| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A case of severe Alexander disease with de novo c. 239 T > C, p.(F80S), in GFAP
|
Matsumoto, Ayumi
|
|
|
40 |
7 |
p. 587-591
|
artikel
|
| 2 |
Agraphia with reversible splenial corpus callosum lesion caused by hypoglycemia
|
Miyakawa, Yukari
|
|
|
40 |
7 |
p. 592-595
|
artikel
|
| 3 |
Announcements and reports
|
|
|
|
40 |
7 |
p. I-II
|
artikel
|
| 4 |
A novel germline PIGA mutation causes early-onset epileptic encephalopathies in Chinese monozygotic twins
|
Xie, Ling-ling
|
|
|
40 |
7 |
p. 596-600
|
artikel
|
| 5 |
Challenges and research progress of the use of mesenchymal stem cells in the treatment of ischemic stroke
|
Jiang, Jipeng
|
|
|
40 |
7 |
p. 612-626
|
artikel
|
| 6 |
Contents
|
|
|
|
40 |
7 |
p. OBC
|
artikel
|
| 7 |
Cover
|
|
|
|
40 |
7 |
p. IBC
|
artikel
|
| 8 |
Early risk factors for mortality in children with seizure and/or impaired consciousness accompanied by fever without known etiology
|
Tomioka, Kazumi
|
|
|
40 |
7 |
p. 552-557
|
artikel
|
| 9 |
Editorial Board
|
|
|
|
40 |
7 |
p. IFC
|
artikel
|
| 10 |
Efficacy of CBD-enriched medical cannabis for treatment of refractory epilepsy in children and adolescents – An observational, longitudinal study
|
Hausman-Kedem, Moran
|
|
|
40 |
7 |
p. 544-551
|
artikel
|
| 11 |
Fazio-Londe syndrome in siblings from India with different phenotypes
|
Gowda, Vykuntaraju K.
|
|
|
40 |
7 |
p. 582-586
|
artikel
|
| 12 |
Four years follow up of ACY1 deficient patient and pedigree study
|
Alessandrì, Maria Grazia
|
|
|
40 |
7 |
p. 570-575
|
artikel
|
| 13 |
Further characterization of CAPOS/CAOS syndrome with the Glu818Lys mutation in the ATP1A3 gene: A case report
|
Hayashida, Takuya
|
|
|
40 |
7 |
p. 576-581
|
artikel
|
| 14 |
Identification of sleep hypoventilation in young individuals with Becker muscular dystrophy: A pilot study
|
Nakamura, Yuko
|
|
|
40 |
7 |
p. 537-543
|
artikel
|
| 15 |
Long-term home non-invasive positive pressure ventilation in children: Results from a single center in Japan
|
Ikeda, Azusa
|
|
|
40 |
7 |
p. 558-565
|
artikel
|
| 16 |
Mutational spectrum of PTS gene and in silico pathological assessment of a novel variant in Mexico
|
Fernández-Lainez, Cynthia
|
|
|
40 |
7 |
p. 530-536
|
artikel
|
| 17 |
Periventricular small cystic lesions in a patient with Coffin-Lowry syndrome who exhibited a novel mutation in the RPS6KA3 gene
|
Miyata, Yohane
|
|
|
40 |
7 |
p. 566-569
|
artikel
|
| 18 |
Rituximab was effective for acute disseminated encephalomyelitis followed by recurrent optic neuritis with anti-myelin oligodendrocyte glycoprotein antibodies
|
Nagashima, Masako
|
|
|
40 |
7 |
p. 607-611
|
artikel
|
| 19 |
Successful hemispherotomy in two refractory epilepsy patients with cerebral hemiatrophy and contralateral EEG abnormalities
|
Takayama, Rumiko
|
|
|
40 |
7 |
p. 601-606
|
artikel
|
| 20 |
The course of awake breathing disturbances across the lifespan in Rett syndrome
|
Tarquinio, Daniel C.
|
|
|
40 |
7 |
p. 515-529
|
artikel
|
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