| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
An atypical patient with Cowden syndrome and PTEN gene mutation presenting with cortical malformation and focal epilepsy
|
Elia, Maurizio
|
|
2012
|
34 |
10 |
p. 873-876
4 p.
|
artikel
|
| 2 |
Announcements and reports
|
|
|
2012
|
34 |
10 |
p. XXVI-XXXI
nvt p.
|
artikel
|
| 3 |
Antiamnesic activity of Syzygium cumini against scopolamine induced spatial memory impairments in rats
|
Alikatte, Kanaka Latha
|
|
2012
|
34 |
10 |
p. 844-851
8 p.
|
artikel
|
| 4 |
A pediatric patient with myopathy associated with antibodies to a signal recognition particle
|
Kawabata, Takayoshi
|
|
2012
|
34 |
10 |
p. 877-880
4 p.
|
artikel
|
| 5 |
A severe form of epidermal nevus syndrome associated with brainstem and cerebellar malformations and neonatal medulloblastoma
|
Okumura, Akihisa
|
|
2012
|
34 |
10 |
p. 881-885
5 p.
|
artikel
|
| 6 |
Attention and executive functions profile in childhood absence epilepsy
|
D’Agati, Elisa
|
|
2012
|
34 |
10 |
p. 812-817
6 p.
|
artikel
|
| 7 |
Author Index to Volume 34
|
|
|
2012
|
34 |
10 |
p. IX-XX
nvt p.
|
artikel
|
| 8 |
Benign myoclonic epilepsy in infancy with preceding afebrile generalized tonic–clonic seizures in Japan
|
Ito, Susumu
|
|
2012
|
34 |
10 |
p. 829-833
5 p.
|
artikel
|
| 9 |
Clinical and genetic characterization of a 2-year-old boy with complete PLP1 deletion
|
Torisu, Hiroyuki
|
|
2012
|
34 |
10 |
p. 852-856
5 p.
|
artikel
|
| 10 |
Complex malformation (Ruggieri–Happle) phenotype with “cutis tricolor” in a 10-year-old girl
|
Nicita, Francesco
|
|
2012
|
34 |
10 |
p. 869-872
4 p.
|
artikel
|
| 11 |
Contents
|
|
|
2012
|
34 |
10 |
p. OBC-
1 p.
|
artikel
|
| 12 |
Contents continued
|
|
|
2012
|
34 |
10 |
p. IBC-
1 p.
|
artikel
|
| 13 |
Corrigendum to “MECP2 gene mutation analysis in the British and Italian Rett Syndrome patients: hot spot map of the most recurrent mutations and bioinformatic analysis of a new MECP2 conserved region” [Brain Dev 2001; 23: S246–50]
|
Vacca, Marcella
|
|
2012
|
34 |
10 |
p. 891-
1 p.
|
artikel
|
| 14 |
Cumulative contents to Volume 34
|
|
|
2012
|
34 |
10 |
p. I-VIII
nvt p.
|
artikel
|
| 15 |
Developmental change of visuo-spatial working memory in children: Quantitative evaluation through an Advanced Trail Making Test
|
Kokubo, Naomi
|
|
2012
|
34 |
10 |
p. 799-805
7 p.
|
artikel
|
| 16 |
Editorial Board
|
|
|
2012
|
34 |
10 |
p. IFC-
1 p.
|
artikel
|
| 17 |
EEG characteristics and visual cognitive function of children with attention deficit hyperactivity disorder (ADHD)
|
Shi, Tongkun
|
|
2012
|
34 |
10 |
p. 806-811
6 p.
|
artikel
|
| 18 |
Effects of lamotrigine on cognition and behavior compared to carbamazepine as monotherapy for children with partial epilepsy
|
Eun, So-Hee
|
|
2012
|
34 |
10 |
p. 818-823
6 p.
|
artikel
|
| 19 |
Exacerbation of idiopathic paroxysmal kinesigenic dyskinesia in remission state caused by secondary hypoparathyroidism with hypocalcemia after thyroidectomy: Evidence for ion channelopathy
|
Jin, Dongkwan
|
|
2012
|
34 |
10 |
p. 840-843
4 p.
|
artikel
|
| 20 |
Focal cortical myoclonus in rolandic cortical dysplasia presenting as hemifacial twitching
|
Honda, Ryoko
|
|
2012
|
34 |
10 |
p. 886-890
5 p.
|
artikel
|
| 21 |
Guide for Authors
|
|
|
2012
|
34 |
10 |
p. XXXII-XXXVI
nvt p.
|
artikel
|
| 22 |
Lateral medullary syndrome in a boy with hereditary dysfibrinogenemia
|
Kibe, Tetsuya
|
|
2012
|
34 |
10 |
p. 857-860
4 p.
|
artikel
|
| 23 |
Nonconvulsive status epilepticus due to drug induced neurotoxicity in chronically ill children
|
Ekici, Arzu
|
|
2012
|
34 |
10 |
p. 824-828
5 p.
|
artikel
|
| 24 |
Pulmonary hypertension in a child with mitochondrial A3243G point mutation
|
Hung, Po-Cheng
|
|
2012
|
34 |
10 |
p. 866-868
3 p.
|
artikel
|
| 25 |
Quantitative computed tomography for enzyme replacement therapy in Pompe disease
|
Yonee, Chihiro
|
|
2012
|
34 |
10 |
p. 834-839
6 p.
|
artikel
|
| 26 |
Subject Index to Volume 34
|
|
|
2012
|
34 |
10 |
p. XXI-XXV
nvt p.
|
artikel
|
| 27 |
Two Japanese patients with Leigh syndrome caused by novel SURF1 mutations
|
Tanigawa, Junpei
|
|
2012
|
34 |
10 |
p. 861-865
5 p.
|
artikel
|
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