Transition from agalsidase beta to migalastat in a female Fabry disease patient with recurrent stroke-like episodes

被引:0
|
作者
Wang, Hua [1 ]
机构
[1] Loma Linda Univ, Sch Med, Loma Linda, CA USA
关键词
D O I
10.1016/j.ymgme.2023.108071
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
332
引用
收藏
页数:2
相关论文
共 50 条
  • [1] Dual therapy with migalastat and agalsidase-beta in a patient with Fabry disease with progressing hypertrophic cardiomyopathy
    Stauffer, Chanan
    Balwani, Manisha
    Desnick, Robert J.
    Fierro, Luca
    Ganesh, Jaya
    MOLECULAR GENETICS AND METABOLISM, 2021, 132 (02) : S103 - S103
  • [2] Clinical outcomes after switching to migalastat from agalsidase alfa or agalsidase beta in patients with Fabry disease: Post hoc analysis from ATTRACT
    Sunder-Plassmann, Gere
    Jovanovic, Ana
    Feldt-Rasmussen, Ulla
    Jain, Vipul
    Peceny, Markus
    Skuban, Nina
    Giugliani, Roberto
    MOLECULAR GENETICS AND METABOLISM, 2019, 126 (02) : S141 - S141
  • [3] Clinical outcomes in patients switching from agalsidase beta to migalastat: A Fabry Registry analysis
    Pisani, Antonio
    Wilson, Kathryn M.
    Batista, Julie L.
    Kantola, Ilkka
    Ortiz, Alberto
    Politei, Juan
    Al-Shaar, Laila
    Maski, Manish
    Crespo, Ana
    Ponce, Elvira
    Linhart, Ales
    JOURNAL OF INHERITED METABOLIC DISEASE, 2024, 47 (05) : 1080 - 1095
  • [4] Clinical outcomes in patients switching from agalsidase beta to migalastat: A Fabry Registry analysis
    Pisani, Antonio
    Wilson, Kathryn
    Batista, Julie
    Kantola, Ilkka
    Arduan, Alberto Ortiz
    Politei, Juan
    Al-Shaar, Laila
    Maski, Manish
    Crespo, Ana
    Ponce, Elvira
    Linhart, Ales
    MOLECULAR GENETICS AND METABOLISM, 2024, 141 (02)
  • [5] Novel MTCYB Mutation in a Young Patient with Recurrent Stroke-like Episodes and Status Epilepticus
    Mancuso, Michelangelo
    Nesti, Claudia
    Ienco, Elena Caldarazzo
    Orsucci, Daniele
    Pizzanelli, Chiara
    Chiti, Alberto
    Giorgi, Filippo S.
    Meschini, Maria Chiara
    Fontanini, Gabriella
    Santorelli, Filippo Maria
    Logerfo, Annalisa
    Romano, Alessandro
    Siciliano, Gabriele
    Bonuccelli, Ubaldo
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2014, 164 (11) : 2922 - 2925
  • [6] CONGENITAL LIVEDO-RETICULARIS AND RECURRENT STROKE-LIKE EPISODES
    BAXTER, P
    GARDNERMEDWIN, D
    GREEN, SH
    MOSS, C
    DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY, 1993, 35 (10): : 917 - 921
  • [7] Forecasting stroke-like episodes and outcomes in mitochondrial disease
    Ng, Yi Shiau
    Lax, Nichola Z.
    Blain, Alasdair P.
    Erskine, Daniel
    Baker, Mark R.
    Polvikoski, Tuomo
    Thomas, Rhys H.
    Morris, Christopher M.
    Lai, Ming
    Whittaker, Roger G.
    Gebbels, Alasdair
    Winder, Amy
    Hall, Julie
    Feeney, Catherine
    Farrugia, Maria Elena
    Hirst, Claire
    Roberts, Mark
    Lawthom, Charlotte
    Chrysostomou, Alexia
    Murphy, Kevin
    Baird, Tracey
    Maddison, Paul
    Duncan, Callum
    Poulton, Joanna
    Nesbitt, Victoria
    Hanna, Michael G.
    Pitceathly, Robert D. S.
    Taylor, Robert W.
    Blakely, Emma L.
    Schaefer, Andrew M.
    Turnbull, Doug M.
    McFarland, Robert
    Gorman, Grainne S.
    BRAIN, 2022, 145 (02) : 542 - 554
  • [8] Recurrent stroke-like episodes of Wilson disease with a novel Val176fs mutation
    Lishou Pan
    Dan Ding
    Huilin Leng
    Xinbo Deng
    Yanming Xu
    Neurological Sciences, 2018, 39 : 973 - 974
  • [9] Recurrent stroke-like episodes of Wilson disease with a novel Val176fs mutation
    Pan, Lishou
    Ding, Dan
    Leng, Huilin
    Deng, Xinbo
    Xu, Yanming
    NEUROLOGICAL SCIENCES, 2018, 39 (05) : 973 - 974
  • [10] Recurrent Episodes of Stroke-Like Symptoms Due to Accidental Intoxication With Doxepin
    Gade, Katrin
    Baehr, Mathias
    Kermer, Pawel
    JOURNAL OF NEUROPSYCHIATRY AND CLINICAL NEUROSCIENCES, 2010, 22 (02) : E23 - E23