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 *

202 related articles for article (PubMed ID: 30595768)

  • 21. 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]  

  • 22. Impact of Genetic Testing in Transthyretin (ATTR) Cardiac Amyloidosis.
    Gopal DM; Ruberg FL; Siddiqi OK
    Curr Heart Fail Rep; 2019 Oct; 16(5):180-188. PubMed ID: 31520266
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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]  

  • 24. Preclinical diagnosis of wild-type transthyretin amyloid cardiomyopathy in a patient undergoing carpal tunnel release.
    Nakashima N; Takashio S; Morioka M; Nishi M; Hirakawa K; Hanatani S; Masuda T; Ueda M; Tsujita K
    J Cardiol Cases; 2021 Nov; 24(5):250-253. PubMed ID: 34868409
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [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
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Conjunctival lymphangiectasia and retinal angiopathy in hereditary transthyretin amyloidosis.
    Patil NS; Iqbal MM; Bursztyn LLCD
    Int J Retina Vitreous; 2022 Jan; 8(1):4. PubMed ID: 34991732
    [TBL] [Abstract][Full Text] [Related]  

  • 27. "Red-flag" symptom clusters in transthyretin familial amyloid polyneuropathy.
    Conceição I; González-Duarte A; Obici L; Schmidt HH; Simoneau D; Ong ML; Amass L
    J Peripher Nerv Syst; 2016 Mar; 21(1):5-9. PubMed ID: 26663427
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Hereditary transthyretin amyloidosis: baseline characteristics of patients in the NEURO-TTR trial.
    Waddington-Cruz M; Ackermann EJ; Polydefkis M; Heitner SB; Dyck PJ; Barroso FA; Wang AK; Berk JL; Dyck PJB; Monia BP; Hughes SG; Tai L; Jesse Kwoh T; Jung SW; Coelho T; Benson MD; Gertz MA
    Amyloid; 2018 Sep; 25(3):180-188. PubMed ID: 30169969
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Cardiomyopathy in a Japanese family with the Glu61Lys transthyretin variant: a new phenotype.
    Noto Y; Tokuda T; Shiga K; Tsuchiya A; Yazaki M; Matoba S; Nakagawa M
    Amyloid; 2009; 16(2):99-102. PubMed ID: 20536403
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Impact of Carpal Tunnel Syndrome Surgery on Early Diagnosis and Treatment of Transthyretin Cardiac Amyloidosis.
    Kuznecova I; Mierkyte G; Janciauskas D; Vajauskas D; Jankauskas A; Pilipaityte L; Rimdeika R; Tamaliunas V; Ereminiene E
    Medicina (Kaunas); 2023 Feb; 59(2):. PubMed ID: 36837536
    [No Abstract]   [Full Text] [Related]  

  • 31. Transthyretin Amyloidosis Presenting With Upper-Extremity Neuropathy and Paucity of Autonomic Impairment.
    Devarapalli S; Zhou DJ; Dyck PJB; Piccione EA
    J Clin Neuromuscul Dis; 2019 Jun; 20(4):207-209. PubMed ID: 31135624
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Phenotype of a second Irish variant causing hereditary amyloidogenic transthyretin amyloidosis.
    Asad M; Bermingham N; McNamara B; Kearney P; Ryan AM
    J Neurol; 2022 Sep; 269(9):4802-4807. PubMed ID: 35428899
    [TBL] [Abstract][Full Text] [Related]  

  • 33. High Hereditary Transthyretin-Related Amyloidosis Prevalence in Crete: Genetic Heterogeneity and Distinct Phenotypes.
    Tzagournissakis M; Foukarakis E; Samonakis D; Tsilimbaris M; Michaelidou K; Mathioudakis L; Marinis A; Giannakoudakis E; Spanaki C; Skoula I; Erimaki S; Amoiridis G; Koutsis G; Koukouraki S; Stylianou K; Plaitakis A; Mitsias PD; Zaganas I
    Neurol Genet; 2022 Oct; 8(5):e200013. PubMed ID: 36101541
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Genomic Screening for Pathogenic Transthyretin Variants Finds Evidence of Underdiagnosed Amyloid Cardiomyopathy From Health Records.
    Carry BJ; Young K; Fielden S; Kelly MA; Sturm AC; Avila JD; Martin CL; Kirchner HL; Fornwalt BK; Haggerty CM;
    JACC CardioOncol; 2021 Oct; 3(4):550-561. PubMed ID: 34746851
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Asp58Ala is the predominant mutation of the TTR gene in Korean patients with hereditary transthyretin-related amyloidosis.
    Jang MA; Lee GY; Kim K; Kim SJ; Kim JS; Lee SY; Kim HJ; Jeon ES
    Ann Hum Genet; 2015 Mar; 79(2):99-107. PubMed ID: 25644864
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Diagnosis and therapeutic approaches to transthyretin amyloidosis.
    Ando Y; Ueda M
    Curr Med Chem; 2012; 19(15):2312-23. PubMed ID: 22471980
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Analysis of transthyretin in human serum by capillary zone electrophoresis electrospray ionization time-of-flight mass spectrometry. Application to familial amyloidotic polyneuropathy type I.
    Pont L; Benavente F; Barbosa J; Sanz-Nebot V
    Electrophoresis; 2015 Jun; 36(11-12):1265-73. PubMed ID: 25820240
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Cardiac amyloidosis: updates in diagnosis and management.
    Mohty D; Damy T; Cosnay P; Echahidi N; Casset-Senon D; Virot P; Jaccard A
    Arch Cardiovasc Dis; 2013 Oct; 106(10):528-40. PubMed ID: 24070600
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Transthyretin cardiac amyloidosis: an under-diagnosed cause of heart failure.
    Molina O G; Judge D; Campbell W; Chahal H; Mugmon M
    J Community Hosp Intern Med Perspect; 2014; 4(5):25500. PubMed ID: 25432650
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Transthyretin-Related Familial Amyloid Polyneuropathy (TTR-FAP): A Single-Center Experience in Sicily, an Italian Endemic Area.
    Mazzeo A; Russo M; Di Bella G; Minutoli F; Stancanelli C; Gentile L; Baldari S; Carerj S; Toscano A; Vita G
    J Neuromuscul Dis; 2015 Jul; 2(s2):S39-S48. PubMed ID: 27858761
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.