Hyperglycemic acidotic coma and death in Kearns-Sayre syndrome (Q42220787)

18 October 2017

title

Hyperglycemic acidotic coma and death in Kearns-Sayre syndrome (English)

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18 October 2017

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Bachynski BN

1

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18 October 2017

Flynn JT

2

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18 October 2017

Rodrigues MM

3

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18 October 2017

Rosenthal S

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18 October 2017

Cullen R

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18 October 2017

Curless RG

6

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18 October 2017

language of work or name

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1 March 1986

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18 October 2017

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18 October 2017

volume

93

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18 October 2017

issue

3

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18 October 2017

page(s)

391-396

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Retinitis Pigmentosa, External Ophthalmoplegia, and Complete Heart Block

18 October 2017

cites work

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Ophthalmoplegia plus. The neurodegenerative disorders associated with progressive external ophthalmoplegia

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

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Spongiform encephalopathy with chronic progressive external ophthalmoplegia. Central ophthalmoplegia mimicking ocular myopathy

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Leukoencephalopathy in oculocraniosomatic neuromuscular disease with ragged-red fibers. Mitochondrial abnormalities demonstrated by computerized tomography

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7 January 2021

Kearns-Sayre syndrome and hypoparathyroidism

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7 January 2021

Kearns-Sayre syndrome with hypoparathyroidism

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Letter: Progressive external ophthalmoplegia: evidence for a disorder in pyruvate-lactate metabolism

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Correction of increased plasma pyruvate and plasma lactate levels using large doses of thiamine in patients with Kearns-Sayre syndrome

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7 January 2021

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

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Demyelinating radiculopathy in the Kearns-Sayre syndrome: a clinicopathological study

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Growth hormone deficiency in mitochondrial cytopathy

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Abrupt neurological deterioration in children with Kearns-Sayre syndrome

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Depressed ventilatory response in oculocraniosomatic neuromuscular disease

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7 January 2021

Hyperglycemic Hyperosmolar Coma: A Syndrome Almost Unique to the Elderly

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Hyperosmolar non-ketotic diabetic syndrome precipitated by treatment with diuretics

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Progressive ophthalmoplegia, glycogen storage, and abnormal mitochondria.

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Improvement of abnormal pyruvate metabolism and cardiac conduction defect with coenzyme Q10 in Kearns-Sayre syndrome

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7 January 2021

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

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

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7 January 2021

10.1016/S0161-6420(86)33744-8

Identifiers

DOI

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