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2. 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]
3. [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]
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. 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]
6. 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]
7. [An Autopsy Case of Amiotrophic Lateral Sclerosis Characterized by Upper Motor Neuron Degeneration and Progressive Pseudobulbar Palsy]. Kikuchi R; Ishihara K; Nagumo K; Sioda J; Kawamura M; Yoshida M Brain Nerve; 2019 Jan; 71(1):75-80. PubMed ID: 30630132 [TBL] [Abstract][Full Text] [Related]
8. Motor neuron disease with predominantly upper extremity involvement: a clinicopathological study. Sasaki S; Iwata M Acta Neuropathol; 1999 Dec; 98(6):645-50. PubMed ID: 10603042 [TBL] [Abstract][Full Text] [Related]
9. [Two siblings of familial amyotrophic lateral sclerosis with multisystemic degeneration characterized by mild involvement of the middle root zone of the posterior column, Clarke's nuclei and spinocerebellar tract]. Yoshida M; Okuda S; Murakami N; Hashizume Y; Sobue G Rinsho Shinkeigaku; 1995 Jun; 35(6):589-99. PubMed ID: 8521632 [TBL] [Abstract][Full Text] [Related]
10. 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]
11. [A 65-year-old woman with dysarthria, dysphagia, weakness, and gait disturbance]. Imai H; Furukawa Y; Sumino S; Mori H; Ueda G; Shirai T; Kondo T; Mizuno Y No To Shinkei; 1995 Apr; 47(4):399-410. PubMed ID: 7772410 [TBL] [Abstract][Full Text] [Related]
12. [An autopsied case of dominantly affecting upper motor neuron with atrophy of the frontal and temporal lobes--with special reference to primary lateral sclerosis]. Konagaya M; Sakai M; Iida M; Hashizume Y Rinsho Shinkeigaku; 1995 Apr; 35(4):384-90. PubMed ID: 7614764 [TBL] [Abstract][Full Text] [Related]
13. 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]
14. [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]
15. 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]
16. Pathological findings in a patient with amyotrophic lateral sclerosis and multifocal motor neuropathy with conduction block. Veugelers B; Theys P; Lammens M; Van Hees J; Robberecht W J Neurol Sci; 1996 Mar; 136(1-2):64-70. PubMed ID: 8815180 [TBL] [Abstract][Full Text] [Related]
17. [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]