(Q46910563)

English

Social outcome in treated individuals with inherited metabolic disorders: UK study

scientific article published in January 2005

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/16435174

Social outcome in treated individuals with inherited metabolic disorders: UK study (English)

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/16435174

author name string

M Bhat

1

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/16435174

C Haase

2

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/16435174

P J Lee

3

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/16435174

publication date

1 January 2005

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/16435174

Journal of Inherited Metabolic Disease

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/16435174

28

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/16435174

6

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/16435174

825-830

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/16435174

The natural history of homocystinuria due to cystathionine beta-synthase deficiency.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16435174

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Early diagnosis of inherited metabolic disorders towards improving outcome: the controversial issue of galactosaemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/16435174

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Intelligence and professional career in young adults treated early for phenylketonuria

1 reference

https://pubmed.ncbi.nlm.nih.gov/16435174

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Successful adjustment to society by adults with phenylketonuria

1 reference

https://pubmed.ncbi.nlm.nih.gov/16435174

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Galactosemia: how does long-term treatment change the outcome?

1 reference

https://pubmed.ncbi.nlm.nih.gov/16435174

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Growing older: the adult metabolic clinic

1 reference

https://pubmed.ncbi.nlm.nih.gov/16435174

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The molecular basis of cystathionine beta-synthase deficiency in Australian patients: genotype-phenotype correlations and response to treatment

1 reference

https://pubmed.ncbi.nlm.nih.gov/16435174

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Care of the adult with phenylketonuria

1 reference

https://pubmed.ncbi.nlm.nih.gov/16435174

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Long‐term prognosis in galactosaemia: Results of a survey of 350 cases

1 reference

https://pubmed.ncbi.nlm.nih.gov/16435174

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Long-term outcome in 134 patients with galactosaemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/16435174

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The relationship of genotype to cognitive outcome in galactosaemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/16435174

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The intellectual abilities of early-treated individuals with pyridoxine-nonresponsive homocystinuria due to cystathionine beta-synthase deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/16435174

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S10545-005-0159-X

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/16435174

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/16435174

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