99 related articles for article (PubMed ID: 1764852)
21. Classification of nerve cells from substantia nigra of patients with Parkinson's disease and amyotrophic lateral sclerosis with the use of X-ray fluorescence microscopy and multivariate methods.
Chwiej J; Fik-Mazgaj K; Szczerbowska-Boruchowska M; Lankosz M; Ostachowicz J; Adamek D; Simionovici A; Bohic S
Anal Chem; 2005 May; 77(9):2895-900. PubMed ID: 15859608
[TBL] [Abstract][Full Text] [Related]
22. Familial amyotrophic lateral sclerosis with bulbar onset and a novel Asp101Tyr Cu/Zn superoxide dismutase gene mutation.
Tan CF; Piao YS; Hayashi S; Obata H; Umeda Y; Sato M; Fukushima T; Nakano R; Tsuji S; Takahashi H
Acta Neuropathol; 2004 Oct; 108(4):332-6. PubMed ID: 15235802
[TBL] [Abstract][Full Text] [Related]
23. Amyotrophic lateral sclerosis. Inclusion bodies in a case of the classic sporadic form.
Sun CN; Araoz C; Lucas G; Morgan PN; White HJ
Ann Clin Lab Sci; 1975; 5(1):38-44. PubMed ID: 163072
[TBL] [Abstract][Full Text] [Related]
24. [A-56-year-old woman with parkinsonism, whose mother had Parkinson's disease].
Shimo Y; Takanashi M; Ohta S; Terashima K; Mori H; Shirai T; Miwa H; Mizuno Y
No To Shinkei; 2001 May; 53(5):495-505. PubMed ID: 11428377
[TBL] [Abstract][Full Text] [Related]
25. Midbrain dopaminergic neuronal degeneration in a transgenic mouse model of familial amyotrophic lateral sclerosis.
Kostic V; Gurney ME; Deng HX; Siddique T; Epstein CJ; Przedborski S
Ann Neurol; 1997 Apr; 41(4):497-504. PubMed ID: 9124807
[TBL] [Abstract][Full Text] [Related]
26. [A 49-year-old man with progressive bulbar palsy and respiratory failure].
Motoi Y; Satoh K; Matsumine H; Wakiya M; Mori H; Shirai T; Kondo T; Mizuno Y
No To Shinkei; 1998 Jan; 50(1):93-100. PubMed ID: 9493205
[TBL] [Abstract][Full Text] [Related]
27. [A 78-year-old man with young onset parkinsonism and sudden death].
Miyasaka H; Mori H; Saikawa T; Shirai T; Kondo T; Imai H; Mizuno Y
No To Shinkei; 1996 May; 48(5):487-95. PubMed ID: 8672309
[TBL] [Abstract][Full Text] [Related]
28. Comparison of pathological alterations in ALS and a murine transgenic model: pathogenetic implications.
Dal Canto MC
Clin Neurosci; 1995-1996; 3(6):332-7. PubMed ID: 9021254
[TBL] [Abstract][Full Text] [Related]
29. Familial ALS with FUS P525L mutation: two Japanese sisters with multiple systems involvement.
Mochizuki Y; Isozaki E; Takao M; Hashimoto T; Shibuya M; Arai M; Hosokawa M; Kawata A; Oyanagi K; Mihara B; Mizutani T
J Neurol Sci; 2012 Dec; 323(1-2):85-92. PubMed ID: 22980027
[TBL] [Abstract][Full Text] [Related]
30. 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]
31. Therapeutic benefits of putrescine-modified catalase in a transgenic mouse model of familial amyotrophic lateral sclerosis.
Reinholz MM; Merkle CM; Poduslo JF
Exp Neurol; 1999 Sep; 159(1):204-16. PubMed ID: 10486188
[TBL] [Abstract][Full Text] [Related]
32. Amyotrophic lateral sclerosis.
Gordon PH; Mitsumoto H; Hays AP
Sci Aging Knowledge Environ; 2003 Sep; 2003(35):dn2. PubMed ID: 12954882
[TBL] [Abstract][Full Text] [Related]
33. Limited corticospinal tract involvement in amyotrophic lateral sclerosis subjects with the A4V mutation in the copper/zinc superoxide dismutase gene.
Cudkowicz ME; McKenna-Yasek D; Chen C; Hedley-Whyte ET; Brown RH
Ann Neurol; 1998 Jun; 43(6):703-10. PubMed ID: 9629839
[TBL] [Abstract][Full Text] [Related]
34. [Two autopsy cases of sporadic amyotrophic lateral sclerosis with 20-year-clinical course without respirators].
Kato S; Oda M; Hayashi H; Komori T; Hirose K; Tanabe H; Arai N
No To Shinkei; 1993 Mar; 45(3):267-72. PubMed ID: 8323821
[TBL] [Abstract][Full Text] [Related]
35. Coexistence of Huntington's disease and familial amyotrophic lateral sclerosis: case presentation.
Rubio A; Steinberg K; Figlewicz DA; MacDonald ME; Greenamyre T; Hamill R; Shoulson I; Powers JM
Acta Neuropathol; 1996 Oct; 92(4):421-7. PubMed ID: 8891076
[TBL] [Abstract][Full Text] [Related]
36. 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]
37. 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]
38. [An autopsy case of multiple system atrophy with many Lewy bodies--striatonigral degeneration, olivo-ponto-cerebellar atrophy and autonomic nerve nucleus involvement in the spinal cord].
Morioka E; Kuroda S; Kuyama K; Otsuki S; Hosokawa K; Namba R
No To Shinkei; 1987 Apr; 39(4):361-6. PubMed ID: 3036191
[TBL] [Abstract][Full Text] [Related]
39. Luyso-pallido-nigral atrophy and amyotrophic lateral sclerosis.
Gray F; Eizenbaum JF; Gherardi R; Degos JD; Poirier J
Acta Neuropathol; 1985; 66(1):78-82. PubMed ID: 3993336
[TBL] [Abstract][Full Text] [Related]
40. [Clinical study of familial forms of amyotrophic lateral sclerosis. Review of the literature].
Moulard B; Camu W; Malafosse A; Billiard M; Baldy-Moulinier M
Rev Neurol (Paris); 1997 Jun; 153(5):314-24. PubMed ID: 9296165
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
