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.
8. A Diagnostic Approach to Spastic ataxia Syndromes. Pedroso JL; Vale TC; França Junior MC; Kauffman MA; Teive H; Barsottini OGP; Munhoz RP Cerebellum; 2022 Dec; 21(6):1073-1084. PubMed ID: 34782953 [TBL] [Abstract][Full Text] [Related]
9. Expanding the clinical and neuroimaging features of NKX6-2-related hereditary spastic ataxia type 8. Hosseini Bereshneh A; Hosseipour S; Rasoulinezhad MS; Pak N; Garshasbi M; Tavasoli AR Eur J Med Genet; 2020 May; 63(5):103868. PubMed ID: 32004679 [TBL] [Abstract][Full Text] [Related]
10. A case of spinocerebellar ataxia accompanied by severe involvement of the motor neuron system. Manabe Y; Shiro Y; Takahashi K; Kashihara K; Abe K Neurol Res; 2000 Sep; 22(6):567-70. PubMed ID: 11045017 [TBL] [Abstract][Full Text] [Related]
11. A FAMILY WITH HEREDITARY SPASTIC ATAXIA: AN INVESTIGATION INTO THE EXISTENCE OF THE SO CALLED "FORMES FRUSTES". van Beusekom ; Staal A; Went LN Acta Neurol Scand; 1965; 41(2):97-119. PubMed ID: 14289917 [No Abstract] [Full Text] [Related]
12. De novo mutations of TUBB2A cause infantile-onset epilepsy and developmental delay. Cai S; Li J; Wu Y; Jiang Y J Hum Genet; 2020 Jul; 65(7):601-608. PubMed ID: 32203252 [TBL] [Abstract][Full Text] [Related]
13. SCA1 patients may present as hereditary spastic paraplegia and must be included in spastic-ataxias group. Pedroso JL; de Souza PV; Pinto WB; Braga-Neto P; Albuquerque MV; Saraiva-Pereira ML; Jardim LB; Barsottini OG Parkinsonism Relat Disord; 2015 Oct; 21(10):1243-6. PubMed ID: 26231471 [TBL] [Abstract][Full Text] [Related]
14. The "broken wishbone" splenial sign: A diagnostic hallmark for SPG54 spastic ataxia. Zaidi SA; Saal HM; Espay AJ; Duker AP J Neurol Sci; 2019 Aug; 403():114-116. PubMed ID: 31271950 [No Abstract] [Full Text] [Related]
17. [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]