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                             37 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 A case of Guillain–Barré syndrome with meningeal irritation Ashikari, Yuka
2016
38 1 p. 163-166
4 p.
artikel
2 ADHD-like behavior in a patient with hypothalamic hamartoma Katayama, Koujyu
2016
38 1 p. 145-148
4 p.
artikel
3 Announcements and reports 2016
38 1 p. I-IV
nvt p.
artikel
4 Childhood Sjögren syndrome presenting as acute brainstem encephalitis Matsui, Yoriko
2016
38 1 p. 158-162
5 p.
artikel
5 Circadian-relevant genes are highly polymorphic in autism spectrum disorder patients Yang, Zhiliang
2016
38 1 p. 91-99
9 p.
artikel
6 Clinical profiles for seizure remission and developmental gains after total corpus callosotomy Iwasaki, Masaki
2016
38 1 p. 47-53
7 p.
artikel
7 Congenital neurogenic muscular atrophy in megaconial myopathy due to a mutation in CHKB gene Castro-Gago, Manuel
2016
38 1 p. 167-172
6 p.
artikel
8 Contents 2016
38 1 p. OBC-
1 p.
artikel
9 Contributions of Japanese patients to development of antisense therapy for DMD Matsuo, Masafumi
2016
38 1 p. 4-9
6 p.
artikel
10 Cover 2016
38 1 p. IBC-
1 p.
artikel
11 Differential diagnosis of ventriculomegaly and brainstem kinking on fetal MRI Amir, Tali
2016
38 1 p. 103-108
6 p.
artikel
12 Distinct but milder phenotypes with choreiform movements in siblings with compound heterozygous mutations in the transcription preinitiation mediator complex subunit 17 (MED17) Hirabayashi, Shinichi
2016
38 1 p. 118-123
6 p.
artikel
13 Dramatic effect of levetiracetam in early-onset epileptic encephalopathy due to STXBP1 mutation Dilena, Robertino
2016
38 1 p. 128-131
4 p.
artikel
14 Dr. Masaya Segawa, Japanese pioneer in child neurology Hoshino, Kyoko
2016
38 1 p. 2-3
2 p.
artikel
15 Editorial Board 2016
38 1 p. IFC-
1 p.
artikel
16 Effects of donepezil and serotonin reuptake inhibitor on acute regression during adolescence in Down syndrome Tamasaki, Akiko
2016
38 1 p. 113-117
5 p.
artikel
17 Efficacy of antiepileptic drugs for the treatment of Dravet syndrome with different genotypes Shi, Xiu-Yu
2016
38 1 p. 40-46
7 p.
artikel
18 Five novel SUCLG1 mutations in three Chinese patients with succinate-CoA ligase deficiency noticed by mild methylmalonic aciduria Liu, Yupeng
2016
38 1 p. 61-67
7 p.
artikel
19 Functional brain maturation of prematurely born, growth discordant monochorionic twins assessed by aEEG Kazanci, Ebru
2016
38 1 p. 100-102
3 p.
artikel
20 Functional outcomes in Rett syndrome Pidcock, Frank S.
2016
38 1 p. 76-81
6 p.
artikel
21 Late-onset epileptic spasms in a patient with 22q13.3 deletion syndrome Ishikawa, Nobutsune
2016
38 1 p. 109-112
4 p.
artikel
22 Multi-frequency localization of aberrant brain activity in autism spectrum disorder Xiang, Jing
2016
38 1 p. 82-90
9 p.
artikel
23 Narcolepsy in a three-year-old girl: A case report Park, Eu Gene
2016
38 1 p. 139-141
3 p.
artikel
24 New year’s greetings Mizuguchi, Masashi
2016
38 1 p. 1-
1 p.
artikel
25 Occurrence of bilaterally independent epileptic spasms after a corpus callosotomy in West syndrome Kobayashi, Katsuhiro
2016
38 1 p. 132-135
4 p.
artikel
26 Pediatric epilepsy following neonatal seizures symptomatic of stroke Suppiej, Agnese
2016
38 1 p. 27-31
5 p.
artikel
27 Phenytoin toxicity in two-month-old Thai infant with CYP2C9 gene polymorphism – A case report Veeravigrom, Montida
2016
38 1 p. 136-138
3 p.
artikel
28 Posterior reversible leukoencephalopathy syndrome with spinal cord involvement in a 9-year-old girl Yiş, Uluç
2016
38 1 p. 154-157
4 p.
artikel
29 Predictive factors for relapse of epileptic spasms after adrenocorticotropic hormone therapy in West syndrome Hayashi, Yumiko
2016
38 1 p. 32-39
8 p.
artikel
30 Pre-movement gating of somatosensory evoked potentials in Segawa disease Kimura, Kazue
2016
38 1 p. 68-75
8 p.
artikel
31 Reply to the letter: “The diagnostic value of MRI in pediatric chronic inflammatory demyelinating polyradiculoneuropathy” Abe, Yuichi
2016
38 1 p. 174-
1 p.
artikel
32 Reversible bilateral striatal lesions following Mycoplasma pneumoniae infection associated with elevated levels of interleukins 6 and 8 Yuan, Zhe-Feng
2016
38 1 p. 149-153
5 p.
artikel
33 Spectrum of migraine variants and beyond: The individual syndromes in children Gupta, Surya N.
2016
38 1 p. 10-26
17 p.
artikel
34 Spectrum of mutations in Glutaryl-CoA dehydrogenase gene in glutaric aciduria type I – Study from South India Radha Rama Devi, A.
2016
38 1 p. 54-60
7 p.
artikel
35 The diagnostic value of MRI in pediatric chronic inflammatory demyelinating polyradiculoneuropathy Yang, Li
2016
38 1 p. 173-
1 p.
artikel
36 The expanding phenotypic spectrum of ARFGEF2 gene mutation: Cardiomyopathy and movement disorder Yilmaz, Sanem
2016
38 1 p. 124-127
4 p.
artikel
37 White matter abnormalities in an adult patient with l-2-hydroxyglutaric aciduria Yamamoto, Toshiyuki
2016
38 1 p. 142-144
3 p.
artikel
                             37 gevonden resultaten
 
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