Letter: Biochemical abnormalities in Leigh's disease (Q39382567)

11 September 2017

title

Letter: Biochemical abnormalities in Leigh's disease (English)

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11 September 2017

J P Blass

1

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11 September 2017

S D Cederbaum

series ordinal

2

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11 September 2017

H G Dunn

series ordinal

3

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11 September 2017

language of work or name

English

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publication date

1 June 1976

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11 September 2017

number of pages

2

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inferred from page(s)

published in

The Lancet

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11 September 2017

volume

1

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11 September 2017

issue

7971

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11 September 2017

page(s)

1237-1238

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Subacute necrotizing encephalomyelopathy in an infant

11 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2876%2992181-4

7 January 2021

Subacute Necrotizing Encephalomyelopathy (Leigh's Disease): a Consideration of Clinical Features and Etiology

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2876%2992181-4

7 January 2021

Thiamine Triphosphate Deficiency in Subacute Necrotizing Encephalomyelopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2876%2992181-4

7 January 2021

Specificity of the urine inhibitor test for Leigh's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2876%2992181-4

7 January 2021

Leigh's encephalomyelopathy: an inborn error of gluconeogenesis

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2876%2992181-4

7 January 2021

Biochemical studies and therapy in subacute necrotizing encephalomyelopathy (Leigh's syndrome)

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2876%2992181-4

7 January 2021

Pathogenesis of Leigh's encephalomyelopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2876%2992181-4

7 January 2021

Subacute necrotizing encephalomyelopathy. Clinical, ultrastructural, biochemical and therapeutic studies in an infant

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2876%2992181-4

7 January 2021

Subdural empyema in infants, children and adults

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2876%2992181-4

7 January 2021

A defect in pyruvate decarboxylase in a child with an intermittent movement disorder

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2876%2992181-4

7 January 2021

An inherited defect affecting the tricarboxylic acid cycle in a patient with congenital lactic acidosis

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2876%2992181-4

7 January 2021

10.1016/S0140-6736(76)92181-4

Identifiers

DOI

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11 September 2017

1 reference