Patients with hereditary ATTR amyloidosis experience an increasing burden of illness as the disease progresses

被引：0
|
作者：
David Adams
Oved Amitay
Teresa Coelho
机构：
[1] Univ Paris-Sud,Hopital de Bicetre, Service de Neurologie and Centre de Reference des Neuropathies Amyloides Familiales (NNERF), INSERM U1195
[2] APHP,Commercial
[3] Alnylam Pharmaceuticals,Unidade Clinica de Paramiloidose
[4] Hospital de Santo Antonio,undefined
来源：
Orphanet Journal of Rare Diseases | / 10卷 / Suppl 1期
关键词：
Employment Status; Amyloidosis; Disease Burden; Polyneuropathy; Perceive Health Status;
D O I：
10.1186/1750-1172-10-S1-P58
中图分类号：
学科分类号：
摘要：
引用
收藏
相关论文
共 50 条
  • [21] Disease burden of ATTR amyloidosis based on the SF-36v2® health survey
    Sanchorawala, Vaishali
    Greatsinger, Alexandra
    Staron, Andrew
    Berk, John
    Mendelson, Lisa
    Joshi, Tracy
    Burke, Natasha
    Tabatabaeepour, Nadia
    Smith, Jess
    Signorovitch, James
    AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS, 2024, 31 : S86 - S86
  • [22] Axonal excitability in hereditary TTR amyloidosis is consistent with sensory disease burden
    Carroll, Antonia
    Howells, James
    Lin, Cindy
    Park, Susanna
    Simon, Neil
    Reilly, Mary
    Vucic, Steve
    Kiernan, Matthew
    JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM, 2020, 25 (04) : 472 - 472
  • [23] Tetraparesis and sensorimotor axonal polyneuropathy due to co-occurrence of Pompe disease and hereditary ATTR amyloidosis
    Zimmermann, Milan
    Deininger, Natalie
    Willikens, Sophia
    Haack, Tobias B.
    Grundmann-Hauser, Kathrin
    Streubel, Berthold
    Schreiber, Melanie
    Lerche, Holger
    Grimm, Alexander
    NEUROLOGICAL SCIENCES, 2021, 42 (04) : 1523 - 1525
  • [24] Tetraparesis and sensorimotor axonal polyneuropathy due to co-occurrence of Pompe disease and hereditary ATTR amyloidosis
    Milan Zimmermann
    Natalie Deininger
    Sophia Willikens
    Tobias B. Haack
    Kathrin Grundmann-Hauser
    Berthold Streubel
    Melanie Schreiber
    Holger Lerche
    Alexander Grimm
    Neurological Sciences, 2021, 42 : 1523 - 1525
  • [25] HEREDITARY ANGIOEDEMA IN AUSTRALIA: PATIENT EXPERIENCE AND BURDEN OF DISEASE
    Katelaris, Constance H.
    King, Nicole
    INTERNAL MEDICINE JOURNAL, 2012, 42 : 9 - 10
  • [26] Pathological and biochemical changes of tissue deposited amyloid protein by liver transplantation in hereditary ATTR amyloidosis patients
    Yazaki, Masahide
    BRAIN PATHOLOGY, 2019, 29 : 61 - 61
  • [27] Preliminary assessment of neuropathy progression in patients with hereditary ATTR amyloidosis after orthotopic liver transplantation (OLT)
    David Adams
    Juan Buades
    Ole Suhr
    Laura Obici
    Teresa Coelho
    Orphanet Journal of Rare Diseases, 10 (Suppl 1)
  • [28] MEASUREMENT PROPERTIES OF THE RASCH-BUILT OVERALL DISABILITY SCALE IN PATIENTS WITH HEREDITARY ATTR AMYLOIDOSIS WITH POLYNEUROPATHY
    Regnault, A.
    Denoncourt, R. N.
    Strahs, A.
    Agarwal, S.
    Marquis, P.
    Cano, S.
    VALUE IN HEALTH, 2017, 20 (05) : A330 - A330
  • [29] The global patient experience of transthyretin amyloidosis (ATTR): symptoms and quality-of-life impacts of ATTR among patients in 11 countries
    Broderick, Lynne
    O'Connor, Meaghan
    Brown, Duncan
    Llonch, Montserrat Vera
    Hsu, Kristen
    McCausland, Kristen
    White, Michelle
    QUALITY OF LIFE RESEARCH, 2021, 30 (SUPPL 1) : S37 - S37
  • [30] Diflunisal is Associated With Improved Mortality in Patients With Wild-Type ATTR Cardiac Amyloidosis: The BU Amyloidosis Center Experience
    Mints, Yuliya Y.
    Berk, John L.
    Connors, Lawreen
    Doros, Gheorghe
    Gopal, Deepa M.
    Kataria, Shivangi
    Lohrmann, Graham
    Pipilas, Alexandra R.
    Ruberg, Frederick L.
    Siddiqi, Omar K.
    CIRCULATION, 2019, 140
12345