| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Announcements and reports
|
|
|
2018
|
40 |
4 |
p. I-II
|
artikel
|
| 2 |
Arima syndrome caused by CEP290 specific variant and accompanied with pathological cilium; clinical comparison with Joubert syndrome and its related diseases
|
Itoh, Masayuki
|
|
2018
|
40 |
4 |
p. 259-267
|
artikel
|
| 3 |
A severe female case of arthrogryposis multiplex congenita with brain atrophy, spastic quadriplegia and intellectual disability caused by ZC4H2 mutation
|
Okubo, Yukimune
|
|
2018
|
40 |
4 |
p. 334-338
|
artikel
|
| 4 |
Avoid mitochondrion-toxic antiepileptic drugs in glycine encephalopathy
|
Finsterer, Josef
|
|
2018
|
40 |
4 |
p. 366
|
artikel
|
| 5 |
Contents
|
|
|
2018
|
40 |
4 |
p. OBC
|
artikel
|
| 6 |
Cover
|
|
|
2018
|
40 |
4 |
p. IBC
|
artikel
|
| 7 |
Cytokine/chemokine elevation during the transition phase from HSV encephalitis to autoimmune anti-NMDA receptor encephalitis
|
Omae, Takanori
|
|
2018
|
40 |
4 |
p. 361-365
|
artikel
|
| 8 |
Differential effects on sodium current impairments by distinct SCN1A mutations in GABAergic neurons derived from Dravet syndrome patients
|
Kim, Hyun Woo
|
|
2018
|
40 |
4 |
p. 287-298
|
artikel
|
| 9 |
Duchenne muscular dystrophy with platypnea-orthodeoxia from Chilaiditi syndrome
|
Ogasawara, Masashi
|
|
2018
|
40 |
4 |
p. 339-342
|
artikel
|
| 10 |
Editorial Board
|
|
|
2018
|
40 |
4 |
p. IFC
|
artikel
|
| 11 |
Excitotoxicity in encephalopathy associated with STEC O-157 infection
|
Ishida, Shigenobu
|
|
2018
|
40 |
4 |
p. 357-360
|
artikel
|
| 12 |
High dose phenobarbitone coma in pediatric refractory status epilepticus; a retrospective case record analysis, a proposed protocol and review of literature
|
Gulati, Sheffali
|
|
2018
|
40 |
4 |
p. 316-324
|
artikel
|
| 13 |
Histopathological proof of the pathogenicity of a rare GFAP mutation in a patient with flaccid paraparesis
|
Brackmann, Florian
|
|
2018
|
40 |
4 |
p. 330-333
|
artikel
|
| 14 |
Hydrocephalus in pyridoxine-dependent epilepsy: New case and literature review
|
Navarro-Abia, Virginia
|
|
2018
|
40 |
4 |
p. 348-352
|
artikel
|
| 15 |
l-Thyroxine-responsive drop attacks in childhood benign hereditary chorea: A case report
|
Shiohama, Tadashi
|
|
2018
|
40 |
4 |
p. 353-356
|
artikel
|
| 16 |
Novel BICD2 mutation in a Japanese family with autosomal dominant lower extremity-predominant spinal muscular atrophy-2
|
Yoshioka, Mieko
|
|
2018
|
40 |
4 |
p. 343-347
|
artikel
|
| 17 |
Predictive value of EEG for febrile seizure recurrence
|
Cappellari, Alberto M.
|
|
2018
|
40 |
4 |
p. 311-315
|
artikel
|
| 18 |
Prevalence of idiopathic epilepsy among school children in Gharbia Governorate, Egypt
|
Alshahawy, Azza Kamal
|
|
2018
|
40 |
4 |
p. 278-286
|
artikel
|
| 19 |
Scalp-recorded high-frequency oscillations in childhood epileptic encephalopathy with continuous spike-and-wave during sleep with different etiologies
|
Gong, Pan
|
|
2018
|
40 |
4 |
p. 299-310
|
artikel
|
| 20 |
Social involvement issues in patients with Becker muscular dystrophy: A questionnaire survey of subjects from a patient registry
|
Mori-Yoshimura, Madoka
|
|
2018
|
40 |
4 |
p. 268-277
|
artikel
|
| 21 |
The presence of diminished white matter and corpus callosal thinning in a case with a SOX9 mutation
|
Matsumoto, Ayumi
|
|
2018
|
40 |
4 |
p. 325-329
|
artikel
|
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