(Q34260274)

1 August 2017

Hudson memorial lecture. Neonatal management of organic acidurias. Clinical update (English)

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1 August 2017

6

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author name string

J M Saudubray

1

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1 August 2017

H Ogier

2

1 reference

1 August 2017

C Charpentier

3

1 reference

1 August 2017

E Depondt

4

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1 August 2017

F X Coudé

5

1 reference

1 August 2017

G Mitchell

7

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1 August 2017

F Rey

8

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1 August 2017

J Rey

9

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1 August 2017

J Frézal

10

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1 August 2017

1 January 1984

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Journal of Inherited Metabolic Disease

1 August 2017

1 reference

1 August 2017

7 Suppl 1

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1 August 2017

2-9

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https://scigraph.springernature.com/pub.10.1007/bf03047365

1 August 2017

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cites work

Propionicacidemia, a New Inborn Error of Metabolism

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FBF03047365

Therapeutic Effects of Glycine in Isovaleric Acidemia

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FBF03047365

Prognosis of congenital methylmalonic aciduria. Correlations between tolerance to proteins, response to vitamin B12 and enzymatic defect (author's transl)

21 January 2018

1 reference

12 December 2020

Correlation between serum propionate and blood ammonia concentrations in propionic acidemia.

1 reference

12 December 2020

Isovalericacidemia: a case report.

1 reference

12 December 2020

Isovaleric acidemia. Study and treatment in 3 brothers

1 reference

12 December 2020

Isolation and Identification of Methylcitrate, a Major Metabolic Product of Propionate in Patients with Propionic Acidemia

1 reference

12 December 2020

The Isolation and Identification of N-Isovalerylglycine from Urine of Patients with Isovaleric Acidemia

1 reference

12 December 2020

Maple syrup urine disease: branched-chain keto-aciduria

1 reference

12 December 2020

Treatment of a neonate with propionic acidaemia and severe hyperammonaemia by peritoneal dialysis

1 reference

12 December 2020

Carnitine deficiency in premature infants receiving total parenteral nutrition: effect of L-carnitine supplementation

1 reference

12 December 2020

Idiopathic hyperglycinemia and hyperglycinuria: a new disorder of amino acid metabolism. I

1 reference

12 December 2020

Multiple exchange transfusions as treatment during the acute period in maple syrup urine disease

1 reference

12 December 2020

Isovaleric acidemia: results of family study and dietary treatment.

1 reference

12 December 2020

The specificity of glycine-N-acylase and acylglycine excretion in the organicacidaemias

1 reference

12 December 2020

Methylmalonic acidemia: 6 years' clinical experience with two variants unresponsive to vitamin B12 therapy

1 reference

12 December 2020

Propionicacidemia. A report on two cases (author's transl)

1 reference

12 December 2020

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

1 reference

12 December 2020

Organic acidaemia and Hyperammonaemia: review

1 reference

12 December 2020

Isovaleric acidemia: use of glycine therapy in neonates

1 reference

12 December 2020

Peritoneal dialysis in maple-syrup-urine disease: studies on branched-chain amino and keto acids

1 reference

12 December 2020

Urea nitrogen excretion in critically ill children.

1 reference

12 December 2020

[Methyl malonic acidemia with hyperuricemic nephropathy]

1 reference

12 December 2020

Dietary treatment and biochemical studies on a neonatal case of propionyl-CoA carboxylase deficiency

1 reference

12 December 2020

Heterogeneity of leucinosis. Correlations between clinical manifestations, protein tolerance and enzyme deficiency

1 reference

12 December 2020

Peritoneal dialysis update

1 reference

12 December 2020

[Emergency treatment of an acute form of leucinosis by peritoneal dialysis]

1 reference

12 December 2020

Glycine therapy in isovaleric acidemia

1 reference

12 December 2020

The therapy of maple syrup urine disease

1 reference

12 December 2020

Maple syrup urine disease--therapeutic use of insulin in catabolic states

1 reference

12 December 2020

Maple syrup urine disease: treatment of the acutely ill newborn

1 reference

12 December 2020

The Natural History of the Inherited Methylmalonic Acidemias

1 reference

12 December 2020

Maple syrup disease; isolation and identification of organic acids in the urine

1 reference

12 December 2020

Propionic acidemia: a clinical update

1 reference

12 December 2020

Acute leucinosis, normal psychomotor development at one year of age

1 reference

12 December 2020

Outcome of early and long-term management of classical maple syrup urine disease

1 reference

12 December 2020

Emergency treatment of inborn amino errors of amino acid metabolism detected in the neonatal period

1 reference

12 December 2020

Value of peritoneal dialysis in the emergency treatment of metabolic diseases of constitutional origin revealed in the neonatal period

1 reference

12 December 2020

Infection in maple-syrup-urine disease

1 reference

12 December 2020

Exchange transfusion in acute episodes of maple syrup urine disease. Studies on branched-chain amino and keto acids

1 reference

12 December 2020

A new syndrome: progressive familial infantile cerebral dysfunction associated with an unusual urinary substance.

1 reference

12 December 2020

Correlation between blood ammonia concentration and organic acid accumulation in isovaleric and propionic acidemia

1 reference

12 December 2020

Inhibition by propionyl-coenzyme A of N-acetylglutamate synthetase in rat liver mitochondria. A possible explanation for hyperammonemia in propionic and methylmalonic acidemia

1 reference

12 December 2020

3-Hydroxypropionate: Significance of β-Oxidation of Propionate in Patients with Propionic Acidemia and Methylmalonic Acidemia

1 reference

12 December 2020

Management of maple syrup urine disease in Canada. Committee for improvement of Hereditary Disease Management

1 reference

12 December 2020

Hyperglycinemia and propionyl CoA carboxylase deficiency and episodic severe illness without consistent ketosis

1 reference

12 December 2020

[Endogenous renal clearance of amino acids: variations in relation to age]

1 reference

12 December 2020

MAPLE SYRUP URINE DISEASE, WITH PARTICULAR REFERENCE TO DIETOTHERAPY

1 reference

12 December 2020

L-carnitine therapy in propionicacidaemia

1 reference

12 December 2020

Occurrence of hyperammonemia in the course of 17 cases of methylmalonic acidemia

1 reference

12 December 2020

Abnormal metabolites of isoleucine in a patient with propionyl-CoA carboxylase deficiency

1 reference

12 December 2020

Isovaleric acidemia: a new genetic defect of leucine metabolism

1 reference

12 December 2020

Peritoneal dialysis in maple syrup urine disease.

1 reference

12 December 2020

[Neonatal leucinosis with favourable course. Therapeutic problems]

1 reference

12 December 2020

DIETARY TREATMENT OF A CHILD WITH MAPLE SYRUP URINE DISEASE (BRANCHED-CHAIN KETOACIDURIA).

1 reference

12 December 2020

Outcome of maple syrup urine disease

1 reference

12 December 2020

Reduction of plasma propionate by peritoneal dialysis

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF03047365

1 reference

Dimensions Publication ID

1 August 2017

0 references

1 reference