Wireless Sensors to Measure Walking in Patients with Facioscapulohumeral Muscular Dystrophy (FSHD)

被引:0
|
作者
Huisinga, Jessie [2 ]
Bruetsch, Adam [2 ]
Currence, Melissa [2 ]
Herbelin, Laura [1 ]
Jawdat, Omar [2 ]
Pasnoor, Mamatha [2 ]
Dimachkie, Mazen [2 ]
Barohn, Richard [2 ]
Statland, Jeffrey [2 ]
机构
[1] KU Med Ctr, Kansas City, KS USA
[2] Univ Kansas, Med Ctr, Kansas City, KS 66103 USA
关键词
D O I
暂无
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
I8.012
引用
收藏
页数:2
相关论文
共 50 条
  • [1] Facioscapulohumeral muscular dystrophy (FSHD)
    van der Maarel, S. M.
    EUROPEAN JOURNAL OF NEUROLOGY, 2017, 24 : 5 - 5
  • [2] Updates on Facioscapulohumeral Muscular Dystrophy (FSHD)
    Chin, Amanda X. Y.
    Quak, Zhi Xuan
    Chan, Yee Cheun
    Quek, Amy M. L.
    Ng, Kay W. P.
    CURRENT TREATMENT OPTIONS IN NEUROLOGY, 2024, 26 (6) : 261 - 275
  • [3] Epigenetics in Facioscapulohumeral Muscular Dystrophy (FSHD)
    Claustres, Mireille
    HUMAN MUTATION, 2009, 30 (10)
  • [4] Orofacial Muscle Weakening in Facioscapulohumeral Muscular Dystrophy (FSHD) Patients
    Konstantonis, Dimitrios
    Kekou, Kyriaki
    Papaefthymiou, Petros
    Vastardis, Heleni
    Konstantoni, Nikoleta
    Athanasiou, Maria
    Svingou, Maria
    Margariti, Anastasia
    Panousopoulou, Angeliki
    CHILDREN-BASEL, 2022, 9 (01):
  • [5] Facioscapulohumeral muscular dystrophy (FSHD) in monozygotic twins
    Piko, H
    Herczegfalvi, A
    Ban, Z
    Karcagi, V
    NEUROMUSCULAR DISORDERS, 2003, 13 (7-8) : 634 - 634
  • [6] Epigenomic Studies of Facioscapulohumeral Muscular Dystrophy (FSHD)
    Zeng, Weihua
    de Greef, Jessica C.
    Chen, Yen-yun
    Chien, Richard
    Kong, Xiangduo
    Winokur, Sara T.
    Ball, Alexander R., Jr.
    van der Maarel, Silvere M.
    Yokomori, Kyoko
    FASEB JOURNAL, 2010, 24
  • [7] Molecular genetics of facioscapulohumeral muscular dystrophy (FSHD)
    Fisher, J
    Upadhyaya, M
    NEUROMUSCULAR DISORDERS, 1997, 7 (01) : 55 - 62
  • [8] Prenatal diagnosis for facioscapulohumeral muscular dystrophy (FSHD)
    Upadhyaya, M
    MacDonald, M
    Ravine, D
    PRENATAL DIAGNOSIS, 1999, 19 (10) : 959 - 965
  • [9] Facioscapulohumeral muscular dystrophy (FSHD): an enigma unravelled?
    Mark Richards
    Frédérique Coppée
    Nick Thomas
    Alexandra Belayew
    Meena Upadhyaya
    Human Genetics, 2012, 131 : 325 - 340
  • [10] Homozygosity for facioscapulohumeral muscular dystrophy (FSHD) gene
    Canki-Klain, N
    Zagar, M
    Lannoy, N
    Verellen-Dumoulin, C
    Zurak, N
    NEUROMUSCULAR DISORDERS, 2001, 11 (6-7) : 634 - 635