Therapeutic advances in hereditary ATTR amyloidosis

被引：0
|
作者：
Hawkins, P. [1 ]
机构：
[1] UCL, Royal Free Hosp, Natl Amyloidosis Ctr, London, England
来源：
NEUROMUSCULAR DISORDERS | 2018年 / 28卷
关键词：
D O I：
10.1016/S0960-8966(18)30292-X
中图分类号：
R74 [神经病学与精神病学];
学科分类号：
摘要：
S02
引用
收藏
页码：S1 / S1
页数：1
相关论文
共 50 条
  • [41] Diverse spectrum of hereditary ATTR amyloidosis: polyneuropathy, cardiomyopathy, and cerebral amyloid angiopathy
    Yamashita, Taro
    Ueda, Mitsuharu
    Ando, Yukio
    BRAIN PATHOLOGY, 2019, 29 : 61 - 61
  • [42] Transthyretin Amyloidosis (ATTR)
    Benson, Merrill D.
    BRAIN PATHOLOGY, 2019, 29 : 61 - 62
  • [43] Advances in the treatment of hereditary transthyretin amyloidosis: A review
    Gertz, Morie A.
    Mauermann, Michelle L.
    Grogan, Martha
    Coelho, Teresa
    BRAIN AND BEHAVIOR, 2019, 9 (09):
  • [44] TTR gene silencing therapy in post liver transplant hereditary ATTR amyloidosis patients
    Moshe-Lilie, Orly
    Dimitrova, Diana
    Heitner, Stephen B.
    Brannagan, Thomas H., III
    Zivkovic, Sasha
    Hanna, Mazen
    Masri, Ahmad
    Polydefkis, Michael
    Berk, John L.
    Gertz, Morie A.
    Karam, Chafic
    AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS, 2020, 27 (04): : 250 - 253
  • [45] A Patient With Hereditary ATTR and a Novel AGel p.Ala578Pro Amyloidosis
    Sridharan, Meera
    Highsmith, W. Edward
    Kurtin, Paul J.
    Zimmermann, Michael T.
    Theis, Jason D.
    Dasari, Surendra
    Dingli, David
    MAYO CLINIC PROCEEDINGS, 2018, 93 (11) : 1678 - 1682
  • [46] Screening for Fabry disease and hereditary ATTR amyloidosis in idiopathic small fiber and mixed neuropathy
    Hietaharju, Aki J.
    Samuelsson, Kristin
    Radovic, Ana
    Press, Rayomand
    Auranen, Mari
    Ylikallio, Emil
    Tyynismaa, Henna
    Karppa, Mikko
    Vetelainen, Matilda
    Peltola, Niina
    Mellgren, Svein I.
    Mygland, Ase
    Tallaksen, Chantal
    Andersen, Henning
    Terkelsen, Astrid J.
    Fontain, Freja
    MOLECULAR GENETICS AND METABOLISM, 2019, 126 (02) : S72 - S73
  • [47] Common transthyretin-derived amyloid fibril structures in patients with hereditary ATTR amyloidosis
    Maximilian Steinebrei
    Julian Baur
    Anaviggha Pradhan
    Niklas Kupfer
    Sebastian Wiese
    Ute Hegenbart
    Stefan O. Schönland
    Matthias Schmidt
    Marcus Fändrich
    Nature Communications, 14
  • [48] NEUROSURGICAL PRESENTATION OF HEREDITARY TRANSTHYRETIN (ATTR) AMYLOIDOSIS: EARLY RECOGNITION FOR EARLIER GENETIC THERAPIES
    Kapoor, M.
    Quaegebeur, Annelies
    Shah, Sachit
    Carr, A. S.
    Reilly, M. M.
    JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 2019, 90 (03): : E40 - E41
  • [49] Common transthyretin-derived amyloid fibril structures in patients with hereditary ATTR amyloidosis
    Steinebrei, Maximilian
    Baur, Julian
    Pradhan, Anaviggha
    Kupfer, Niklas
    Wiese, Sebastian
    Hegenbart, Ute
    Schoenland, Stefan O.
    Schmidt, Matthias
    Faendrich, Marcus
    NATURE COMMUNICATIONS, 2023, 14 (01)
  • [50] Neurofilament light chain as a biomarker for monitoring response to change in treatment in hereditary ATTR amyloidosis
    Sato, Mitsuto
    Mochizuki, Yusuke
    Takahashi, Yusuke
    Takasone, Ken
    Aldinc, Emre
    Ticau, Simina
    Jia, Gang
    Sekijima, Yoshiki
    AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS, 2023, 30 (03): : 351 - 352
12345