Choroidal and retinal angiopathy in V30M hereditary transthyretin amyloidosis

被引：0
|
作者：
Rousseau, Antoine [1 ,2 ]
Terrada, Celine [3 ,4 ]
Touhami, Sara [1 ]
Barreau, Emmanuel [1 ,2 ]
Rothschild, Pierre-Raphael [5 ]
Valleix, Sophie [6 ]
Errera, Marie-Helene [7 ]
Cauquil, Cecile [2 ,8 ]
Guiochon-Mantel, Anne [2 ,9 ]
Adams, David [2 ,8 ]
Labetoulle, Marc [1 ,2 ]
机构：
[1] Univ Paris Sud, DHU Vis & Handicap, Hop Bicetre, AP HP,Ophthalmol, Le Kremlin Bicetre, France
[2] Ctr Reference Neuropathies Amyloides Familiales &, Le Kremlin Bicetre, France
[3] Hop Lariboisiere, Ophthalmol, Paris, France
[4] Ctr Reference Malad Vasc Rares Syst Nerveux Cent, Paris, France
[5] Paris Ouest Univ, Cochin Hosp, AP HP, Ophthalmol, Paris, France
[6] Paris Ouest Univ, Cochin Hosp, AP HP, Lab Biochim & Genet Mol, Paris, France
[7] DHU Vis & Handicaps, Quinze Vingts Natl Eye Ctr, Ophthalmol, Paris, France
[8] Univ Paris Sud, Hop Bicetre, AP HP, Neurol, Le Kremlin Bicetre, France
[9] Univ Paris Sud, Hop Bicetre, AP HP, Biochim & Genet Mol, Le Kremlin Bicetre, France
来源：
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE | 2017年 / 58卷 / 08期
关键词：
D O I：
暂无
中图分类号：
R77 [眼科学];
学科分类号：
100212 ;
摘要：
1556
引用
收藏
页数：4
相关论文
共 50 条
  • [1] Coexistence of transthyretin- and Aβ-type cerebral amyloid angiopathy in a patient with hereditary transthyretin V30M amyloidosis
    Sakai, Kenji
    Asakawa, Miwako
    Takahashi, Ryoichi
    Ishida, Chiho
    Nakamura, Ritsuko
    Hamaguchi, Tsuyoshi
    Ono, Kenjiro
    Iwasa, Kazuo
    Yamada, Masahito
    BRAIN PATHOLOGY, 2019, 29 : 18 - 18
  • [2] Coexistence of transthyretin- and Aβ-type cerebral amyloid angiopathy in a patient with hereditary transthyretin V30M amyloidosis
    Sakai, Kenji
    Asakawa, Miwako
    Takahashi, Ryoichi
    Ishida, Chiho
    Nakamura, Ritsuko
    Hamaguchi, Tsuyoshi
    Ono, Kenjiro
    Iwasa, Kazuo
    Yamada, Masahito
    JOURNAL OF THE NEUROLOGICAL SCIENCES, 2017, 381 : 144 - 146
  • [3] Hereditary transthyretin amyloidosis V30M: intrafamilial phenotypic variability
    Dourado Sotero, F.
    Campos, C.
    Conceicao, I.
    EUROPEAN JOURNAL OF NEUROLOGY, 2019, 26 : 541 - 541
  • [4] Brain MRI in patients with V30M hereditary transthyretin amyloidosis
    Sousa, Luisa
    Pinto, Catarina
    Azevedo, Ana
    Igreja, Liliana
    Marta, Ana
    Fernandes, Joana
    Oliveira, Pedro
    Cardoso, Marcio
    Alves, Cristina
    da Silva, Ana Martins
    Pinto, Miguel Mendonca
    Sousa, Ana Paula
    Coelho, Teresa
    Taipa, Ricardo
    AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS, 2024, 31 (04): : 285 - 290
  • [5] Amyloid fibril composition is related to the phenotype of hereditary transthyretin V30M amyloidosis
    Ihse, E.
    Ybo, A.
    Suhr, O. B.
    Lindqvist, P.
    Backman, C.
    Westermark, P.
    JOURNAL OF PATHOLOGY, 2008, 216 (02): : 253 - 261
  • [6] Nerve ultrasonography features in hereditary transthyretin amyloidosis with V30M mutation and polyneuropathy
    Alessandro Salvalaggio
    Daniele Coraci
    Mario Cacciavillani
    Luca Padua
    Chiara Briani
    Neurological Sciences, 2021, 42 : 2547 - 2548
  • [7] Nerve ultrasonography features in hereditary transthyretin amyloidosis with V30M mutation and polyneuropathy
    Salvalaggio, Alessandro
    Coraci, Daniele
    Cacciavillani, Mario
    Padua, Luca
    Briani, Chiara
    NEUROLOGICAL SCIENCES, 2021, 42 (06) : 2547 - 2548
  • [8] NEUROARTHROPATHY SECONDARY TO TRANSTHYRETIN AMYLOIDOSIS (ATTR V30M)
    Wilmes, D.
    Wautier, D.
    Jonckheere, S.
    Cornu, O.
    Yombi, J. C.
    ACTA CLINICA BELGICA, 2012, 67 (05): : 372 - 374
  • [9] Hereditary amyloidosis related to transthyretin V30M: disease progression in treated and untreated patients
    Conceicao, I.
    Miranda, B.
    Castro, J.
    de Carvalho, M.
    EUROPEAN JOURNAL OF NEUROLOGY, 2018, 25 (11) : 1320 - E115
  • [10] Portuguese-type amyloidosis (transthyretin amyloidosis, ATTR V30M)
    Lobato, L
    JOURNAL OF NEPHROLOGY, 2003, 16 (03) : 438 - 442
12345