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Acta Neuropathologica
|
October 5, 2001
Familial frontotemporal dementia and parkinsonism with a novel N296H mutation in exon 10 of the tau gene and a widespread tau accumulation in the glial cells
E Iseki, T Matsumura, W Marui, et al.
Neurological Research
|
December 29, 1998
Japanese Creutzfeldt-Jakob disease patients exhibiting high incidence of the E200K PRNP mutation and located in the basin of a river
T Miyakawa, K Inoue, E Iseki, et al.
Journal of the Neurological Sciences
|
March 1, 1996
Neuropathological evaluation and apolipoprotein E gene polymorphism analysis in diffuse Lewy body disease
C Kawanishi, K Suzuki, T Odawara, et al.
Journal of Medical Genetics
|
April 16, 1998
Pancreatic exocrine dysfunction associated with mitochondrial tRNA(Leu)(UUR) mutation
H Onishi, T Hanihara, N Sugiyama, et al.
Neuroscience Letters
|
March 21, 1997
Glial tau-positive structures lack the sequence encoded by exon 3 of the tau protein gene
T Nishimura, K Ikeda, H Akiyama, et al.
Journal of the Neurological Sciences
|
June 24, 2000
Familial frontotemporal dementia with a P301L tau mutation in Japan
K Kodama, S Okada, E Iseki, et al.
Neuropathology and Applied Neurobiology
|
July 27, 2006
Comparison of extent of tau pathology in patients with frontotemporal dementia with Parkinsonism linked to chromosome 17 (FTDP-17), frontotemporal lobar degeneration with Pick bodies and early onset Alzheimer's disease
A-M Shiarli, R Jennings, J Shi, et al.
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of 6
Search research articles
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Showing results (51-60 of 57) with videos related to
Sort By:
Page
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You have reached the last page of results.
This site can display upto 57 results.
Acta Neuropathologica
|
October 5, 2001
Familial frontotemporal dementia and parkinsonism with a novel N296H mutation in exon 10 of the tau gene and a widespread tau accumulation in the glial cells
E Iseki, T Matsumura, W Marui, et al.
Neurological Research
|
December 29, 1998
Japanese Creutzfeldt-Jakob disease patients exhibiting high incidence of the E200K PRNP mutation and located in the basin of a river
T Miyakawa, K Inoue, E Iseki, et al.
Journal of the Neurological Sciences
|
March 1, 1996
Neuropathological evaluation and apolipoprotein E gene polymorphism analysis in diffuse Lewy body disease
C Kawanishi, K Suzuki, T Odawara, et al.
Journal of Medical Genetics
|
April 16, 1998
Pancreatic exocrine dysfunction associated with mitochondrial tRNA(Leu)(UUR) mutation
H Onishi, T Hanihara, N Sugiyama, et al.
Neuroscience Letters
|
March 21, 1997
Glial tau-positive structures lack the sequence encoded by exon 3 of the tau protein gene
T Nishimura, K Ikeda, H Akiyama, et al.
Journal of the Neurological Sciences
|
June 24, 2000
Familial frontotemporal dementia with a P301L tau mutation in Japan
K Kodama, S Okada, E Iseki, et al.
Neuropathology and Applied Neurobiology
|
July 27, 2006
Comparison of extent of tau pathology in patients with frontotemporal dementia with Parkinsonism linked to chromosome 17 (FTDP-17), frontotemporal lobar degeneration with Pick bodies and early onset Alzheimer's disease
A-M Shiarli, R Jennings, J Shi, et al.
Page
of 6