BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

152 related articles for article (PubMed ID: 10842718)

  • 1. Heart failure caused by a novel amyloidogenic mutation of the transthyretin gene: ATTR Ala45Ser.
    Janunger T; Anan I; Holmgren G; Lövheim O; Ohlsson PI; Suhr OB; Tashima K
    Amyloid; 2000 Jun; 7(2):137-40. PubMed ID: 10842718
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Late onset cardiomyopathy as presenting sign of ATTR A45G amyloidosis caused by a novel TTR mutation (p.A65G).
    Klaassen SHC; Lemmink HH; Bijzet J; Glaudemans AWJM; Bos R; Plattel W; van den Berg MP; Slart RHJA; Nienhuis HLA; van Veldhuisen DJ; Hazenberg BPC
    Cardiovasc Pathol; 2017; 29():19-22. PubMed ID: 28460244
    [TBL] [Abstract][Full Text] [Related]  

  • 3. ATTR amyloid in the carpal tunnel ligament is frequently of wildtype transthyretin origin.
    Gioeva Z; Urban P; Meliss RR; Haag J; Axmann HD; Siebert F; Becker K; Radtke HG; Röcken C
    Amyloid; 2013 Mar; 20(1):1-6. PubMed ID: 23244293
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Transthyretin: Its function and amyloid formation.
    Ueda M
    Neurochem Int; 2022 May; 155():105313. PubMed ID: 35218869
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. A new diagnostic procedure to detect unknown transthyretin (TTR) mutations in familial amyloidotic polyneuropathy (FAP).
    Yamashita T; Ando Y; Bernt Suhr O; Nakamura M; Sakashita N; Ohlsson PI; Terazaki H; Obayashi K; Uchino M; Ando M
    J Neurol Sci; 2000 Feb; 173(2):154-9. PubMed ID: 10675660
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Transthyretin Tyr69-to-Ile mutation (double-nucleotide substitution in codon 69) in a Japanese familial amyloidosis patient with cardiomyopathy and carpal tunnel syndrome.
    Takei Y; Hattori T; Yazaki M; Tokuda T; Urasawa N; Kanai S; Ikeda S
    Amyloid; 2003 Mar; 10(1):25-8. PubMed ID: 12762138
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Cardiac Amyloidosis Due to Transthyretin Protein: A Review.
    Ruberg FL; Maurer MS
    JAMA; 2024 Mar; 331(9):778-791. PubMed ID: 38441582
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A novel compound heterozygote (FAP ATTR Arg104His/ATTR Val30Met) with high serum transthyretin (TTR) and retinol binding protein (RBP) levels.
    Terazaki H; Ando Y; Misumi S; Nakamura M; Ando E; Matsunaga N; Shoji S; Okuyama M; Ideta H; Nakagawa K; Ishizaki T; Ando M; Saraiva MJ
    Biochem Biophys Res Commun; 1999 Oct; 264(2):365-70. PubMed ID: 10529370
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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; 12(3):184-8. PubMed ID: 16194874
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A transthyretin mutation (Tyr78Phe) associated with peripheral neuropathy, carpal tunnel syndrome and skin amyloidosis.
    Magy N; Liepnieks JJ; Gil H; Kantelip B; Dupond JL; Kluve-Beckerman B; Benson MD
    Amyloid; 2003 Mar; 10(1):29-33. PubMed ID: 12762139
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Hereditary ATTR Amyloidosis with Cardiomyopathy Caused by the Novel Variant Transthyretin Y114S (p.Y134S).
    Nakase T; Yamashita T; Matsuo Y; Nomura T; Sasada K; Masuda T; Misumi Y; Takamatsu K; Oda S; Furukawa Y; Obayashi K; Matsui H; Ando Y; Ueda M
    Intern Med; 2019 Sep; 58(18):2695-2698. PubMed ID: 31178489
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Nodular cutaneous amyloidosis and carpal tunnel syndrome due to the amyloidogenic transthyretin His 114 variant.
    Mochizuki H; Kamakura K; Masaki T; Hirata A; Tokuda T; Yazaki M; Motoyoshi K; Ikeda S
    Amyloid; 2001 Jun; 8(2):105-10. PubMed ID: 11409031
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Prevalence of germline mutations in the TTR gene in a consecutive series of surgical pathology specimens with ATTR amyloid.
    Eriksson M; Büttner J; Todorov T; Yumlu S; Schönland S; Hegenbart U; Kristen AV; Dengler T; Lohse P; Helmke B; Schmidt H; Röcken C
    Am J Surg Pathol; 2009 Jan; 33(1):58-65. PubMed ID: 18830126
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Tenosynovial and Cardiac Amyloidosis in Patients Undergoing Carpal Tunnel Release.
    Sperry BW; Reyes BA; Ikram A; Donnelly JP; Phelan D; Jaber WA; Shapiro D; Evans PJ; Maschke S; Kilpatrick SE; Tan CD; Rodriguez ER; Monteiro C; Tang WHW; Kelly JW; Seitz WH; Hanna M
    J Am Coll Cardiol; 2018 Oct; 72(17):2040-2050. PubMed ID: 30336828
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Report of five rare or previously unknown amyloidogenic transthyretin mutations disclosed in Sweden.
    Suhr OB; Andersen O; Aronsson T; Jonasson J; Kalimo H; Lundahl C; Lundgren HE; Melberg A; Nyberg J; Olsson M; Sandberg A; Westermark P
    Amyloid; 2009 Dec; 16(4):208-14. PubMed ID: 19922332
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A new transthyretin variant (Glu61Gly) associated with cardiomyopathy.
    Rosenzweig M; Skinner M; Prokaeva T; Théberge R; Costello C; Drachman BM; Connors LH
    Amyloid; 2007 Mar; 14(1):65-71. PubMed ID: 17453626
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Familial amyloid cardiomyopathy masquerading as chronic Guillain-Barre syndrome: things are not always what they seem.
    Hu D; Liu L; Yuan S; Yi Y; Peng D
    Front Med; 2017 Jun; 11(2):293-296. PubMed ID: 28425041
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A new amyloidogenic transthyretin variant, [D38A], detected by electrospray ionization/mass spectrometry.
    Kishikawa M; Nakanishi T; Miyazaki A; Shimizu A; Kusaka H; Fukui M; Nishiue T
    Amyloid; 1999 Dec; 6(4):278-81. PubMed ID: 10611949
    [TBL] [Abstract][Full Text] [Related]  

  • 20. New transthyretin variants SER 91 and SER 116 associated with familial amyloidotic polyneuropathy. Mutations in brief no. 151. Online.
    Misrahi AM; Plante V; Lalu T; Serre L; Adams D; Lacroix DC; Saïd G
    Hum Mutat; 1998; 12(1):71. PubMed ID: 10627135
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.