(Q70308999)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7067593%20AND%20SRC:MED&resulttype=core&format=json

10 October 2019

title

Kearns syndrome: a heterogeneous group of disorders with CPEO, or a nosological entity? (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7067593%20AND%20SRC:MED&resulttype=core&format=json

10 October 2019

author name string

L A Bastiaensen

1

1 reference

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10 October 2019

C W Frenken

2

1 reference

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10 October 2019

H J Ter Laak

3

1 reference

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10 October 2019

H H Jaspar

4

1 reference

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10 October 2019

A M Stadhouders

5

1 reference

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10 October 2019

W Ruitenbeek

6

1 reference

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10 October 2019

J H Veerkamp

7

1 reference

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10 October 2019

publication date

1 January 1982

1 reference

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Documenta Ophthalmologica

10 October 2019

published in

1 reference

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10 October 2019

volume

52

1 reference

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10 October 2019

issue

3-4

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10 October 2019

page(s)

207-225

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https://scigraph.springernature.com/pub.10.1007/bf01675852

10 October 2019

exact match

0 references

cites work

A Familial Mitochondrial Myopathy With Central Defect in Neural Transmission

1 reference

12 December 2020

Autosomal dominant Kearns-Sayre syndrome.

1 reference

12 December 2020

Kearns syndrome or Kearns disease. Further evidence of a genuine entity in a case with uncommon features

1 reference

12 December 2020

Morphologic and metabolic studies in a case of oculo-cranio-somatic neuromuscular disease

1 reference

12 December 2020

Familial Kearns-Sayre syndrome

1 reference

12 December 2020

Spongy degeneration of the CNS: an instance of the rare juvenile form

1 reference

12 December 2020

Familial progressive external ophthalmoplegia with abnormal muscle mitochondria

1 reference

12 December 2020

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

1 reference

12 December 2020

A case of ocular myopathy associated with abnormal findings in computerized tomography of the brain and ischemic exercise test, & hypoacusis (author's transl)

1 reference

12 December 2020

Familial mitochondrial myopathy with cataract

1 reference

12 December 2020

Ophthalmoplegia-plus, a real nosological entity

1 reference

12 December 2020

Progressive external ophthalmoplegia. Evidence for a generalised mitochondrial disease with a defect in pyruvate metabolism

1 reference

12 December 2020

Ocular myopathy associated with retinitis pigmentosa

1 reference

12 December 2020

Progressive ophthalmoplegia, glycogen storage, and abnormal mitochondria.

1 reference

12 December 2020

[Differential diagnosis of ocular myopathies]

1 reference

12 December 2020

Kearns-Sayre syndrome and hypoparathyroidism

1 reference

12 December 2020

A generalized disorder of nervous system, skeletal muscle and heart resembling Refsum's disease and Hurler's syndrome. II. Ultrastructure

1 reference

12 December 2020

Congenital oculoskeletal myopathy with abnormal muscle and liver mitochondria

1 reference

12 December 2020

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

1 reference

12 December 2020

[The Kearns-Sayre syndrome. A case report (author's transl)]

1 reference

12 December 2020

Neurological associations of chronic heart block

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF01675852

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7067593%20AND%20SRC:MED&resulttype=core&format=json

10 October 2019

1 reference