BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

179 related articles for article (PubMed ID: 30638075)

  • 1. Sudoscan in the evaluation and follow-up of patients and carriers with TTR mutations: experience from an Italian Centre.
    Luigetti M; Bisogni G; Romano A; Di Paolantonio A; Barbato F; Primicerio G; Rossini PM; Servidei S; Sabatelli M
    Amyloid; 2018 Dec; 25(4):242-246. PubMed ID: 30638075
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Assessment of autonomic innervation of the foot in familial amyloid polyneuropathy.
    Zouari HG; Ng Wing Tin S; Wahab A; Damy T; Lefaucheur JP
    Eur J Neurol; 2019 Jan; 26(1):94-e10. PubMed ID: 30102818
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The diagnostic accuracy of Sudoscan in transthyretin familial amyloid polyneuropathy.
    Castro J; Miranda B; Castro I; de Carvalho M; Conceição I
    Clin Neurophysiol; 2016 May; 127(5):2222-7. PubMed ID: 27072093
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The value of electrochemical skin conductance measurement using Sudoscan® in the assessment of patients with familial amyloid polyneuropathy.
    Lefaucheur JP; Zouari HG; Gorram F; Nordine T; Damy T; Planté-Bordeneuve V
    Clin Neurophysiol; 2018 Aug; 129(8):1565-1569. PubMed ID: 29883834
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Neurophysiological markers of small fibre neuropathy in TTR-FAP mutation carriers.
    Lefaucheur JP; Ng Wing Tin S; Kerschen P; Damy T; Planté-Bordeneuve V
    J Neurol; 2013 Jun; 260(6):1497-503. PubMed ID: 23306657
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Detailed clinical, physiological and pathological phenotyping can impact access to disease-modifying treatments in ATTR carriers.
    Beauvais D; Labeyrie C; Cauquil C; Francou B; Eliahou L; Not A; Echaniz-Laguna A; Adam C; Slama MS; Benmalek A; Leonardi L; Rouzet F; Adams D; Algalarrondo V; Beaudonnet G
    J Neurol Neurosurg Psychiatry; 2024 May; 95(6):489-499. PubMed ID: 37875336
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Quantitative sudomotor test helps differentiate transthyretin familial amyloid polyneuropathy from chronic inflammatory demyelinating polyneuropathy.
    Fortanier E; Delmont E; Verschueren A; Attarian S
    Clin Neurophysiol; 2020 May; 131(5):1129-1133. PubMed ID: 32217467
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Correlation between Sudoscan and COMPASS 31: assessment of autonomic dysfunction on hATTR V30M patients.
    Conceição I; de Castro I; Castro J
    Amyloid; 2019; 26(sup1):23. PubMed ID: 31343356
    [No Abstract]   [Full Text] [Related]  

  • 10. Monitoring effectiveness and safety of Tafamidis in transthyretin amyloidosis in Italy: a longitudinal multicenter study in a non-endemic area.
    Cortese A; Vita G; Luigetti M; Russo M; Bisogni G; Sabatelli M; Manganelli F; Santoro L; Cavallaro T; Fabrizi GM; Schenone A; Grandis M; Gemelli C; Mauro A; Pradotto LG; Gentile L; Stancanelli C; Lozza A; Perlini S; Piscosquito G; Calabrese D; Mazzeo A; Obici L; Pareyson D
    J Neurol; 2016 May; 263(5):916-924. PubMed ID: 26984605
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Early skin denervation in hereditary and iatrogenic transthyretin amyloid neuropathy.
    Masuda T; Ueda M; Suenaga G; Misumi Y; Tasaki M; Izaki A; Yanagisawa Y; Inoue Y; Motokawa H; Matsumoto S; Mizukami M; Arimura A; Deguchi T; Nishio Y; Yamashita T; Inomata Y; Obayashi K; Ando Y
    Neurology; 2017 Jun; 88(23):2192-2197. PubMed ID: 28490654
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Early diagnostic tools in hereditary amyloidosis related to transthyretin (hATTR) V30M autonomic neuropathy.
    de Campos CF; Conceição I; Castro I
    Amyloid; 2019; 26(sup1):35-36. PubMed ID: 31343294
    [No Abstract]   [Full Text] [Related]  

  • 13. Early diagnosis of ATTR amyloidosis through targeted follow-up of identified carriers of TTR gene mutations.
    Conceição I; Damy T; Romero M; Galán L; Attarian S; Luigetti M; Sadeh M; Sarafov S; Tournev I; Ueda M
    Amyloid; 2019 Mar; 26(1):3-9. PubMed ID: 30793974
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Serum neurofilament light chain as a reliable biomarker of hereditary transthyretin-related amyloidosis-A Swiss reference center experience.
    Loser V; Benkert P; Vicino A; Lim Dubois Ferriere P; Kuntzer T; Pasquier J; Maceski A; Kuhle J; Theaudin M
    J Peripher Nerv Syst; 2023 Mar; 28(1):86-97. PubMed ID: 36471582
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Small fibre neuropathy assessments in early stages of hATTR amyloidosis.
    González-Duarte A; Cárdenas-Soto K; Fueyo O; Bañuelos CE; Gibbons C; Freeman R
    Amyloid; 2019; 26(sup1):55-56. PubMed ID: 31343296
    [No Abstract]   [Full Text] [Related]  

  • 17. Familial ATTR amyloidosis: microalbuminuria as a predictor of symptomatic disease and clinical nephropathy.
    Lobato L; Beirão I; Silva M; Bravo F; Silvestre F; Guimarães S; Sousa A; Noël LH; Sequeiros J
    Nephrol Dial Transplant; 2003 Mar; 18(3):532-8. PubMed ID: 12584275
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Transthyretin (ATTR) amyloidosis: clinical spectrum, molecular pathogenesis and disease-modifying treatments.
    Sekijima Y
    J Neurol Neurosurg Psychiatry; 2015 Sep; 86(9):1036-43. PubMed ID: 25604431
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Pupillometric findings in ATTRv patients and carriers: results from a single-centre experience.
    Romano A; Guglielmino V; Di Paolantonio A; Bisogni G; Sabatelli M; Della Marca G; Minnella AM; Maceroni M; Bellavia S; Scala I; Sabatelli E; Rollo E; Luigetti M
    Amyloid; 2022 Dec; 29(4):270-275. PubMed ID: 36066019
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Misdiagnosis in late versus early onset hATTR amyloidosis patients: experience from a reference centre.
    Falcão de Campos C; Parreira S; Conceição I
    Amyloid; 2019; 26(sup1):37-38. PubMed ID: 31343293
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 9.