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.
17. SPOAN syndrome: a novel mutation and new ocular findings; a case report. Bazvand F; Keramatipour M; Riazi-Esfahani H; Mahmoudi A BMC Neurol; 2021 Jan; 21(1):24. PubMed ID: 33451298 [TBL] [Abstract][Full Text] [Related]
18. Intrathecal baclofen therapy for the symptomatic treatment of hereditary spastic paraplegia. Margetis K; Korfias S; Boutos N; Gatzonis S; Themistocleous M; Siatouni A; Dalivigka Z; Flaskas T; Stranjalis G; Boviatsis E; Sakas D Clin Neurol Neurosurg; 2014 Aug; 123():142-5. PubMed ID: 24973568 [TBL] [Abstract][Full Text] [Related]
19. Complicated hereditary spastic paraplegia with peripheral neuropathy, optic atrophy and mental retardation. Miyama S; Arimoto K; Kimiya S; Tomi H Neuropediatrics; 2000 Aug; 31(4):214-7. PubMed ID: 11071149 [TBL] [Abstract][Full Text] [Related]
20. Clinical observations in autosomal recessive spastic paraplegia in childhood and further evidence for genetic heterogeneity. Topaloğlu H; Pinarli G; Erdem H; Gücüyener K; Karaduman A; Topçu M; Akarsu AN; Ozgüç M Neuropediatrics; 1998 Aug; 29(4):189-94. PubMed ID: 9762694 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]