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                             19 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 Acute encephalopathy in two cases with severe congenital hydrocephalus Tanoue, Koji
2011
33 7 p. 616-619
4 p.
artikel
2 A familial case of LEOPARD syndrome associated with a high-functioning autism spectrum disorder Watanabe, Yoriko
2011
33 7 p. 576-579
4 p.
artikel
3 Announcement: JSCN Best Paper Awards 2011
33 7 p. I-
1 p.
artikel
4 Announcements and reports 2011
33 7 p. II-VI
nvt p.
artikel
5 Atypical childhood absence epilepsy with preceding or simultaneous generalized tonic clonic seizures Wakamoto, Hiroyuki
2011
33 7 p. 589-592
4 p.
artikel
6 Cerebrospinal fluid and serum levels of vitamin B6 in status epilepticus children Hasumi, Hiroki
2011
33 7 p. 580-588
9 p.
artikel
7 Contents 2011
33 7 p. IBC-
1 p.
artikel
8 Editorial Board 2011
33 7 p. IFC-
1 p.
artikel
9 Epilepsy and trimethylaminuria: A new case report and literature review Pellicciari, Alessandro
2011
33 7 p. 593-596
4 p.
artikel
10 Head circumference and body growth in autism spectrum disorders Fukumoto, Aya
2011
33 7 p. 569-575
7 p.
artikel
11 Infant ERP amplitudes change over the course of an experimental session: Implications for cognitive processes and methodology Stets, Manuela
2011
33 7 p. 558-568
11 p.
artikel
12 Lesions in the central tegmental tract in autopsy cases of developmental brain disorders Shioda, Mutsuki
2011
33 7 p. 541-547
7 p.
artikel
13 Migraine triggered by epileptic discharges in a Rasmussen’s encephalitis patient after surgery Fusco, Lucia
2011
33 7 p. 597-600
4 p.
artikel
14 Paths to the making of an academic clinical investigator—Part 2 Rapin, Isabelle
2011
33 7 p. 537-540
4 p.
artikel
15 Pitfalls in diagnosing psychogenic nonepileptic seizures in a sexually abused child Nagamitsu, Shinichiro
2011
33 7 p. 601-603
3 p.
artikel
16 Renal agenesis and external iliac artery stenosis in an infant with moyamoya disease Ramesh, Konanki
2011
33 7 p. 612-615
4 p.
artikel
17 Serial MRI changes in a patient with infantile Alexander disease and prolonged survival Shiihara, Takashi
2011
33 7 p. 604-607
4 p.
artikel
18 Somatic mosaicism for Y120X mutation in the MECP2 gene causes atypical Rett syndrome in a male Pieras, Juan I
2011
33 7 p. 608-611
4 p.
artikel
19 Value of clinical assessment in the diagnostic evaluation of Global Developmental Delay (GDD) using a Likelihood Ratio Model Wong, Virginia C.N.
2011
33 7 p. 548-557
10 p.
artikel
                             19 gevonden resultaten
 
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