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                             20 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 Amelioration of intractable epilepsy by adjunct vagus nerve stimulation therapy in a girl with a CDKL5 mutation Baba, Shimpei
2017
39 4 p. 341-344
4 p.
artikel
2 Anatomical, animal, and cellular evidence for Zika-induced pathogenesis of fetal microcephaly Wang, Jing-Zhang
2017
39 4 p. 294-297
4 p.
artikel
3 Announcements and reports 2017
39 4 p. I-IV
nvt p.
artikel
4 A small pons as a characteristic finding in Down syndrome: A quantitative MRI study Fujii, Yuta
2017
39 4 p. 298-305
8 p.
artikel
5 A ten-year follow-up cohort study of childhood epilepsy: Changes in epilepsy diagnosis with age Hanaoka, Yoshiyuki
2017
39 4 p. 312-320
9 p.
artikel
6 Clinically mild encephalitis/encephalopathy with a reversible splenial lesion of corpus callosum in Chinese children Fang, Qiong
2017
39 4 p. 321-326
6 p.
artikel
7 Contents 2017
39 4 p. OBC-
1 p.
artikel
8 Cover 2017
39 4 p. IBC-
1 p.
artikel
9 Dramatic response after functional hemispherectomy in a patient with epileptic encephalopathy carrying a de novo COL4A1 mutation Hino-Fukuyo, Naomi
2017
39 4 p. 337-340
4 p.
artikel
10 Dropped head congenital muscular dystrophy caused by de novo mutations in LMNA Karaoglu, Pakize
2017
39 4 p. 361-364
4 p.
artikel
11 Early-Onset Epileptic Encephalopathy in infants with different forms of Congenital Disorders of Glycosylation (CDG) Fiumara, Agata
2017
39 4 p. 366-367
2 p.
artikel
12 Editorial Board 2017
39 4 p. IFC-
1 p.
artikel
13 Efficacy of sodium channel blockers in SCN2A early infantile epileptic encephalopathy Dilena, Robertino
2017
39 4 p. 345-348
4 p.
artikel
14 Epilepsia partialis continua in MELAS/Leigh overlap syndrome Finsterer, Josef
2017
39 4 p. 365-
1 p.
artikel
15 Gastric perforation and critical illness polyneuropathy after steroid treatment in a patient with encephalitis/encephalopathy with transient splenial lesion Ikeno, Mitsuru
2017
39 4 p. 356-360
5 p.
artikel
16 Hyperekplexia: Report on phenotype and genotype of 16 Jordanian patients Masri, Amira
2017
39 4 p. 306-311
6 p.
artikel
17 Massive lamotrigine poisoning. A case report Grosso, Salvatore
2017
39 4 p. 349-351
3 p.
artikel
18 Novel mutation in a patient with late onset GLUT1 deficiency syndrome Juozapaite, Sandra
2017
39 4 p. 352-355
4 p.
artikel
19 Postnatal irradiation-induced hippocampal neuropathology, cognitive impairment and aging Tang, Feng Ru
2017
39 4 p. 277-293
17 p.
artikel
20 Short-term efficacy and tolerability of methylphenidate in children with traumatic brain injury and attention problems Ekinci, Ozalp
2017
39 4 p. 327-336
10 p.
artikel
                             20 gevonden resultaten
 
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