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 *

139 related articles for article (PubMed ID: 37768132)

  • 1. Hereditary transthyretin cardiac amyloidosis proven by endomyocardial biopsy: a single-centre retrospective study and literature review.
    Yu TP; Hou J; Yang TJ; Chen XQ; Chen YC
    Acta Cardiol; 2024 Jun; 79(4):436-443. PubMed ID: 37768132
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Hereditary transthyretin-related amyloidosis is frequent in polyneuropathy and cardiomyopathy of no obvious aetiology.
    Skrahina V; Grittner U; Beetz C; Skripuletz T; Juenemann M; Krämer HH; Hahn K; Rieth A; Schaechinger V; Patten M; Tanislav C; Achenbach S; Assmus B; Knebel F; Gingele S; Skrahin A; Hartkamp J; Förster TM; Roesner S; Pereira C; Rolfs A
    Ann Med; 2021 Dec; 53(1):1787-1796. PubMed ID: 34658264
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Hereditary Transthyretin Amyloidosis in Eight Chinese Families.
    Meng LC; Lyu H; Zhang W; Liu J; Wang ZX; Yuan Y
    Chin Med J (Engl); 2015 Nov; 128(21):2902-5. PubMed ID: 26521788
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Clinical phenotypes and genetic features of hereditary transthyretin amyloidosis patients in China.
    He X; Tian Z; Guan H; Zhang S
    Orphanet J Rare Dis; 2022 Sep; 17(1):337. PubMed ID: 36056432
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Ophthalmic manifestations in a Chinese family with familial amyloid polyneuropathy due to a TTR Gly83Arg mutation.
    Liu T; Zhang B; Jin X; Wang W; Lee J; Li J; Yuan H; Cheng X
    Eye (Lond); 2014 Jan; 28(1):26-33. PubMed ID: 24113303
    [TBL] [Abstract][Full Text] [Related]  

  • 6. DISCOVERY: prevalence of transthyretin (
    Akinboboye O; Shah K; Warner AL; Damy T; Taylor HA; Gollob J; Powell C; Karsten V; Vest J; Maurer MS
    Amyloid; 2020 Dec; 27(4):223-230. PubMed ID: 32456532
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Sporadic Cardiac Amyloidosis by Amyloidogenic Transthyretin V122I Variant.
    Nehashi T; Oikawa M; Amami K; Kanno Y; Yokokawa T; Misaka T; Yamada S; Kunii H; Nakazato K; Ishida T; Takeishi Y
    Int Heart J; 2019 Nov; 60(6):1441-1443. PubMed ID: 31666456
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Transthyretin Glu54Leu - an unknown mutation within the Swedish population associated with amyloid cardiomyopathy and a unique fibril type.
    Hellman U; Lång K; Ihse E; Jonasson J; Olsson M; Lundgren HE; Pilebro B; Westermark P; Wixner J; Anan I
    Scand J Clin Lab Invest; 2019 Oct; 79(6):372-376. PubMed ID: 31169435
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Technetium pyrophosphate myocardial uptake and peripheral neuropathy in a rare variant of familial transthyretin (TTR) amyloidosis (Ser23Asn): a case report and literature review.
    Castaño A; Bokhari S; Brannagan TH; Wynn J; Maurer MS
    Amyloid; 2012 Mar; 19(1):41-6. PubMed ID: 22149423
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Characterization and natural history of different phenotypes in hereditary transthyretin amyloidosis: 40-year experience at a single Italian referral centre.
    Caponetti AG; Sguazzotti M; Accietto A; Saturi G; Ponziani A; Giovannetti A; Massa P; Ruotolo I; Sena G; Zaccaro A; Parisi V; Bonfiglioli R; Guaraldi P; Gagliardi C; Cortelli P; Galie N; Biagini E; Longhi S
    Eur J Prev Cardiol; 2024 May; 31(7):866-876. PubMed ID: 38204330
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Cardiac amyloidosis: a review and report of a new transthyretin (prealbumin) variant.
    Hesse A; Altland K; Linke RP; Almeida MR; Saraiva MJ; Steinmetz A; Maisch B
    Br Heart J; 1993 Aug; 70(2):111-5. PubMed ID: 8038017
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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; 24(2):92-95. PubMed ID: 28494620
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Amyloid Cardiomyopathy in the Rare Transthyretin Tyr78Phe Mutation.
    Tini G; Vianello PF; Gemelli C; Grandis M; Canepa M
    J Cardiovasc Transl Res; 2019 Dec; 12(6):514-516. PubMed ID: 30604309
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Spectrum of transthyretin gene mutations and clinical characteristics of Polish patients with cardiac transthyretin amyloidosis.
    Gawor M; Holcman K; Franaszczyk M; Lipowska M; Michałek P; Teresińska A; Bilińska ZT; Rubiś P; Kostkiewicz M; Szot W; Podolec P; Grzybowski J
    Cardiol J; 2022; 29(6):985-993. PubMed ID: 32789836
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A novel TTR mutation (p.Ala65Val) underlying late-onset hereditary transthyretin (ATTRv) amyloidosis with mixed cardiac and neuropathic phenotype: a case report.
    Thimm A; Oubari S; Hoffmann J; Carpinteiro A; Papathanasiou M; Luedike P; Kessler L; Rischpler C; Röcken C; Diebold I; Rassaf T; Schmidt H; Kleinschnitz C; Hagenacker T
    BMC Neurol; 2022 Dec; 22(1):469. PubMed ID: 36494773
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The genetic heterogeneity of hereditary transthyretin amyloidosis in a sample of the Brazilian population.
    Lavigne-Moreira C; Marques VD; Gonçalves MVM; de Oliveira MF; Tomaselli PJ; Nunez JC; do Nascimento OJM; Barreira AA; Marques W
    J Peripher Nerv Syst; 2018 Jun; 23(2):134-137. PubMed ID: 29520877
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Hereditary transthyretin amyloidosis in mainland China: a unicentric retrospective study.
    Du K; Li F; Wang H; Miao Y; Lv H; Zhang W; Wang Z; Yuan Y; Meng L
    Ann Clin Transl Neurol; 2021 Apr; 8(4):831-841. PubMed ID: 33739616
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Hereditary cardiac amyloidosis associated with Pro24Ser transthyretin mutation: a case report.
    Yamamoto H; Hashimoto T; Kawamura S; Hiroe M; Yamashita T; Ando Y; Yokochi T
    J Med Case Rep; 2018 Dec; 12(1):370. PubMed ID: 30553273
    [TBL] [Abstract][Full Text] [Related]  

  • 19. THAOS - The Transthyretin Amyloidosis Outcomes Survey: initial report on clinical manifestations in patients with hereditary and wild-type transthyretin amyloidosis.
    Coelho T; Maurer MS; Suhr OB
    Curr Med Res Opin; 2013 Jan; 29(1):63-76. PubMed ID: 23193944
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genotype-Phenotype Correlations in ATTR Amyloidosis: A Clinical Update.
    Monda E; Cirillo C; Verrillo F; Palmiero G; Falco L; Aimo A; Emdin M; Merlo M; Limongelli G
    Heart Fail Clin; 2024 Jul; 20(3):317-323. PubMed ID: 38844302
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.