Quantitative oculomotor assessment and non-motor biomarkers in late-onset Tay-Sachs and Sandhoff disease

被引：0
|
作者：
Stephen, Christopher [1 ,2 ]
Balkwill, David [2 ,4 ]
James, Peter [1 ,2 ]
Sassower, Kenneth [1 ,2 ]
Schmahmann, Jeremy [1 ,2 ]
Lewis, Richard [2 ,4 ]
Eichler, Florian [2 ,3 ]
机构：
[1] Massachusetts Gen Hosp, Neurol, Boston, MA 02114 USA
[2] Harvard Med Sch, Boston, MA USA
[3] Massachusetts Gen Hosp, Child Neurol, Boston, MA 02114 USA
[4] Massachusetts Eye & Ear Infirm, Jenks Vestibular Lab, Boston, MA 02114 USA
来源：
NEUROLOGY | 2018年 / 90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：
P1.066
引用
收藏
页数：2
相关论文
共 50 条
  • [21] Pontocerebellar atrophy is the hallmark neuroradiological finding in late-onset Tay-Sachs disease
    Jitka Májovská
    Anita Hennig
    Igor Nestrasil
    Susanne A. Schneider
    Helena Jahnová
    Manuela Vaněčková
    Martin Magner
    Petr Dušek
    Neurological Sciences, 2022, 43 : 3273 - 3281
  • [22] The Natural History of Late Onset Tay-Sachs Disease
    Yerramilli-Rao, Padmaja
    Giannikopoulos, Ourania
    Kublis, Kim
    Pan, Jessica
    Eichler, Florian
    MOLECULAR GENETICS AND METABOLISM, 2012, 105 (02) : S67 - S67
  • [23] Retrospective survey of late onset Tay-Sachs disease
    Karaa, A. Amel
    Haxton, Elizabeth
    Yerramilli-Rao, Padmaja
    Giannikopoulos, Ourania
    Pollak, Lauren
    Morgan, Amy
    Sharma, Nutan
    Kubilus, Kim
    Khan, Susan
    Sathe, Swati
    Tifft, Cynthia
    Pan, Jessica
    Eichler, Florian
    MOLECULAR GENETICS AND METABOLISM, 2016, 117 (02) : S64 - S65
  • [24] The Natural History of Late Onset Tay-Sachs Disease
    Yerramilli-Rao, Padmaja
    Giannikopoulos, Ourania
    Kublis, Kim
    Pan, Jessica
    Eichler, Florian
    NEUROLOGY, 2012, 78
  • [25] Late-onset Tay-Sachs disease presenting with a neuromuscular phenotype-a case series
    Fullam, Sarah
    Togher, Zara
    Power, Alan
    Kennelly, Laura
    McHugh, John C.
    O'Dowd, Sean
    Tubridy, Niall
    Hardiman, Orla
    Costigan, Donal
    Ryan, Aisling
    Lefter, Stela
    Connolly, Sean
    Murphy, Sinead M.
    EUROPEAN JOURNAL OF NEUROLOGY, 2024, 31 (01)
  • [26] MRI volumetric studies of cerebellar atrophy in late-onset Tay-Sachs disease (LOTS)
    Moore, Willa F.
    Shapiro, Barbara E.
    Leigh, R. John
    Ying, Sarah H.
    NEUROLOGY, 2008, 70 (11) : A264 - A264
  • [27] Dysarthria and Stutter as Presenting Symptoms of Late-Onset Tay-Sachs Disease in Three Siblings
    Grim, Kristina K.
    Phillips, Gregory D.
    Renner, David R.
    MOVEMENT DISORDERS CLINICAL PRACTICE, 2015, 2 (03): : 289 - 290
  • [28] Late-onset Tay-Sachs disease:: natural history and treatment with OGT 918 (Zavesca™)
    Kolodny, EH
    Neudorfer, O
    Gianutsos, J
    Zaroff, C
    Barnett, N
    Zeng, B
    Raghavan, S
    Torres, P
    Pastores, G
    JOURNAL OF NEUROCHEMISTRY, 2004, 90 : 54 - 54
  • [29] Late-onset Tay-Sachs disease: The spectrum of peripheral neuropathy in 30 affected patients
    Shapiro, Barbara E.
    Logigian, Eric L.
    Kolodny, Edwin H.
    Pastores, Gregory M.
    MUSCLE & NERVE, 2008, 38 (02) : 1012 - 1015
  • [30] Re: Neurocognitive testing in late-onset Tay-Sachs disease: A pilot study Response
    Elstein, Deborah
    Doniger, Glen M.
    Simon, Ely
    Korn-Lubetzki, Isabelle
    Navon, Ruth
    Zimran, Ari
    JOURNAL OF INHERITED METABOLIC DISEASE, 2009, 32 (02) : 311 - 311
12345