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                             17 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 A case of acute encephalopathy with biphasic seizures and late reduced diffusion associated with Streptococcus pneumoniae meningoencephalitis Kuwata, Seiko
2012
34 6 p. 529-532
4 p.
artikel
2 An investigation into kana reading development in normal and dyslexic Japanese children using length and lexicality effects Sambai, Ami
2012
34 6 p. 520-528
9 p.
artikel
3 Announcements and reports 2012
34 6 p. I-VI
nvt p.
artikel
4 A novel mutation in an atypical presentation of the rare infantile Farber disease Al Jasmi, Fatma
2012
34 6 p. 533-535
3 p.
artikel
5 A study of educational underachievement in Indian children with epilepsy Singh, Harpal
2012
34 6 p. 504-510
7 p.
artikel
6 Atonic variant of benign childhood epilepsy with centrotemporal spikes (atonic-BECTS): A distinct electro-clinical syndrome Cherian, Ajith
2012
34 6 p. 511-519
9 p.
artikel
7 Comments on the article by Mizuno Y. et al. entitled “Congenital infection-like syndrome with intracranial calcification” Asai, Daisuke
2012
34 6 p. 539-
1 p.
artikel
8 Congenital infection-like syndrome with intracranial calcification: Absence of TINF2 mutation Mizuno, Yoko
2012
34 6 p. 540-
1 p.
artikel
9 Contents 2012
34 6 p. OBC-
1 p.
artikel
10 Cutaneous adverse drug reaction in patients with epilepsy after acute encephalitis Mogami, Yukiko
2012
34 6 p. 496-503
8 p.
artikel
11 Decreased benzodiazepine receptor and increased GABA level in cortical tubers in tuberous sclerosis complex Mori, Kenji
2012
34 6 p. 478-486
9 p.
artikel
12 Early-onset neurodegeneration with brain iron accumulation due to PANK2 mutation Rossi, Daniela
2012
34 6 p. 536-538
3 p.
artikel
13 Editorial Board 2012
34 6 p. IFC-
1 p.
artikel
14 IBC 2012
34 6 p. IBC-
1 p.
artikel
15 Maturation of EEG oscillations in children with sodium channel mutations Holmes, Gregory L.
2012
34 6 p. 469-477
9 p.
artikel
16 MECP2 mutations and clinical correlations in Greek children with Rett syndrome and associated neurodevelopmental disorders Psoni, Stavroula
2012
34 6 p. 487-495
9 p.
artikel
17 Ohtahara syndrome with emphasis on recent genetic discovery Pavone, Piero
2012
34 6 p. 459-468
10 p.
artikel
                             17 gevonden resultaten
 
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