| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A case of Bardet-Biedl syndrome complicated with intracranial hypertension in a Japanese child
|
Saida, Ken
|
|
2014
|
36 |
8 |
p. 721-724
4 p.
|
artikel
|
| 2 |
A female carrier of ornithine carbamoyltransferase deficiency masquerading as attention deficit-hyperactivity disorder
|
Kim, Se Hee
|
|
2014
|
36 |
8 |
p. 734-737
4 p.
|
artikel
|
| 3 |
A haploinsufficiency of FOXG1 identified in a boy with congenital variant of Rett syndrome
|
Kumakura, Akira
|
|
2014
|
36 |
8 |
p. 725-729
5 p.
|
artikel
|
| 4 |
An autopsy case of microencephaly, bizarre putaminal lesion, and cerebellar atrophy with heart and liver diseases
|
Okoshi, Yumi
|
|
2014
|
36 |
8 |
p. 707-710
4 p.
|
artikel
|
| 5 |
Announcements and Reports
|
|
|
2014
|
36 |
8 |
p. I-IV
nvt p.
|
artikel
|
| 6 |
Anti-NMDAR autoimmune encephalitis
|
Miya, Kazushi
|
|
2014
|
36 |
8 |
p. 645-652
8 p.
|
artikel
|
| 7 |
Call for Papers
|
|
|
2014
|
36 |
8 |
p. V-
1 p.
|
artikel
|
| 8 |
Contents
|
|
|
2014
|
36 |
8 |
p. OBC-
1 p.
|
artikel
|
| 9 |
Cover
|
|
|
2014
|
36 |
8 |
p. IBC-
1 p.
|
artikel
|
| 10 |
Delayed myelination is not a constant feature of Allan–Herndon–Dudley syndrome: Report of a new case and review of the literature
|
Azzolini, Sara
|
|
2014
|
36 |
8 |
p. 716-720
5 p.
|
artikel
|
| 11 |
Dibutyl phthalate-induced neurotoxicity in the brain of immature and mature rat offspring
|
Li, Xiujuan
|
|
2014
|
36 |
8 |
p. 653-660
8 p.
|
artikel
|
| 12 |
Disruption of Aspm causes microcephaly with abnormal neuronal differentiation
|
Fujimori, Akira
|
|
2014
|
36 |
8 |
p. 661-669
9 p.
|
artikel
|
| 13 |
Early clinical features and diagnosis of Dravet syndrome in 138 Chinese patients with SCN1A mutations
|
Xu, Xiaojing
|
|
2014
|
36 |
8 |
p. 676-681
6 p.
|
artikel
|
| 14 |
Editorial Board
|
|
|
2014
|
36 |
8 |
p. IFC-
1 p.
|
artikel
|
| 15 |
Leigh syndrome with Fukuyama congenital muscular dystrophy: A case report
|
Kondo, Hidehito
|
|
2014
|
36 |
8 |
p. 730-733
4 p.
|
artikel
|
| 16 |
Neuropsychological and neuroimaging phenotype induced by a CAMTA1 mutation
|
Magnin, Eloi
|
|
2014
|
36 |
8 |
p. 711-715
5 p.
|
artikel
|
| 17 |
Novel SETX variants in a patient with ataxia, neuropathy, and oculomotor apraxia are associated with normal sensitivity to oxidative DNA damaging agents
|
Vantaggiato, Chiara
|
|
2014
|
36 |
8 |
p. 682-689
8 p.
|
artikel
|
| 18 |
Pseudotumor cerebri/idiopathic intracranial hypertension in children: An experience of a tertiary care hospital
|
Değerliyurt, Aydan
|
|
2014
|
36 |
8 |
p. 690-699
10 p.
|
artikel
|
| 19 |
Psychometric properties of Japanese version of the Swanson, Nolan, and Pelham, version-IV Scale-Teacher Form: A study of school children in community samples
|
Inoue, Yuki
|
|
2014
|
36 |
8 |
p. 700-706
7 p.
|
artikel
|
| 20 |
Serum tau protein level serves as a predictive factor for neurological prognosis in neonatal asphyxia
|
Takahashi, Kazumasa
|
|
2014
|
36 |
8 |
p. 670-675
6 p.
|
artikel
|
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