(Q41009526)

25 September 2017

Clinical outcome of long-term management of patients with vitamin B12-unresponsive methylmalonic acidemia (English)

1 reference

25 September 2017

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van der Meer SB

1

1 reference

25 September 2017

Poggi F

2

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25 September 2017

Spada M

3

1 reference

25 September 2017

Bonnefont JP

4

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25 September 2017

Ogier H

5

1 reference

25 September 2017

Hubert P

6

1 reference

25 September 2017

Depondt E

7

1 reference

25 September 2017

Rapoport D

8

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25 September 2017

Rabier D

9

1 reference

25 September 2017

Charpentier C

10

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25 September 2017

language of work or name

English

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publication date

1 December 1994

1 reference

The Journal of Pediatrics

25 September 2017

1 reference

25 September 2017

125

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25 September 2017

6 Pt 1

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25 September 2017

903-908

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Methylmalonic Aciduria: Metabolic Block Localization and Vitamin B 12 Dependency

25 September 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2805%2982005-0

Inherited methylmalonyl CoA mutase apoenzyme deficiency in human fibroblasts: evidence for allelic heterogeneity, genetic compounds, and codominant expression

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2805%2982005-0

Methylmalonic aciduria. An inborn error of metabolism leading to chronic metabolic acidosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2805%2982005-0

Dietary therapy in two patients with vitamin B12-unresponsive methylmalonic acidemia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2805%2982005-0

The management and long term outcome of organic acidaemias

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2805%2982005-0

The Natural History of the Inherited Methylmalonic Acidemias

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2805%2982005-0

An evaluation of protein requirements in methylmalonic acidaemia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2805%2982005-0

Studies on requirements for amino acids in infants with disorders of amino acid metabolism. I. Effect of alanine

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2805%2982005-0

Abnormality of odd-numbered long-chain fatty acids in erythrocyte membrane lipids from patients with disorders of propionate metabolism

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2805%2982005-0

Contribution of odd-chain fatty acid oxidation to propionate production in disorders of propionate metabolism.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2805%2982005-0

Metabolic response to carnitine in methylmalonic aciduria. An effective strategy for elimination of propionyl groups

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2805%2982005-0

The use of metronidazole in management of methylmalonic and propionic acidaemias

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2805%2982005-0

Chronic renal failure in methylmalonic acidaemia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2805%2982005-0

Cardiomyopathy in propionic acidaemia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2805%2982005-0

Correction of methylmalonyl-CoA mutase deficiency in Mut0 fibroblasts and constitution of gene expression in primary human hepatocytes by retroviral-mediated gene transfer

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2805%2982005-0

10.1016/S0022-3476(05)82005-0

7 January 2021

Identifiers

DOI

1 reference

25 September 2017

1 reference