| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Biochemical Analyses of Cerebrospinal Fluid for the Diagnosis of Neurometabolic Conditions. What Can We Expect?
|
Batllori, Marta
|
|
2016
|
23 |
4 |
p. 273-284
12 p.
|
artikel
|
| 2 |
Creatine Defects and Central Nervous System
|
Fons, Carmen
|
|
2016
|
23 |
4 |
p. 285-289
5 p.
|
artikel
|
| 3 |
Diseases of the Synaptic Vesicle: A Potential New Group of Neurometabolic Disorders Affecting Neurotransmission
|
Cortès-Saladelafont, E.
|
|
2016
|
23 |
4 |
p. 306-320
15 p.
|
artikel
|
| 4 |
Epilepsy in Inborn Errors of Metabolism With Therapeutic Options
|
Campistol, Jaume
|
|
2016
|
23 |
4 |
p. 321-331
11 p.
|
artikel
|
| 5 |
Impaired Neurotransmission in Early-treated Phenylketonuria Patients
|
González, María Julieta
|
|
2016
|
23 |
4 |
p. 332-340
9 p.
|
artikel
|
| 6 |
Introduction
|
Campistol, Jaume
|
|
2016
|
23 |
4 |
p. 255-256
2 p.
|
artikel
|
| 7 |
Neonatal Screening for Inherited Metabolic Diseases in 2016
|
Villoria, Judit Garcia
|
|
2016
|
23 |
4 |
p. 257-272
16 p.
|
artikel
|
| 8 |
Neuromuscular Manifestations in Mitochondrial Diseases in Children
|
Nascimento, Andrés
|
|
2016
|
23 |
4 |
p. 290-305
16 p.
|
artikel
|
| 9 |
Pyridoxal Phosphate Supplementation in Neuropediatric Disorders
|
Cortès-Saladelafont, Elisenda
|
|
2016
|
23 |
4 |
p. 351-358
8 p.
|
artikel
|
| 10 |
Treatable Inborn Errors of Metabolism Due to Membrane Vitamin Transporters Deficiency
|
Ortigoza Escobar, Juan Darío
|
|
2016
|
23 |
4 |
p. 341-350
10 p.
|
artikel
|
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