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Journal Abstract Search
203 related items for PubMed ID: 5173358
1. Dominant olivopontocerebellar atrophy with dementia and extrapyramidal signs: report of a family through three generations. Konigsmark BW, Lipton HL. Birth Defects Orig Artic Ser; 1971 Feb; 7(1):178-91. PubMed ID: 5173358 [Abstract] [Full Text] [Related]
4. [Extrapyramidal manifestations in hereditary olivopontocerebellar atrophy--clinical study of 10 cases in three affected pedigrees]. Sasaki H, Wakisaka A, Doi S, Hamada K, Hamada T, Shima K, Tashiro K. Hokkaido Igaku Zasshi; 1992 Jan; 67(1):55-66. PubMed ID: 1559661 [Abstract] [Full Text] [Related]
5. Olivopontocerebellar atrophy in children: a report of seven cases in two families. Colan RV, Snead OC, Ceballos R. Ann Neurol; 1981 Oct; 10(4):355-63. PubMed ID: 7316488 [Abstract] [Full Text] [Related]
6. [Olivopontocerebellar atrophy in the context of progressive cerebellar atrophies (a clinico-anatomical study)]. Ionel C. Rev Med Interna Neurol Psihiatr Neurochir Dermatovenerol Neurol Psihiatr Neurochir; 1990 Oct; 35(1):51-60. PubMed ID: 2237007 [Abstract] [Full Text] [Related]
7. Dominant olivopontocerebellar atrophy with dementia and extrapyramidal signs: report of a family through three generations. Konigsmark BW, Lipton HL. J Neuropathol Exp Neurol; 1971 Jan; 30(1):133-4. PubMed ID: 5100702 [No Abstract] [Full Text] [Related]
10. [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]
11. Hereditary spastic ataxia: report of a family through four generations. Ishino H, Sato M, Terao A, Hayahara T, Otsuki S. Folia Psychiatr Neurol Jpn; 1971 Sep; 25(4):269-81. PubMed ID: 5172645 [No Abstract] [Full Text] [Related]
13. An apology and an introduction to the olivopontocerebellar atrophies. Duvoisin RC. Adv Neurol; 1984 Sep; 41():5-12. PubMed ID: 6496230 [Abstract] [Full Text] [Related]
15. Olivopontocerebellar atrophy. A review of 117 cases. Berciano J. J Neurol Sci; 1982 Feb; 53(2):253-72. PubMed ID: 7057212 [Abstract] [Full Text] [Related]
16. Hereditary cerebellar cortical and extrapyramidal nuclear abiotrophy in Kerry Blue Terriers. deLahunta A, Averill DR. J Am Vet Med Assoc; 1976 Jun 15; 168(12):1119-24. PubMed ID: 931776 [Abstract] [Full Text] [Related]
17. Neuronal loss in the basal nucleus of Meynert in a patient with olivopontocerebellar atrophy. Tagliavini F, Pilleri G. Acta Neuropathol; 1985 Jun 15; 66(2):127-33. PubMed ID: 4013667 [Abstract] [Full Text] [Related]
18. Hereditary olivopontocerebellar atrophy with retinal degeneration. Report of a family through six generations. Weiner LP, Konigsmark BW, Stoll J, Magladery JW. Arch Neurol; 1967 Apr 15; 16(4):364-76. PubMed ID: 6021917 [No Abstract] [Full Text] [Related]
19. A variety of olivopontocerebellar atrophy distinguished by slow eye movements and peripheral neuropathy. Wadia NH. Adv Neurol; 1984 Apr 15; 41():149-77. PubMed ID: 6093483 [No Abstract] [Full Text] [Related]
20. The orthostatic hypotension syndrome of Shy-Drager. A clinicopathologic report. Schwarz GA. Arch Neurol; 1967 Feb 15; 16(2):123-39. PubMed ID: 6018044 [No Abstract] [Full Text] [Related] Page: [Next] [New Search]