Thiamine-Responsive and Non-responsive Patients with PDHC-E1 Deficiency: A Retrospective Assessment (Q34734686)

24718837

4 August 2017

title

Thiamine-Responsive and Non-responsive Patients with PDHC-E1 Deficiency: A Retrospective Assessment (English)

1 reference

4 August 2017

4

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13 June 2020

author name string

Sanne van Dongen

1

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13 June 2020

Ruth M Brown

2

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13 June 2020

Garry K Brown

3

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13 June 2020

Avihu Boneh

5

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13 June 2020

publication date

10 April 2014

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24718837

Journal of Inherited Metabolic Disorders Reports

4 August 2017

published in

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13 June 2020

volume

15

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13 June 2020

page(s)

13-27

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The spectrum of pyruvate dehydrogenase complex deficiency: clinical, biochemical and genetic features in 371 patients

13 June 2020

cites work

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Intermittent-relapsing pyruvate dehydrogenase complex deficiency: a case with clinical, biochemical, and neuroradiological reversibility.

7 July 2018

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Pyruvate dehydrogenase complex deficiency: four neurological phenotypes with differing pathogenesis

7 July 2018

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A Korean female patient with thiamine-responsive pyruvate dehydrogenase complex deficiency due to a novel point mutation (Y161C)in the PDHA1 gene

7 July 2018

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Mitochondrial modulation: reversible phosphorylation takes center stage?

7 July 2018

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A novel Y243S mutation in the pyruvate dehydrogenase El alpha gene subunit: correlation with thiamine pyrophosphate interaction

7 July 2018

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Caveats when considering ketogenic diets for the treatment of pyruvate dehydrogenase complex deficiency

7 July 2018

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Outcome of thiamine treatment in a child with Leigh disease due to thiamine-responsive pyruvate dehydrogenase deficiency

7 July 2018

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Mutations in the X-linked pyruvate dehydrogenase (E1) alpha subunit gene (PDHA1) in patients with a pyruvate dehydrogenase complex deficiency

7 July 2018

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

7 July 2018

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Outcome of pyruvate dehydrogenase deficiency treated with ketogenic diets. Studies in patients with identical mutations.

7 July 2018

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Pyruvate dehydrogenase complex deficiency due to a point mutation (P188L) within the thiamine pyrophosphate binding loop of the E1 alpha subunit

7 July 2018

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7 July 2018

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Function of the nonidentical subunits of mammalian pyruvate dehydrogenase

7 July 2018

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Alpha-keto acid dehydrogenase complexes. X. Regulation of the activity of the pyruvate dehydrogenase complex from beef kidney mitochondria by phosphorylation and dephosphorylation

7 July 2018

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Immunochemical analysis of normal and mutant forms of human pyruvate dehydrogenase

7 July 2018

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"Cerebral" lactic acidosis: defects in pyruvate metabolism with profound brain damage and minimal systemic acidosis

7 July 2018

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

7 July 2018

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Lacticacidaemia due to pyruvate dehydrogenase deficiency, with evidence of protein polymorphism in the alpha-subunit of the enzyme.

7 July 2018

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

7 July 2018

1 reference

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The clinical and biochemical spectrum of human pyruvate dehydrogenase complex deficiency

7 July 2018

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X-linked pyruvate dehydrogenase E1 alpha subunit deficiency in heterozygous females: variable manifestation of the same mutation

7 July 2018

1 reference

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A cognitively normal PDH-deficient 18-year-old man carrying the R263G mutation in the PDHA1 gene.

7 July 2018

1 reference

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Somatic mosaicism for a PDHA1 mutation in a female with pyruvate dehydrogenase deficiency

26 October 2018

1 reference

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Pyruvate dehydrogenase deficiency presenting as intermittent isolated acute ataxia

26 October 2018

1 reference

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Thiamine-responsive pyruvate dehydrogenase deficiency in two patients caused by a point mutation (F205L and L216F) within the thiamine pyrophosphate binding region

26 October 2018

1 reference

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Diagnosis and molecular analysis of three male patients with thiamine-responsive pyruvate dehydrogenase complex deficiency

26 October 2018

1 reference

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

26 October 2018

1 reference

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Leigh syndrome: clinical features and biochemical and DNA abnormalities.

26 October 2018

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Characterization of point mutations in patients with pyruvate dehydrogenase deficiency: role of methionine-181, proline-188, and arginine-349 in the alpha subunit

26 October 2018

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12 December 2020

Pyruvate dehydrogenase deficiency in a child responsive to thiamine treatment

1 reference

12 December 2020

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

1 reference

12 December 2020

Optimal handling of blood samples for routine measurement of lactate and pyruvate

1 reference

12 December 2020

Thiamine Responsive Pyruvate Dehydrogenase Deficiency

1 reference

12 December 2020

Recurrent muscle weakness and ataxia in thiamine-responsive pyruvate dehydrogenase complex deficiency

1 reference

12 December 2020

Identifiers

DOI

10.1007/8904_2014_293

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24718837%20AND%20SRC:MED&resulttype=core&format=json

13 June 2020

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13 June 2020

24718837

1 reference