168 related articles for article (PubMed ID: 2752643)
1. [Xeroderma pigmentosum presenting clinical features of spinocerebellar degeneration].
Tomimoto H; Hirose S; Akiguchi I; Nishigoori C; Kameyama M
Rinsho Shinkeigaku; 1989 Feb; 29(2):172-6. PubMed ID: 2752643
[TBL] [Abstract][Full Text] [Related]
2. Neurological manifestations in xeroderma pigmentosum.
Mimaki T; Itoh N; Abe J; Tagawa T; Sato K; Yabuuchi H; Takebe H
Ann Neurol; 1986 Jul; 20(1):70-5. PubMed ID: 3740815
[TBL] [Abstract][Full Text] [Related]
3. Primary degeneration of the granular layer of the cerebellum. A study of 14 patients and review of the literature.
Pascual-Castroviejo I; Gutierrez M; Morales C; Gonzalez-Mediero I; Martínez-Bermejo A; Pascual-Pascual SI
Neuropediatrics; 1994 Aug; 25(4):183-90. PubMed ID: 7824090
[TBL] [Abstract][Full Text] [Related]
4. [A 60-year-old man with intention tremor as an initial symptom followed by cerebellar ataxia, peripheral neuropathy and dementia].
Machida Y; Lijima M; Nakamura K; Ota S; Hattori N; Mizuno Y
No To Shinkei; 2005 Aug; 57(8):710-9. PubMed ID: 16146216
[TBL] [Abstract][Full Text] [Related]
5. [A case of adult-onset Huntington disease presenting with spasticity and cerebellar ataxia, mimicking spinocerebellar degeneration].
Kageyama Y; Yamamoto S; Ueno M; Ichikawa K
Rinsho Shinkeigaku; 2003; 43(1-2):16-9. PubMed ID: 12820545
[TBL] [Abstract][Full Text] [Related]
6. [Cystinuria with symptoms of cerebellar atrophy--a case report].
Tanaka Y; Tsuda M; Miyazaki M; Kuzuhara S
Rinsho Shinkeigaku; 1991 Mar; 31(3):318-20. PubMed ID: 1893674
[TBL] [Abstract][Full Text] [Related]
7. Spinocerebellar degeneration and cerebral hypomyelination in a family.
Chatkupt S; Wolansky LJ; Jotkowitz A; Shih LY; Cook SD
Am J Med Genet; 1995 Jun; 60(3):188-91. PubMed ID: 7573169
[TBL] [Abstract][Full Text] [Related]
8. [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]
9. [A 63-year-old woman with muscle weakness, myotonia, and parkinsonism].
Okuma Y; Tanaka S; Nomura Y; Mori H; Yan H; Shirai T; Kondo T; Segawa M; Mizuno Y
No To Shinkei; 1996 Mar; 48(3):287-97. PubMed ID: 8868342
[TBL] [Abstract][Full Text] [Related]
10. [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]
11. [A 64-year-old woman with progressive gait disturbance and dementia for one year].
Sugita Y; Matsumine H; Wakiya M; Mori H; Suda K; Kondo T; Mizuno Y
No To Shinkei; 1998 Sep; 50(9):861-70. PubMed ID: 9789311
[TBL] [Abstract][Full Text] [Related]
12. [Familial idiopathic vitamin E deficiency associated with cerebellar atrophy].
Aoki K; Washimi Y; Fujimori N; Maruyama K; Yanagisawa N
Rinsho Shinkeigaku; 1990 Sep; 30(9):966-71. PubMed ID: 2265507
[TBL] [Abstract][Full Text] [Related]
13. [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]
14. [(Neurological CPC.55). A 60-year-old woman with progressive cerebellar ataxia, myoclonus, and dementia].
Morikawa N; Mori H; Sumino S; Kodera M; Shirai T; Kondo T; Mizuno Y
No To Shinkei; 1997 Jul; 49(7):663-71. PubMed ID: 9234257
[TBL] [Abstract][Full Text] [Related]
15. [Clinical types of spinocerebellar degeneration and evaluation with MR imaging].
Kojima S
Rinsho Shinkeigaku; 1993 Dec; 33(12):1294-6. PubMed ID: 8174328
[TBL] [Abstract][Full Text] [Related]
16. [A case of juvenile Sandhoff disease].
Mitsuo K; Koutake N; Kobayashi T; Iwashita H; Goto I
Rinsho Shinkeigaku; 1990 Feb; 30(2):179-83. PubMed ID: 2350930
[TBL] [Abstract][Full Text] [Related]
17. Neurological manifestations in two related xeroderma pigmentosum group D patients: complications of the late-onset type of the juvenile form.
Stojkovic T; Defebvre L; Quilliet X; Eveno E; Sarasin A; Mezzina M; Destée A
Mov Disord; 1997 Jul; 12(4):616-9. PubMed ID: 9251090
[No Abstract] [Full Text] [Related]
18. [A whole family affected by xeroderma pigmentosum: clinical and genetic particularities].
Zghal M; Fazaa B; Zghal A; Mokhtar I; Sarasin A; Kamoun MR; Gharbi MR
Ann Dermatol Venereol; 2003 Jan; 130(1 Pt 1):31-6. PubMed ID: 12605154
[TBL] [Abstract][Full Text] [Related]
19. [A case with posterior column ataxia associated with cerebellar ataxia and sensory neuropathy].
Kikuchi Y; Ogawa M; Shigetoh H; Kawai M; Satoyoshi E
Rinsho Shinkeigaku; 1999 Sep; 39(9):944-7. PubMed ID: 10614159
[TBL] [Abstract][Full Text] [Related]
20. [A case presenting clinical features of spinocerebellar degeneration with dentatorubral tract involvement in MRI. Clinical conference].
Kumagai T
No To Shinkei; 2003 Aug; 55(8):723-30. PubMed ID: 13677309
[No Abstract] [Full Text] [Related]
[Next] [New Search]
