| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
ACTH has beneficial effects on stuttering in ADHD and ASD patients with ESES: A retrospective study
|
Altunel, Attila
|
|
2017
|
39 |
2 |
p. 130-137
8 p.
|
artikel
|
| 2 |
Announcements and reports
|
|
|
2017
|
39 |
2 |
p. I-IV
nvt p.
|
artikel
|
| 3 |
A novel homozygous HOXB1 mutation in a Turkish family with hereditary congenital facial paresis
|
Sahin, Yavuz
|
|
2017
|
39 |
2 |
p. 166-170
5 p.
|
artikel
|
| 4 |
Behavioral outcomes of school-aged full-term small-for-gestational-age infants: A nationwide Japanese population-based study
|
Takeuchi, Akihito
|
|
2017
|
39 |
2 |
p. 101-106
6 p.
|
artikel
|
| 5 |
Contents
|
|
|
2017
|
39 |
2 |
p. OBC-
1 p.
|
artikel
|
| 6 |
Cover
|
|
|
2017
|
39 |
2 |
p. IBC-
1 p.
|
artikel
|
| 7 |
Determination of restless legs syndrome prevalence in children aged 13–16years in the provincial center of Kayseri
|
Per, Huseyin
|
|
2017
|
39 |
2 |
p. 154-160
7 p.
|
artikel
|
| 8 |
Disparities in visuo-spatial constructive abilities in Williams syndrome patients with typical deletion on chromosome 7q11.23
|
Muramatsu, Yukako
|
|
2017
|
39 |
2 |
p. 145-153
9 p.
|
artikel
|
| 9 |
Early cardiac involvement in an infantile Sandhoff disease case with novel mutations
|
Lee, Hsiu-Fen
|
|
2017
|
39 |
2 |
p. 171-176
6 p.
|
artikel
|
| 10 |
Editorial Board
|
|
|
2017
|
39 |
2 |
p. IFC-
1 p.
|
artikel
|
| 11 |
Hypersomnolence-hyperkinetic movement disorder in a child with compound heterozygous mutation in 4-aminobutyrate aminotransferase (ABAT) gene
|
Nagappa, Madhu
|
|
2017
|
39 |
2 |
p. 161-165
5 p.
|
artikel
|
| 12 |
Infantile neuroaxonal dystrophy and PLA2G6-associated neurodegeneration: An update for the diagnosis
|
Iodice, Alessandro
|
|
2017
|
39 |
2 |
p. 93-100
8 p.
|
artikel
|
| 13 |
Mandibulofacial dysostosis with microcephaly: A case presenting with seizures
|
Matsuo, Mari
|
|
2017
|
39 |
2 |
p. 177-181
5 p.
|
artikel
|
| 14 |
Muscle development in healthy children evaluated by bioelectrical impedance analysis
|
Uchiyama, Tomoka
|
|
2017
|
39 |
2 |
p. 122-129
8 p.
|
artikel
|
| 15 |
Neurodevelopmental outcome of term infants with perinatal asphyxia with hypoxic ischemic encephalopathy stage II
|
Adhikari, Sudhir
|
|
2017
|
39 |
2 |
p. 107-111
5 p.
|
artikel
|
| 16 |
Predicting the reading skill of Japanese children
|
Ogino, Tatsuya
|
|
2017
|
39 |
2 |
p. 112-121
10 p.
|
artikel
|
| 17 |
Reply to: Uniparental disomy of chromosome 1 unmasks recessive mutations of PPT1 in a boy with neuronal ceroid lipofuscinosis type 1
|
Niida, Yo
|
|
2017
|
39 |
2 |
p. 184-185
2 p.
|
artikel
|
| 18 |
Spectral characteristics of intracranial electroencephalographic activity in patients with Lennox–Gastaut syndrome
|
Lee, Dongpyo
|
|
2017
|
39 |
2 |
p. 138-144
7 p.
|
artikel
|
| 19 |
Uniparental disomy of chromosome 1 unmasks recessive mutations of PPT1 in a boy with neuronal ceroid lipofuscinosis type 1
|
Travaglini, Lorena
|
|
2017
|
39 |
2 |
p. 182-183
2 p.
|
artikel
|
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