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1
Hereditary spastic paraparesis: a review of new developments.
J Neurol Neurosurg Psychiatry. 2000 Aug;69(2):150-60. doi: 10.1136/jnnp.69.2.150.
2
[Congenital autosomal-recessive familial spastic paraplegia].
Zh Nevropatol Psikhiatr Im S S Korsakova. 1991;91(8):97-9.
3
Hereditary spastic paraplegia. A diagnostic reminder.
Dev Med Child Neurol. 1993 May;35(5):452-5. doi: 10.1111/j.1469-8749.1993.tb11669.x.
4
Clinical Reasoning: Childhood-onset atrophy and spasticity.
Neurology. 2016 Mar 29;86(13):e140-3. doi: 10.1212/WNL.0000000000002519.
5
Complicated autosomal recessive hereditary spastic paraplegia: a complex picture is emerging.
Neurology. 2008 Apr 15;70(16 Pt 2):1375-6. doi: 10.1212/01.wnl.0000310433.12618.e4.
6
Hereditary spastic paraplegias.
Hong Kong Med J. 2009 Jun;15(3):217-20.
7
X-linked adrenoleukodystrophy presenting as autosomal dominant pure hereditary spastic paraparesis.
J Neurol Neurosurg Psychiatry. 2004 May;75(5):686-8. doi: 10.1136/jnnp.2003.022970.
8
MRI of autosomal dominant pure spastic paraplegia.
Neuroradiology. 1997 Oct;39(10):724-7. doi: 10.1007/s002340050495.
9
[Ataxias and hereditary spastic paraplegias].
Nervenarzt. 2017 Jul;88(7):720-727. doi: 10.1007/s00115-017-0357-4.
10
Spinal cord magnetic resonance imaging in autosomal dominant hereditary spastic paraplegia.
Neuroradiology. 2005 Oct;47(10):730-4. doi: 10.1007/s00234-005-1415-3. Epub 2005 Sep 6.

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Microglia and CD8+ T cell activation precede neuronal loss in a murine model of spastic paraplegia 15.
J Exp Med. 2025 Jul 7;222(7). doi: 10.1084/jem.20232357. Epub 2025 Apr 23.
2
Spastic Paraplegia Type 78 Associated With ATP13A2 Gene Variants in Compound Heterozygosity.
Mol Genet Genomic Med. 2025 Feb;13(2):e70073. doi: 10.1002/mgg3.70073.
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A rare case of hereditary spastic paraplegia: Case report.
Radiol Case Rep. 2024 Nov 15;20(1):837-840. doi: 10.1016/j.radcr.2024.09.158. eCollection 2025 Jan.
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ESCRT-III: a versatile membrane remodeling machinery and its implications in cellular processes and diseases.
Anim Cells Syst (Seoul). 2024 Jul 25;28(1):367-380. doi: 10.1080/19768354.2024.2380294. eCollection 2024.
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Clinical analysis in patients with hereditary spastic paraplegia.
Front Neurol. 2023 Jun 15;14:1198728. doi: 10.3389/fneur.2023.1198728. eCollection 2023.
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Novel mutation of gene in a Chinese family with hereditary spastic paraplegia: A case report.
World J Clin Cases. 2023 May 16;11(14):3288-3294. doi: 10.12998/wjcc.v11.i14.3288.
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Genetic characterization of primary lateral sclerosis.
J Neurol. 2023 Aug;270(8):3970-3980. doi: 10.1007/s00415-023-11746-7. Epub 2023 May 3.
10
Leukodystrophy-Like Presentation in a Child: A Case of Hereditary Spastic Paraparesis-35.
Ann Indian Acad Neurol. 2022 Jul-Aug;25(4):745-746. doi: 10.4103/aian.aian_120_22. Epub 2022 Mar 25.

本文引用的文献

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Hereditary spastic paraplegia.
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A sex-linked recessive form of spastic paraplegia.
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Familial spastic paraplegia with amyotrophy, oligophrenia, and central retinal degeneration.
Arch Neurol. 1959 Aug;1:133-40. doi: 10.1001/archneur.1959.03840020007002.
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Familial spastic paraplegia; its relation to mental and cardiac abnormalities.
Lancet. 1957 Jul 27;273(6987):169-70. doi: 10.1016/s0140-6736(57)90618-9.
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Hereditary (familial) spastic paraplegia; further clinical and pathologic observations.
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Hereditary spastic paraplegia; report of a family with associated extrapyramidal signs.
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Hereditary (familial) spastic paraplegia.
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