| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A case of subacute combined degeneration of the spinal cord due to folic acid and copper deficiency
|
Nakamura, Takuji
|
|
2019
|
41 |
1 |
p. 111-115
|
artikel
|
| 2 |
Announcements and reports
|
|
|
2019
|
41 |
1 |
p. I-II
|
artikel
|
| 3 |
A novel homozygous mutation of CLCN2 in a patient with characteristic brain MRI images – A first case of CLCN2-related leukoencephalopathy in Japan
|
Hoshi, Miyuki
|
|
2019
|
41 |
1 |
p. 101-105
|
artikel
|
| 4 |
Atypical PEX16 peroxisome biogenesis disorder with mild biochemical disruptions and long survival
|
Zaabi, Nuha Al
|
|
2019
|
41 |
1 |
p. 57-65
|
artikel
|
| 5 |
Avoid valproate in patients with IARS2 mutations
|
Finsterer, Josef
|
|
2019
|
41 |
1 |
p. 121
|
artikel
|
| 6 |
Characteristics of Japanese patients with X-linked adrenoleukodystrophy and concerns of their families from the 1st registry system
|
Sakurai, Ken
|
|
2019
|
41 |
1 |
p. 50-56
|
artikel
|
| 7 |
Clasmatodendrosis is associated with dendritic spines and does not represent autophagic astrocyte death in influenza-associated encephalopathy
|
Tachibana, Masaya
|
|
2019
|
41 |
1 |
p. 85-95
|
artikel
|
| 8 |
Contents
|
|
|
2019
|
41 |
1 |
p. OBC
|
artikel
|
| 9 |
Cover
|
|
|
2019
|
41 |
1 |
p. IBC
|
artikel
|
| 10 |
Cyclic alternating pattern in infants with congenital hypothyroidism
|
Santana-Miranda, Rafael
|
|
2019
|
41 |
1 |
p. 66-71
|
artikel
|
| 11 |
Dense array EEG estimated the epileptic focus in a patient with epilepsy secondary to tuberous sclerosis complex
|
Amano, Yuki
|
|
2019
|
41 |
1 |
p. 116-120
|
artikel
|
| 12 |
Editorial Board
|
|
|
2019
|
41 |
1 |
p. IFC
|
artikel
|
| 13 |
Elimination of amyloid precursor protein in senile plaques in the brain of a patient with Alzheimer-type dementia and Down syndrome
|
Arai, Yasuhiro
|
|
2019
|
41 |
1 |
p. 106-110
|
artikel
|
| 14 |
Everolimus for epilepsy and autism spectrum disorder in tuberous sclerosis complex: EXIST-3 substudy in Japan
|
Mizuguchi, Masashi
|
|
2019
|
41 |
1 |
p. 1-10
|
artikel
|
| 15 |
Identification of a novel PAFAH1B1 missense mutation as a cause of mild lissencephaly with basal ganglia calcification
|
Shi, Chang-he
|
|
2019
|
41 |
1 |
p. 29-35
|
artikel
|
| 16 |
Incidence of infantile spinal muscular atrophy on Shikoku Island of Japan
|
Okamoto, Kentaro
|
|
2019
|
41 |
1 |
p. 36-42
|
artikel
|
| 17 |
Maternal risk factors associated with neural tube defects in Tigray regional state of Ethiopia
|
Berihu, Birhane Alem
|
|
2019
|
41 |
1 |
p. 11-18
|
artikel
|
| 18 |
Neonatal seizures and white matter injury: Role of rotavirus infection and probiotics
|
Yeom, Jung Sook
|
|
2019
|
41 |
1 |
p. 19-28
|
artikel
|
| 19 |
Renal dysfunction is rare in Fukuyama congenital muscular dystrophy
|
Ishigaki, Keiko
|
|
2019
|
41 |
1 |
p. 43-49
|
artikel
|
| 20 |
Reply to: Avoid valproate in patients with IARS2 mutations
|
Takezawa, Yusuke
|
|
2019
|
41 |
1 |
p. 122
|
artikel
|
| 21 |
Risk factors and motor outcome of paediatric stroke patients
|
Karalok, Zeynep Selen
|
|
2019
|
41 |
1 |
p. 96-100
|
artikel
|
| 22 |
Risk factors of cognitive impairment in pediatric epilepsy patients with focal cortical dysplasia
|
Kimura, Nobusuke
|
|
2019
|
41 |
1 |
p. 77-84
|
artikel
|
| 23 |
The effects of antihistamines on the semiology of febrile seizures
|
Takasu, Michihiko
|
|
2019
|
41 |
1 |
p. 72-76
|
artikel
|
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