(Q34301609)

1 August 2017

title

Familial hypertryptophanemia in two siblings (English)

1 reference

1 August 2017

1 reference

John R. Martin

1

0 references

Clive S. Mellor

2

0 references

F. Clarke Fraser

3

0 references

J. R. Martin

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7628119

20 June 2024

C. S. Mellor

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7628119

20 June 2024

F. C. Fraser

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7628119

20 June 2024

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=7628119

20 June 2024

publication date

1 April 1995

1 reference

full work available at URL

1 August 2017

23 April 2008

0 references

https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fj.1399-0004.1995.tb03956.x

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1995.TB03956.X

https://onlinelibrary.wiley.com/doi/pdf/10.1111/j.1399-0004.1995.tb03956.x

20 June 2024

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1995.TB03956.X

20 June 2024

1 reference

1 August 2017

volume

47

1 reference

1 August 2017

issue

4

1 reference

1 August 2017

page(s)

180-183

1 reference

Articular mobility in an African population

1 August 2017

cites work

1

1 reference

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Behavioral consequences of congenital rubella.

20 June 2024

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The blue diaper syndrome: Familial hypercalcemia with nephrocalcinosis and indicanuria

20 June 2024

3

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1995.TB03956.X

Familial essential tryptophan metabolism disorder (Essential hereditary vitamin B6 deficiency)

20 June 2024

5

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1995.TB03956.X

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

20 June 2024

6

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1995.TB03956.X

L-tryptophan: a common denominator of biochemical and neurological events of acute hepatic porphyria?

20 June 2024

8

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1995.TB03956.X

Dermatoglyphics and syndromes

20 June 2024

10

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1995.TB03956.X

Tryptophan metabolism. A hitherto unreported abnormality occurring in a family

20 June 2024

11

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1995.TB03956.X

The Hartnup phenotype: Mendelian transport disorder, multifactorial disease

20 June 2024

12

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1995.TB03956.X

The eosinophilia-myalgia syndrome associated with ingestion of L-tryptophan

20 June 2024

14

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1995.TB03956.X

Tryptophan metabolism via the kynurenine pathway in patients with the eosinophilia-myalgia syndrome

20 June 2024

15

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1995.TB03956.X

Familial hypertryptophanemia, tryptophanuria and indoleketonuria

20 June 2024

16

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1995.TB03956.X

A Defect in Tryptophan Metabolism

20 June 2024

19

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1995.TB03956.X

20 June 2024

Identifiers

0 references

1 reference