| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A case of juvenile Canavan disease with distinct pons involvement
|
Çakar, Nafiye Emel
|
|
|
42 |
2 |
p. 222-225
|
artikel
|
| 2 |
Analysis of spinal muscular atrophy-like patients by targeted resequencing
|
Hosokawa, Shinichi
|
|
|
42 |
2 |
p. 148-156
|
artikel
|
| 3 |
A new missense mutation in DPF2 gene related to Coffin Siris syndrome 7: Description of a mild phenotype expanding DPF2-related clinical spectrum and differential diagnosis among similar syndromes epigenetically determined
|
Milone, Roberta
|
|
|
42 |
2 |
p. 192-198
|
artikel
|
| 4 |
Atypical gamma functional connectivity pattern during light sleep in children with attention deficit hyperactivity disorder
|
Ueda, Riyo
|
|
|
42 |
2 |
p. 129-139
|
artikel
|
| 5 |
Children with autism spectrum disorder comorbid with attention-deficit/hyperactivity disorder examined by the Wisconsin card sorting test: Analysis by age-related differences
|
Kado, Yoko
|
|
|
42 |
2 |
p. 113-120
|
artikel
|
| 6 |
Contents
|
|
|
|
42 |
2 |
p. OBC
|
artikel
|
| 7 |
Cover
|
|
|
|
42 |
2 |
p. IBC
|
artikel
|
| 8 |
d-Glycerate kinase deficiency in a neuropediatric patient
|
Sass, Jörn Oliver
|
|
|
42 |
2 |
p. 226-230
|
artikel
|
| 9 |
Effects of valproic acid and levetiracetam monotherapy on carotid intima-media and epicardial adipose tissue thickness in non-obese children with epilepsy
|
Karatoprak, Elif
|
|
|
42 |
2 |
p. 165-170
|
artikel
|
| 10 |
Japanese encephalitis-induced anti-N-methyl-d-aspartate receptor encephalitis: A hospital-based prospective study
|
Ma, Jiannan
|
|
|
42 |
2 |
p. 179-184
|
artikel
|
| 11 |
Metabolic crisis after trivial head trauma in late-onset isolated sulfite oxidase deficiency: Report of two new cases and review of published patients
|
Sharawat, Indar Kumar
|
|
|
42 |
2 |
p. 157-164
|
artikel
|
| 12 |
Neurodevelopmental disorder associated with de novo SCN3A pathogenic variants: two new cases and review of the literature
|
Inuzuka, Luciana Midori
|
|
|
42 |
2 |
p. 211-216
|
artikel
|
| 13 |
Novel biallelic FA2H mutations in a Japanese boy with fatty acid hydroxylase-associated neurodegeneration
|
Kawaguchi, Masahiro
|
|
|
42 |
2 |
p. 217-221
|
artikel
|
| 14 |
Phenotype–genotype correlations in patients with GNB1 gene variants, including the first three reported Japanese patients to exhibit spastic diplegia, dyskinetic quadriplegia, and infantile spasms
|
Endo, Wakaba
|
|
|
42 |
2 |
p. 199-204
|
artikel
|
| 15 |
PIGA related disorder as a range of phenotypes rather than two distinct subtypes
|
Cash, Shelby J.
|
|
|
42 |
2 |
p. 205-210
|
artikel
|
| 16 |
Safety and immediate effects of Hybrid Assistive Limb in children with cerebral palsy: A pilot study
|
Nakagawa, Shogo
|
|
|
42 |
2 |
p. 140-147
|
artikel
|
| 17 |
Serum and cerebrospinal fluid cytokines in children with acute encephalopathy
|
Kawahara, Yuta
|
|
|
42 |
2 |
p. 185-191
|
artikel
|
| 18 |
Sodium phenylbutyrate improved the clinical state in an adult patient with arginase 1 deficiency
|
Matsufuji, Mayumi
|
|
|
42 |
2 |
p. 231-235
|
artikel
|
| 19 |
Support and development of autistic children with selective eating habits
|
Yamane, Kiyoko
|
|
|
42 |
2 |
p. 121-128
|
artikel
|
| 20 |
The effects of antihistamine on the duration of the febrile seizure: A single center study with a systematic review and meta-analysis
|
Sugitate, Ryo
|
|
|
42 |
2 |
p. 103-112
|
artikel
|
| 21 |
Two autopsy cases of sudden unexpected death from Dravet syndrome with novel de novo SCN1A variants
|
Hata, Yukiko
|
|
|
42 |
2 |
p. 171-178
|
artikel
|
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