| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A 2-bp deletion in exon 74 of the dystrophin gene does not clearly induce muscle weakness
|
Kimura, Shigemi
|
|
2009
|
31 |
2 |
p. 169-172
4 p.
|
artikel
|
| 2 |
A catalog of SCN1A variants
|
Lossin, Christoph
|
|
2009
|
31 |
2 |
p. 114-130
17 p.
|
artikel
|
| 3 |
A MECP2 mutation in a highly conserved aminoacid causing mental retardation in a male
|
Campos Jr., Mário
|
|
2009
|
31 |
2 |
p. 176-178
3 p.
|
artikel
|
| 4 |
An exploration of symmetry in early autism spectrum disorders: Analysis of lying
|
Esposito, Gianluca
|
|
2009
|
31 |
2 |
p. 131-138
8 p.
|
artikel
|
| 5 |
Announcements and reports
|
|
|
2009
|
31 |
2 |
p. I-IV
nvt p.
|
artikel
|
| 6 |
Callosal lesions and delirious behavior during febrile illness
|
Okumura, Akihisa
|
|
2009
|
31 |
2 |
p. 158-162
5 p.
|
artikel
|
| 7 |
Cardiac troponin I for accurate evaluation of cardiac status in myopathic patients
|
Castro-Gago, Manuel
|
|
2009
|
31 |
2 |
p. 184-
1 p.
|
artikel
|
| 8 |
Complex partial status epilepticus in children with epilepsy
|
Kikumoto, Kenichi
|
|
2009
|
31 |
2 |
p. 148-157
10 p.
|
artikel
|
| 9 |
Convulsing toward the pathophysiology of autism
|
Tuchman, Roberto
|
|
2009
|
31 |
2 |
p. 95-103
9 p.
|
artikel
|
| 10 |
Editorial Board
|
|
|
2009
|
31 |
2 |
p. IFC-
1 p.
|
artikel
|
| 11 |
Event-related potentials of self-face recognition in children with pervasive developmental disorders
|
Gunji, Atsuko
|
|
2009
|
31 |
2 |
p. 139-147
9 p.
|
artikel
|
| 12 |
Increased brain lactate during stroke-like episode in a patient with congenital disorder of glycosylation type Ia
|
Baalen, Andreas van
|
|
2009
|
31 |
2 |
p. 183-
1 p.
|
artikel
|
| 13 |
Novel de novo splice-site mutation of SCN1A in a patient with partial epilepsy with febrile seizures plus
|
Kumakura, Akira
|
|
2009
|
31 |
2 |
p. 179-182
4 p.
|
artikel
|
| 14 |
OBC (Contents)
|
|
|
2009
|
31 |
2 |
p. OBC-
1 p.
|
artikel
|
| 15 |
Recent advances in neurobiology of Tuberous Sclerosis Complex
|
Napolioni, Valerio
|
|
2009
|
31 |
2 |
p. 104-113
10 p.
|
artikel
|
| 16 |
Segawa disease with a novel heterozygous mutation in exon 5 of the GCH-1 gene (E183K)
|
Ikeda, T.
|
|
2009
|
31 |
2 |
p. 173-175
3 p.
|
artikel
|
| 17 |
Sleep spindle alterations in patients with malformations of cortical development
|
Selvitelli, Megan F.
|
|
2009
|
31 |
2 |
p. 163-168
6 p.
|
artikel
|
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