Eplontersen: a promising breakthrough in treating hereditary transthyretin amyloidosis-related polyneuropathy

被引:0
|
作者
Qazi, Muhammad Saeed [1 ]
Tariq, Muhammad Burhan [2 ]
Farhan, Kanza [2 ]
Salomon, Izere [3 ]
机构
[1] Main LUMHS, Bilawal Med Coll Boys BMC, Jamshoro, Pakistan
[2] Jinnah Sindh Med Univ, Sindh Med Coll, Karachi, Pakistan
[3] Univ Rwanda, Coll Med & Hlth Sci, Kigali, Rwanda
来源
ANNALS OF MEDICINE AND SURGERY | 2024年 / 86卷 / 08期
关键词
D O I
10.1097/MS9.0000000000002330
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
引用
收藏
页码:4336 / 4337
页数:2
相关论文
共 50 条
  • [31] Health-related quality of life in hereditary transthyretin amyloidosis polyneuropathy: a prospective, observational study
    Ines, Monica
    Coelho, Teresa
    Conceicao, Isabel
    Ferreira, Lara
    de Carvalho, Mamede
    Costa, Joao
    ORPHANET JOURNAL OF RARE DISEASES, 2020, 15 (01)
  • [32] Clinical characteristics of patients with transthyretin gene mutations and polyneuropathy manifestations of hereditary transthyretin amyloidosis
    Khella, Sami
    Shah, Keyur
    Delgado, Diego
    Marti, Catherine
    Keller, Andrew
    Jefferies, John
    Towne, Meghan
    Gabriel, Aaron
    Narayana, Arvind
    Olugemo, Kemi
    JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM, 2021, 26 (03) : 390 - 391
  • [33] Diagnostic challenges in hereditary transthyretin amyloidosis with polyneuropathy: avoiding misdiagnosis of a treatable hereditary neuropathy
    Cortese, Andrea
    Vegezzi, Elisa
    Lozza, Alessandro
    Alfonsi, Enrico
    Montini, Alessandra
    Moglia, Arrigo
    Merlini, Giampaolo
    Obici, Laura
    JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 2017, 88 (05): : 457 - 458
  • [34] Treatment Satisfaction for Gene Silencing Pharmacotherapies in Hereditary Transthyretin Amyloidosis with Polyneuropathy
    Brown, D.
    Kessler, A. Sikora
    Llonch, M. Vera
    Yarlas, A.
    McCausland, K.
    EUROPEAN JOURNAL OF NEUROLOGY, 2021, 28 : 547 - 547
  • [35] Kind and distribution of cutaneous sensation loss in hereditary transthyretin amyloidosis with polyneuropathy
    Pinto, Marcus V.
    Dyck, P. James B.
    Gove, Linde E.
    McCauley, Bryan M.
    Ackermann, Elizabeth J.
    Hughes, Steven G.
    Waddington-Cruz, Marcia
    Dyck, Peter J.
    JOURNAL OF THE NEUROLOGICAL SCIENCES, 2018, 394 : 78 - 83
  • [36] Responder analysis for neuropathic assessments in patients with hereditary transthyretin amyloidosis with polyneuropathy
    Yarlas, Aaron
    Lovley, Andrew
    Vera-Llonch, Montserrat
    JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM, 2020, 25 (04) : 478 - 478
  • [37] Five-Year Results With Patisiran for Hereditary Transthyretin Amyloidosis With Polyneuropathy
    Adams, David
    Wixner, Jonas
    Polydefkis, Michael
    Berk, John L.
    Conceicao, Isabel M.
    Dispenzieri, Angela
    Peltier, Amanda
    Ueda, Mitsuharu
    Bender, Shaun
    Capocelli, Kelley
    Jay, Patrick Y.
    Yureneva, Elena
    Obici, Laura
    Patisiran Global OLE Study Grp
    JAMA NEUROLOGY, 2025, 82 (03) : 228 - 236
  • [38] A Review of Patisiran (ONPATTRO®) for the Treatment of Polyneuropathy in People with Hereditary Transthyretin Amyloidosis
    Urits, Ivan
    Swanson, Daniel
    Swett, Michael C.
    Patel, Anjana
    Berardino, Kevin
    Amgalan, Ariunzaya
    Berger, Amnon A.
    Kassem, Hisham
    Kaye, Alan
    Viswanath, Omar
    NEUROLOGY AND THERAPY, 2020, 9 (02) : 301 - 315
  • [39] A Review of Patisiran (ONPATTRO®) for the Treatment of Polyneuropathy in People with Hereditary Transthyretin Amyloidosis
    Ivan Urits
    Daniel Swanson
    Michael C. Swett
    Anjana Patel
    Kevin Berardino
    Ariunzaya Amgalan
    Amnon A. Berger
    Hisham Kassem
    Alan D. Kaye
    Omar Viswanath
    Neurology and Therapy, 2020, 9 : 301 - 315
  • [40] Quantitative muscle ultrasound as a disease biomarker in hereditary transthyretin amyloidosis with polyneuropathy
    Tan, Siew Yin
    Tan, Cheng Yin
    Yahya, Mohd Azly
    Low, Soon Chai
    Shahrizaila, Nortina
    Goh, Khean Jin
    NEUROLOGICAL SCIENCES, 2024, 45 (07) : 3449 - 3459