(Q42122614)

English

Discussion on some clinical, genetic and biochemical aspects of metabolic disorders of the nervous system: metabolic disease of the nervous system: clinical aspects

scientific article published on October 1958

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

16 October 2017

Discussion on some clinical, genetic and biochemical aspects of metabolic disorders of the nervous system: metabolic disease of the nervous system: clinical aspects (English)

1 reference

Europe PubMed Central

PMC publication ID

16 October 2017

metabolic disease

1 reference

based on heuristic

inferred from title

author name string

MATTHEWS WB

1

1 reference

Europe PubMed Central

PMC publication ID

16 October 2017

language of work or name

0 references

publication date

1 October 1958

1 reference

Europe PubMed Central

PMC publication ID

16 October 2017

Journal of the Royal Society of Medicine

1 reference

Europe PubMed Central

PMC publication ID

16 October 2017

51

1 reference

Europe PubMed Central

PMC publication ID

16 October 2017

10

1 reference

Europe PubMed Central

PMC publication ID

16 October 2017

859-863

1 reference

Europe PubMed Central

PMC publication ID

16 October 2017

Phenylketonuria with normal intelligence and Gowers' muscular dystrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1889852

29 May 2018

Penicillamine, a new oral therapy for Wilson's disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1889852

29 May 2018

Hereditary pellagra-like skin rash with temporary cerebellar ataxia, constant renal amino-aciduria, and other bizarre biochemical features

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1889852

29 May 2018

Is hepatolenticular degeneration a clinico-pathological entity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1889852

29 May 2018

Congenital galactosaemia and mental health.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1889852

17 August 2018

A disease, probably hereditary characterised by severe mental deficiency and a constant gross abnormality of aminoacid metabolism.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1889852

17 August 2018

Diabetic amyotrophy.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1889852

17 August 2018

Familial idiopathic methaemoglobinaemia, associated with mental deficiency and neurological abnormalities.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1889852

17 August 2018

Cobalt, copper and molybdenum in the nutrition of animals and plants

1 reference

https://pubmed.ncbi.nlm.nih.gov/13601739

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital methemoglobinemia in the newborn period

1 reference

https://pubmed.ncbi.nlm.nih.gov/13601739

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Nervous manifestations of porphyria.]

1 reference

https://pubmed.ncbi.nlm.nih.gov/13601739

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic and environmental control of enzyme formation

1 reference

https://pubmed.ncbi.nlm.nih.gov/13601739

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Laboratory diagnosis of congenital galactosaemia at birth

1 reference

https://pubmed.ncbi.nlm.nih.gov/13601739

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Tests of ceruloplasmin substitution in hepatocerebral degeneration (Wilson's disease)]

1 reference

https://pubmed.ncbi.nlm.nih.gov/13601739

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Porphyria; a South African screening experiment

1 reference

https://pubmed.ncbi.nlm.nih.gov/13601739

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Intermittent aldosteronism in periodic paralysis; dependence of attacks on retention of sodium, and failure to induce attacks by restriction of dietary sodium

1 reference

https://pubmed.ncbi.nlm.nih.gov/13601739

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The treatment of acute porphyria with chelating agents: a report of 21 cases

1 reference

https://pubmed.ncbi.nlm.nih.gov/13601739

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Detection by Phenylalanine Tolerance Tests of Heterozygous Carriers of Phenylketonuria

1 reference

https://pubmed.ncbi.nlm.nih.gov/13601739

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

16 October 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

16 October 2017

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