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Academic Journal

The first reports of FA2H-associated neurodegeneration from two unrelated Iranian families.

Authors : Hashemi, Narges (AUTHOR); Abadi, Reza Nejad Shahrokh (AUTHOR); Alavi, Afagh (AUTHOR)

Subjects: IRANIANS; FAMILIAL spastic paraplegia; IRON oresIRAN

Source: Neurological Sciences. Dec2023, Vol. 44 Issue 12, p4359-4362. 4p.

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Academic Journal

Two sisters with recessive dystrophic epidermolysis bullosa caused by novel variants in COL7A1.

Authors : Zhou, Mandi¹ (AUTHOR) ; Zheng, Zhixin^2,3 (AUTHOR); Teng, Jinglei^2,3 (AUTHOR)

Subjects: *EPIDERMOLYSIS bullosa; *FAMILIAL spastic paraplegia; *SISTERS

Source: Skin Research & Technology. Jun2024, Vol. 30 Issue 6, p1-3. 3p.

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Academic Journal

A founder mutation in COQ7, p.(Leu111Pro), causes pure hereditary spastic paraplegia (HSP) in the Iranian population.

Authors : Sadr, Zahra (AUTHOR); Zare-Abdollahi, Davood (AUTHOR); Rohani, Mohammad (AUTHOR)

Subjects: IRANIANS; FAMILIAL spastic paraplegia; GENETIC mutation

Source: Neurological Sciences. Jul2023, Vol. 44 Issue 7, p2599-2602. 4p. 2 Charts.

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Academic Journal

Mobile digital gait analysis captures effects of botulinum toxin in hereditary spastic paraplegia.

Authors : Ibrahim, Alzhraa A. (AUTHOR); Ollenschläger, Malte (AUTHOR); Klebe, Stephan (AUTHOR)

Subjects: FAMILIAL spastic paraplegia; BOTULINUM toxin; BOTULINUM A toxins

Source: European Journal of Neurology. Aug2024, Vol. 31 Issue 8, p1-10. 10p.

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Academic Journal

Relationship between brain white matter damage and grey matter atrophy in hereditary spastic paraplegia types 4 and 5.

Authors : Tu, Yuqing (AUTHOR); Liu, Ying (AUTHOR); Fan, Shuping (AUTHOR)

Subjects: FAMILIAL spastic paraplegia; WHITE matter (Nerve tissue); ATROPHY

Source: European Journal of Neurology. Aug2024, Vol. 31 Issue 8, p1-11. 11p.

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Academic Journal

Movement disorders in hereditary spastic paraplegia (HSP): a systematic review and individual participant data meta-analysis.

Authors : Fereshtehnejad, Seyed-Mohammad (AUTHOR); Saleh, Philip A. (AUTHOR); Oliveira, Lais M. (AUTHOR)

Subjects: FAMILIAL spastic paraplegia; MOVEMENT disorders; SCHOENLEIN-Henoch purpura

Source: Neurological Sciences. Mar2023, Vol. 44 Issue 3, p947-959. 13p. 1 Color Photograph, 1 Diagram, 4 Charts, 2 Graphs.

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Academic Journal

Spinal cord stimulation may improve gait and cognition in hereditary spastic paraplegia with mental retardation: a case report.

Authors : Tufo, Tommaso (AUTHOR); Ciavarro, Marco (AUTHOR); Di Giuda, Daniela (AUTHOR)

Subjects: FAMILIAL spastic paraplegia; SPINAL cord; SINGLE-photon emission computed tomography

Source: Neurological Sciences. Mar2023, Vol. 44 Issue 3, p961-966. 6p. 1 Diagram, 2 Charts.

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Academic Journal

Novel ERLIN2 variant expands the phenotype of Spastic Paraplegia 18.

Authors : de Souza, Guilherme Carvalho (AUTHOR); Malta, Maria Carolina (AUTHOR); Santos, Mirele Raíssa Silva (AUTHOR)

Subjects: PARAPLEGIA; FAMILIAL spastic paraplegia; MEDICAL geneticsBRAZIL

Source: Neurological Sciences. Jun2024, Vol. 45 Issue 6, p2705-2710. 6p.

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Academic Journal

A novel ATP13A2 variant causing complicated hereditary spastic paraplegia.

Authors : Zhang, Fan (AUTHOR); Liu, Peng (AUTHOR); Li, Jiaxiang (AUTHOR)

Subjects: FAMILIAL spastic paraplegia; PARKINSON'S disease; WHOLE genome sequencing

Source: Neurological Sciences. Apr2024, Vol. 45 Issue 4, p1749-1753. 5p.

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Academic Journal

Progressive motor neuron syndromes with single CNS lesions and CSF oligoclonal bands: never forget solitary sclerosis!

Authors : Giacopuzzi Grigoli, Eleonora (AUTHOR); Cinnante, Claudia (AUTHOR); Doneddu, Pietro Emiliano (AUTHOR)

Subjects: NATIONAL Football League; FAMILIAL spastic paraplegia; MOTOR neurons

Source: Neurological Sciences. Dec2022, Vol. 43 Issue 12, p6951-6954. 4p. 1 Black and White Photograph.

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