| no |
title |
author |
magazine |
year |
volume |
issue |
page(s) |
type |
| 1 |
A novel ATP1A2 variant associated with severe stepwise regression, hemiplegia, epilepsy and movement disorders in two unrelated patients
|
Calame, Daniel G.
|
|
|
31 |
C |
p. 21-26
|
article
|
| 2 |
A patient centered view of randomized control trial data: An example with fenfluramine for Dravet syndrome
|
Auvin, Stéphane
|
|
|
31 |
C |
p. 104
|
article
|
| 3 |
Brain morphological abnormalities in children with cyclin-dependent kinase-like 5 deficiency disorder
|
Tang, Yingying
|
|
|
31 |
C |
p. 46-53
|
article
|
| 4 |
CASK related disorder: Epilepsy and developmental outcome
|
Giacomini, Thea
|
|
|
31 |
C |
p. 61-69
|
article
|
| 5 |
Commentary on “Exome sequencing and electro-clinical features in pediatric patients with very early-onset retinal dystrophies: A cohort study”
|
Heydari, Kimia
|
|
|
31 |
C |
p. 106-107
|
article
|
| 6 |
Editorial Board
|
|
|
|
31 |
C |
p. i
|
article
|
| 7 |
Epidemiology of traumatic brain injury in children 15 years and younger in South-Eastern Norway in 2015–16. Implications for prevention and follow-up needs
|
Dahl, Hilde Margrete
|
|
|
31 |
C |
p. 70-77
|
article
|
| 8 |
Evaluating next-generation sequencing in neuromuscular diseases with neonatal respiratory distress
|
François-Heude, Marie-Céline
|
|
|
31 |
C |
p. 78-87
|
article
|
| 9 |
Exome sequencing and electro-clinical features in pediatric patients with very early-onset retinal dystrophies: A cohort study
|
Suppiej, A.
|
|
|
31 |
C |
p. 1-9
|
article
|
| 10 |
Fenfluramine responder analyses and numbers needed to treat: Translating epilepsy trial data into clinical practice
|
Sullivan, Joseph
|
|
|
31 |
C |
p. 10-14
|
article
|
| 11 |
Melatonin for neuroprotection in neonatal encephalopathy: A systematic review & meta-analysis of clinical trials
|
Ahmed, Javed
|
|
|
31 |
C |
p. 38-45
|
article
|
| 12 |
Novel presentations associated with a PDHA1 variant – Alternating hemiplegia in Hemizygote proband and Guillain Barre Syndrome in Heterozygote mother
|
Sen, Kuntal
|
|
|
31 |
C |
p. 27-30
|
article
|
| 13 |
Nusinersen does not improve lung function in a cohort of children with spinal muscular atrophy – A single-center retrospective study
|
Heitschmidt, Laura
|
|
|
31 |
C |
p. 88-91
|
article
|
| 14 |
Optimizing neonatal outcomes with melatonin - Huge promise but slow progress
|
Pang, Raymand
|
|
|
31 |
C |
p. 102-103
|
article
|
| 15 |
Pediatric SMA patients with complex spinal anatomy: Implementation and evaluation of a decision-tree algorithm for administration of nusinersen
|
Carrera-García, Laura
|
|
|
31 |
C |
p. 92-101
|
article
|
| 16 |
Recessive VAMP1 mutations associated with severe congenital myasthenic syndromes – A recognizable clinical phenotype
|
Polavarapu, Kiran
|
|
|
31 |
C |
p. 54-60
|
article
|
| 17 |
The phenotypic variability and natural history of NARS2 associated disease
|
Sofou, Kalliopi
|
|
|
31 |
C |
p. 31-37
|
article
|
| 18 |
Ultrasound estimation of brain volume in preterm infants
|
van Wezel-Meijler, Gerda
|
|
|
31 |
C |
p. 105
|
article
|
| 19 |
Uncomplicated intraventricular hemorrhage is not associated with lower estimated cerebral volume at term age
|
Graça, André M.
|
|
|
31 |
C |
p. 15-20
|
article
|
Journal description