(Q40128767)

17 September 2017

title

Congenital lactic acidosis due to pyruvate carboxylase deficiency: Absence of an inhibitor of TPP-ATP phosphoryl transferase (English)

1 reference

Congenital lactic acidosis

3 January 2023

0 references

1 reference

1 reference

pyruvate carboxylase deficiency disease

inferred from title

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A203466

3 January 2023

author name string

K. Tada

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A203466

3 January 2023

G. Takada

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A203466

3 January 2023

K. Omura

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A203466

3 January 2023

Y. Itokawa

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A203466

3 January 2023

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=203466

3 January 2023

publication date

1 January 1978

1 reference

17 September 2017

17 January 1978

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=203466

full work available at URL

3 January 2023

http://link.springer.com/content/pdf/10.1007/BF00445770.pdf

file format

Portable Document Format

1 reference

http://link.springer.com/article/10.1007/BF00445770/fulltext.html

3 January 2023

1 reference

http://link.springer.com/content/pdf/10.1007/BF00445770

3 January 2023

1 reference

European Journal of Pediatrics

3 January 2023

published in

1 reference

17 September 2017

volume

127

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17 September 2017

issue

2

1 reference

17 September 2017

page(s)

141-147

1 reference

https://scigraph.springernature.com/pub.10.1007/bf00445770

17 September 2017

exact match

0 references

cites work

Abnormally high levels of lactate and pyruvate in cerebrospinal fluid of hyperalaninemia with hyperpyruvicemia.

1 reference

12 December 2020

Pathogenesis of Leigh's encephalomyelopathy.

1 reference

12 December 2020

Lactate metabolism. Studies of a child with a serious congenital deviation

1 reference

12 December 2020

Pyruvate carboxylase in human liver. Apparent loss of a component of catalytic activity in a form of lactic acidosis with hypoglycemia.

1 reference

12 December 2020

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

1 reference

12 December 2020

Pyruvate Dehydrogenase Phosphatase Deficiency: A Cause of Congenital Chronic Lactic Acidosis in Infancy

1 reference

12 December 2020

Lactic acidosis in three sibs due to defects in both pyruvate dehydrogenase and alpha-ketoglutarate dehydrogenase complexes

1 reference

12 December 2020

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

1 reference

12 December 2020

Absence of pyruvate decarboxylase activity in man: a cause of congenital lactic acidosis

1 reference

12 December 2020

Experience with Phosphoryl Transferase Inhibition in Subacute Necrotizing Encephalomyelopathy

1 reference

12 December 2020

Hepatic fructose-1,6-diphosphatase deficiency. A cause of lactic acidosis and hypoglycemia in infancy

1 reference

12 December 2020

Hyperalaninemia hyperpyruvicemia and lactic acidosis due to pyruvate carboxylase deficiency of the liver; treatment with thiamine and lipoic acid.

1 reference

12 December 2020

Leigh's encephalomyelopathy: an inborn error of gluconeogenesis

1 reference

12 December 2020

Brain and cerebrospinal fluid lactate concentration in respiratory acidosis and alkalosis

1 reference

12 December 2020

Thiamine Triphosphate Deficiency in Subacute Necrotizing Encephalomyelopathy

1 reference

12 December 2020

Fatal lactic acidosis in a newborn attributable to a congenital defect of pyruvate dehydrogenase

1 reference

12 December 2020

Neonatal congenital lactic acidosis with pyruvate carboxylase deficiency in two siblings

1 reference

12 December 2020

PYRUVATE CARBOXYLASE. I. NATURE OF THE REACTION

1 reference

12 December 2020

Lactic acidosis with necrotizing encephalopathy in two sibs

1 reference

12 December 2020

Renal function studies and kidney pyruvate carboxylase in subacute necrotizing encephalomyelopathy (Leigh's syndrome).

1 reference

12 December 2020

Hyperalaninemia with Pyruvicemia due to Pyruvate Carboxylase Deficiency of the Liver

1 reference

12 December 2020

Hyperalaninemia with Pyruvicemia (Preliminary Report)

1 reference

12 December 2020

Enzyme-inhibiting factor in subacute necrotizing encephalomyelopathy

1 reference

12 December 2020

Hyperalaninemia with pyruvicemia in a patient suggestive of Leigh's encephalomyelopathy.

1 reference

12 December 2020

Subacute necrotizing encephalomyelopathy in an infant

1 reference

12 December 2020

Thiamine-responsive lactice acidosis in a patient with deficient low-KM pyruvate carboxylase activity in liver

1 reference

12 December 2020

Cellulose: Refutation of a Folded-Chain Structure

4

1 reference

3 January 2023

Identifiers

DOI

10.1007/BF00445770

1 reference

17 September 2017

1 reference