| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A dilemma in pediatric migraine: Headache or school performance? – A comparison of topiramate and flunarizine
|
Akca, Ünal
|
|
|
47 |
4 |
p.
|
artikel
|
| 2 |
Association between epilepsy and attention deficit/hyperactivity disorder – correlation between interictal epileptiform discharges and behavioral disturbances
|
Kanemura, Hideaki
|
|
|
47 |
4 |
p.
|
artikel
|
| 3 |
Awareness and knowledge of pediatricians regarding genetic testing for Fragile X syndrome in Japan: A National Survey of Pediatricians Managing Developmental Delay/Intellectual disability
|
Okazaki, Tetsuya
|
|
|
47 |
4 |
p.
|
artikel
|
| 4 |
Biallelic novel CCDC186 loss-of-function variant disrupting the gene function causes neurodevelopmental phenotype and review of the literature
|
Gezdirici, Alper
|
|
|
47 |
4 |
p.
|
artikel
|
| 5 |
Characteristics of febrile seizure after the end of the COVID-19 global health emergency
|
Numoto, Shingo
|
|
|
47 |
4 |
p.
|
artikel
|
| 6 |
Characteristics of withdrawal seizures in children with refractory status epilepticus who responded favorably to continuous midazolam therapy
|
Takeuchi, Hirokazu
|
|
|
47 |
4 |
p.
|
artikel
|
| 7 |
Drug-resistant epilepsy in children post-neonatal seizures: Clinical profiles and predictors
|
Saenchai, Warisara
|
|
|
47 |
4 |
p.
|
artikel
|
| 8 |
Early hypoglycemia is not an independent risk factor for 2-year neurodevelopmental impairment in appropriate-for-gestational age preterm infants < 32 weeks
|
Palazzo, Martina
|
|
|
47 |
4 |
p.
|
artikel
|
| 9 |
Endocrinological study of low-dose adrenocorticotropic hormone therapy without tapering in infantile epileptic spasms syndrome
|
Morita, Shumpei
|
|
|
47 |
4 |
p.
|
artikel
|
| 10 |
Epilepsy phenotypes and responses to antiseizure medications in pediatric patients with EEF1A2-related epilepsy
|
Yun, Hee-Jeong
|
|
|
47 |
4 |
p.
|
artikel
|
| 11 |
Focus on epilepsy and epilepsy syndromes in children with autism spectrum disorders: a study of 74 patients
|
Caraballo, Roberto H.
|
|
|
47 |
4 |
p.
|
artikel
|
| 12 |
Genetic analysis of leukodystrophies in children: towards improved diagnostic yield
|
Saitsu, Hirotomo
|
|
|
47 |
4 |
p.
|
artikel
|
| 13 |
Hand-arm bimanual intensive therapy versus modified constraint-induced movement therapy in children with hemiparetic cerebral palsy: A randomized controlled trial
|
Panda, Prateek Kumar
|
|
|
47 |
4 |
p.
|
artikel
|
| 14 |
Hematopoietic stem cell gene therapy of neurometabolic lysosomal storage diseases
|
Consiglieri, Giulia
|
|
|
47 |
4 |
p.
|
artikel
|
| 15 |
Letter to the editor: ‘Prevalence and management of gastrointestinal complications of Duchenne muscular dystrophy: A retrospective cohort study’
|
Atamanalp, Sabri Selcuk
|
|
|
47 |
4 |
p.
|
artikel
|
| 16 |
L-NAME improves the morphology and necrosis of skeletal muscle by activating PINK1-PARKIN mediated mitophagy in mdx mice
|
Li, Junxia
|
|
|
47 |
4 |
p.
|
artikel
|
| 17 |
Long-term outcome prediction after pediatric cardiac arrest by continuous electroencephalography
|
Ohashi, Eri
|
|
|
47 |
4 |
p.
|
artikel
|
| 18 |
Low excretor glutaric acidemia type 1 with transient lesions in the basal ganglia
|
Miyata, Yohane
|
|
|
47 |
4 |
p.
|
artikel
|
| 19 |
MECP2 duplication syndrome: Recent advances in pathophysiology and therapeutic perspectives
|
Akaba, Yuichi
|
|
|
47 |
4 |
p.
|
artikel
|
| 20 |
Molecular pathologies and therapies for Pelizaeus-Merzbacher disease
|
Inoue, Ken
|
|
|
47 |
4 |
p.
|
artikel
|
| 21 |
Motor skills and neurological soft signs: Are they only clinical differences or reflection of distinct etiopathogenesis in tic disorder and primary stereotypic movement disorder?
|
Akbas Aliyev, Ecem Selin
|
|
|
47 |
4 |
p.
|
artikel
|
| 22 |
National study on pediatric acute encephalopathy in Japan (April 2020 to October 2023): Insights from the third study
|
Omata, Taku
|
|
|
47 |
4 |
p.
|
artikel
|
| 23 |
Natural history of timed rise from floor in young individuals with Duchenne muscular dystrophy: A single-center retrospective study
|
Yoneno, Shota
|
|
|
47 |
4 |
p.
|
artikel
|
| 24 |
Prevalence and management of gastrointestinal complications in Duchenne muscular dystrophy: A retrospective cohort study
|
Aihara, Yu
|
|
|
47 |
4 |
p.
|
artikel
|
| 25 |
Recognition of Japanese kanji words in children with specific learning disorders: a preliminary study using magnetoencephalography
|
Egashira, Yuka
|
|
|
47 |
4 |
p.
|
artikel
|
| 26 |
Relationship between cerebrospinal fluid cytokines/chemokines and clinical impact of myelin oligodendrocyte glycoprotein antibody-associated disorders in children
|
Lee, SunMin
|
|
|
47 |
4 |
p.
|
artikel
|
| 27 |
The first case of Al-Raqad syndrome in Japan is associated with a homozygous DCPS exonic variant resulting in aberrant splicing
|
Nozaki, Haruka
|
|
|
47 |
4 |
p.
|
artikel
|
| 28 |
Tuberous sclerosis complex: Clinical, genetic and 7T-MRI neuroimaging findings
|
Campanario da Silva Pereira, Conceição
|
|
|
47 |
4 |
p.
|
artikel
|
| 29 |
Unraveling the connections between migraine and psychiatric comorbidities: A narrative review
|
Yum, Jungyon
|
|
|
47 |
4 |
p.
|
artikel
|
| 30 |
Valproate and lamotrigine combination therapy in children with drug-resistant focal epilepsy: an observational analysis focusing on neuroimaging abnormalities
|
Watanabe, Shiena
|
|
|
47 |
4 |
p.
|
artikel
|
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