Cardiac Monitoring of Transplanted Patients for FAP Val30Met

被引：0
|
作者：
Della-Guardia, Bianca [1 ]
Almeida, Marcio D. [1 ]
Felga, Guilherme E. G. [1 ]
Curvelo, Lilian A. [1 ]
Evangelista, Andreia S. [1 ]
Matielo, Celso E. L. [1 ]
Pandullo, Fernando L. [1 ]
Coelho, Maria P. V. [1 ]
Afonso, Rogerio C. [1 ]
Ferraz-Neto, Ben-Hur [1 ]
机构：
[1] Hosp Israelita Albert Einstein, Liver Transplantat Unit, Sao Paulo, Brazil
来源：
LIVER TRANSPLANTATION | 2012年 / 18卷
关键词：
D O I：
暂无
中图分类号：
R57 [消化系及腹部疾病];
学科分类号：
摘要：
引用
收藏
页码：S166 / S166
页数：1
相关论文
共 50 条
  • [41] DPD scintigraphy fails to detect transthyretin cardiac amyloidosis in Val30Met mutation carriers with early onset disease
    Olivella, A.
    Yun, S.
    Belahnech, Y.
    Diez-Lopez, C.
    Garcia-Romero, E.
    Roca Elias, J.
    Manito, N.
    Rodriguez-Palomares, J.
    Gonzalez-Costello, J.
    EUROPEAN JOURNAL OF HEART FAILURE, 2021, 23 : 246 - 247
  • [42] DETECTION OF Val30Met MUTATION BY REAL-TIME PCR IN BRAZILIAN FAMILIES
    Castro, Vanessa F. D.
    Sitnik, Roberta
    Almeida, Marcio D.
    Pinho, Joao R. R.
    Della-Guardia, Bianca
    Alfonso, Rogerio C.
    Ferraz-Neto, Ben-Hur
    LIVER TRANSPLANTATION, 2009, 15 (07) : S123 - S123
  • [43] Angiographic Signatures of the Predominant Form of Familial Transthyretin Amyloidosis (Val30Met Mutation)
    Rousseau, Antoine
    Terrada, Celine
    Touhami, Sara
    Barreau, Emmanuel
    Rothschild, Pierre-Raphael
    Valleix, Sophie
    Benoudiba, Farida
    Errera, Marie-Helene
    Cauquil, Cecile
    Guiochon-Mantel, Anne
    Adams, David
    Labetoulle, Marc
    AMERICAN JOURNAL OF OPHTHALMOLOGY, 2018, 192 : 169 - 177
  • [44] Evidence of the presence of amyloid substance in the blood of familial amyloidotic polyneuropathy patients with ATTR Val30Met mutation
    Liu, Jinping
    Lan, Jie
    Zhao, Peng
    Zheng, Fang
    Song, Jingjing
    Zhang, Peilan
    Sun, Xuguo
    INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL PATHOLOGY, 2014, 7 (11): : 7795 - 7800
  • [45] Heterogeneity of penetrance in familial amyloid polyneuropathy, ATTR Val30Met, in the Swedish population
    Hellman, Urban
    Alarcon, Flora
    Lundgren, Hans-Erik
    Suhr, Ole B.
    Bonaiti-Pellie, Catherine
    Plante-Bordeneuve, Violaine
    AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS, 2008, 15 (03): : 181 - 186
  • [46] Suture trabeculotomy ab interno for secondary glaucoma in Japanese patients with Val30Met hereditary transthyretin amyloidosis
    Takahiro Kawaji
    Tomoki Sato
    Scientific Reports, 12
  • [47] Presence of autoantibody against ATTR Val30Met after sequential after transplantation
    Ando, Y
    Terazaki, H
    Haraoka, K
    Tajiri, T
    Nakamura, M
    Obayashi, K
    Misumi, S
    Shoji, S
    Hata, K
    Nakagawa, K
    Ishizaki, T
    Uemoto, S
    Inomata, Y
    Tanaka, K
    Okabe, H
    TRANSPLANTATION, 2002, 73 (05) : 751 - 755
  • [48] The significance of carpal tunnel syndrome in transthyretin Val30Met familial amyloid polyneuropathy
    Koike, Haruki
    Morozumi, Saori
    Kawagashira, Yuichi
    Iijima, Masahiro
    Yamamoto, Masahiko
    Hattori, Naoki
    Tanaka, Fumiaki
    Nakamura, Tomohiko
    Hirayama, Masaaki
    Ando, Yukio
    Ikeda, Shu-Ichi
    Sobue, Gen
    AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS, 2009, 16 (03): : 142 - 148
  • [49] The functional and structural evaluation of small fibers in asymptomatic carriers of TTR p.Val50Met (Val30Met) mutation
    Bekircan-Kurt, Can Ebru
    Yilmaz, Ezgi
    Arslan, Doruk
    Yildiz, Fatma Gokcem
    Dikmetas, Ozlem
    Ergul-Ulger, Zeynep
    Kocabeyoglu, Sibel
    Irkec, Murat
    Hekimsoy, Vedat
    Tokgozoglu, Lale
    Tan, Ersin
    Erdem-Ozdamar, Sevim
    NEUROMUSCULAR DISORDERS, 2022, 32 (01) : 50 - 56
  • [50] Hereditary amyloidosis by transthyretin: diagnosis of heterozygous mutation Val30Met in two brothers
    Giglio, G.
    Antuzzi, G.
    Carrozza, F.
    Obici, L.
    Musacchio, M.
    AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS, 2010, 17 : 134 - 135
12345