| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Aggregate formation analysis of GFAPR416W found in one case of Alexander disease
|
Tulyeu, Janyerkye
|
|
2019
|
41 |
2 |
p. 195-200
|
artikel
|
| 2 |
Announcements and reports
|
|
|
2019
|
41 |
2 |
p. I-II
|
artikel
|
| 3 |
A novel DDC gene deletion mutation in two Chinese mainland siblings with aromatic l-amino acid decarboxylase deficiency
|
Dai, Lifang
|
|
2019
|
41 |
2 |
p. 205-209
|
artikel
|
| 4 |
An unusual manifestation of Sjögren syndrome encephalitis
|
Iwai, Kenji
|
|
2019
|
41 |
2 |
p. 217-220
|
artikel
|
| 5 |
ATP13A2-related juvenile-onset Parkinson disease
|
Suleiman, Jehan
|
|
2019
|
41 |
2 |
p. 223
|
artikel
|
| 6 |
Behavioral profiles in Rett syndrome: Data from the natural history study
|
Buchanan, Caroline B.
|
|
2019
|
41 |
2 |
p. 123-134
|
artikel
|
| 7 |
Combining visual sensory functions and visuospatial orienting functions in children with visual pathology: A longitudinal study
|
Kooiker, Marlou J.G.
|
|
2019
|
41 |
2 |
p. 135-149
|
artikel
|
| 8 |
Contents
|
|
|
2019
|
41 |
2 |
p. OBC
|
artikel
|
| 9 |
Cover
|
|
|
2019
|
41 |
2 |
p. IBC
|
artikel
|
| 10 |
Editorial Board
|
|
|
2019
|
41 |
2 |
p. IFC
|
artikel
|
| 11 |
Effects of human umbilical cord blood CD34+ cell transplantation in neonatal hypoxic-ischemia rat model
|
Yu, Yan
|
|
2019
|
41 |
2 |
p. 173-181
|
artikel
|
| 12 |
Factors associated with electroencephalographic and clinical remission of benign childhood epilepsy with centrotemporal spikes
|
Lee, Eun Hye
|
|
2019
|
41 |
2 |
p. 158-162
|
artikel
|
| 13 |
Genetic analysis of undiagnosed ataxia-telangiectasia-like disorders
|
Kashimada, Ayako
|
|
2019
|
41 |
2 |
p. 150-157
|
artikel
|
| 14 |
Mitochondrial dysfunction in ATP13A2 carriers
|
Finsterer, Josef
|
|
2019
|
41 |
2 |
p. 221-222
|
artikel
|
| 15 |
Multi affected pedigree with congenital microcephaly: WES revealed PNKP gene mutation
|
Entezam, Mona
|
|
2019
|
41 |
2 |
p. 182-186
|
artikel
|
| 16 |
Reading disability due to an ocular motor disorder: A case of an adolescent girl with a previous diagnosis of dyslexia
|
Kurokami, Tsunehiko
|
|
2019
|
41 |
2 |
p. 187-190
|
artikel
|
| 17 |
Reply to the Letter, “Leigh syndrome with spinal cord involvement due to a hemizygous NDUFA1 mutation”
|
Osaka, Hitoshi
|
|
2019
|
41 |
2 |
p. 224
|
artikel
|
| 18 |
Severe neurologic and hepatic toxicity in a newborn prenatally exposed to methamphetamine. A case report
|
Maranella, Eugenia
|
|
2019
|
41 |
2 |
p. 191-194
|
artikel
|
| 19 |
The association of epileptic focus estimated by magnetoencephalography with cognitive function in non-lesional epilepsy with continuous spikes and waves during slow wave sleep (ECSWS) children
|
Magara, Shinichi
|
|
2019
|
41 |
2 |
p. 163-172
|
artikel
|
| 20 |
Transient extreme spindles in a young child with anti-NMDAR encephalitis: A case report
|
Tokunaga, Sachi
|
|
2019
|
41 |
2 |
p. 210-213
|
artikel
|
| 21 |
Transient posterior cerebral arteriopathy: An unusual case enterovirus-related
|
Piccolo, Benedetta
|
|
2019
|
41 |
2 |
p. 214-216
|
artikel
|
| 22 |
X-linked Charcot–Marie–Tooth disease type 5 with recurrent weakness after febrile illness
|
Nishikura, Noriko
|
|
2019
|
41 |
2 |
p. 201-204
|
artikel
|
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