(Q68876683)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4451038%20AND%20SRC:MED&resulttype=core&format=json

28 September 2019

title

[Mitochondrial anomalies with peculiar distribution in a muscular dystrophy with pelvic onset (author's transl)] (English)

1 reference

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28 September 2019

1 reference

H Carrier

1

1 reference

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28 September 2019

A Garde

2

1 reference

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28 September 2019

M Tommasi

3

1 reference

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28 September 2019

N Kopp

4

1 reference

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28 September 2019

J F Savet

5

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28 September 2019

publication date

1 January 1974

1 reference

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28 September 2019

published in

Acta Neuropathologica

1 reference

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28 September 2019

volume

30

1 reference

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28 September 2019

issue

4

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28 September 2019

page(s)

295-303

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https://scigraph.springernature.com/pub.10.1007/bf00697012

28 September 2019

exact match

0 references

cites work

Mitochondrial myopathy

1 reference

12 December 2020

A case of severe hypermetabolism of nonthyroid origin with a defect in the maintenance of mitochondrial respiratory control: a correlated clinical, biochemical, and morphological study

1 reference

12 December 2020

External Ophthalmoplegia, Pigmentary Degeneration of the Retina, and Cardiomyopathy: A Newly Recognized Syndrome.

1 reference

12 December 2020

Atypical muscle mitochondria in oculoskeletal myopathy

1 reference

12 December 2020

2 cases of mitochondrial myopathy: clinical, histological and histochemical aspects

1 reference

12 December 2020

Mitochondrial ultrastructure with crystalloid inclusions in an unusual type of human myopathy

1 reference

12 December 2020

[Ultrastructure and topochemistry of giant mitochondria and their inclusions in myopathies]

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Ophthalmoplegia plus. The neurodegenerative disorders associated with progressive external ophthalmoplegia

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Oculopharyngeal involvement in familial neurogenic muscular atrophy

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Electron microscopic and enzyme histochemical studies of cerebellum, ocular and skeletal muscles in chronic progressive ophthalmoplegia with cerebellar ataxia.

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

[A case of congenital myopathy with mitochondrial abnormalities. Clinical and ultrastructural study]

1 reference

12 December 2020

The pharynx and esophagus in ocular muscular dystrophy.

1 reference

12 December 2020

Myopathy with atypical mitochondria in type I skeletal muscle fibers. A histochemical and ultrastructural study

1 reference

12 December 2020

Two childhood myopathies with abnormal mitochondria. I. Megaconial myopathy. II. Pleoconial myopathy

1 reference

12 December 2020

Late onset mitochondrial myopathy

1 reference

12 December 2020

Severe hypermetabolism with primary abnormality of skeletal muscle mitochondria

1 reference

12 December 2020

Chronic progressive external ophthalmoplegia. A critical review

1 reference

12 December 2020

Skeletal muscle disease with abnormal mitochondria

1 reference

12 December 2020

Ultrastructural features of intracellular lipid in normal human muscle

1 reference

12 December 2020

A new mitochondrial myopathy in a patient with salt craving.

1 reference

12 December 2020

Progressive ophthalmoplegia, glycogen storage, and abnormal mitochondria.

1 reference

12 December 2020

Myopathy with mitochondrial abnormalities localizated in type I fibers. Clinical, histochemical and ultrastructural data apropos of a diffuse atrophic form with ocular onset

1 reference

12 December 2020

Progressive ophthalmoplegia. Report of cases

1 reference

12 December 2020

Oculocraniosomatic neuromuscular disease with "ragged-red" fibers.

1 reference

12 December 2020

OCULAR MYOPATHY WITH DYSPHAGIA

1 reference

12 December 2020

Oculopharyngeal muscular dystrophy. A familial disease of late life characterized by dysphagia and progressive ptosis of the evelids

1 reference

12 December 2020

The Oculopharyngeal Syndrome

1 reference

12 December 2020

THE GENERAL OCCURENCE OF MITOCHONDRIAL DNA

1 reference

12 December 2020

A generalized disorder of nervous system, skeletal muscle and heart resembling Refsum's disease and Hurler's syndrome. I. Clinical, pathologic and biochemical characteristics

1 reference

12 December 2020

Myopathy with abnormal structure and function of muscle mitochondria

1 reference

12 December 2020

"Megaconial" mitochondria observed in a case of chronic polymyositis

1 reference

12 December 2020

Progressive dystrophy of the external ocular muscles (ocular myopathy).

1 reference

12 December 2020

Ocular myopathy. A familial case of oculo-pharyngeal and skeletal muscular dystrophy with late onset

1 reference

12 December 2020

New myopathy with mitochondrial enzyme hyperactivity. Histochemical demonstration

1 reference

12 December 2020

Morphologic features of hypermetabolic mitochondrial disease. A light microscopic, histochemical and electron microscopic study

1 reference

12 December 2020

Familial Myopathy With Abnormal Muscle Mitochondria

1 reference

12 December 2020

Descending ocular myopathy.

1 reference

12 December 2020

The Kearns-Shy syndrome. A multisystem disease with mitochondrial abnormality demonstrated in skeletal muscle and skin

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00697012

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4451038%20AND%20SRC:MED&resulttype=core&format=json

28 September 2019

1 reference