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                             19 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 A case of Ohtahara syndrome with mitochondrial respiratory chain complex I deficiency Seo, Joo Hee
2010
32 3 p. 253-257
5 p.
artikel
2 Acknowledgement to Reviewers in 2009 2010
32 3 p. VI-VII
nvt p.
artikel
3 A de novo 11p12-p15.4 duplication in a patient with pharmacoresistant epilepsy, mental retardation, and dysmorphisms Coppola, Antonietta
2010
32 3 p. 248-252
5 p.
artikel
4 Announcements and reports 2010
32 3 p. I-V
nvt p.
artikel
5 A special report of the 10th AOCCN Kim, Dong Wook
2010
32 3 p. 263-264
2 p.
artikel
6 Association between Tourette syndrome and comorbidities in Japan Kano, Yukiko
2010
32 3 p. 201-207
7 p.
artikel
7 Bilateral pallidal stimulation in children and adolescents with primary generalized dystonia – Report of six patients and literature-based analysis of predictive outcomes variables Borggraefe, Ingo
2010
32 3 p. 223-228
6 p.
artikel
8 Comprehensive genetic analyses of PLP1 in patients with Pelizaeus–Merzbacher disease applied by array-CGH and fiber-FISH analyses identified new mutations and variable sizes of duplications Shimojima, Keiko
2010
32 3 p. 171-179
9 p.
artikel
9 Contents 2010
32 3 p. IBC-
1 p.
artikel
10 Delayed gyration with pontocerebellar hypoplasia type 1 Okanishi, Tohru
2010
32 3 p. 258-262
5 p.
artikel
11 Editorial Board 2010
32 3 p. IFC-
1 p.
artikel
12 Effect of iron deficiency anemia on visual evoked potential of growing children Monga, Madhulika
2010
32 3 p. 213-216
4 p.
artikel
13 Effects of antiepileptic drugs on mRNA levels of BDNF and NT-3 and cell neogenesis in the developing rat brain Shi, Xiu-Yu
2010
32 3 p. 229-235
7 p.
artikel
14 Efficacy and tolerability of adjunctive therapy with zonisamide in childhood intractable epilepsy Lee, Yun Jin
2010
32 3 p. 208-212
5 p.
artikel
15 Ischemia induced neural stem cell proliferation and differentiation in neonatal rat involved vascular endothelial growth factor and transforming growth factor-beta pathways Sun, Jinqiao
2010
32 3 p. 191-200
10 p.
artikel
16 Sonic hedgehog (SHH) mutation in patients within the spectrum of holoprosencephaly Bertolacini, Claudia Danielli Pereira
2010
32 3 p. 217-222
6 p.
artikel
17 Two novel gap junction protein alpha 12 gene mutations in two Chinese patients with Pelizaeus–Merzbacher-like disease Wang, Jingmin
2010
32 3 p. 236-243
8 p.
artikel
18 Unilaterally and rapidly progressing white matter lesion and elevated cytokines in a patient with Tay–Sachs disease Hayase, Tomomi
2010
32 3 p. 244-247
4 p.
artikel
19 X-linked adrenoleukodystrophy: Clinical course and minimal incidence in South Brazil Jardim, Laura Bannach
2010
32 3 p. 180-190
11 p.
artikel
                             19 gevonden resultaten
 
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