(Q43564493)

24 November 2017

title

Features of carnitine palmitoyltransferase type I deficiency (English)

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24 November 2017

author

Peter Theodore Clayton

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ORCID Public Data File 2021

author name string

S E Olpin

1

1 reference

24 November 2017

J Allen

2

1 reference

24 November 2017

J R Bonham

3

1 reference

24 November 2017

S Clark

4

1 reference

24 November 2017

P T Clayton

5

1 reference

24 November 2017

J Calvin

6

1 reference

24 November 2017

M Downing

7

1 reference

24 November 2017

K Ives

8

1 reference

24 November 2017

S Jones

9

1 reference

24 November 2017

N J Manning

10

1 reference

24 November 2017

R J Pollitt

11

1 reference

24 November 2017

S J Standing

12

1 reference

24 November 2017

M S Tanner

13

1 reference

24 November 2017

publication date

1 February 2001

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Journal of Inherited Metabolic Disease

24 November 2017

published in

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24 November 2017

volume

24

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24 November 2017

issue

1

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24 November 2017

page(s)

35-42

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https://scigraph.springernature.com/pub.10.1023/a:1005694320063

24 November 2017

exact match

0 references

cites work

Hepatic and Muscular Presentations of Carnitine Palmitoyl Transferase Deficiency: Two Distinct Entities

1 reference

12 December 2020

The mitochondrial carnitine palmitoyltransferase system. From concept to molecular analysis

1 reference

12 December 2020

Characterisation of carnitine palmitoyltransferases in patients with a carnitine palmitoyltransferase deficiency: implications for diagnosis and therapy

1 reference

12 December 2020

Fine chromosome mapping of the genes for human liver and muscle carnitine palmitoyltransferase I (CPT1A and CPT1B).

1 reference

12 December 2020

Fasting hypoglycemia resulting from hepatic carnitine palmitoyl transferase deficiency.

1 reference

12 December 2020

Normal muscle CPT1 and CPT2 activities in hepatic presentation patients with CPT1 deficiency in fibroblasts. Tissue specific isoforms of CPT1?

1 reference

12 December 2020

Brief report: renal tubular acidosis in carnitine palmitoyltransferase type 1 deficiency

1 reference

12 December 2020

A comparison of [9,10-3H]palmitic and [9,10-3H]myristic acids for the detection of defects of fatty acid oxidation in intact cultured fibroblasts

1 reference

12 December 2020

Atypical features of the hepatic form of carnitine palmitoyltransferase deficiency in a Hutterite family

1 reference

12 December 2020

Improved detection of long-chain fatty acid oxidation defects in intact cells using [9,10-3H]oleic acid

1 reference

12 December 2020

Chronic cardiomyopathy and weakness or acute coma in children with a defect in carnitine uptake

1 reference

12 December 2020

Rat heart expresses two forms of mitochondrial carnitine palmitoyltransferase I. The minor component is identical to the liver enzyme

1 reference

12 December 2020

Renal tubular dysfunction in multiple acyl-CoA dehydrogenase deficiency

1 reference

12 December 2020

Rate-dependent distal renal tubular acidosis and carnitine palmitoyltransferase I deficiency

1 reference

12 December 2020

Molecular basis of hepatic carnitine palmitoyltransferase I deficiency

1 reference

12 December 2020

Identifiers

DOI

10.1023/A:1005694320063

1 reference

Dimensions Publication ID

24 November 2017

1046996603

0 references

1 reference