These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
124 related articles for article (PubMed ID: 31591173)
21. [Olivo-ponto-cerebellar atrophy (a clinico-morphologic and biochemical study of one case)]. Drobysheva NA; Grushina AG; Kut'lina VA Zh Nevropatol Psikhiatr Im S S Korsakova; 1974; 74(12):1793-8. PubMed ID: 4450909 [No Abstract] [Full Text] [Related]
22. [A 29-year-old man with diabetes insipidus and cerebellar ataxia and development of spinal cord swelling 15 years after the onset]. Ohkuma Y; Sato K; Ohtomo T; Ohishi H; Mitsuoka H; Mori H; Hirai S; Takubo H; Takeda N; Sato K; Mizuno Y No To Shinkei; 1997 May; 49(5):473-81. PubMed ID: 9163763 [TBL] [Abstract][Full Text] [Related]
23. Is the "cerebellar" incoordination of Refsum's disease due to structural lesions in the cerebellum? Salisachs P J Neurol Neurosurg Psychiatry; 1982 May; 45(5):473-4. PubMed ID: 6177839 [No Abstract] [Full Text] [Related]
25. Acute cerebellar ataxia following meningococcal group C conjugate vaccination. Cutroneo PM; Italiano D; Trifirò G; Tortorella G; Russo A; Isola S; Caputi AP; Spina E J Child Neurol; 2014 Jan; 29(1):128-30. PubMed ID: 23275434 [TBL] [Abstract][Full Text] [Related]
26. 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; 25(4):269-81. PubMed ID: 5172645 [No Abstract] [Full Text] [Related]
27. [An autopsy case of Marie's hereditary ataxia]. Ishino H; Sato M; Mii T; Terano A; Hayahara T Seishin Shinkeigaku Zasshi; 1971 Oct; 73(10):747-57. PubMed ID: 5168989 [No Abstract] [Full Text] [Related]
28. [Differential diagnosis of cerebellar and spinal ataxia in horse. A case of cerebellar ataxia in a foal]. Böhm D Berl Munch Tierarztl Wochenschr; 1975 Mar; 88(5):81-6. PubMed ID: 1120060 [No Abstract] [Full Text] [Related]
29. Stiff-person syndrome associated with cerebellar ataxia and high glutamic acid decarboxylase antibody titer. Kono S; Miyajima H; Sugimoto M; Suzuki Y; Takahashi Y; Hishida A Intern Med; 2001 Sep; 40(9):968-71. PubMed ID: 11579968 [TBL] [Abstract][Full Text] [Related]
31. Adult celiac disease presenting as cerebellar syndrome. Finelli PF; McEntee WJ; Ambler M; Kestenbaum D Neurology; 1980 Mar; 30(3):245-9. PubMed ID: 7189024 [TBL] [Abstract][Full Text] [Related]
32. Superficial bedside brain biopsy can be a safe and practical approach to confirm a rare form of prion disease in cerebellar ataxia: A case study. Rusina R; Netuka D; Johanidesová S; Smětáková M; Mouchová Z; Matěj R J Neurol Sci; 2017 Apr; 375():73-75. PubMed ID: 28320192 [No Abstract] [Full Text] [Related]
33. Ataxia in childhood. Brett EM Physiotherapy; 1975 Nov; 61(11):329-31. PubMed ID: 1197408 [No Abstract] [Full Text] [Related]
37. Clinical Reasoning: Progressive cognitive decline, cerebellar ataxia, recurrent myoclonus, and epilepsy. Xiao F; Fan J; Tan J; Wang XF Neurology; 2018 May; 90(20):e1827-e1831. PubMed ID: 29760005 [No Abstract] [Full Text] [Related]
38. [An autopsy case of hereditary ataxia (hereditary spastic ataxia)]. Yagishita S; Nakano T; Iwabuchi K; Sakai H No To Shinkei; 1985 Jun; 37(6):603-9. PubMed ID: 4041292 [TBL] [Abstract][Full Text] [Related]
39. Clinical Reasoning: A 54-year-old woman with dementia, myoclonus, and ataxia. Ali F; Murray JA; Adams AC; Flanagan EP Neurology; 2017 Jul; 89(2):e7-e12. PubMed ID: 28696937 [No Abstract] [Full Text] [Related]
40. The clinical features and classification of the late onset autosomal dominant cerebellar ataxias. A study of 11 families, including descendants of the 'the Drew family of Walworth'. Harding AE Brain; 1982 Mar; 105(Pt 1):1-28. PubMed ID: 7066668 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]