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                             14 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 A new case of concurrent existence of PRRT2-associated paroxysmal movement disorders with c.649dup variant and 16p11.2 microdeletion syndrome Komatsu, Kazuyuki

44 7 p. 474-479
artikel
2 Announcements
44 7 p. iii
artikel
3 Contents
44 7 p. OBC
artikel
4 Copy number assessment of SMN1 based on real-time PCR with high-resolution melting: fast and highly reliable testing Xu, Ying

44 7 p. 462-468
artikel
5 Cover
44 7 p. IBC
artikel
6 De novo POLR2A p.(Ile457Thr) variant associated with early-onset encephalopathy and cerebellar atrophy: expanding the phenotypic spectrum Giacomini, Thea

44 7 p. 480-485
artikel
7 Early maladaptive schemas differing according to sex may contribute to migraine among the youth Güler Aksu, Gülen

44 7 p. 427-437
artikel
8 Early therapeutic plasma exchange may lead to complete neurological recovery in moderate to severe influenza-associated acute necrotizing encephalopathy Okajima, Kie

44 7 p. 492-497
artikel
9 Editorial Board
44 7 p. IFC
artikel
10 Impairment of autonomic emotional response for executive function in children with ADHD: A multi-modal fNIRS and pupillometric study during the Wisconsin Card Sorting Test Kaga, Yoshimi

44 7 p. 438-445
artikel
11 Paroxysmal limb dystonias associated with GABBR2 pathogenic variant: A case-based literature review D'Onofrio, Gianluca

44 7 p. 469-473
artikel
12 Prevalent MLC1 mutation causing autosomal recessive megalencephalic leukoencephalopathy in consanguineous Palestinian families Khalaf-Nazzal, Reham

44 7 p. 454-461
artikel
13 Pseudotumor cerebri syndrome in children: Clinical characteristic and re-classification Masri, Amira

44 7 p. 446-453
artikel
14 Recurrent pneumonia in three patients with MECP2 duplication syndrome with aspiration as the possible cause Sugitate, Ryo

44 7 p. 486-491
artikel
                             14 gevonden resultaten
 
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