Atypical amyotrophic lateral sclerosis with dementia mimicking frontal Pick's disease: a report of an autopsy case with a clinical course of 15 years

2001 ◽  
Vol 101 (6) ◽  
pp. 625-630 ◽  
Author(s):  
K. Tsuchiya ◽  
K. Ikeda ◽  
C. Haga ◽  
T. Kobayashi ◽  
Y. Morimatsu ◽  
...  
Keyword(s):  
Amyotrophic Lateral Sclerosis ◽  
Clinical Course ◽  
Pick's Disease ◽  
Pick’S Disease ◽  
Autopsy Case ◽  
Lateral Sclerosis

Morphometrical reappraisal of motor neuron system of Pick's disease and amyotrophic lateral sclerosis with dementia

2002 ◽  
Vol 104 (1) ◽  
pp. 21-28 ◽  
Author(s):  
Kenji Ikeda ◽  
Haruhiko Akiyama ◽  
Tetsuaki Arai ◽  
Hideki Ueno ◽  
Kuniaki Tsuchiya ◽  
...  
Keyword(s):  
Amyotrophic Lateral Sclerosis ◽  
Motor Neuron ◽  
Pick's Disease ◽  
Pick’S Disease ◽  
Neuron System ◽  
Lateral Sclerosis

scholarly journals Progress in Clinical Neurosciences: Frontotemporal Dementia-Pick's Disease

2006 ◽  
Vol 33 (2) ◽  
pp. 141-148 ◽  
Author(s):  
Andrew Kertesz
Keyword(s):  
Amyotrophic Lateral Sclerosis ◽  
Frontotemporal Dementia ◽  
Unsolved Problem ◽  
Corticobasal Degeneration ◽  
Primary Progressive Aphasia ◽  
Pick's Disease ◽  
Pick’S Disease ◽  
Diagnostic Features ◽  
Pick Bodies ◽  
Lateral Sclerosis

ABSTRACT:Frontotemporal dementia (clinical Pick's disease) is a relatively common, but underdiagnosed degenerative disease in the presenium. Estimated prevalence ranges from 6-12% of dementias. The behavioural, aphasic and extrapyramidal presentations are labeled FTD-behavioural variant, Primary Progressive Aphasia (PPA) and Corticobasal Degeneration/Progressive Supranuclear Palsy (CBD/PSP). The diagnostic features and course of each are described and their overlap in the evolution of the illness is emphasized. The neuropathology ranges from the most common tau negative ubiquitin positive amyotrophic lateral sclerosis (ALS) type inclusions to the tau positive classical Pick bodies and more or less distinct changes of PSP and CBD. The genetics of the relatively frequent tau mutations and the yet unsolved problem of tau negative families are discussed. The tau negative cases tend to be associated with the behavioural presentation and semantic dementia and the tau positive ones with PPA and the CBD/PSP syndrome. However the overlap is too great to split the disease. A glossary to navigate the proliferating terminology is included.

Pick's disease with amyotrophic lateral sclerosis (ALS): report of two autopsy cases and literature review

1997 ◽  
Vol 148 (1) ◽  
pp. 107-112 ◽  
Author(s):  
Kazuhiro Niizato ◽  
Kuniaki Tsuchiya ◽  
Itaru Tominaga ◽  
Yuji Kato ◽  
Kenji Ikeda
Keyword(s):  
Amyotrophic Lateral Sclerosis ◽  
Literature Review ◽  
Pick's Disease ◽  
Pick’S Disease ◽  
Lateral Sclerosis

Pick's disease: A case clinically resembling amyotrophic lateral sclerosis

Neurology ◽  
1991 ◽  
Vol 41 (11) ◽  
pp. 1831-1831 ◽  
Author(s):  
M. Sam ◽  
L. Gutmann ◽  
S. S. Schochet ◽  
H. Doshi
Keyword(s):  
Amyotrophic Lateral Sclerosis ◽  
Pick's Disease ◽  
Pick’S Disease ◽  
Lateral Sclerosis

scholarly journals An Autopsy Case of Amyotrophic Lateral Sclerosis with Waldenström Macroglobulinemia and Anti-MAG Gammopathy

2011 ◽  
Vol 3 (3) ◽  
pp. 294-300 ◽  
Author(s):  
Snejana Jurici ◽  
Annie Laquerrière ◽  
Anne-Laure Bedat-Millet ◽  
Fabrice Jardin ◽  
Lucile Musset ◽  
...  
Keyword(s):  
Amyotrophic Lateral Sclerosis ◽  
Autopsy Case ◽  
Waldenström Macroglobulinemia ◽  
Waldenstrom Macroglobulinemia ◽  
Lateral Sclerosis

A novel SOD1 mutation in a young amyotrophic lateral sclerosis patient with a very slowly progressive clinical course

2010 ◽  
Vol 42 (4) ◽  
pp. 596-597 ◽  
Author(s):  
Eleni Georgoulopoulou ◽  
Cinzia Gellera ◽  
Cinzia Bragato ◽  
Patrizia Sola ◽  
Annalisa Chiari ◽  
...  
Keyword(s):  
Amyotrophic Lateral Sclerosis ◽  
Clinical Course ◽  
Amyotrophic Lateral Sclerosis Patient ◽  
Sod1 Mutation ◽  
Lateral Sclerosis
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