| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A case of severe autosomal dominant spinal muscular atrophy with lower extremity predominance caused by a de novo BICD2 mutation
|
Ueda, Yuki
|
|
|
43 |
1 |
p. 135-139
|
artikel
|
| 2 |
Administration of nusinersen via paramedian approach for spinal muscular atrophy
|
Iwayama, Hideyuki
|
|
|
43 |
1 |
p. 121-126
|
artikel
|
| 3 |
Analysis of factors related to low health-related quality of life in children with epilepsy using a self-assessed Japanese version of the KIDSCREEN-52
|
Furuichi, Yasuko
|
|
|
43 |
1 |
p. 78-88
|
artikel
|
| 4 |
A rare infective cause of stroke in an immunocompetent child
|
Gupta, Juhi
|
|
|
43 |
1 |
p. 152-156
|
artikel
|
| 5 |
Cannabidiol-enriched oil in children and adults with treatment-resistant epilepsy-does tolerance exist?
|
Uliel-Sibony, Shimrit
|
|
|
43 |
1 |
p. 89-96
|
artikel
|
| 6 |
Chaperone therapy for molecular pathology in lysosomal diseases
|
Suzuki, Yoshiyuki
|
|
|
43 |
1 |
p. 45-54
|
artikel
|
| 7 |
Circulating markers of oxidative stress are associated with a muscle injury in patients with muscular dystrophy Duchenne
|
Almeida-Becerril, Tomas
|
|
|
43 |
1 |
p. 111-120
|
artikel
|
| 8 |
Contents
|
|
|
|
43 |
1 |
p. OBC
|
artikel
|
| 9 |
Corrigendum to ‘Targeted gene panel sequencing in early infantile onset developmental and epileptic encephalopathy’ [Brain Dev. 42(6) (2020) 438–448]
|
Na, Ji-Hoon
|
|
|
43 |
1 |
p. 179
|
artikel
|
| 10 |
Cover
|
|
|
|
43 |
1 |
p. IBC
|
artikel
|
| 11 |
Diagnostic yield of capillary compared to venous glucose in the diagnosis of hypoglycorrhachia in children: A prospective, observational study
|
Farfán-Albarracín, Juan David
|
|
|
43 |
1 |
p. 63-68
|
artikel
|
| 12 |
Dominant SCN2A mutation with variable phenotype in two generations
|
Passi, Gouri Rao
|
|
|
43 |
1 |
p. 166-169
|
artikel
|
| 13 |
Editorial Board
|
|
|
|
43 |
1 |
p. IFC
|
artikel
|
| 14 |
Efficacy of perampanel for epileptic seizures and daily behavior in a patient with Leigh syndrome: A case report
|
Kimura, Shuhei
|
|
|
43 |
1 |
p. 157-159
|
artikel
|
| 15 |
Eight years follow-up of a generalized epilepsy patient with eating-induced late-onset epileptic spasms and atypical absence with myoclonic jerks
|
Wang, Xiaoli
|
|
|
43 |
1 |
p. 160-165
|
artikel
|
| 16 |
Epilepsy in Angelman syndrome: A scoping review
|
Samanta, Debopam
|
|
|
43 |
1 |
p. 32-44
|
artikel
|
| 17 |
Epilepsy in patients with advanced Fukuyama congenital muscular dystrophy
|
Kuwayama, Ryoko
|
|
|
43 |
1 |
p. 106-110
|
artikel
|
| 18 |
Gallbladder cancer with ascites in a child with metachromatic leukodystrophy
|
Koshu, Kiri
|
|
|
43 |
1 |
p. 140-143
|
artikel
|
| 19 |
Guidelines for the diagnosis and treatment of acute encephalopathy in childhood
|
Mizuguchi, Masashi
|
|
|
43 |
1 |
p. 2-31
|
artikel
|
| 20 |
Lenticular nuclei to thalamic ratio on PET is useful for diagnosis of GLUT1 deficiency syndrome
|
Natsume, Jun
|
|
|
43 |
1 |
p. 69-77
|
artikel
|
| 21 |
Low threshold to Vestibular and Oral Sensory stimuli might affect quality of sleep among children with autism spectrum disorder
|
Kosaka, Takuya
|
|
|
43 |
1 |
p. 55-62
|
artikel
|
| 22 |
Natural history in spinal muscular atrophy Type I in Taiwanese population: A longitudinal study
|
Ou, Shan-Fu
|
|
|
43 |
1 |
p. 127-134
|
artikel
|
| 23 |
New year’s greetings
|
Kobayashi, Katsuhiro
|
|
|
43 |
1 |
p. 1
|
artikel
|
| 24 |
Predictors of malnutrition in children with neurodisabilities
|
Panda, Prateek Kumar
|
|
|
43 |
1 |
p. 176-177
|
artikel
|
| 25 |
Predictors of malnutrition in children with neurodisabilities; Reply
|
Hasegawa, Mari
|
|
|
43 |
1 |
p. 178
|
artikel
|
| 26 |
Professor Kenneth F. Swaiman
|
|
|
|
43 |
1 |
p. 180
|
artikel
|
| 27 |
Reply to: “Letter: Two cases of persistent falcine and occipital sinuses”
|
Inui, Takehiko
|
|
|
43 |
1 |
p. 175
|
artikel
|
| 28 |
The changes in the topological properties of brain structural network based on diffusion tensor imaging in pediatric epilepsy patients with vagus nerve stimulators: A graph theoretical analysis
|
Zhu, Jin
|
|
|
43 |
1 |
p. 97-105
|
artikel
|
| 29 |
Tremor as an early sign of hereditary spastic paraplegia due to mutations in ALDH18A1
|
Kalmár, Tibor
|
|
|
43 |
1 |
p. 144-151
|
artikel
|
| 30 |
Two cases of persistent falcine and occipital sinuses
|
Balak, Naci
|
|
|
43 |
1 |
p. 174
|
artikel
|
| 31 |
Two cases of persistent falcine and occipital sinuses
|
Inui, Takehiko
|
|
|
43 |
1 |
p. 170-173
|
artikel
|
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