307 related articles for article (PubMed ID: 25407076)
1. [An autopsy case with progressive muscular atrophy: an subtype of lower motor predominant amyotrophic lateral sclerosis].
Kosaka T; Tawara S; Harada M; Takahashi T; Murayama T
Brain Nerve; 2014 Nov; 66(11):1405-9. PubMed ID: 25407076
[TBL] [Abstract][Full Text] [Related]
2. Sporadic amyotrophic lateral sclerosis of long duration mimicking spinal progressive muscular atrophy exists: additional autopsy case with a clinical course of 19 years.
Tsuchiya K; Sano M; Shiotsu H; Akiyama H; Watabiki S; Taki K; Kondo H; Nakano I; Ikeda K
Neuropathology; 2004 Sep; 24(3):228-35. PubMed ID: 15484701
[TBL] [Abstract][Full Text] [Related]
3. Sporadic amyotrophic lateral sclerosis of long duration mimicking spinal progressive muscular atrophy: a clinicopathological study.
Tsuchiya K; Shintani S; Kikuchi M; Kondo H; Kamaya T; Ohbu S; Kato S; Hayashi H; Ikeda K; Nakano I
J Neurol Sci; 1999 Jan; 162(2):174-8. PubMed ID: 10202983
[TBL] [Abstract][Full Text] [Related]
4. [Neurological CPC.57. An 80-year-old woman with four years history of muscle atrophy involving lower extremities predominantly on the right side].
Miwa H; Mori H; Sumino S; Matsuoka S; Shirai T; Imai H; Mizuno Y
No To Shinkei; 1997 Sep; 49(9):857-65. PubMed ID: 9311007
[TBL] [Abstract][Full Text] [Related]
5. [An autopsy case with lower motor neuron disease showing a transient-appearance of anti-GM1 antibody and an improvement of conduction block after gamma-globulin administration].
Kikuchi H; Kawano Y; Dohura K; Kawamura T; Taniwaki T; Yamada T; Kato M; Iwaki T; Kira J
No To Shinkei; 1999 May; 51(5):455-64. PubMed ID: 10396755
[TBL] [Abstract][Full Text] [Related]
6. TAR DNA-binding protein 43 pathology in a case clinically diagnosed with facial-onset sensory and motor neuronopathy syndrome: an autopsied case report and a review of the literature.
Sonoda K; Sasaki K; Tateishi T; Yamasaki R; Hayashi S; Sakae N; Ohyagi Y; Iwaki T; Kira J
J Neurol Sci; 2013 Sep; 332(1-2):148-53. PubMed ID: 23849263
[TBL] [Abstract][Full Text] [Related]
7. Sporadic amyotrophic lateral sclerosis with circumscribed temporal atrophy: a report of an autopsy case without dementia and with ubiquitinated intraneuronal inclusions.
Tsuchiya K; Takahashi M; Shiotsu H; Akiyama H; Haga C; Watabiki S; Taki K; Nakano I; Ikeda K
Neuropathology; 2002 Dec; 22(4):308-16. PubMed ID: 12564772
[TBL] [Abstract][Full Text] [Related]
8. Sporadic amyotrophic lateral sclerosis with multiple system degeneration: a report of an autopsy case without respirator administration.
Machida Y; Tsuchiya K; Anno M; Haga C; Ito T; Shimo Y; Wakeshima T; Iritani S; Ikeda K
Acta Neuropathol; 1999 Nov; 98(5):512-5. PubMed ID: 10541875
[TBL] [Abstract][Full Text] [Related]
9. Flail arm syndrome with cytoplasmic vacuoles in remaining anterior horn motor neurons: A peculiar variant of amyotrophic lateral sclerosis.
Hino S; Sasaki S
Neuropathology; 2015 Dec; 35(6):582-6. PubMed ID: 26149762
[TBL] [Abstract][Full Text] [Related]
10. Amyotrophic lateral sclerosis in an adult following acute paralytic poliomyelitis in early childhood.
Shimada A; Lange DJ; Hays AP
Acta Neuropathol; 1999 Mar; 97(3):317-21. PubMed ID: 10090681
[TBL] [Abstract][Full Text] [Related]
11. Amyotrophic lateral sclerosis of long clinical course clinically presenting with progressive muscular atrophy.
Matsubara T; Oda M; Takahashi T; Watanabe C; Tachiyama Y; Morino H; Kawakami H; Kaji R; Maruyama H; Murayama S; Izumi Y
Neuropathology; 2019 Feb; 39(1):47-53. PubMed ID: 30511354
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. An autopsy case of early-stage amyotrophic lateral sclerosis with TDP-43 immunoreactive neuronal, but not glial, inclusions.
Kon T; Mori F; Oyama Y; Tanji K; Kimura T; Takahashi S; Wakabayashi K
Neuropathology; 2019 Jun; 39(3):224-230. PubMed ID: 31020724
[TBL] [Abstract][Full Text] [Related]
14. Autopsy findings in the early stage of amyotrophic lateral sclerosis with "dropped head" syndrome.
Tanikawa S; Tanino M; Wang L; Ishikawa M; Miyazaki M; Tsuda M; Orba Y; Sawa H; Matoba K; Nakamura N; Nagashima K; Hall WW; Tanaka S
Neuropathology; 2019 Oct; 39(5):374-377. PubMed ID: 31373095
[TBL] [Abstract][Full Text] [Related]
15. Concomitant alpha-synuclein pathology in an autopsy case of amyotrophic lateral sclerosis presenting with orthostatic hypotension and cardiac arrests.
Yamada T; Itoh K; Matsuo K; Yamamoto Y; Hosokawa Y; Koizumi T; Shiga K; Mizuno T; Nakagawa M; Fushiki S
Neuropathology; 2014 Apr; 34(2):164-9. PubMed ID: 23898972
[TBL] [Abstract][Full Text] [Related]
16. Primary lateral sclerosis: upper-motor-predominant amyotrophic lateral sclerosis with frontotemporal lobar degeneration--immunohistochemical and biochemical analyses of TDP-43.
Kosaka T; Fu YJ; Shiga A; Ishidaira H; Tan CF; Tani T; Koike R; Onodera O; Nishizawa M; Kakita A; Takahashi H
Neuropathology; 2012 Aug; 32(4):373-84. PubMed ID: 22098653
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Forme fruste or incipient form of widespread-type amyotrophic lateral sclerosis, or motor neuron disease with pallido-nigro-luysian atrophy? An autopsy case report.
Hashimoto T; Matsubara S; Mochizuki Y; Tsuji S; Mizutani T; Oyanagi K
Neuropathology; 2008 Jun; 28(3):309-16. PubMed ID: 18179405
[TBL] [Abstract][Full Text] [Related]
19. A fatal neuromuscular disease in an adult patient after poliomyelitis in early childhood: consideration of the pathology of post-polio syndrome.
Kosaka T; Kuroha Y; Tada M; Hasegawa A; Tani T; Matsubara N; Koike R; Toyoshima Y; Takahashi H
Neuropathology; 2013 Feb; 33(1):93-101. PubMed ID: 22672529
[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]