Diversity in the Charcot-Marie-Tooth disease population in the UK and US: insights from a digital real-world observational study

被引：0
|
作者：
Ziemssen, T. [1 ]
Attarian, S. [2 ]
Thomas, F. P. [3 ]
Moore, A. [4 ]
Tanesse, D. [5 ]
Paoli, X. [6 ]
Bertrand, V. [6 ]
Boutalbi, Y. [6 ]
Bagshaw, E. [7 ]
Kousoulakou, H. [7 ]
Larkin, M. [7 ]
机构：
[1] Carl Gustav Carus Univ Hosp, Dresden, Germany
[2] Hop Marseille, Marseilles, France
[3] Hackensack Univ Med Ctr, Hackensack, NJ USA
[4] Hereditary Neuropathy Fdn, New York, NY USA
[5] European CMT Federat, Fougeres, France
[6] Pharnext SA, Issy Les Moulineaux, France
[7] Vitaccess, Oxford, England
来源：
EUROPEAN JOURNAL OF NEUROLOGY | 2019年 / 26卷
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：
EPO1320
引用
收藏
页码：539 / 539
页数：1
相关论文
共 50 条
  • [41] Hip Dysplasia in Charcot-Marie-Tooth Disease: Insights From a Large Cohort of Children and Adolescents
    Tan, Khian Aun
    Ryan, Monique M.
    Kennedy, Rachel A.
    Carroll, Kate
    de Valle, Katy
    Kollias, Carrie M.
    Yiu, Eppie M.
    JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM, 2025, 30 (01)
  • [42] Prevalence of Symptomatic Charcot-Marie-Tooth Disease in Iceland: A Study of a Well-Defined Population
    Gudmundsson, Bjarni
    Olafsson, Elias
    Jakobsson, Finnbogi
    Luovigsson, Petur
    NEUROEPIDEMIOLOGY, 2010, 34 (01) : 13 - 17
  • [43] CHARCOT-MARIE-TOOTH DISEASE: FREQUENCY OF GENETIC SUBTYPES IN A SOUTHERN ITALY POPULATION
    Manganelli, F.
    Tozza, S.
    Pisciotta, C.
    Bellone, E.
    Iodice, R.
    Dubbioso, R.
    Nolano, M.
    Geroldi, A.
    Capponi, A.
    Mandich, P.
    Santoro, L.
    JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM, 2014, 19 : S20 - S20
  • [44] Charcot-Marie-Tooth disease: frequency of genetic subtypes in a Southern Italy population
    Manganelli, Fiore
    Tozza, Stefano
    Pisciotta, Chiara
    Bellone, Emilia
    Iodice, Rosa
    Nolano, Maria
    Geroldi, Alessandro
    Capponi, Simona
    Mandich, Paola
    Santoro, Lucio
    JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM, 2014, 19 (04) : 292 - 298
  • [45] CHARCOT-MARIE-TOOTH DISEASE - STUDY OF A LARGE KINSHIP WITH AN INTERMEDIATE FORM
    ROSSI, A
    PARADISO, C
    CIONI, R
    RIZZUTO, N
    GUAZZI, G
    JOURNAL OF NEUROLOGY, 1985, 232 (02) : 91 - 98
  • [46] Charcot-Marie-Tooth disease and sleep apnoea syndrome:: a family study
    Dematteis, M
    Pépin, JL
    Jeanmart, M
    Deschaux, C
    Labarre-Vila, A
    Lévy, P
    LANCET, 2001, 357 (9252): : 267 - 272
  • [47] Charcot-Marie-Tooth disease and related disorders: a natural history study
    Laura, M.
    Murphy, S. M.
    Rossor, A.
    Hiscock, A.
    Main, M.
    Shy, M. E.
    Muntoni, F.
    Reilly, M. M.
    NEUROMUSCULAR DISORDERS, 2011, 21 : S17 - S17
  • [48] An epidemiological genetic study of Charcot-Marie-Tooth disease in western Japan
    Kurihara, S
    Adachi, Y
    Wada, K
    Awaki, E
    Harada, H
    Nakashima, K
    NEUROEPIDEMIOLOGY, 2002, 21 (05) : 246 - 250
  • [49] Exploratory Study of Physical Activity in Persons With Charcot-Marie-Tooth Disease
    Anens, Elisabeth
    Emtner, Margareta
    Hellstrom, Karin
    ARCHIVES OF PHYSICAL MEDICINE AND REHABILITATION, 2015, 96 (02): : 260 - 268
  • [50] A pilot study of proximal strength training in Charcot-Marie-Tooth disease
    Ramdharry, Gita M.
    Pollard, Alexander
    Anderson, Cheryl
    Laura, Matilde
    Murphy, Sinead M.
    Dudziec, Magdalena
    Dewar, Elizabeth L.
    Hutton, Elspeth
    Grant, Robert
    Reilly, Mary M.
    JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM, 2014, 19 (04) : 328 - 332
12345