publication . Article . Other literature type . 2015

Neuropsychological Investigation in Chinese Patients with Progressive Muscular Atrophy

Cui, Bo; Cui, Liying; Liu, Mingsheng; Li, Xiaoguang; Ma, Junfang; Fang, Jia; Ding, Qingyun;
Open Access
  • Published: 04 Jun 2015 Journal: PLOS ONE, volume 10, page e0128883 (eissn: 1932-6203, Copyright policy)
  • Publisher: Public Library of Science (PLoS)
Abstract
Background Progressive muscular atrophy (PMA) is a rare type of degenerative motor neuron disease (MND) of which the onset happens in adult period. Despite its well-defined clinical characteristics, its neuropsychological profile has remained poorly understood, considering the consensus of cognitive and behavioral impairment reached in amyotrophic lateral sclerosis (ALS). Methods We conducted a cross-sectional evaluation of Chinese PMA patients with a series of comprehensive batteries emphasizing the executive and attention function, and covering other domains of memory, language, visuospatial function, calculation and behavior as well. Their performances were c...
Subjects
free text keywords: Dementia, medicine.disease, medicine, Neuropsychology, Atrophy, Motor neuron, medicine.anatomical_structure, Amyotrophic lateral sclerosis, Cognition, Psychiatry, medicine.medical_specialty, Young adult, Progressive muscular atrophy, business.industry, business, Physical medicine and rehabilitation, R, Science, Q, Research Article
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40 references, page 1 of 3

1 Ince PG, Evans J, Knopp M, Forster G, Hamdalla HH, Wharton SB, et al Corticospinal tract degeneration in the progressive muscular atrophy variant of ALS. Neurology. 2003;60:1252–8. 12707426 [PubMed]

2 Murphy JM, Henry RG, Langnlore S, Kramer JH, Miller BL, Lomen-Hoerth C. Continuum of frontal lobe impairment in amyotrophic lateral sclerosis. Arch Neurol. 2007;64:530–4. 17420314 [PubMed]

3 Phukan J, Pender NP, and Hardiman O. Cognitive impairment in amyotrophic lateral sclerosis. Lancet Neurol.2007;6:994–100. 17945153 [OpenAIRE] [PubMed]

4 Lomen-Hoerth C. Clinical phenomenology and neuroimaging correlates in ALS-FTD.J Mol Neurosci. 2011;45:656–62. 10.1007/s12031-011-9636-x 21971978 [OpenAIRE] [PubMed] [DOI]

5 Brooks BR, Miller RG, Swash M, Musat M, World Federation of Neurology Research Group on Motor Neuron Diseases. El Escorial revisited: revised criteria for the diagnosis of amyotrophic lateral sclerosis. Amyotroph Lateral Scler Other Motor Neuron Disord. 2000;1:293–9. 11464847 [PubMed]

6 Brooks BR. El Escorial World Federation of Neurology criteria for the diagnosis of amyotrophic lateral sclerosis. Subcommittee on Motor Neuron Diseases/Amyotrophic Lateral Sclerosis of the World Federation of Neurology Research Group on Neuromuscular Diseases and the El Escorial "Clinical limits of amyotrophic lateral sclerosis" workshop contributors. J Neurol Sci. 1994;124 Suppl: 96–107. 7807156 [PubMed]

7 Cui F, Liu M, Chen Y, Huang X, Cui L Fan D, et al Epidemiological characteristics of motor neuron disease in Chinese patients. Acta Neurol Scand. 2014;130:111–7. 10.1111/ane.12240 24689740 [OpenAIRE] [PubMed] [DOI]

8 Visser J, van den Berg-Vos RM, Franssen H, van den Berg LH, Wokke JH, de Jong JM, et al Disease course and prognostic factors of progressive muscular atrophy. Arch Neurol. 2007;64:522–8 17420313 [PubMed]

9 Liu MS, Cui LY, Fan DS, Chinese ALS Association. Age at onset of amyotrophic lateral sclerosis in China. Acta Neurol Scand. 2014;129:163–7. 10.1111/ane.12157 23819875 [PubMed] [DOI]

10 Cedarbaum JM, Stambler N, Malta E, Fuller C, Hilt D, Thurmond B, et al The ALSFRS-R: a revised ALS functional rating scale that incorporates assessments of respiratory function. BDNF ALS Study Group (Phase III). J Neurol Sci. 1999;169:13–21. 10540002 [OpenAIRE] [PubMed]

11 Hillel AD, Miller RM, Yorkston K, McDonald E, Norris FH, Konikow N. Amyotrophic lateral sclerosis severity scale. Neuroepidemiology. 1989;8:142–50. 2725806 [PubMed]

12 Zhang ZX, Hong X, Li H, Zhao JH, Huang JB Wei J, et al [The Mini-Mental State Examination in population aged 55 years and over in urban and rural areas of Beijing]. Chin J Neurol. 1993;32:149–53. Chinese.

13 Butters N, Granholm E, Salmon DP, Grant I, Wolfe J. Episodic and semantic memory: a comparison of amnesic and demented patients. J Clin Exp Neuropsychol. 1987;9:479–97. 2959682 [PubMed]

14 Shi LL, Hong X, Ni J, Wu LY, Zhang ZX, Wei J. [Validity of verbal fluency in diagnosis of Alzheimer Disease]. Chin J Ment Health. 2009;23:701–5.Chinese

15 Abrahams S, Goldstein LH, Kew JJ, Brooks DJ, Lloyd CM, Frith CD, et al Frontal lobe dysfunction in amyotrophic lateral sclerosis. A PET study. Brain. 1996;119:2105–20. 9010014 [OpenAIRE] [PubMed]

40 references, page 1 of 3
Abstract
Background Progressive muscular atrophy (PMA) is a rare type of degenerative motor neuron disease (MND) of which the onset happens in adult period. Despite its well-defined clinical characteristics, its neuropsychological profile has remained poorly understood, considering the consensus of cognitive and behavioral impairment reached in amyotrophic lateral sclerosis (ALS). Methods We conducted a cross-sectional evaluation of Chinese PMA patients with a series of comprehensive batteries emphasizing the executive and attention function, and covering other domains of memory, language, visuospatial function, calculation and behavior as well. Their performances were c...
Subjects
free text keywords: Dementia, medicine.disease, medicine, Neuropsychology, Atrophy, Motor neuron, medicine.anatomical_structure, Amyotrophic lateral sclerosis, Cognition, Psychiatry, medicine.medical_specialty, Young adult, Progressive muscular atrophy, business.industry, business, Physical medicine and rehabilitation, R, Science, Q, Research Article
Related Organizations
Download fromView all 4 versions
PLoS ONE
Article . 2015
Provider: Crossref
PLoS ONE
Article
Provider: UnpayWall
PLoS ONE
Article . 2015
40 references, page 1 of 3

1 Ince PG, Evans J, Knopp M, Forster G, Hamdalla HH, Wharton SB, et al Corticospinal tract degeneration in the progressive muscular atrophy variant of ALS. Neurology. 2003;60:1252–8. 12707426 [PubMed]

2 Murphy JM, Henry RG, Langnlore S, Kramer JH, Miller BL, Lomen-Hoerth C. Continuum of frontal lobe impairment in amyotrophic lateral sclerosis. Arch Neurol. 2007;64:530–4. 17420314 [PubMed]

3 Phukan J, Pender NP, and Hardiman O. Cognitive impairment in amyotrophic lateral sclerosis. Lancet Neurol.2007;6:994–100. 17945153 [OpenAIRE] [PubMed]

4 Lomen-Hoerth C. Clinical phenomenology and neuroimaging correlates in ALS-FTD.J Mol Neurosci. 2011;45:656–62. 10.1007/s12031-011-9636-x 21971978 [OpenAIRE] [PubMed] [DOI]

5 Brooks BR, Miller RG, Swash M, Musat M, World Federation of Neurology Research Group on Motor Neuron Diseases. El Escorial revisited: revised criteria for the diagnosis of amyotrophic lateral sclerosis. Amyotroph Lateral Scler Other Motor Neuron Disord. 2000;1:293–9. 11464847 [PubMed]

6 Brooks BR. El Escorial World Federation of Neurology criteria for the diagnosis of amyotrophic lateral sclerosis. Subcommittee on Motor Neuron Diseases/Amyotrophic Lateral Sclerosis of the World Federation of Neurology Research Group on Neuromuscular Diseases and the El Escorial "Clinical limits of amyotrophic lateral sclerosis" workshop contributors. J Neurol Sci. 1994;124 Suppl: 96–107. 7807156 [PubMed]

7 Cui F, Liu M, Chen Y, Huang X, Cui L Fan D, et al Epidemiological characteristics of motor neuron disease in Chinese patients. Acta Neurol Scand. 2014;130:111–7. 10.1111/ane.12240 24689740 [OpenAIRE] [PubMed] [DOI]

8 Visser J, van den Berg-Vos RM, Franssen H, van den Berg LH, Wokke JH, de Jong JM, et al Disease course and prognostic factors of progressive muscular atrophy. Arch Neurol. 2007;64:522–8 17420313 [PubMed]

9 Liu MS, Cui LY, Fan DS, Chinese ALS Association. Age at onset of amyotrophic lateral sclerosis in China. Acta Neurol Scand. 2014;129:163–7. 10.1111/ane.12157 23819875 [PubMed] [DOI]

10 Cedarbaum JM, Stambler N, Malta E, Fuller C, Hilt D, Thurmond B, et al The ALSFRS-R: a revised ALS functional rating scale that incorporates assessments of respiratory function. BDNF ALS Study Group (Phase III). J Neurol Sci. 1999;169:13–21. 10540002 [OpenAIRE] [PubMed]

11 Hillel AD, Miller RM, Yorkston K, McDonald E, Norris FH, Konikow N. Amyotrophic lateral sclerosis severity scale. Neuroepidemiology. 1989;8:142–50. 2725806 [PubMed]

12 Zhang ZX, Hong X, Li H, Zhao JH, Huang JB Wei J, et al [The Mini-Mental State Examination in population aged 55 years and over in urban and rural areas of Beijing]. Chin J Neurol. 1993;32:149–53. Chinese.

13 Butters N, Granholm E, Salmon DP, Grant I, Wolfe J. Episodic and semantic memory: a comparison of amnesic and demented patients. J Clin Exp Neuropsychol. 1987;9:479–97. 2959682 [PubMed]

14 Shi LL, Hong X, Ni J, Wu LY, Zhang ZX, Wei J. [Validity of verbal fluency in diagnosis of Alzheimer Disease]. Chin J Ment Health. 2009;23:701–5.Chinese

15 Abrahams S, Goldstein LH, Kew JJ, Brooks DJ, Lloyd CM, Frith CD, et al Frontal lobe dysfunction in amyotrophic lateral sclerosis. A PET study. Brain. 1996;119:2105–20. 9010014 [OpenAIRE] [PubMed]

40 references, page 1 of 3
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publication . Article . Other literature type . 2015

Neuropsychological Investigation in Chinese Patients with Progressive Muscular Atrophy

Cui, Bo; Cui, Liying; Liu, Mingsheng; Li, Xiaoguang; Ma, Junfang; Fang, Jia; Ding, Qingyun;