婴儿期小脑-丘脑-脊髓变性：韦尼克-霍夫曼病的一种罕见变异型 - Suppr

Suppr

超能文献

CEREBELLO-THALAMO-SPINAL DEGENERATION IN INFANCY: AN UNUSUAL VARIANT OF WERDNIG-HOFFMANN DISEASE.

作者信息

NORMAN R M, KAY J M

出版信息

Arch Dis Child. 1965 Jun;40(211):302-8. doi: 10.1136/adc.40.211.302.

DOI:10.1136/adc.40.211.302

PMID:14294750

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2019395/

Abstract

摘要

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b8a4/2019395/5e5e787720f5/archdisch01576-0071-a.jpg

相似文献

CEREBELLO-THALAMO-SPINAL DEGENERATION IN INFANCY: AN UNUSUAL VARIANT OF WERDNIG-HOFFMANN DISEASE.

Arch Dis Child. 1965 Jun;40(211):302-8. doi: 10.1136/adc.40.211.302.

[CASE OF MYELOPATHIC MUSCULAR ATROPHY THOUGHT AT FIRST TO BE PROGRESSIVE MUSCULAR DYSTROPHY--A VIEW OF THE RELATION BETWEEN KUGELBERG-WELANDER'S MUSCULAR ATROPHY AND WERDNIG-HOFFMANN DISEASE].

Nihon Shonika Gakkai Zasshi. 1963 Nov 1;67:745-8.

[Cerebral agyria-pachygyria in a child with Werdnig-Hoffmann disease].

Rev Neurol (Paris). 1999 Sep;155(8):589-91.

[Infantile spinal muscular atrophy. Description of 2 cases of Werdnig-Hoffmann disease].

Minerva Pediatr. 1987 Sep 30;39(17-18):709-14.

Cerebellar hypoplasia in Werdnig-Hoffmann disease.

Arch Dis Child. 1961 Feb;36(185):96-101. doi: 10.1136/adc.36.185.96.

Chromatolytic neurons in Werdnig-Hoffmann disease contain phosphorylated neurofilaments.

Acta Neuropathol. 1988;77(1):91-4. doi: 10.1007/BF00688247.

Spinal Muscular Atrophy: Autopsy Based Neuropathological Demonstration.

Neurol India. 2020 Jul-Aug;68(4):882-885. doi: 10.4103/0028-3886.293477.

Infantile neuronal degeneration masquerading as Werdnig-Hoffmann disease.

Ann Neurol. 1980 Sep;8(3):317-24. doi: 10.1002/ana.410080316.

Infantile progressive spinal muscular atrophy with ophthalmoplegia and pyramidal symptoms.

Pediatr Neurol. 1994 Jun;10(4):320-4. doi: 10.1016/0887-8994(94)90130-9.

Adult-onset motor neuron disease and infantile Werdnig-Hoffmann disease (spinal muscular atrophy type 1) in the same family.

Neurology. 1992 Aug;42(8):1477-80. doi: 10.1212/wnl.42.8.1477.

引用本文的文献

Cerebellar pathology contributes to neurodevelopmental deficits in spinal muscular atrophy.

Res Sq. 2025 Jun 23:rs.3.rs-6819992. doi: 10.21203/rs.3.rs-6819992/v2.

The Dual Nature of Onuf's Nucleus: Neuroanatomical Features and Peculiarities, in Health and Disease.

Front Neuroanat. 2020 Sep 4;14:572013. doi: 10.3389/fnana.2020.572013. eCollection 2020.

Infantile cerebello-optic atrophy. Neuropathology of the progressive encephalopathy syndrome with edema, hypsarrhythmia and optic atrophy (the PEHO syndrome).

Acta Neuropathol. 1993;85(3):241-7. doi: 10.1007/BF00227717.

A neuropathologic study of Werdnig-Hoffmann disease with special reference to the thalamus and posterior roots.

Acta Neuropathol. 1983;60(1-2):99-106. doi: 10.1007/BF00685353.

Amyotrophic cerebellar hypoplasia: a specific form of infantile spinal atrophy.

Acta Neuropathol. 1984;63(4):282-6. doi: 10.1007/BF00687334.

Is Werdnig-Hoffmann disease a pure lower motor neuron disorder?

Acta Neuropathol. 1985;65(3-4):270-80. doi: 10.1007/BF00687008.

Anterior horn cell disease associated with pontocerebellar hypoplasia in infants.

J Neurol Neurosurg Psychiatry. 1977 Apr;40(4):370-8. doi: 10.1136/jnnp.40.4.370.

本文引用的文献

[Spinal amyotrophia in children (Werdnig-Hoffmann paralysis) as hereditary degeneration].

Rev Neurol (Paris). 1951 Jan;84(1):14-31.

Cerebellar hypoplasia in Werdnig-Hoffmann disease.

Arch Dis Child. 1961 Feb;36(185):96-101. doi: 10.1136/adc.36.185.96.

[Forty cases of Werdnig-Hoffmann disease with eleven anatomical examinations].

Rev Neurol (Paris). 1955 Oct;93(4):621-44.

文献AI研究员

20分钟写一篇综述，助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型，支持多种主流文档格式。

立即体验