no |
title |
author |
magazine |
year |
volume |
issue |
page(s) |
type |
1 |
Acute presentations of inherited metabolic disorders: investigation and initial management
|
Ghosh, Arunabha |
|
2019 |
29 |
3 |
p. 99-104 |
article |
2 |
‘Ammonia, lactate and blood gases – A user's guide’
|
Davison, James E. |
|
2019 |
29 |
3 |
p. 142-145 |
article |
3 |
Editorial Board
|
|
|
2019 |
29 |
3 |
p. i |
article |
4 |
Familial hypercholesterolaemia: what’s new?
|
Ramaswami, Uma |
|
2019 |
29 |
3 |
p. 127-136 |
article |
5 |
Inherited mitochondrial disease
|
Davison, James |
|
2019 |
29 |
3 |
p. 116-122 |
article |
6 |
Medium-chain acyl-CoA dehydrogenase deficiency
|
Jameson, Elisabeth |
|
2019 |
29 |
3 |
p. 123-126 |
article |
7 |
Newborn screening for inborn errors of metabolism
|
Korenev, Sergei |
|
2019 |
29 |
3 |
p. 105-110 |
article |
8 |
Phenylketonuria
|
Cleary, Maureen Anne |
|
2019 |
29 |
3 |
p. 111-115 |
article |
9 |
Pollen food syndrome
|
Edwards, Sally E. |
|
2019 |
29 |
3 |
p. 137-141 |
article |
10 |
Self-assessment
|
Diviney, James |
|
2019 |
29 |
3 |
p. 146-149 |
article |