Frontotemporal lobar degeneration with motor neuron disease showing severe and circumscribed atrophy of anterior temporal lobes

Abstract Frontotemporal lobar degeneration (FTLD) is characterized by a variety of behavioral and psychiatric symptoms based on the dysfunction of frontal and/or temporal lobes. A 63-year-old Japanese man without a family history of neurological diseases developed progressive symptoms of frontotempo...

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Veröffentlicht in:	Journal of the neurological sciences 2010-10, Vol.297 (1), p.92-96
Hauptverfasser:	Kuwahara, Hiroya, Tsuchiya, Kuniaki, Saito, Yukinobu, Kobayashi, Zen, Miyazaki, Hiroshi, Izumiyama, Yoko, Akiyama, Haruhiko, Arai, Tetsuaki, Mizusawa, Hidehiro
Format:	Artikel
Sprache:	eng
Schlagworte:	Amyotrophic lateral sclerosis Antibodies Asian Continental Ancestry Group Atrophy Biological and medical sciences Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases DNA-Binding Proteins - metabolism Frontotemporal dementia Frontotemporal lobar degeneration Frontotemporal Lobar Degeneration - complications Humans Magnetic Resonance Imaging - methods Male Medical sciences Melanins - metabolism Middle Aged Motor neuron disease Motor Neuron Disease - complications Neurology TDP-43 Temporal lobe Temporal Lobe - pathology Ubiquitin - metabolism
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