| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Announcements and reports
|
|
|
2017
|
39 |
10 |
p. I-III
|
artikel
|
| 2 |
A patient with Muenke syndrome manifesting migrating neonatal seizures
|
Okubo, Yukimune
|
|
2017
|
39 |
10 |
p. 873-876
|
artikel
|
| 3 |
Cardiac involvement in Fukuyama muscular dystrophy is less severe than in Duchenne muscular dystrophy
|
Yamamoto, Tetsushi
|
|
2017
|
39 |
10 |
p. 861-868
|
artikel
|
| 4 |
Childhood idiopathic spinal cord infarction: Description of 7 cases and review of the literature
|
Bar, Claire
|
|
2017
|
39 |
10 |
p. 818-827
|
artikel
|
| 5 |
Contents
|
|
|
2017
|
39 |
10 |
p. OBC
|
artikel
|
| 6 |
Cover
|
|
|
2017
|
39 |
10 |
p. IBC
|
artikel
|
| 7 |
Editorial Board
|
|
|
2017
|
39 |
10 |
p. IFC
|
artikel
|
| 8 |
Effectiveness of vitamin K2 on osteoporosis in adults with cerebral palsy
|
Kodama, Yuichi
|
|
2017
|
39 |
10 |
p. 846-850
|
artikel
|
| 9 |
Exploring a method for evaluation of preschool and school children with autism spectrum disorder through checking their understanding of the speaker’s emotions with the help of prosody of the voice
|
Horie, Mayumi
|
|
2017
|
39 |
10 |
p. 836-845
|
artikel
|
| 10 |
Miglustat therapy in a case of early-infantile Niemann-Pick type C
|
Usui, Miho
|
|
2017
|
39 |
10 |
p. 886-890
|
artikel
|
| 11 |
Myoclonic epilepsy in infancy with preceding or concurrent afebrile generalized tonic-clonic seizures in Chinese children
|
Yang, Zhixian
|
|
2017
|
39 |
10 |
p. 828-835
|
artikel
|
| 12 |
[No title]
|
Kaga, Makiko
|
|
2017
|
39 |
10 |
p. 817
|
artikel
|
| 13 |
Novel FKRP mutations in a Japanese MDC1C sibship clinically diagnosed with Fukuyama congenital muscular dystrophy
|
Yoshioka, Mieko
|
|
2017
|
39 |
10 |
p. 869-872
|
artikel
|
| 14 |
Spinal muscular atrophy carriers with two SMN1 copies
|
Ar Rochmah, Mawaddah
|
|
2017
|
39 |
10 |
p. 851-860
|
artikel
|
| 15 |
Successful corpus callosotomy for Doose syndrome
|
Kanai, Sotaro
|
|
2017
|
39 |
10 |
p. 882-885
|
artikel
|
| 16 |
The therapeutic implication of a novel SCN2A mutation associated early-onset epileptic encephalopathy with Rett-like features
|
Liang, Jao-Shwann
|
|
2017
|
39 |
10 |
p. 877-881
|
artikel
|
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