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The p.D417N variant of TUBB4A as a possible cause of hereditary spastic paraplegia: a case report.

• Authors : Matteoni, Enrico¹ (AUTHOR) ; Canosa, Antonio^1,2,3 (AUTHOR); Tessa, Alessandra⁴ (AUTHOR)

Subjects: *TUBULINS; *BASAL ganglia; *EUKARYOTIC cells

• Source: Egyptian Journal of Neurology, Psychiatry & Neurosurgery. 11/1/2024, Vol. 60 Issue 1, p1-5. 5p.

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Investigating the genetic basis of hereditary spastic paraplegia and cerebellar Ataxia in Pakistani families.

• Authors : Azeem, Arfa¹ (AUTHOR); Ahmed, Asif Naveed¹ (AUTHOR); Khan, Niamat¹ (AUTHOR)

• Source: BMC Neurology. 9/20/2024, Vol. 24 Issue 1, p1-12. 12p.

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Adult-Onset Hereditary Spastic Paraplegia 15 in a Saudi Patient with A Compound Heterozygous Variant in the ZFYVE26 Gene.

• Authors : ALGAHTANI, Hussein^1,2,3 ; SHIRAH, Bader⁴; ALJOHANI, Rahaf³

• Source: Maedica - a Journal of Clinical Medicine. 2022, Vol. 17 Issue 3, p730-734. 5p.

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CAPN1 and hereditary spastic paraplegia: a novel variant in an Iranian family and overview of the genotype-phenotype correlation.

• Authors : Rahimi Bidgoli, Mohammad Masoud¹ (AUTHOR); Javanparast, Leila¹ (AUTHOR); Rohani, Mohammad² (AUTHOR)

• Source: International Journal of Neuroscience. Oct2021, Vol. 131 Issue 10, p962-974. 13p.

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Liver X receptor-agonist treatment rescues degeneration in a Drosophila model of hereditary spastic paraplegia.

• Authors : Byrne, Dwayne J.^1,2 (AUTHOR); Garcia-Pardo, M. Elena¹ (AUTHOR); Cole, Nelson B.² (AUTHOR)

• Source: Acta Neuropathologica Communications. 3/28/2022, Vol. 10 Issue 1, p1-20. 20p.

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Description of clinical features and genetic analysis of one ultra-rare (SPG64) and two common forms (SPG5A and SPG15) of hereditary spastic paraplegia families.

• Authors : Pashaei, Mahdieh¹ (AUTHOR); Davarzani, Atefeh¹ (AUTHOR); Hajati, Reza¹ (AUTHOR)

• Source: Journal of Neurogenetics. Jun2021, Vol. 35 Issue 2, p84-94. 11p.

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The investigation of genetic and clinical features in patients with hereditary spastic paraplegia in central‐Southern China.

• Authors : Wang, Chen¹ (AUTHOR); Zhang, Yun‐Jian¹ (AUTHOR); Xu, Ci‐Hao² (AUTHOR)

• Source: Molecular Genetics & Genomic Medicine. May2021, Vol. 9 Issue 5, p1-10. 10p.

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Balance rehabilitation with a virtual reality protocol for patients with hereditary spastic paraplegia: Protocol for a clinical trial.

• Authors : Zeigelboim, Bianca Simone¹ (AUTHOR); José, Maria Renata¹ (AUTHOR); Santos, Geslaine Janaina Bueno dos² (AUTHOR)

Subjects: *RESEARCH protocols; *VIRTUAL reality; *FAMILIAL spastic paraplegia

• Source: PLoS ONE. 4/1/2021, Vol. 16 Issue 4, p1-13. 13p.

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Two novel truncating variants in UBAP1 are responsible for hereditary spastic paraplegia.

• Authors : Bian, Xinchao¹ (AUTHOR); Cheng, Guangying² (AUTHOR); Sun, Xinbo¹ (AUTHOR)

Subjects: *FAMILIAL spastic paraplegia; *NEURODEGENERATION

• Source: PLoS ONE. 6/30/2021, Vol. 16 Issue 6, p1-11. 11p.

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Hereditary spastic paraplegia.

• Authors : Murala, Sireesha¹ (AUTHOR) ; Nagarajan, Elanagan² (AUTHOR); Bollu, Pradeep C.¹ (AUTHOR)

• Source: Neurological Sciences. 2021, Vol. 42 Issue 3, p883-894. 12p. 4 Charts.

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