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Hereditary (familial) spastic paraplegia.

作者信息

SCHWARZ G A

出版信息

AMA Arch Neurol Psychiatry. 1952 Nov;68(5):655-62. doi: 10.1001/archneurpsyc.1952.02320230081010.

DOI:10.1001/archneurpsyc.1952.02320230081010

PMID:12984880

Abstract

摘要

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Hereditary (familial) spastic paraplegia.

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引用本文的文献

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Bibliography of human genetics.

Am J Hum Genet. 1953 Sep;5(3):284-91.

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Spinal somatosensory evoked potentials in hereditary spastic paraplegia.

J Neurol Neurosurg Psychiatry. 1981 Mar;44(3):243-6. doi: 10.1136/jnnp.44.3.243.

[Familial spastic spinal paralysis].

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相似文献

Hereditary (familial) spastic paraplegia.

AMA Arch Neurol Psychiatry. 1952 Nov;68(5):655-62. doi: 10.1001/archneurpsyc.1952.02320230081010.

Prevalence of hereditary ataxia and spastic paraplegia in southeast Norway: a population-based study.

Brain. 2009 Jun;132(Pt 6):1577-88. doi: 10.1093/brain/awp056. Epub 2009 Mar 31.

Advances in hereditary spastic paraplegia.

Curr Opin Neurol. 1997 Aug;10(4):313-8. doi: 10.1097/00019052-199708000-00006.

Hereditary spastic paraplegia: identification of an SPG3A gene mutation in a Chinese family.

Hong Kong Med J. 2009 Aug;15(4):304-7.

Hereditary spastic paraplegia with hypoplastic corpus callosum in a Turkish family.

J Child Neurol. 2007 Feb;22(2):214-7. doi: 10.1177/0883073807300293.

Hereditary spastic paraplegia caused by compound heterozygous mutations outside the motor domain of the KIF1A gene.

Eur J Neurol. 2017 May;24(5):741-747. doi: 10.1111/ene.13279. Epub 2017 Mar 22.

Gait evolution in a family with hereditary spastic paraplegia.

Eur J Paediatr Neurol. 2015 Jan;19(1):87-92. doi: 10.1016/j.ejpn.2014.08.001. Epub 2014 Aug 30.

Loss-of-function mutations in the ATP13A2/PARK9 gene cause complicated hereditary spastic paraplegia (SPG78).

Brain. 2017 Feb;140(2):287-305. doi: 10.1093/brain/aww307.

A founder mutation p.H701P identified as a major cause of SPG7 in Norway.

Eur J Neurol. 2016 Apr;23(4):763-71. doi: 10.1111/ene.12937. Epub 2016 Jan 12.

Hereditary Spastic Paraplegia: Clinical and Genetic Hallmarks.

Cerebellum. 2017 Apr;16(2):525-551. doi: 10.1007/s12311-016-0803-z.

引用本文的文献

Multimodal MRI Longitudinal Assessment of White and Gray Matter in Different SPG Types of Hereditary Spastic Paraparesis.

Front Neurosci. 2020 Jun 4;14:325. doi: 10.3389/fnins.2020.00325. eCollection 2020.

Brain white matter involvement in hereditary spastic paraplegias: analysis with multiple diffusion tensor indices.

AJNR Am J Neuroradiol. 2014 Aug;35(8):1533-8. doi: 10.3174/ajnr.A3897. Epub 2014 Apr 30.

Hereditary spastic paraplegia: clinico-pathologic features and emerging molecular mechanisms.

Acta Neuropathol. 2013 Sep;126(3):307-28. doi: 10.1007/s00401-013-1115-8. Epub 2013 Jul 30.

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.

CEREBRAL PALSY IN CHILDREN OF VERY LOW BIRTH WEIGHT.

Arch Dis Child. 1963 Dec;38(202):579-88. doi: 10.1136/adc.38.202.579.

Bibliography of human genetics.

Am J Hum Genet. 1953 Sep;5(3):284-91.

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.

Hereditary "pure" spastic paraplegia: a clinical and genetic study of 22 families.

J Neurol Neurosurg Psychiatry. 1981 Oct;44(10):871-83. doi: 10.1136/jnnp.44.10.871.

Spinal somatosensory evoked potentials in hereditary spastic paraplegia.

J Neurol Neurosurg Psychiatry. 1981 Mar;44(3):243-6. doi: 10.1136/jnnp.44.3.243.

[Familial spastic spinal paralysis].

Dtsch Z Nervenheilkd. 1968 Jun 5;193(4):287-323.