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                             20 gevonden resultaten
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
                             20 gevonden resultaten
 
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