376 related articles for article (PubMed ID: 20022024)
1. Neuronal and glial tau pathology in early frontotemporal lobar degeneration-tau, Pick's disease subtype.
Mimuro M; Yoshida M; Miyao S; Harada T; Ishiguro K; Hashizume Y
J Neurol Sci; 2010 Mar; 290(1-2):177-82. PubMed ID: 20022024
[TBL] [Abstract][Full Text] [Related]
2. KP1 expression of ghost Pick bodies, amyloid P-positive astrocytes and selective nigral degeneration in early onset Picks disease.
Kobayashi K; Hayashi M; Fukutani Y; Miyazu K; Shiozawa M; Muramori F; Aoki T; Koshino Y
Clin Neuropathol; 1999; 18(5):240-9. PubMed ID: 10505433
[TBL] [Abstract][Full Text] [Related]
3. Sporadic four-repeat tauopathy with frontotemporal lobar degeneration, Parkinsonism, and motor neuron disease: a distinct clinicopathological and biochemical disease entity.
Fu YJ; Nishihira Y; Kuroda S; Toyoshima Y; Ishihara T; Shinozaki M; Miyashita A; Piao YS; Tan CF; Tani T; Koike R; Iwanaga K; Tsujihata M; Onodera O; Kuwano R; Nishizawa M; Kakita A; Ikeuchi T; Takahashi H
Acta Neuropathol; 2010 Jul; 120(1):21-32. PubMed ID: 20140439
[TBL] [Abstract][Full Text] [Related]
4. Glycogen synthase kinase-3 is associated with neuronal and glial hyperphosphorylated tau deposits in Alzheimer's disease, Pick's disease, progressive supranuclear palsy and corticobasal degeneration.
Ferrer I; Barrachina M; Puig B
Acta Neuropathol; 2002 Dec; 104(6):583-91. PubMed ID: 12410379
[TBL] [Abstract][Full Text] [Related]
5. Astrocytic degeneration relates to the severity of disease in frontotemporal dementia.
Broe M; Kril J; Halliday GM
Brain; 2004 Oct; 127(Pt 10):2214-20. PubMed ID: 15282215
[TBL] [Abstract][Full Text] [Related]
6. [Clinico-pathological investigation of two patients with dementia with motor neuron disease].
Yamamoto R; Iseki E; Murayama N; Minegishi M; Kimura M; Eto K; Arai H; Ohbu S; Hatanaka D; Hino H; Fujisawa K
Brain Nerve; 2007 Mar; 59(3):263-9. PubMed ID: 17370652
[TBL] [Abstract][Full Text] [Related]
7. Sporadic four-repeat tauopathy with frontotemporal degeneration, parkinsonism and motor neuron disease.
Piao YS; Tan CF; Iwanaga K; Kakita A; Takano H; Nishizawa M; Lashley T; Revesz T; Lees A; de Silva R; Tsujihata M; Takahashi H
Acta Neuropathol; 2005 Dec; 110(6):600-9. PubMed ID: 16328530
[TBL] [Abstract][Full Text] [Related]
8. Anti-tau phospho-specific Ser262 antibody recognizes a variety of abnormal hyper-phosphorylated tau deposits in tauopathies including Pick bodies and argyrophilic grains.
Ferrer I; Barrachina M; Puig B
Acta Neuropathol; 2002 Dec; 104(6):658-64. PubMed ID: 12410387
[TBL] [Abstract][Full Text] [Related]
9. Frontotemporal dementia with co-occurrence of astrocytic plaques and tufted astrocytes, and severe degeneration of the cerebral white matter: a variant of corticobasal degeneration?
Tan CF; Piao YS; Kakita A; Yamada M; Takano H; Tanaka M; Mano A; Makino K; Nishizawa M; Wakabayashi K; Takahashi H
Acta Neuropathol; 2005 Mar; 109(3):329-38. PubMed ID: 15841415
[TBL] [Abstract][Full Text] [Related]
10. Familial frontotemporal dementia: a report of three cases of severe cerebral atrophy with rare inclusions that are negative for tau and synuclein, but positive for ubiquitin.
Chang HT; Cortez S; Vonsattel JP; Stopa EG; Schelper RL
Acta Neuropathol; 2004 Jul; 108(1):10-6. PubMed ID: 15108011
[TBL] [Abstract][Full Text] [Related]
11. An autopsy case of diffuse neurofibrillary tangles with calcification: early stage pathologic findings.
Iwasaki Y; Ito M; Mori K; Deguchi A; Nagaoka M; Yoshida M; Hashizume Y
Neuropathology; 2009 Dec; 29(6):697-703. PubMed ID: 19389080
[TBL] [Abstract][Full Text] [Related]
12. Regional and cellular pathology in frontotemporal dementia: relationship to stage of disease in cases with and without Pick bodies.
Kersaitis C; Halliday GM; Kril JJ
Acta Neuropathol; 2004 Dec; 108(6):515-23. PubMed ID: 15368070
[TBL] [Abstract][Full Text] [Related]
13. Severity of gliosis in Pick's disease and frontotemporal lobar degeneration: tau-positive glia differentiate these disorders.
Schofield E; Kersaitis C; Shepherd CE; Kril JJ; Halliday GM
Brain; 2003 Apr; 126(Pt 4):827-40. PubMed ID: 12615642
[TBL] [Abstract][Full Text] [Related]
14. [Rivastigmine in a case of autopsy proved frontotemporal dementia (Pick's disease)].
Calatayud-Noguera T; Astudillo-González A; Alvarez-Carriles JC; Temprano-Fernández T; Cortés-Velarde M; Oliva-Nacarino P
Rev Neurol; 2009 Jun 1-15; 48(11):582-4. PubMed ID: 19472156
[TBL] [Abstract][Full Text] [Related]
15. Coexistence of amyotrophic lateral sclerosis and argyrophilic grain disease: a non-demented autopsy case showing circumscribed temporal atrophy and involvement of the amygdala.
Yokota O; Tsuchiya K; Noguchi Y; Akabane H; Ishizu H; Saito Y; Akiyama H
Neuropathology; 2007 Dec; 27(6):539-50. PubMed ID: 18021374
[TBL] [Abstract][Full Text] [Related]
16. Ubiquitin-positive frontotemporal lobar degeneration presenting with progressive Gogi (word-meaning) aphasia. A neuropsychological, radiological and pathological evaluation of a Japanese semantic dementia patient.
Sakurai Y; Tsuchiya K; Oda T; Hori K; Tominaga I; Akiyama H; Bando M; Haga C; Iwata M; Mannen T
J Neurol Sci; 2006 Dec; 250(1-2):3-9. PubMed ID: 17045299
[TBL] [Abstract][Full Text] [Related]
17. Primary progressive aphasia as the initial manifestation of corticobasal degeneration and unusual tauopathies.
Ferrer I; Hernández I; Boada M; Llorente A; Rey MJ; Cardozo A; Ezquerra M; Puig B
Acta Neuropathol; 2003 Nov; 106(5):419-35. PubMed ID: 12955398
[TBL] [Abstract][Full Text] [Related]
18. Phosphorylated mitogen-activated protein kinase (MAPK/ERK-P), protein kinase of 38 kDa (p38-P), stress-activated protein kinase (SAPK/JNK-P), and calcium/calmodulin-dependent kinase II (CaM kinase II) are differentially expressed in tau deposits in neurons and glial cells in tauopathies.
Ferrer I; Blanco R; Carmona M; Puig B
J Neural Transm (Vienna); 2001; 108(12):1397-415. PubMed ID: 11810404
[TBL] [Abstract][Full Text] [Related]
19. Expression of transcription factors c-Fos, c-Jun, CREB-1 and ATF-2, and caspase-3 in relation with abnormal tau deposits in Pick's disease.
Nieto-Bodelón M; Santpere G; Torrejón-Escribano B; Puig B; Ferrer I
Acta Neuropathol; 2006 Apr; 111(4):341-50. PubMed ID: 16496165
[TBL] [Abstract][Full Text] [Related]
20. Primary lateral sclerosis: a rare upper-motor-predominant form of amyotrophic lateral sclerosis often accompanied by frontotemporal lobar degeneration with ubiquitinated neuronal inclusions? Report of an autopsy case and a review of the literature.
Tan CF; Kakita A; Piao YS; Kikugawa K; Endo K; Tanaka M; Okamoto K; Takahashi H
Acta Neuropathol; 2003 Jun; 105(6):615-20. PubMed ID: 12734667
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
