(Q35085922)

6 August 2017

1 reference

title

Emergency management of inherited metabolic diseases (English)

1 reference

6 August 2017

Prietsch V

1

1 reference

6 August 2017

Lindner M

2

1 reference

6 August 2017

Zschocke J

3

1 reference

6 August 2017

Nyhan WL

4

1 reference

6 August 2017

Hoffmann GF

5

1 reference

6 August 2017

1 November 2002

1 reference

Journal of Inherited Metabolic Disease

6 August 2017

1 reference

6 August 2017

25

1 reference

6 August 2017

7

1 reference

6 August 2017

531-546

1 reference

https://scigraph.springernature.com/pub.10.1023/a:1022040422590

6 August 2017

0 references

cites work

Assessment of energy expenditure in metabolic disorders

1 reference

12 December 2020

Secondary carnitine deficiency in hyperammonemic attacks of ornithine transcarbamylase deficiency

1 reference

12 December 2020

Resting energy expenditure in disorders of propionate metabolism.

1 reference

12 December 2020

Pharmacologic amino acid acylation in the acute hyperammonemia of propionic acidemia

1 reference

12 December 2020

Continuous venovenous hemofiltration in the management of acute decompensation in inborn errors of metabolism

1 reference

12 December 2020

Inhibition of pyruvate carboxylase by sequestration of coenzyme A with sodium benzoate

1 reference

12 December 2020

Postoperative metabolic decompensation in maple syrup urine disease is completely prevented by insulin

1 reference

12 December 2020

Branched-chain amino acid-free parenteral nutrition in the treatment of acute metabolic decompensation in patients with maple syrup urine disease

1 reference

12 December 2020

A case of carbamylphosphate synthetase-I deficiency associated with secondary carnitine deficiency--L-carnitine treatment of CPS-I deficiency

1 reference

12 December 2020

Alternative pathway therapy for urea cycle disorders

1 reference

12 December 2020

Metabolic decompensation and lactic acidosis in propionic acidaemia complicated by thiamine deficiency

1 reference

12 December 2020

Modulation of the activity of rat liver acetylglutamate synthase by pH and arginine concentration

1 reference

12 December 2020

Continuous venovenous haemodiafiltration in the acute phase of neonatal maple syrup urine disease.

1 reference

12 December 2020

Very long chain acyl-CoA dehydrogenase deficiency: successful treatment of acute cardiomyopathy

1 reference

12 December 2020

L-carnitine enhances excretion of propionyl coenzyme A as propionylcarnitine in propionic acidemia

1 reference

12 December 2020

Thiamine response in maple syrup urine disease

1 reference

12 December 2020

On the Possible Mechanism of Phenylacetate Neurotoxicity: Inhibition of Choline Acetyltransferase by Phenylacetyl-CoA

1 reference

12 December 2020

Sodium benzoate inhibits fatty acid oxidation in rat liver: effect on ammonia levels

1 reference

12 December 2020

Anabolic effect of human growth hormone: management of inherited disorders of catabolic pathways

1 reference

12 December 2020

Dialysis in neonates with inborn errors of metabolism

1 reference

12 December 2020

Acute illness in maple syrup urine disease: dynamics of protein metabolism and implications for management.

1 reference

12 December 2020

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

1 reference

12 December 2020

The treatment of congenital lactic acidoses

1 reference

12 December 2020

Nasogastric drip feeding as the only treatment of neonatal maple syrup urine disease

1 reference

12 December 2020

Neonatal hemodialysis: effective therapy for the encephalopathy of inborn errors of metabolism

1 reference

12 December 2020

Disposition of sodium benzoate in newborn infants with hyperammonemia

1 reference

12 December 2020

Intercurrent illness in inborn errors of intermediary metabolism

1 reference

12 December 2020

Absence of acidosis in the initial presentation of propionic acidaemia

1 reference

12 December 2020

Continuous venovenous haemofiltration in the acute treatment of inborn errors of metabolism

1 reference

12 December 2020

Treatment of the acute crisis in maple syrup urine disease

1 reference

12 December 2020

Urinary excretion of l-carnitine and acylcarnitines by patients with disorders of organic acid metabolism: evidence for secondary insufficiency of l-carnitine

1 reference

12 December 2020

Clearance of toxic metabolites during therapy for inborn errors of metabolism

1 reference

12 December 2020

L-carnitine therapy in isovaleric acidemia

1 reference

12 December 2020

Effective hemodialysis and hemofiltration driven by an extracorporeal membrane oxygenation pump in infants with hyperammonemia

1 reference

12 December 2020

Primary treatment of propionic acidemia complicated by acute thiamine deficiency

1 reference

12 December 2020

Identifiers

DOI

10.1023/A:1022040422590

1 reference

Dimensions Publication ID

6 August 2017

0 references

1 reference