(Q38941235)

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Congenital non-progressive encephalopathy and deafness with intermittent episodes of coma and hyperkynureninuria

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scholarly article

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Europe PubMed Central

PubMed publication ID

7 September 2017

Congenital non-progressive encephalopathy and deafness with intermittent episodes of coma and hyperkynureninuria (English)

1 reference

Europe PubMed Central

PubMed publication ID

7 September 2017

congenital disorder

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1 reference

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inferred from title

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based on heuristic

inferred from title

author name string

R Cheminal

1

1 reference

Europe PubMed Central

PubMed publication ID

7 September 2017

B Echenne

2

1 reference

Europe PubMed Central

PubMed publication ID

7 September 2017

H Bellet

3

1 reference

Europe PubMed Central

PubMed publication ID

7 September 2017

M Duran

4

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Europe PubMed Central

PubMed publication ID

7 September 2017

publication date

1 January 1996

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Europe PubMed Central

PubMed publication ID

7 September 2017

Journal of Inherited Metabolic Disease

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Europe PubMed Central

PubMed publication ID

7 September 2017

19

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Europe PubMed Central

PubMed publication ID

7 September 2017

1

1 reference

Europe PubMed Central

PubMed publication ID

7 September 2017

25-30

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Europe PubMed Central

PubMed publication ID

7 September 2017

Kynurenine metabolites of tryptophan: implications for neurologic diseases

1 reference

https://pubmed.ncbi.nlm.nih.gov/8830173

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Kynurenines and Seizures

1 reference

https://pubmed.ncbi.nlm.nih.gov/8830173

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

HYDROXYKYNURENINURIA: A CASE OF ABNORMAL TRYPTOPHAN METABOLISM PROBABLY DUE TO A DEFICIENCY OF KYNURENINASE

1 reference

https://pubmed.ncbi.nlm.nih.gov/8830173

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Urinary excretion of tryptophan metabolites in the healthy infant

1 reference

https://pubmed.ncbi.nlm.nih.gov/8830173

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Family exhibiting cerebellar-like ataxia, photosensitivity and shortness of stature - a new inborn error of tryptophan metabolism

1 reference

https://pubmed.ncbi.nlm.nih.gov/8830173

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lethal familial pellagra-like skin lesion associated with neurologic and developmental impairment and the development of cataracts.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8830173

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cytotoxicity of 3-Hydroxykynurenine: Implications for CNS Damage in Neonatal Vitamin B-6 Deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/8830173

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cytotoxicity of 3-hydroxykynurenine in a neuronal hybrid cell line

1 reference

https://pubmed.ncbi.nlm.nih.gov/8830173

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Excretion and isolation of kynurenine and 3-hydroxykynurenine from human pathological urine

1 reference

https://pubmed.ncbi.nlm.nih.gov/8830173

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Quinolinic acid and other kynurenines in the central nervous system

1 reference

https://pubmed.ncbi.nlm.nih.gov/8830173

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF01799345

1 reference

Europe PubMed Central

PubMed publication ID

7 September 2017

Dimensions Publication ID

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PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

7 September 2017

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