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Volumn 260, Issue 6, 2013, Pages 1667-1669

Amyotrophic lateral sclerosis presenting with apraxia of speech

Author keywords

[No Author keywords available]

Indexed keywords

AGED; AMYOTROPHIC LATERAL SCLEROSIS; APRAXIA OF SPEECH; ATROPHY; CASE REPORT; COMPUTER ASSISTED TOMOGRAPHY; DENERVATION; DYSPHAGIA; ELECTROMYOGRAPHY; FASCICULATION; FEMALE; FUNCTIONAL NEUROIMAGING; HUMAN; HYPERREFLEXIA; LETTER; MIDDLE TEMPORAL GYRUS; NERVE CONDUCTION; PRIMARY MOTOR CORTEX; PRIORITY JOURNAL; QUADRIPLEGIA; SINGLE PHOTON EMISSION COMPUTER TOMOGRAPHY; TENDON REFLEX; TONGUE DISEASE;

EID: 84878835857     PISSN: 03405354     EISSN: 14321459     Source Type: Journal    
DOI: 10.1007/s00415-013-6920-4     Document Type: Letter
Times cited : (4)

References (6)
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    • Is lesion of Exner's area linked to progressive agraphia in amyotrophic lateral sclerosis with dementia? An autopsy case report
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    • Ishihara K, Ichikawa H, Suzuki Y, Shiota J, Nakano I, Kawamura M (2010) Is lesion of Exner's area linked to progressive agraphia in amyotrophic lateral sclerosis with dementia? An autopsy case report. Behav Neurol 23:153-158
    • (2010) Behav Neurol , vol.23 , pp. 153-158
    • Ishihara, K.1    Ichikawa, H.2    Suzuki, Y.3    Shiota, J.4    Nakano, I.5    Kawamura, M.6
  • 3
    • 84855383680 scopus 로고    scopus 로고
    • Co-occurrence of progressive anarthria with an S393L TARDBP mutation and ALS within a family
    • 21830990 10.3109/17482968.2011.598168 1:CAS:528:DC%2BC38Xjs1Wkug%3D%3D
    • Praline J, Vourch P, Guennoc AM, Veyrat-Durebex C, Corcia P (2012) Co-occurrence of progressive anarthria with an S393L TARDBP mutation and ALS within a family. Amyotroph Lateral Scler 13:155-157
    • (2012) Amyotroph Lateral Scler , vol.13 , pp. 155-157
    • Praline, J.1    Vourch, P.2    Guennoc, A.M.3    Veyrat-Durebex, C.4    Corcia, P.5
  • 4
    • 80054832080 scopus 로고    scopus 로고
    • Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS
    • 21944778 10.1016/j.neuron.2011.09.011 1:CAS:528:DC%2BC3MXhtlKrtL%2FP
    • DeJesus-Hernandez M, Mackenzie IR, Boeve BF et al (2011) Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS. Neuron 72:245-256
    • (2011) Neuron , vol.72 , pp. 245-256
    • Dejesus-Hernandez, M.1    Mackenzie, I.R.2    Boeve, B.F.3
  • 6
    • 84867044452 scopus 로고    scopus 로고
    • The diagnosis and understanding of apraxia of speech: Why including neurodegenerative etiologies may be important
    • 23033445 10.1044/1092-4388(2012/11-0309)
    • Duffy JR, Josephs KA (2012) The diagnosis and understanding of apraxia of speech: why including neurodegenerative etiologies may be important. J Speech Lang Hear Res 55:S1518-S1522
    • (2012) J Speech Lang Hear Res , vol.55
    • Duffy, J.R.1    Josephs, K.A.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.