Dysarthria and Stutter as Presenting Symptoms of Late-Onset Tay-Sachs Disease in Three Siblings-Reference-Cited by-同舟云学术

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Dysarthria and Stutter as Presenting Symptoms of Late-Onset Tay-Sachs Disease in Three Siblings

Published:2015-06-30 Issue:3 Volume:2 Page:289-290
ISSN:2330-1619
Container-title:Movement Disorders Clinical Practice
language:en
Short-container-title:Mov Disord Clin Pract

Author:

Grim Kristina K.¹,Phillips Gregory D.¹,Renner David R.¹

Affiliation:

1. Department of Neurology; University of Utah; Salt Lake City Utah USA

Funder

University of Utah Department of Neurology

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/mdc3.12194/fullpdf

Reference8 articles.

1. Late-onset hexosaminidase A deficiency mimicking primary lateral sclerosis;Godeiro-Junior;Arq Neuropsiquiatr,2009

2. Progressive cerebellar ataxia, proximal neurogenic weakness and ocular motor disturbances: hexosaminidase A deficiency with late clinical onset in four siblings;Hund;J Neurol Sci,1997

3. The natural history of juvenile or subacute GM2 gangliosidosis: 21 new cases and literature review of 134 previously reported;Maegawa;Pediatrics,2006

4. Late-onset Tay-Sachs disease presenting as a childhood stutter;Shapiro;J Neurol Neurosurg Psychiatry,2009

5. Ataxia and weakness in a young woman;Beh;Arch Neurol,2012

Cited by 11 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Quantitative brain morphometry identifies cerebellar, cortical, and subcortical gray and white matter atrophy in late‐onset Tay‐Sachs disease;Journal of Inherited Metabolic Disease;2023-12-19

2. Letter response: Intra-familial phenotype variability in Late-Onset Tay-Sachs disease;Tremor and Other Hyperkinetic Movements;2023

3. Relationship between neurochemical concentrations and neurofunctional measures in late-onset GM2 gangliosidosis;2022-09-12

4. The landscape of functional brain network impairments in late-onset GM2 gangliosidosis;2022-09-12

5. Neurodegeneration with progressive dystonia: Juvenile-onset Tay–Sachs disease;Annals of Indian Academy of Neurology;2022

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