nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
Announcements and reports
|
|
|
2018 |
40 |
5 |
p. I-II |
artikel |
2 |
ATP1A3-related epileptic encephalopathy responding to ketogenic diet
|
Schirinzi, Tommaso |
|
2018 |
40 |
5 |
p. 433-438 |
artikel |
3 |
Contents
|
|
|
2018 |
40 |
5 |
p. OBC |
artikel |
4 |
Cover
|
|
|
2018 |
40 |
5 |
p. IBC |
artikel |
5 |
De novo HDAC8 mutation causes Rett-related disorder with distinctive facial features and multiple congenital anomalies
|
Saikusa, Tomoko |
|
2018 |
40 |
5 |
p. 406-409 |
artikel |
6 |
Detection of fast (40–150 Hz) oscillations from the ictal scalp EEG data of myoclonic seizures in pediatric patients
|
Kobayashi, Katsuhiro |
|
2018 |
40 |
5 |
p. 397-405 |
artikel |
7 |
Diagnostic challenge for the rare lysosomal storage disease: Late infantile GM1 gangliosidosis
|
Lee, Jin Sook |
|
2018 |
40 |
5 |
p. 383-390 |
artikel |
8 |
Editorial Board
|
|
|
2018 |
40 |
5 |
p. IFC |
artikel |
9 |
Efficacy and safety of everolimus in patients younger than 12 months with congenital subependymal giant cell astrocytoma
|
Kuki, Ichiro |
|
2018 |
40 |
5 |
p. 415-420 |
artikel |
10 |
EPO improved neurologic outcome in rat pups late after traumatic brain injury
|
Schober, Michelle E. |
|
2018 |
40 |
5 |
p. 367-375 |
artikel |
11 |
Familial cases of progressive myoclonic epilepsy caused by maternal somatic mosaicism of a recurrent KCNC1 p.Arg320His mutation
|
Kim, Hyuna |
|
2018 |
40 |
5 |
p. 429-432 |
artikel |
12 |
Guillain-Barré syndrome and optic neuritis after Mycoplasma pneumoniae infection
|
Matsunaga, Manaka |
|
2018 |
40 |
5 |
p. 439-442 |
artikel |
13 |
Hemiconvulsion-hemiplegia-epilepsy evolving to contralateral hemi-Lennox-Gastaut-like phenotype
|
Myers, Kenneth A. |
|
2018 |
40 |
5 |
p. 425-428 |
artikel |
14 |
Is vatiquinone truly beneficial for Leigh syndrome?
|
Finsterer, Josef |
|
2018 |
40 |
5 |
p. 443 |
artikel |
15 |
Quantitative microstructural cerebral changes in neurofibromatosis type 1
|
Bültmann, Eva |
|
2018 |
40 |
5 |
p. 376-382 |
artikel |
16 |
Reply to the letter to the editor by Josef Finsterer and Sinda Zarrouk-Mahjoub
|
Osaka, Hitoshi |
|
2018 |
40 |
5 |
p. 444 |
artikel |
17 |
Rett-like features and cortical visual impairment in a Japanese patient with HECW2 mutation
|
Nakamura, Haruhiko |
|
2018 |
40 |
5 |
p. 410-414 |
artikel |
18 |
Successful use of non-invasive positive pressure ventilation in a patient with the severe form of X-linked myotubular myopathy
|
Inoue, Kenji |
|
2018 |
40 |
5 |
p. 421-424 |
artikel |
19 |
The assessment of sniff nasal inspiratory pressure in patients with Duchenne muscular dystrophy in China
|
Zhang, Shu |
|
2018 |
40 |
5 |
p. 391-396 |
artikel |