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                             19 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 Aggravation of atonic seizures by rufinamide: A case report Bektaş, Gonca
2016
38 7 p. 654-657
4 p.
artikel
2 A girl with infantile neuronal ceroid lipofuscinosis caused by novel PPT1 mutation and paternal uniparental isodisomy of chromosome 1 Niida, Yo
2016
38 7 p. 674-677
4 p.
artikel
3 ALDH18A1-related cutis laxa syndrome with cyclic vomiting Nozaki, Fumihito
2016
38 7 p. 678-684
7 p.
artikel
4 Announcements and reports 2016
38 7 p. II-IV
nvt p.
artikel
5 Contents 2016
38 7 p. OBC-
1 p.
artikel
6 Cover 2016
38 7 p. IBC-
1 p.
artikel
7 Editorial Board 2016
38 7 p. IFC-
1 p.
artikel
8 Infantile spinal muscular atrophy with respiratory distress type I presenting without respiratory involvement: Novel mutations and review of the literature Luan, Xinghua
2016
38 7 p. 685-689
5 p.
artikel
9 JSCN ICNC 2016 Travel Award 2016
38 7 p. I-
1 p.
artikel
10 Manifestations and characteristics of congenital adrenal hyperplasia-associated encephalopathy Abe, Yuichi
2016
38 7 p. 638-647
10 p.
artikel
11 Outcome of ketogenic diets in GLUT1 deficiency syndrome in Japan: A nationwide survey Fujii, Tatsuya
2016
38 7 p. 628-637
10 p.
artikel
12 Plasma exchange in pediatric anti-NMDAR encephalitis: A systematic review Suppiej, Agnese
2016
38 7 p. 613-622
10 p.
artikel
13 Post-vaccination MDEM associated with MOG antibody in a subclinical Chlamydia infected boy Azumagawa, Kohji
2016
38 7 p. 690-693
4 p.
artikel
14 Potential risk factors for dexmedetomidine withdrawal seizures in infants after surgery for congenital heart disease Takahashi, Yoshihiro
2016
38 7 p. 648-653
6 p.
artikel
15 17q21.31 microdeletion syndrome: Description of a case further contributing to the delineation of Koolen-de Vries syndrome Bernardo, Pia
2016
38 7 p. 663-668
6 p.
artikel
16 Successful treatment of migrating partial seizures in Wolf–Hirschhorn syndrome with bromide Itakura, Ayako
2016
38 7 p. 658-662
5 p.
artikel
17 Temple syndrome: A patient with maternal hetero-UPD14, mixed iso- and hetero-disomy detected by SNP microarray typing of patient-father duos Shin, Eun-hye
2016
38 7 p. 669-673
5 p.
artikel
18 The lack of antiepileptic drugs and worsening of seizures among physically handicapped patients with epilepsy during the Great East Japan Earthquake Kobayashi, Satoru
2016
38 7 p. 623-627
5 p.
artikel
19 Vessel wall enhancement in the diagnosis and management of primary angiitis of the central nervous system in children Ohno, Koyo
2016
38 7 p. 694-698
5 p.
artikel
                             19 gevonden resultaten
 
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