(Q44396636)

English

Outcome and survival of 88 patients with urea cycle disorders: a retrospective evaluation

scientific article published on 27 March 2003

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scholarly article

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Europe PubMed Central

PubMed publication ID

2 December 2017

Outcome and survival of 88 patients with urea cycle disorders: a retrospective evaluation (English)

1 reference

Europe PubMed Central

PubMed publication ID

2 December 2017

author name string

Claude Bachmann

1

1 reference

Europe PubMed Central

PubMed publication ID

2 December 2017

publication date

27 March 2003

1 reference

Europe PubMed Central

PubMed publication ID

2 December 2017

European Journal of Pediatrics

1 reference

Europe PubMed Central

PubMed publication ID

2 December 2017

162

1 reference

Europe PubMed Central

PubMed publication ID

2 December 2017

6

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Europe PubMed Central

PubMed publication ID

2 December 2017

410-416

1 reference

Europe PubMed Central

PubMed publication ID

2 December 2017

Neonatal screening for inborn errors of metabolism: cost, yield and outcome.

1 reference

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Some ethical and design challenges of screening programs and screening tests

1 reference

https://pubmed.ncbi.nlm.nih.gov/12684900

12 December 2020

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Prospective treatment of urea cycle disorders.

1 reference

https://pubmed.ncbi.nlm.nih.gov/12684900

12 December 2020

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Long-term treatment of girls with ornithine transcarbamylase deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/12684900

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Screening for inborn errors of metabolism. Report of a WHO Scientific Group

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https://pubmed.ncbi.nlm.nih.gov/12684900

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Neurodevelopmental outcome of long-term therapy of urea cycle disorders in Japan

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Liver transplantation in urea cycle disorders

1 reference

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New pathways of nitrogen excretion in inborn errors of urea synthesis

1 reference

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Long-term follow-up of 12 patients with the late-onset variant of argininosuccinic acid lyase deficiency: no impairment of intellectual and psychomotor development during therapy

1 reference

https://pubmed.ncbi.nlm.nih.gov/12684900

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Ornithine carbamoyl transferase deficiency: findings, models and problems

1 reference

https://pubmed.ncbi.nlm.nih.gov/12684900

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Ammonium-induced impairment of axonal growth is prevented through glial creatine.

1 reference

https://pubmed.ncbi.nlm.nih.gov/12684900

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Neurologic outcome in children with inborn errors of urea synthesis. Outcome of urea-cycle enzymopathies

1 reference

https://pubmed.ncbi.nlm.nih.gov/12684900

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Long-term survival of patients with argininosuccinate synthetase deficiency.

1 reference

https://pubmed.ncbi.nlm.nih.gov/12684900

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Extracorporeal dialysis in neonatal hyperammonemia: modalities and prognostic indicators.

1 reference

https://pubmed.ncbi.nlm.nih.gov/12684900

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based on heuristic

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Neonatal biochemical screening for disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/12684900

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Arginine therapy of argininosuccinase deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/12684900

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Identifiers

10.1007/S00431-003-1188-9

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

2 December 2017

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