Generalized giant axonal neuropathy-Reference-Cited by-同舟云学术

Generalized giant axonal neuropathy

Published:1977 Issue:3 Volume:40 Page:213-218
ISSN:0001-6322
Container-title:Acta Neuropathologica
language:en
Short-container-title:Acta Neuropathol

Author:

Peiffer J�rgen,Schlote Wolfgang,Bischoff Albert,Boltshauser Eugen,M�ller G�nter

Publisher

Springer Science and Business Media LLC

Subject

Cellular and Molecular Neuroscience,Neurology (clinical),Pathology and Forensic Medicine

Link

http://link.springer.com/content/pdf/10.1007/BF00691956.pdf

Reference38 articles.

1. Aguilar, M. J., Chadwick, D. L., Okuyama, K., Kamoshita, S.: Kinky Hair Disease. I. Clinical and Pathological Features. J. Neuropath. Exp. Neur.25, 507?522 (1966)

2. Ametani, T.: Infantile Neuroaxonal Dystrophy (INAD): Light and Electron Microscopic Observation of an Autopsy Case. Neuropädiatrie1, 63?70 (1974)

3. Asbury, A. K., Gale, M. K., Cox, S. C., Baringer, J. R., Berg, B. O.: Giant Axonal Neuropathy ? A Unique Case with Segmental Neurofilamentous Masses. Acta neuropath. (Berl.)20, 237?247 (1972)

4. Bérard-Badier, M., Gambarelli, D., Pinsard, N., Hassoun, J., Toga, M.: Infantile Neuroaxonal Dystrophy or Seitelberger's Disease. II. Peripheral Nerve Involvement: Electron Microscopic Study in one Case. Acta neuropath. (Berl.) Suppl.V, 30?39 (1971)

5. Berg, B. O., Rosenberg, S. H., Asbury, A. K.: Giant Axonal Neuropathy. Pediatrics49, 894?899 (1972)

Cited by 93 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Intermediate filament dysregulation in astrocytes in the human disease model of KLHL16 mutation in giant axonal neuropathy (GAN);Molecular Biology of the Cell;2023-11-01

2. Intermediate filament dysregulation and astrocytopathy in the human disease model ofKLHL16mutation in giant axonal neuropathy (GAN);2023-03-14

3. Two novel pathogenic mutations of GAN gene identified in a chinese family with giant axonal neuropathy: a case report;Molecular Biology Reports;2022-06-28

4. Giant axonal neuropathy with novel GAN pathogenic variant in a patient of consanguineous origin from Poonch Jammu and Kashmir-India;Molecular Biology Reports;2021-02

5. An AARS variant as the likely cause of Swedish type hereditary diffuse leukoencephalopathy with spheroids;Acta Neuropathologica Communications;2019-11-27