(Q33776497)

English

Concomitant administration of sodium dichloroacetate and thiamine in west syndrome caused by thiamine-responsive pyruvate dehydrogenase complex deficiency

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scholarly article

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Europe PubMed Central

PubMed publication ID

29 July 2017

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Europe PubMed Central

Concomitant administration of sodium dichloroacetate and thiamine in west syndrome caused by thiamine-responsive pyruvate dehydrogenase complex deficiency (English)

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

dichloroacetate

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author name string

Naito E

1

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

Ito M

2

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

Yokota I

3

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

Saijo T

4

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

Chen S

5

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

Maehara M

6

1 reference

Europe PubMed Central

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29 July 2017

Kuroda Y

7

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Europe PubMed Central

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29 July 2017

publication date

1 December 1999

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Europe PubMed Central

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29 July 2017

number of pages

4

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Journal of the Neurological Sciences

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Europe PubMed Central

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29 July 2017

171

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Europe PubMed Central

PubMed publication ID

29 July 2017

1

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PubMed publication ID

29 July 2017

56-59

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PubMed publication ID

29 July 2017

Mutation of E1 alpha gene in a female patient with pyruvate dehydrogenase deficiency due to rapid degradation of E1 protein

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2899%2900250-6

7 January 2021

Pyruvate carboxylase deficiency: acute exacerbation after ACTH treatment of infantile spasms

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2899%2900250-6

7 January 2021

Progressive generalized brain atrophy and infantile spasms associated with cytochrome c oxidase deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2899%2900250-6

7 January 2021

Molecular analysis of abnormal pyruvate dehydrogenase in a patient with thiamine-responsive congenital lactic acidemia

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2899%2900250-6

7 January 2021

X-chromosome localization of the functional gene for the E1 alpha subunit of the human pyruvate dehydrogenase complex

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2899%2900250-6

7 January 2021

Biochemical and genetic studies of four patients with pyruvate dehydrogenase E1 alpha deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2899%2900250-6

7 January 2021

Biochemical and molecular analysis of an X-linked case of Leigh syndrome associated with thiamin-responsive pyruvate dehydrogenase deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2899%2900250-6

7 January 2021

DNA diagnosis of pyruvate dehydrogenase deficiency in female patients with congenital lactic acidaemia

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2899%2900250-6

7 January 2021

Cerebral dysgenesis and lactic acidemia: an MRI/MRS phenotype associated with pyruvate dehydrogenase deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2899%2900250-6

7 January 2021

Variable clinical presentation in patients with defective E1 component of pyruvate dehydrogenase complex

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2899%2900250-6

7 January 2021

Identifiers

10.1016/S0022-510X(99)00250-6

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

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