| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A fact-finding survey of the recommendation on sedation during physiological examinations such as electroencephalogram in Japan
|
Korematsu, Seigo
|
|
|
43 |
2 |
p. 208-213
|
artikel
|
| 2 |
A longitudinal cohort study of childhood MMR vaccination and seizure disorder among American children
|
Geier, David A.
|
|
|
43 |
2 |
p. 251-267
|
artikel
|
| 3 |
A novel stop-gain CUL3 mutation in a Japanese patient with autism spectrum disorder
|
Iwafuchi, Sota
|
|
|
43 |
2 |
p. 303-307
|
artikel
|
| 4 |
Bell’s palsy in a pediatric patient with hyper IgM syndrome and severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)
|
Theophanous, Christos
|
|
|
43 |
2 |
p. 357-359
|
artikel
|
| 5 |
Biallelic XPR1 mutation associated with primary familial brain calcification presenting as paroxysmal kinesigenic dyskinesia with infantile convulsions
|
Tang, Li-Ou
|
|
|
43 |
2 |
p. 331-336
|
artikel
|
| 6 |
Clinical characteristics of KCNQ2 encephalopathy
|
Kim, Hyo Jeong
|
|
|
43 |
2 |
p. 244-250
|
artikel
|
| 7 |
Clinical phenotypes of spinal muscular atrophy patients with hybrid SMN gene
|
Niba, Emma Tabe Eko
|
|
|
43 |
2 |
p. 294-302
|
artikel
|
| 8 |
Clinical utility of the FilmArray meningitis/encephalitis panel in children at a tertiary center in South Korea
|
Park, Su Eun
|
|
|
43 |
2 |
p. 234-243
|
artikel
|
| 9 |
Clinical variations of epileptic syndrome associated with PACS2 variant
|
Mizuno, Tomoko
|
|
|
43 |
2 |
p. 343-347
|
artikel
|
| 10 |
Contents
|
|
|
|
43 |
2 |
p. OBC
|
artikel
|
| 11 |
Cover
|
|
|
|
43 |
2 |
p. IBC
|
artikel
|
| 12 |
Diabetes mellitus in an adolescent girl with intellectual disability caused by novel single base pair duplication in the PTRH2 gene: Expanding the clinical spectrum of IMNEPD
|
Parida, Preetinanda
|
|
|
43 |
2 |
p. 314-319
|
artikel
|
| 13 |
Do low birth weight infants not see eyes? Face recognition in infancy
|
Yamamoto, Mayumi
|
|
|
43 |
2 |
p. 186-191
|
artikel
|
| 14 |
Early prediction of encephalopathic transformation in children with benign epilepsy with centro-temporal spikes
|
Porat Rein, Adi
|
|
|
43 |
2 |
p. 268-279
|
artikel
|
| 15 |
Editorial Board
|
|
|
|
43 |
2 |
p. IFC
|
artikel
|
| 16 |
Efficacy of bezafibrate for preventing myopathic attacks in patients with very long-chain acyl-CoA dehydrogenase deficiency
|
Shiraishi, Hideaki
|
|
|
43 |
2 |
p. 214-219
|
artikel
|
| 17 |
Immunodeficiency in a patient with microcephalic osteodysplastic primordial dwarfism type I as compared to Roifman syndrome
|
Hagiwara, Hidetoshi
|
|
|
43 |
2 |
p. 337-342
|
artikel
|
| 18 |
Initial treatment of seizures in children in an emergency department in rural Japan
|
Shiraki, Anna
|
|
|
43 |
2 |
p. 288-293
|
artikel
|
| 19 |
Magnetic resonance neurography in diagnosing childhood chronic inflammatory demyelinating polyradiculoneuropathy
|
Yoshii, Shoko
|
|
|
43 |
2 |
p. 352-356
|
artikel
|
| 20 |
Perampanel may be beneficial in Leigh syndrome by its anti-oxidative but not anti-epileptic effect
|
Finsterer, Josef
|
|
|
43 |
2 |
p. 360
|
artikel
|
| 21 |
PNPT1 mutations may cause Aicardi-Goutières-Syndrome
|
Bamborschke, Daniel
|
|
|
43 |
2 |
p. 320-324
|
artikel
|
| 22 |
Postoperative improvement of executive function and adaptive behavior in children with intractable epilepsy
|
Ueda, Riyo
|
|
|
43 |
2 |
p. 280-287
|
artikel
|
| 23 |
Reply to the letter: “Perampanel may be beneficial in leigh syndrome by its anti-oxidative but not anti-epileptic effect”
|
Kimura, Shuhei
|
|
|
43 |
2 |
p. 361-362
|
artikel
|
| 24 |
Reversible splenial lesion syndrome associated with SARS-CoV-2 infection in two children
|
Bektaş, Gonca
|
|
|
43 |
2 |
p. 230-233
|
artikel
|
| 25 |
Severe pallid breath-holding spells treated with low-dose theophylline
|
Sato, Ayami
|
|
|
43 |
2 |
p. 348-351
|
artikel
|
| 26 |
Shuffling babies and autism spectrum disorder
|
Okai, Yu
|
|
|
43 |
2 |
p. 181-185
|
artikel
|
| 27 |
Spectrum of PAH gene mutations and genotype-phenotype correlation in patients with phenylalanine hydroxylase deficiency from Shanxi province
|
Tao, Yilun
|
|
|
43 |
2 |
p. 220-229
|
artikel
|
| 28 |
The effect of different dietary structure on gastrointestinal dysfunction in children with cerebral palsy and epilepsy based on gut microbiota
|
Huang, Congfu
|
|
|
43 |
2 |
p. 192-199
|
artikel
|
| 29 |
The first Korean cases of combined oxidative phosphorylation deficiency 35 with two novel TRIT1 mutations in two siblings confirmed by clinical and molecular investigation
|
Yoo, Sukdong
|
|
|
43 |
2 |
p. 325-330
|
artikel
|
| 30 |
Valine-restricted diet for patients with ECHS1 deficiency: Divergent clinical outcomes in two Japanese siblings
|
Sato-Shirai, Ikuko
|
|
|
43 |
2 |
p. 308-313
|
artikel
|
| 31 |
Vitamins K and D deficiency in severe motor and intellectually disabled patients
|
Sakai, Tomoko
|
|
|
43 |
2 |
p. 200-207
|
artikel
|
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