BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

213 related articles for article (PubMed ID: 34207092)

  • 1. Ocular Involvement in Hereditary Transthyretin Amyloidosis: A Case Series Describing Novel Potential Biomarkers.
    Minnella AM; Rissotto R; Maceroni M; Romano A; Fasciani R; Luigetti M; Sabatelli M; Rizzo S; Falsini B
    Genes (Basel); 2021 Jun; 12(6):. PubMed ID: 34207092
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Deposits on Retinal Surface Seen on OCT in Ocular Amyloidosis.
    Kakihara S; Hirano T; Matsuda Y; Takano D; Imai A; Miyahara T; Murata T
    Ophthalmol Retina; 2021 Oct; 5(10):1005-1008. PubMed ID: 33422693
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Multimodal retinal imaging in a Chinese kindred with familial amyloid polyneuropathy secondary to transthyretin Ile107Met mutation.
    Lv W; Chen J; Chen W; Hou P; Pang CP; Chen H
    Eye (Lond); 2014 Apr; 28(4):452-8. PubMed ID: 24480837
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Ocular Manifestations in a Chinese Pedigree of Familial Amyloidotic Polyneuropathy Carrying the Transthyretin Mutation c.401A>G (p.Tyr134Cys).
    Zhuang X; Sun Z; Gao F; Wang M; Tang W; Liu W; Wang K; Wu J; Jiang R; Xu G
    Genes (Basel); 2022 May; 13(5):. PubMed ID: 35627273
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Ocular Manifestations of Familial Transthyretin Amyloidosis.
    Reynolds MM; Veverka KK; Gertz MA; Dispenzieri A; Zeldenrust SR; Leung N; Pulido JS
    Am J Ophthalmol; 2017 Nov; 183():156-162. PubMed ID: 28911993
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Transthyretin Ala36Pro mutation in a Chinese pedigree of familial transthyretin amyloidosis with elevated vitreous and serum vascular endothelial growth factor.
    Zou X; Dong F; Zhang S; Tian R; Sui R
    Exp Eye Res; 2013 May; 110():44-9. PubMed ID: 23438977
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Ophthalmological involvement in wild-type transthyretin amyloidosis: A multimodal imaging study.
    Frizziero L; Salvalaggio A; Cosmo E; Cipriani A; Midena E; Briani C
    J Peripher Nerv Syst; 2023 Dec; 28(4):586-596. PubMed ID: 37552555
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Subclinical retinal angiopathy associated with hereditary transthyretin amyloidosis - assessed with optical coherence tomography angiography.
    Marques JH; Coelho J; Malheiro J; Pessoa B; Beirão JM
    Amyloid; 2021 Mar; 28(1):66-71. PubMed ID: 32996337
    [TBL] [Abstract][Full Text] [Related]  

  • 9. OCULAR MANIFESTATIONS OF ASP38ALA AND THR59LYS FAMILIAL TRANSTHYRETIN AMYLOIDOSIS.
    Choi KJ; Son KY; Kang SW; Kim D; Choi JO; Kim HJ; Kim JS; Jeon ES; Kim AY; Kang MC; Kim SJ
    Retina; 2022 Feb; 42(2):396-403. PubMed ID: 34483316
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Ocular Involvement in Hereditary Amyloidosis.
    Minnella AM; Rissotto R; Antoniazzi E; Di Girolamo M; Luigetti M; Maceroni M; Bacherini D; Falsini B; Rizzo S; Obici L
    Genes (Basel); 2021 Jun; 12(7):. PubMed ID: 34206500
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Vutrisiran: A Review in Polyneuropathy of Hereditary Transthyretin-Mediated Amyloidosis.
    Nie T; Heo YA; Shirley M
    Drugs; 2023 Oct; 83(15):1425-1432. PubMed ID: 37728865
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Corneal confocal microscopy identifies corneal nerve loss and increased Langerhans cells in presymptomatic carriers and patients with hereditary transthyretin amyloidosis.
    Thimm A; Carpinteiro A; Oubari S; Papathanasiou M; Kessler L; Rischpler C; Malik RA; Herrmann K; Reinhardt HC; Rassaf T; Kleinschnitz C; Hagenacker T; Stettner M
    J Neurol; 2023 Jul; 270(7):3483-3491. PubMed ID: 37014422
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Ganglion cell loss in early glaucoma, as assessed by photopic negative response, pattern electroretinogram, and spectral-domain optical coherence tomography.
    Cvenkel B; Sustar M; Perovšek D
    Doc Ophthalmol; 2017 Aug; 135(1):17-28. PubMed ID: 28567618
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Familial Oculo-Leptomeningeal Transthyretin Amyloidosis Caused by Leu55Arg Mutation.
    Kleefeld F; Knebel F; Eurich D; Schatka I; Blüthner E; Schönfeld S; Amthauer H; Hahn K
    J Neuromuscul Dis; 2020; 7(4):515-519. PubMed ID: 32741838
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Ocular Morpho-Functional Evaluation in ATTRv Pre-Symptomatic Carriers: A Case Series.
    Maceroni M; Falsini B; Luigetti M; Romano A; Guglielmino V; Fasciani R; Placidi G; D'Agostino E; Sasso P; Rizzo S; Minnella AM
    Diagnostics (Basel); 2023 Jan; 13(3):. PubMed ID: 36766465
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Ophthalmological manifestations in hereditary transthyretin (ATTR V30M) carriers: a review of 513 cases.
    Beirão JM; Malheiro J; Lemos C; Beirão I; Costa P; Torres P
    Amyloid; 2015; 22(2):117-22. PubMed ID: 26096568
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Population Pharmacokinetic-Pharmacodynamic Modeling of Inotersen, an Antisense Oligonucleotide for Treatment of Patients with Hereditary Transthyretin Amyloidosis.
    Yu RZ; Collins JW; Hall S; Ackermann EJ; Geary RS; Monia BP; Henry SP; Wang Y
    Nucleic Acid Ther; 2020 Jun; 30(3):153-163. PubMed ID: 32286934
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A case of transthyretin-related cerebral amyloid angiopathy. The other side of hereditary transthyretin amyloidosis.
    Lemarchant B; Lebouvier T; Delbeuck X; Gibier JB; Tard C
    Acta Neurol Belg; 2022 Apr; 122(2):571-573. PubMed ID: 35040071
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Epigenetic profiling of Italian patients identified methylation sites associated with hereditary transthyretin amyloidosis.
    De Lillo A; Pathak GA; De Angelis F; Di Girolamo M; Luigetti M; Sabatelli M; Perfetto F; Frusconi S; Manfellotto D; Fuciarelli M; Polimanti R
    Clin Epigenetics; 2020 Nov; 12(1):176. PubMed ID: 33203445
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.