Improved growth and nutrition status in children with methylmalonic or propionic acidemia fed an elemental medical food (Q44624376)

4 December 2017

Improved growth and nutrition status in children with methylmalonic or propionic acidemia fed an elemental medical food (English)

1 reference

4 December 2017

1 reference

9

1 reference

4 December 2017

2

Phyllis B Acosta

0 references

author name string

Steven Yannicelli

1

1 reference

4 December 2017

Antonio Velazquez

3

1 reference

4 December 2017

Hans-Georg Bock

4

1 reference

4 December 2017

Barbara Marriage

5

1 reference

4 December 2017

Thaddeus W Kurczynski

6

1 reference

4 December 2017

Marvin Miller

7

1 reference

4 December 2017

Mark Korson

8

1 reference

4 December 2017

Lane Rutledge

10

1 reference

4 December 2017

Laurie Bernstein

11

1 reference

4 December 2017

Jeffrey Chinsky

12

1 reference

4 December 2017

Patricia Galvin-Parton

13

1 reference

4 December 2017

Georgianne L Arnold

14

1 reference

4 December 2017

1 September 2003

1 reference

Molecular Genetics and Metabolism

4 December 2017

1 reference

4 December 2017

80

1 reference

4 December 2017

181-188

1 reference

4 December 2017

1-2

1 reference

Increased urinary metabolite excretion during fasting in disorders of propionate metabolism

4 December 2017

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2003.08.012

Long-term follow-up of 77 patients with isolated methylmalonic acidaemia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2003.08.012

Parenteral nutrition in propionic and methylmalonic acidemia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2003.08.012

The management and long term outcome of organic acidaemias

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2003.08.012

Normal growth and development with unrestricted protein intake after severe infantile propionic acidaemia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2003.08.012

Apparent decreased energy requirements in children with organic acidemias: preliminary observations

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2003.08.012

Clinical outcome and long-term management of 17 patients with propionic acidaemia.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2003.08.012

Neonatal-onset propionic acidemia: neurologic and developmental profiles, and implications for management.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2003.08.012

A case of fulminant ecthyma gangrenosum associated with Pseudomonas aeruginosa infection in a patient with methylmalonic acidemia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2003.08.012

Body composition of reference children from birth to age 10 years

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2003.08.012

Comparison of an elemental and polymeric enteral diet in patients with normal gastrointestinal function

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2003.08.012

Dependence of the utilization of a phenylalanine-free amino acid mixture on different amounts of single dose ingested. A case report

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2003.08.012

The Threonine Requirement of the Normal Infant

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2003.08.012

Resting energy expenditure in disorders of propionate metabolism.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2003.08.012

Congenital microcephaly and seizures due to 3-phosphoglycerate dehydrogenase deficiency: outcome of treatment with amino acids

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2003.08.012

Evaluation of branched-chain amino acid intake in children with maple syrup urine disease and methylmalonic aciduria

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2003.08.012

Inhibition of glycine-serine interconversion in cultured human fibroblasts by products of isoleucine catabolism.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2003.08.012

The Plasma Aminogram. I. Influence of the Level of Protein Intake and a Comparison of Whole Protein and Amino Acid Diets

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2003.08.012

Methylmalonic aciduria. An inborn error leading to metabolic acidosis, long-chain ketonuria and intermittent hyperglycinemia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2003.08.012

Propionic acidaemia: clinical, biochemical and therapeutic aspects. Experience in 30 patients

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2003.08.012

Acrodermatitis enteropathica-like cutaneous lesions in organic aciduria

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2003.08.012

The kinetics of amino acid absorption and alteration of plasma composition of free amino acids after intestinal perfusion of amino acid mixtures

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2003.08.012

Intercurrent illness in inborn errors of intermediary metabolism

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2003.08.012

Interpretation of vitamin A status in apparently healthy Pakistani children by using markers of subclinical infection

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2003.08.012

10.1016/J.YMGME.2003.08.012

7 January 2021

Identifiers

DOI

1 reference

4 December 2017

1 reference