(Q39602156)

13 September 2017

3-Hydroxy-3-methylglutaryl-coenzyme A lyase deficiency: report of five new patients (English)

1 reference

13 September 2017

K M Gibson

1

1 reference

13 September 2017

J Breuer

2

1 reference

13 September 2017

K Kaiser

3

1 reference

13 September 2017

W L Nyhan

4

1 reference

13 September 2017

E E McCoy

5

1 reference

13 September 2017

P Ferreira

6

1 reference

13 September 2017

C L Greene

7

1 reference

13 September 2017

M G Blitzer

8

1 reference

13 September 2017

E Shapira

9

1 reference

13 September 2017

F Reverte

10

1 reference

13 September 2017

1 January 1988

1 reference

Journal of Inherited Metabolic Disease

13 September 2017

1 reference

13 September 2017

11

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13 September 2017

1

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13 September 2017

76-87

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https://scigraph.springernature.com/pub.10.1007/bf01800058

13 September 2017

0 references

cites work

Hydroqnnethylglutaryl CoA lyase deficiency: Features resembling Reye syndrome

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FBF01800058

Deficiency of propionyl-Co A carboxylase and methylcrotonyl-Co A carboxylase in a patient with methylcrotonylglycinuria

21 January 2018

1 reference

12 December 2020

Acetoacetyl CoA thiolase deficiency presenting as ketotic hypoglycemia

1 reference

12 December 2020

Atypical presentation and neuropathological studies in 3-hydroxy-3-methylglutaryl-CoA lyase deficiency

1 reference

12 December 2020

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

1 reference

12 December 2020

Dizygotic twins with 3-hydroxy-3-methylglutaric aciduria; unusual presentation, family studies and dietary management

1 reference

12 December 2020

Patient with Defect in Leucine Metabolism

1 reference

12 December 2020

Cerebral blood flow and exchange of oxygen, glucose, ketone bodies, lactate, pyruvate and amino acids in infants

1 reference

12 December 2020

Genetic complementation analysis of 3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiency in cultured fibroblasts

1 reference

12 December 2020

L-Carnitine Insufficiency in Disorders of Organic acid Metabolism: Response to L-Carnitine by Patients with Methylmalonic Aciduria and 3-Hydroxy-3-methylglutaric Aciduria

1 reference

12 December 2020

3-Hydroxy-3-Methylglutaric Aciduria

1 reference

12 December 2020

3-Hydroxy-3-methylglutaryl-CoA lyase deficiency

1 reference

12 December 2020

3-Hydroxy-3-methylglutaryl-coenzyme a lyase deficiency: a review

1 reference

12 December 2020

Measurement of "true" glucose production rates in infancy and childhood with 6,6-dideuteroglucose

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF01800058

1 reference

13 September 2017

1 reference