脊髓性肌萎缩症：韦尼克-霍夫曼病中的胎儿样组织病理学模式。 - Suppr

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超能文献

Spinal muscular atrophy: foetal-like histopathological pattern in Werdnig-Hoffmann disease.

作者信息

Hausmanowa-Petrusewicz I, Fidzianska A

出版信息

Bull N Y Acad Med. 1974 Dec;50(11):1157-72.

PMID:4529631

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1749458/

Abstract

摘要

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcf5/1749458/fabd88a3d770/bullnyacadmed00178-0026-a.jpg

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Spinal muscular atrophy: foetal-like histopathological pattern in Werdnig-Hoffmann disease.脊髓性肌萎缩症：韦尼克-霍夫曼病中的胎儿样组织病理学模式。

Bull N Y Acad Med. 1974 Dec;50(11):1157-72.

Werdnig-Hoffmann disease.韦尼克-霍夫曼病

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[Ultrastructural findings and characterization of isoenzymes in the muscle in case of Werdnig-Hoffmann disease].

Arch De Vecchi Anat Patol. 1967 Dec;50(3):629-44.

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[A case of Werdnig-Hoffmann disease in a newborn infant].[一例新生儿患韦尼克-霍夫曼病的病例]

Pediatria (Napoli). 1977 Dec 31;85(4):625-44.

[Werdnig-Hoffmann's disease. Study on 53 cases (author's transl)].

An Esp Pediatr. 1975 Jul-Aug;8(4):371-84.

[Progressive muscular spinal atrophy of Werdnig-Hoffmann].[韦尼克-霍夫曼进行性脊髓性肌萎缩症]

Folia Hered Pathol (Milano). 1968:113-26.

[Type II proximal spinal muscular atrophy. Clinical, electrophysiological, histopathological and histochemical studies].[II型近端脊髓性肌萎缩症。临床、电生理、组织病理学及组织化学研究]

Minerva Pediatr. 1974 Jun 23;26(22):1125-45.

Werdnig-Hoffmann disease.韦尼克-霍夫曼病

Cent Afr J Med. 1980 May;26(5):107-11.

引用本文的文献

Spectrum of neuropathophysiology in spinal muscular atrophy type I.I型脊髓性肌萎缩症的神经病理生理学谱

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Failure of lower motor neuron radial outgrowth precedes retrograde degeneration in a feline model of spinal muscular atrophy.下运动神经元的放射状生长失败先于猫肌萎缩性脊髓侧索硬化症模型中的逆行性变性。

J Comp Neurol. 2012 Jun 1;520(8):1737-50. doi: 10.1002/cne.23010.

Ultrastructural abnormalities of muscle and neuromuscular junction differentiation in a bovine congenital neuromuscular disease.一种牛先天性神经肌肉疾病中肌肉和神经肌肉接头分化的超微结构异常

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本文引用的文献

INFANTILE MUSCULAR ATROPHY. A PROSPECTIVE STUDY WITH PARTICULAR REFERENCE TO A SLOWLY PROGRESSIVE VARIETY.婴儿型肌肉萎缩症。一项前瞻性研究，特别关注一种缓慢进展型。

Brain. 1964 Dec;87:707-18. doi: 10.1093/brain/87.4.707.

Hereditary proximal spinal muscular atrophy, a clinical entity simulating progressive muscular dystrophy.遗传性近端脊髓性肌萎缩症，一种类似进行性肌营养不良的临床病症。

Acta Psychiatr Neurol Scand. 1955;30(1-2):395-406.

Benign spinal muscular atrophy arising in childhood and adolescence.

J Neurol Sci. 1967 Jul-Aug;5(1):121-58. doi: 10.1016/0022-510x(67)90013-5.

[The problem of the infantile and juvenile forms of spinal muscular atrophy].[婴儿型和少年型脊髓性肌萎缩症的问题]

Rev Neurol (Paris). 1966 Apr;114(4):295-306.

Electromyography and muscle biopsy in infantile spinal muscular atrophy.婴儿脊髓性肌萎缩症的肌电图检查与肌肉活检

Brain. 1970;93(1):15-30. doi: 10.1093/brain/93.1.15.

Spinal muscular atrophy type II. A separate genetic and clinical entity from type I (Werdnig-Hoffmann disease) and type 3 (Kugelberg-Welander disease).

Clin Genet. 1971;2(4):203-9.

Creatine phospholinase activity in spinal muscular atrophy.

J Neurol Sci. 1968 Mar-Apr;6(2):261-7. doi: 10.1016/0022-510x(68)90095-6.

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