439 related articles for article (PubMed ID: 7614764)
41. Kennedy's disease: a lower motor neuron model to identify upper motor neuron physiology in ALS.
Eisen A
Clin Neurophysiol; 2008 May; 119(5):971-2. PubMed ID: 18308629
[No Abstract] [Full Text] [Related]
42. Frontotemporal lobar degeneration with ubiquitin pathology: an autopsy case presenting with semantic dementia and upper motor neuron signs with a clinical course of 19 years.
Yokota O; Tsuchiya K; Itoh Y; Ishizu H; Akiyama H; Ikeda M; Kuzuhara S; Otomo E
Acta Neuropathol; 2006 Dec; 112(6):739-49. PubMed ID: 17016698
[TBL] [Abstract][Full Text] [Related]
43. [Vacuolar myelopathy with symmetrical involvement of the fasciculus cuneatus, in a case of amyotrophic lateral sclerosis with multisystemic degeneration].
Yamashita M; Yamamoto T
No To Shinkei; 2002 Aug; 54(8):685-91. PubMed ID: 12355880
[TBL] [Abstract][Full Text] [Related]
44. Nigral degeneration in a case of amyotrophic lateral sclerosis: evidence of Lewy body-like and skein-like inclusions in the pigmented neurons.
Su M; Yoshida Y; Ishiguro H; Hirota K
Clin Neuropathol; 1999; 18(6):293-300. PubMed ID: 10580555
[TBL] [Abstract][Full Text] [Related]
45. Alzheimer disease pathology in amyotrophic lateral sclerosis.
Hamilton RL; Bowser R
Acta Neuropathol; 2004 Jun; 107(6):515-22. PubMed ID: 15024584
[TBL] [Abstract][Full Text] [Related]
46. [Amyotrophic lateral sclerosis with dementia (ALSD)].
Nakano I
Rinsho Shinkeigaku; 2006 Nov; 46(11):822-4. PubMed ID: 17432190
[TBL] [Abstract][Full Text] [Related]
47. [A clinicopathological study of two respirator-aided long-survival cases of amyotrophic lateral sclerosis].
Yoshida M; Murakami N; Hashizume Y; Itoh E; Takahashi A
Rinsho Shinkeigaku; 1992 Mar; 32(3):259-65. PubMed ID: 1628448
[TBL] [Abstract][Full Text] [Related]
48. [Differential diagnosis and atypical subsets of amyotrophic lateral sclerosis].
Pradat PF; Bruneteau G
Rev Neurol (Paris); 2006 Jun; 162 Spec No 2():4S81-4S90. PubMed ID: 17128093
[TBL] [Abstract][Full Text] [Related]
49. [A 70-year-old man with a progressive gait disturbance and gaze palsy].
Nakamura T; Yoritaka A; Sumino S; Suzuki H; Mori H; Suda K; Takubo H; Mizuno Y
No To Shinkei; 1997 Jan; 49(1):93-100. PubMed ID: 9027910
[TBL] [Abstract][Full Text] [Related]
50. [An 81-year-old woman with progressive motor disturbance, extrapyramidal features, dementia, and oculomotor palsy].
Urabe T; Mori H; Sumino S; Miwa H; Wakiya M; Shirai T; Takubo H; Mizuno Y
No To Shinkei; 1998 Mar; 50(3):291-301. PubMed ID: 9566008
[TBL] [Abstract][Full Text] [Related]
51. [A nosological study of a patient showing ataxia & lower motor neuron involvement].
Murakami N; Yoshida M; Hashizume Y; Muroga T; Takahashi A
Rinsho Shinkeigaku; 1989 Sep; 29(9):1116-21. PubMed ID: 2598537
[TBL] [Abstract][Full Text] [Related]
52. [What's new in primary lateral sclerosis?].
Le Forestier N; Maisonobe T; Spelle L; Lesort A; Salachas F; Chassande B; Bouche P; Samson Y; Meininger V
Rev Neurol (Paris); 2000 Apr; 156(4):364-71. PubMed ID: 10795013
[TBL] [Abstract][Full Text] [Related]
53. Asymmetric involvement of the spinal cord involving both large and small anterior horn cells in a case of familial amyotrophic lateral sclerosis.
Kato T; Hirano A; Kurland LT
Clin Neuropathol; 1987; 6(2):67-70. PubMed ID: 3036409
[TBL] [Abstract][Full Text] [Related]
54. Granulofilamentous profiles in lower motor neurons: a sporadic case of amyotrophic lateral sclerosis with many Lewy body-like inclusions.
Kusaka H; Matsumoto S; Imai T
Clin Neuropathol; 1992; 11(1):20-4. PubMed ID: 1312402
[TBL] [Abstract][Full Text] [Related]
55. Progressive supranuclear palsy presenting as primary lateral sclerosis but lacking parkinsonism, gaze palsy, aphasia, or dementia.
Nagao S; Yokota O; Nanba R; Takata H; Haraguchi T; Ishizu H; Ikeda C; Takeda N; Oshima E; Sakane K; Terada S; Ihara Y; Uchitomi Y
J Neurol Sci; 2012 Dec; 323(1-2):147-53. PubMed ID: 23026537
[TBL] [Abstract][Full Text] [Related]
56. Familial motor neuron disease with prominent onion-bulb-like structures and axonal swelling restricted to the spinal ventral root: autopsy findings in two siblings.
Tokuyama W; Yagishita S; Ryo M; Kusunoki J; Hasegawa K; Yoshida T; Mikami T; Okayasu I
Neuropathology; 2010 Feb; 30(1):61-70. PubMed ID: 19496941
[TBL] [Abstract][Full Text] [Related]
57. Degeneration of the substantia nigra in familial amyotrophic lateral sclerosis.
Wolf HK; Crain BJ; Siddique T
Clin Neuropathol; 1991; 10(6):291-6. PubMed ID: 1764852
[TBL] [Abstract][Full Text] [Related]
58. Clinicopathologic features of autosomal recessive amyotrophic lateral sclerosis associated with optineurin mutation.
Kamada M; Izumi Y; Ayaki T; Nakamura M; Kagawa S; Kudo E; Sako W; Maruyama H; Nishida Y; Kawakami H; Ito H; Kaji R
Neuropathology; 2014 Feb; 34(1):64-70. PubMed ID: 23889540
[TBL] [Abstract][Full Text] [Related]
59. Degeneration of serotonergic neurons in amyotrophic lateral sclerosis: a link to spasticity.
Dentel C; Palamiuc L; Henriques A; Lannes B; Spreux-Varoquaux O; Gutknecht L; René F; Echaniz-Laguna A; Gonzalez de Aguilar JL; Lesch KP; Meininger V; Loeffler JP; Dupuis L
Brain; 2013 Feb; 136(Pt 2):483-93. PubMed ID: 23114367
[TBL] [Abstract][Full Text] [Related]
60. [An autopsied case of corticobasal degeneration with onset of nonfluent aphasia revealing symmetrical cerebral involvement].
Ishihara K; Mimura M; Ishigaki S; Shiota J; Nakano I; Kawamura M
Brain Nerve; 2012 Aug; 64(8):943-9. PubMed ID: 22868886
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]