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2. [A family with Menzel's disease showing dementia and various extrapyramidal symptoms]. Iwabuchi K, Nagatomo H, Tanabe T, Oda T, Itoh H, Hanihara T, Yagishita S. No To Shinkei; 1993 Sep; 45(9):841-9. PubMed ID: 8217410 [Abstract] [Full Text] [Related]
3. [Linkage study of hereditary spinocerebellar ataxia, and probable correlation for the loci to the disease phenotypes]. Sasaki H. Rinsho Shinkeigaku; 1993 Dec; 33(12):1285-7. PubMed ID: 8174326 [Abstract] [Full Text] [Related]
4. [Spinocerebellar ataxia 1--clinical study of 17 patients in a large pedigree]. Sasaki H, Wakisaka A, Koyama T, Hamada T, Shima K, Tashiro K, Hashimoto K, Miyagishi T. No To Shinkei; 1993 Jun; 45(6):502-8. PubMed ID: 8363844 [Abstract] [Full Text] [Related]
5. Machado-Joseph disease: an autosomal dominant motor system degeneration. Rosenberg RN. Mov Disord; 1992 Jun; 7(3):193-203. PubMed ID: 1620135 [Abstract] [Full Text] [Related]
6. [A clinical study of a family affected with HLA-linked hereditary spinocerebellar ataxia]. Sasaki H, Hamada T, Wakisaka A, Tashiro K. No To Shinkei; 1990 Nov; 42(11):1103-11. PubMed ID: 2076357 [Abstract] [Full Text] [Related]
7. Structural and immunocytochemical features of olivopontocerebellar atrophy caused by the spinocerebellar ataxia type 1 (SCA-1) mutation define a unique phenotype. Robitaille Y, Schut L, Kish SJ. Acta Neuropathol; 1995 Nov; 90(6):572-81. PubMed ID: 8615077 [Abstract] [Full Text] [Related]
8. [Siblings with spinocerebellar ataxia type 1 (SCA 1)--diagnosis by detecting the expansion of CAG repeat on chromosome 6p]. Hanihara T, Takahashi T, Inoue K, Yamada Y, Iwabuchi K. Rinsho Shinkeigaku; 1994 May; 34(5):508-10. PubMed ID: 7924069 [Abstract] [Full Text] [Related]
9. [Clinical study of gene locus heterogeneity in hereditary olivopontocerebellar atrophy (OPCA)--report of 2 pedigrees affected with non SCA1 type OPCA]. Sasaki H, Wakisaka A, Tashiro K, Hamada T, Shima K. Rinsho Shinkeigaku; 1991 Nov; 31(11):1170-6. PubMed ID: 1813183 [Abstract] [Full Text] [Related]
10. [Autopsy cases of hereditary ataxia pathologically diagnosed as the Japanese type of Joseph disease--cliniconeuropathological findings]. Kogure T, Oda T, Katoh Y. Seishin Shinkeigaku Zasshi; 1990 Nov; 92(3):161-83. PubMed ID: 2353076 [Abstract] [Full Text] [Related]
13. [Some problems on the clinical phenotype of Machado-Joseph disease in relation between their ages at onset]. Iwabuchi K, Kogure T, Oda T, Kato Y, Ohtani K, Endo K, Kosaka K, Amano N, Yagishita S. No To Shinkei; 1993 Mar; 45(3):246-54. PubMed ID: 8323819 [Abstract] [Full Text] [Related]
15. [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 [Abstract] [Full Text] [Related]
16. [Study on argyrophilic inclusions of multisystem atrophy (Oppenheimer)]. Iwabuchi K, Kosaka K, Haga C, Tuchiya K, Amano N, Itoh K, Yagishita S, Mizutani Y. No To Shinkei; 1991 Jun; 43(6):561-8. PubMed ID: 1654964 [Abstract] [Full Text] [Related]