Histopathologic and biochemical analysis of classic Pelizaeus-Merzbacher disease

Author:

Iyoda Kuniaki,Tanaka Junichi,Suzuki Yoshiyuki,Nagao Yoshiro,Ohtahara Shunsuke

Publisher

Elsevier BV

Subject

Clinical Neurology,Developmental Neuroscience,Neurology,Pediatrics, Perinatology, and Child Health

Reference11 articles.

1. Über eine eigentümliche form spastischer lähmung mit zerebralerscheinumgen auf hereditärer grundlage (multiple sklerose);Pelizaeus;Arch Psychiatr Nervenkr,1885

2. Eine eigenartige familiär-hereditäre erkrankungsform (aplasia axialis extra corticalis congenita);Merzbacher;Zentralbl Ges Neurol Psychiatry,1910

3. Pelizaeus-Merzbacher disease;Seitelberger,1970

4. Immunohistochemical study of Pelizaeus-Merzbacher disease in comparison with Jimpy mouse;Tanaka;Neuropathology,1987

5. Brainstem auditory evoked potentials in chronic degenerative central nervous system disorders;Markand,1980

Cited by 6 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. Ketogenic diet ameliorates axonal defects and promotes myelination in Pelizaeus–Merzbacher disease;Acta Neuropathologica;2019-03-27

2. Novel pathologic findings in patients with Pelizaeus-Merzbacher disease;Neuroscience Letters;2016-08

3. Pelizaeus-Merzbacher disease;The Indian Journal of Pediatrics;1997-09

4. Proteolipid Protein Is Necessary in Peripheral as Well as Central Myelin;Neuron;1997-07

5. Pelizaeus-Merzbacher Disease;Magnetic Resonance of Myelin, Myelination, and Myelin Disorders;1995

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