(Q48152885)

9 February 2018

title

Neuropathology of myoclonus epilepsy associated with ragged-red fibers (Fukuhara's disease). (English)

1 reference

9 February 2018

author name string

S Takeda

1

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9 February 2018

K Wakabayashi

2

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9 February 2018

E Ohama

3

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9 February 2018

F Ikuta

4

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9 February 2018

publication date

1 January 1988

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9 February 2018

published in

Acta Neuropathologica

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9 February 2018

volume

75

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9 February 2018

issue

5

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9 February 2018

page(s)

433-440

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9 February 2018

https://scigraph.springernature.com/pub.10.1007/bf00687129

exact match

0 references

cites work

Retinitis Pigmentosa, External Ophthalmoplegia, and Complete Heart Block

1 reference

https://api.crossref.org/works/10.1007%2FBF00687129

Mitochondrial encephalomyopathy with lactate-pyruvate elevation and brain infarctions

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF00687129

Familial myoclonus epilepsy and choreoathetosis: hereditary dentatorubral-pallidoluysian atrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF00687129

Molecular genetics, pseudogenetics, and clinical neurology. The Robert Wartenberg Lecture.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF00687129

Joseph disease: a multisystem degenerative disorder of the nervous system

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF00687129

Hereditary multisystemic degeneration with unusual combination of cerebellipetal, dentato-rubral, and nigro-subthalamo-pallidal degenerations.

21 January 2018

1 reference

12 December 2020

[An autopsy case of degenerative type myoclonus epilepsy associated with Friedreich's ataxia and mitochondrial myopathy (author's transl)]

1 reference

12 December 2020

Subacute necrotizing encephalomyelopathy. A review and a study of two families

1 reference

12 December 2020

Myoclonus, cerebellar disorder, neuropathy, mitochondria1 myopathy, and ACTH deficiency

1 reference

12 December 2020

Myoclonus epilepsy associated with ragged-red fibres (mitochondrial abnormalities ): disease entity or a syndrome? Light-and electron-microscopic studies of two cases and review of literature

1 reference

12 December 2020

Retinitis pigmentosa, external ophthalmophegia, and complete heart block: unusual syndrome with histologic study in one of two cases

1 reference

12 December 2020

Myoencephalopathies with abnormal mitochondria: a review

1 reference

12 December 2020

Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes: A distinctive clinical syndrome

1 reference

12 December 2020

Mitochondrial encephalomyopathies: a group of neuromuscular disorders with defects in oxidative metabolism.

1 reference

12 December 2020

Mitochondrial angiopathy in cerebral blood vessels of mitochondrial encephalomyopathy

1 reference

12 December 2020

Nigro-spino-dentatal degeneration with nuclear ophthalmoplegia. A unique and partially treatable clinico-pathological entity.

1 reference

12 December 2020

Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes with acanthocytosis: a clinicopathological study of a unique case.

1 reference

12 December 2020

Dentato-rubro-pallido-luysian atrophy: a clinico-pathological study

1 reference

12 December 2020

Mitochondrial myopathies

1 reference

12 December 2020

Lumping or splitting? "Ophthalmoplegia-plus" or Kearns-Sayre syndrome?

1 reference

12 December 2020

Brain Lesions in Friedreich's Ataxia

1 reference

12 December 2020

Subacute necrotizing encephalomyelopathy in an infant

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00687129

1 reference

9 February 2018

1 reference

9 February 2018