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Page 1

Novel genetic variant in hereditary spastic paraparesis.

Knight KAW, Barbour-Hastie C, Gane A, O'Riordan J. Knight KAW, et al. BMJ Case Rep. 2024 Apr 17;17(4):e252396. doi: 10.1136/bcr-2022-252396. BMJ Case Rep. 2024. PMID: 38631813

Autoimmune Hemolytic Anemia Due to Spondyloenchondrodysplasia with Spastic Paraparesis and Intracranial Calcification due to Mutation in ACP5.

Aylan Gelen S, Kara B, Eser Şimsek I, Güngör M, Zengin E, Sarper N. Aylan Gelen S, et al. J Pediatr Genet. 2021 Nov 2;13(1):50-56. doi: 10.1055/s-0041-1736560. eCollection 2024 Mar. J Pediatr Genet. 2021. PMID: 38567175 Free PMC article.

HTLV-1 associated myelopathy/tropical spastic paraparesis (HAM/TSP): Case based discussion of risk factors, clinical, and therapeutic considerations.

Saab L, DiCapua D, Zubair AS. Saab L, et al. J Neurol Sci. 2024 Apr 15;459:122973. doi: 10.1016/j.jns.2024.122973. Epub 2024 Mar 19. J Neurol Sci. 2024. PMID: 38520941 Review.

Nonpharmacological interventions and outcomes in the management of complications of human T-cell lymphotropic virus type 1-related myelopathy/tropical spastic paraparesis: A systematic review.

Davoudi M, Boostani R, Manzari ZS. Davoudi M, et al. J Res Med Sci. 2024 Feb 23;28:87. doi: 10.4103/jrms.jrms_300_22. eCollection 2023. J Res Med Sci. 2024. PMID: 38510783 Free PMC article. Review.

Hereditary spastic paraparesis type 18 (SPG18): new ERLIN2 variants in a series of Italian patients, shedding light upon genetic and phenotypic variability.

Cioffi E, Gioiosa V, Tessa A, Petrucci A, Trovato R, Santorelli FM, Casali C. Cioffi E, et al. Neurol Sci. 2024 Mar 1. doi: 10.1007/s10072-024-07423-w. Online ahead of print. Neurol Sci. 2024. PMID: 38427163

Hereditary spastic paraparesis type 46 (SPG46): new GBA2 variants in a large Italian case series and review of the literature.

Cioffi E, Coppola G, Musumeci O, Gallone S, Silvestri G, Rossi S, Piemonte F, D'Amico J, Tessa A, Santorelli FM, Casali C. Cioffi E, et al. Neurogenetics. 2024 Feb 9. doi: 10.1007/s10048-024-00749-9. Online ahead of print. Neurogenetics. 2024. PMID: 38334933 Review.

Intrathecal baclofen for the management of hereditary spastic paraparesis: a systematic review.

Viana Pinto L, Romeiro I, Gouveia F, Ramalho J, Ribeiro Silva S, Táboas Simões MI, Rodrigues Leal J. Viana Pinto L, et al. Int J Rehabil Res. 2024 Mar 1;47(1):3-9. doi: 10.1097/MRR.0000000000000607. Epub 2024 Jan 20. Int J Rehabil Res. 2024. PMID: 38251093

A rare case of adult-onset spastic paraparesis associated with Klinefelter syndrome.

Adams L, De Bleecker J. Adams L, et al. BMC Neurol. 2024 Jan 15;24(1):29. doi: 10.1186/s12883-024-03525-2. BMC Neurol. 2024. PMID: 38225593 Free PMC article.

A Novel SPAST Variant Associated with Isolated Spastic Paraplegia.

Høyer H, Nakken O, Holmøy T. Høyer H, et al. Case Rep Genet. 2023 Dec 31;2023:4553365. doi: 10.1155/2023/4553365. eCollection 2023. Case Rep Genet. 2023. PMID: 38186854 Free PMC article.

Hereditary Spastic Paraplegia Type 11-Clinical, Genetic and Neuroimaging Characteristics.

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