140 related articles for article (PubMed ID: 2350930)
21. A Japanese family with early-onset ataxia with motor and sensory neuropathy.
Kobayashi S; Takuma H; Murayama S; Sakurai M; Kanazawa I
J Neurol Sci; 2007 Mar; 254(1-2):44-8. PubMed ID: 17258771
[TBL] [Abstract][Full Text] [Related]
22. [Autosomal recessive hereditary cortical cerebellar atrophy with striatal degeneration--two siblings showing choreoathetoid movement, ataxia, dementia, and amenorrhea].
Iwabuchi K; Nakazawa Y; Akai J; Yagishita S; Amano N
No To Shinkei; 1994 Jun; 46(6):563-71. PubMed ID: 8068439
[TBL] [Abstract][Full Text] [Related]
23. [A case of hereditary motor and sensory neuropathy of neuronal type with retardation of motor development].
Nakano S; Ohnishi A; Yamamoto T; Oishi T; Murai Y
Rinsho Shinkeigaku; 1990 Apr; 30(4):448-51. PubMed ID: 2387117
[TBL] [Abstract][Full Text] [Related]
24. [A 32-year-old man who developed a posterior fossa mass 12 years after the radiation therapy for cerebellar arteriovenous malformation].
Koshimura I; Takeda N; Ohtomo T; Shimada J; Sugano K; Mori H; Mizuno Y; Sato K
No To Shinkei; 1996 Jan; 48(1):81-9. PubMed ID: 8679325
[TBL] [Abstract][Full Text] [Related]
25. [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]
26. [A case of hereditary motor and sensory neuropathy with pyramidal tract sign, optic nerve atrophy and mental retardation].
Adachi T; Imaoka K; Shirasawa A; Yamaguchi S; Kobayashi S
Rinsho Shinkeigaku; 1998 Dec; 38(12):1037-41. PubMed ID: 10349345
[TBL] [Abstract][Full Text] [Related]
27. [A case of juvenile onset ataxia with dystonia, myoclonus, sensorineural hearing loss and mental retardation].
Koide R; Yoshimura N; Soma Y; Tsuji S
Rinsho Shinkeigaku; 1993 Aug; 33(8):909-11. PubMed ID: 8261707
[TBL] [Abstract][Full Text] [Related]
28. [A patient with motor neuron syndrome clinically similar to amyotrophic lateral sclerosis, presenting spontaneous recovery].
Miyoshi K; Ohyagi Y; Amano T; Inoue I; Miyoshi S; Tsuji S; Yamada T; Kira J
Rinsho Shinkeigaku; 2000 Nov; 40(11):1090-5. PubMed ID: 11332188
[TBL] [Abstract][Full Text] [Related]
29. [An apparently sporadic case with spinocerebellar ataxia type 1 (SCA1)].
Futamura N; Matsumura R; Murata K; Suzumura A; Takayanagi T
Rinsho Shinkeigaku; 1997 Aug; 37(8):708-10. PubMed ID: 9404150
[TBL] [Abstract][Full Text] [Related]
30. Progressive dystonia symptomatic of juvenile GM2 gangliosidosis.
Nardocci N; Bertagnolio B; Rumi V; Angelini L
Mov Disord; 1992; 7(1):64-7. PubMed ID: 1532632
[TBL] [Abstract][Full Text] [Related]
31. [A 34-year-old woman with delayed motor milestones, high arched palate, and proximal muscle weakness].
Yamamoto T; Kitada T; Hirasawa E; Mori H; Mizuno Y
No To Shinkei; 1996 Jul; 48(7):677-84. PubMed ID: 8753005
[TBL] [Abstract][Full Text] [Related]
32. [A case of severe involvement of the motor neuron system accompanied with cerebellar ataxia].
Horiuchi I; Furuya H; Yoshimura T; Kobayashi T; Kusunoki S
Rinsho Shinkeigaku; 1997 Feb; 37(2):123-6. PubMed ID: 9164144
[TBL] [Abstract][Full Text] [Related]
33. [A 63 year-old man with progressive gait disturbance and dysarthria].
Nakamura N; Ohta S; Matsumoto M; Mori H; Takubo H; Mizuno Y
No To Shinkei; 1996 Sep; 48(9):865-75. PubMed ID: 8888038
[TBL] [Abstract][Full Text] [Related]
34. [A case of spinocerebellar degeneration with bilateral MLF syndrome and dystonia].
Ohtake T; Nagashima T; Yamane M; Tanabe H
Rinsho Shinkeigaku; 1989 Jan; 29(1):112-4. PubMed ID: 2743681
[TBL] [Abstract][Full Text] [Related]
35. [A 40-year-old woman with progressive dementia and abnormal behavior].
Hattori T; Tanaka S; Shimo Y; Anno M; Ohta S; Ishi K; Mori H; Ohkuma Y; Mizuno Y
No To Shinkei; 1999 Feb; 51(2):185-94. PubMed ID: 10198910
[TBL] [Abstract][Full Text] [Related]
36. [Late cerebellar ataxia associated with fragile X premutation].
Chaussenot A; Borg M; Bayreuther C; Lebrun C
Rev Neurol (Paris); 2008 Nov; 164(11):957-63. PubMed ID: 18808779
[TBL] [Abstract][Full Text] [Related]
37. [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]
38. [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]
39. New cases of adult-onset Sandhoff disease with a cerebellar or lower motor neuron phenotype.
Delnooz CC; Lefeber DJ; Langemeijer SM; Hoffjan S; Dekomien G; Zwarts MJ; Van Engelen BG; Wevers RA; Schelhaas HJ; van de Warrenburg BP
J Neurol Neurosurg Psychiatry; 2010 Sep; 81(9):968-72. PubMed ID: 20798201
[TBL] [Abstract][Full Text] [Related]
40. [A case of hereditary motor and sensory neuropathy type I with optic atrophy, neural deafness and pyramidal tract signs].
Saito T; Nishioka M; Ogino M; Endo K; Kowa H
Rinsho Shinkeigaku; 1993 May; 33(5):519-24. PubMed ID: 8365058
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]