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 |