PubMed ID: 16194874
    [Abstract] [Full Text] [Related]

  • 36. Relation of clinical, echocardiographic and electrocardiographic features of cardiac amyloidosis to the presence of the transthyretin V122I allele in older African-American men.
    Jacobson D, Tagoe C, Schwartzbard A, Shah A, Koziol J, Buxbaum J.
    Am J Cardiol; 2011 Aug 01; 108(3):440-4. PubMed ID: 21600538
    [Abstract] [Full Text] [Related]

  • 37. Genetic testing improves identification of transthyretin amyloid (ATTR) subtype in cardiac amyloidosis.
    Brown EE, Lee YZJ, Halushka MK, Steenbergen C, Johnson NM, Almansa J, Tedford RJ, Cingolani O, Russell SD, Sharma K, Judge DP.
    Amyloid; 2017 Jun 01; 24(2):92-95. PubMed ID: 28494620
    [Abstract] [Full Text] [Related]

  • 38. Cardiac amyloidosis: a practical approach to diagnosis and management.
    Kapoor P, Thenappan T, Singh E, Kumar S, Greipp PR.
    Am J Med; 2011 Nov 01; 124(11):1006-15. PubMed ID: 22017778
    [Abstract] [Full Text] [Related]

  • 39. Non-coding variants contribute to the clinical heterogeneity of TTR amyloidosis.
    Iorio A, De Lillo A, De Angelis F, Di Girolamo M, Luigetti M, Sabatelli M, Pradotto L, Mauro A, Mazzeo A, Stancanelli C, Perfetto F, Frusconi S, My F, Manfellotto D, Fuciarelli M, Polimanti R.
    Eur J Hum Genet; 2017 Sep 01; 25(9):1055-1060. PubMed ID: 28635949
    [Abstract] [Full Text] [Related]

  • 40. Transthyretin-derived senile systemic amyloidosis: clinicopathologic and structural considerations.
    Westermark P, Bergström J, Solomon A, Murphy C, Sletten K.
    Amyloid; 2003 Aug 01; 10 Suppl 1():48-54. PubMed ID: 14640042
    [Abstract] [Full Text] [Related]

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