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.
42. Atypical Gerstmann-Straüssler syndrome or familial spinocerebellar ataxia and Alzheimer's disease? de Courten-Myers G; Mandybur TI Neurology; 1987 Feb; 37(2):269-75. PubMed ID: 3808307 [TBL] [Abstract][Full Text] [Related]
43. [Familial atrophic form of spinocerebellar ataxia]. Gaj T; Grendus-Tota B Neurol Neurochir Pol; 1973; 7(5):679-83. PubMed ID: 4763007 [No Abstract] [Full Text] [Related]
44. A case of Gerstmann-Sträussler-Scheinker syndrome with the P105L prion protein gene mutation presenting with ataxia and extrapyramidal signs without spastic paraparesis. Iwasaki Y; Kizawa M; Hori N; Kitamoto T; Sobue G Clin Neurol Neurosurg; 2009 Sep; 111(7):606-9. PubMed ID: 19443103 [TBL] [Abstract][Full Text] [Related]
45. An autopsy case of spinocerebellar ataxia type 6 with mental symptoms of schizophrenia and dementia. Tashiro H; Suzuki SO; Hitotsumatsu T; Iwaki T Clin Neuropathol; 1999; 18(4):198-204. PubMed ID: 10442462 [TBL] [Abstract][Full Text] [Related]
46. Syndrome of bilateral ophthalmoplegia and ataxia (a varient of Fisher's syndrome) (case report). Bomb BS; Bedi HK; Saifee AA J Assoc Physicians India; 1979 Feb; 27(2):175-7. PubMed ID: 511838 [No Abstract] [Full Text] [Related]
48. Clinical phenotype and neuroimaging findings in a French family with hereditary ferritinopathy (FTL498-499InsTC). Ory-Magne F; Brefel-Courbon C; Payoux P; Debruxelles S; Sibon I; Goizet C; Labauge P; Menegon P; Uro-Coste E; Ghetti B; Delisle MB; Vidal R; Rascol O Mov Disord; 2009 Aug; 24(11):1676-83. PubMed ID: 19514068 [TBL] [Abstract][Full Text] [Related]
49. A newly formed amyloidogenic fragment due to a stop codon mutation causes familial British dementia. Ghiso J; Vidal R; Rostagno A; Mead S; Révész T; Plant G; Frangione B Ann N Y Acad Sci; 2000 Apr; 903():129-37. PubMed ID: 10818498 [TBL] [Abstract][Full Text] [Related]
50. A Novel ITM2B Mutation Associated with Familial Chinese Dementia. Liu X; Chen KL; Wang Y; Huang YY; Chen SD; Dong Q; Cui M; Yu JT J Alzheimers Dis; 2021; 81(2):499-505. PubMed ID: 33814452 [TBL] [Abstract][Full Text] [Related]
51. [An autopsy case of Crow-Fukase syndrome with massive appearance of amyloid bodies in the central nervous systems]. Tomi H; Mukoyama M; Kamei N; Sunohara N; Satoyoshi E Rinsho Shinkeigaku; 1988 Aug; 28(8):887-90. PubMed ID: 3240625 [No Abstract] [Full Text] [Related]
54. [A novel variation in ATP1A3 gene in a child with CAPOS syndrome]. Zhang F; Wang J; Zou LP; Zhang MN; Dun S; Yang G Zhonghua Er Ke Za Zhi; 2020 Mar; 58(3):233-235. PubMed ID: 32135597 [TBL] [Abstract][Full Text] [Related]
55. Clinical presentation of rapidly progressive familial Danish dementia. Zhou Z; Ainger TJ; Han DY Neurocase; 2018; 24(5-6):287-289. PubMed ID: 30843473 [TBL] [Abstract][Full Text] [Related]
56. Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome: a histopathologic case report. Szmulewicz DJ; Merchant SN; Halmagyi GM Otol Neurotol; 2011 Oct; 32(8):e63-5. PubMed ID: 21451431 [No Abstract] [Full Text] [Related]
58. Miniplaques and shapeless cerebral amyloid deposits in a case of Gerstmann-Sträussler-Scheinker's syndrome. Boellaard JW; Doerr-Schott J; Schlote W Acta Neuropathol; 1993; 86(5):532-5. PubMed ID: 8310806 [TBL] [Abstract][Full Text] [Related]