| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Acute flaccid myelitis caused by enterovirus D68: Case definitions for use in clinical practice
|
Kramer, Rolf
|
|
2019
|
23 |
2 |
p. 235-239
|
artikel
|
| 2 |
A population-based and case-controlled study of children and adolescents with narcolepsy: Health-related quality of life, adaptive behavior and parental stress
|
Szakács, Attila
|
|
2019
|
23 |
2 |
p. 288-295
|
artikel
|
| 3 |
Attention measures of patients with Rett Syndrome need to overcome the challenges in evaluating the oculomotor function using electronystagmography
|
Fabio, Rosa Angela
|
|
2019
|
23 |
2 |
p. 232
|
artikel
|
| 4 |
Challenges in evaluating the oculomotor function in individuals with Rett syndrome using electronystagmography
|
de Breet, Laurèl H.M.
|
|
2019
|
23 |
2 |
p. 262-269
|
artikel
|
| 5 |
Characteristic clinical and ultrastructural findings in nesprinopathies
|
Kölbel, Heike
|
|
2019
|
23 |
2 |
p. 254-261
|
artikel
|
| 6 |
Clinical deterioration despite syringomyelia resolution after successful foramen magnum decompression for Chiari malformation - Case series
|
Shetty, J.
|
|
2019
|
23 |
2 |
p. 333-337
|
artikel
|
| 7 |
Cognitive-behavioural treatment of functional neurological symptoms (conversion disorder) in children and adolescents: A case series
|
McFarlane, Fiona A.
|
|
2019
|
23 |
2 |
p. 317-328
|
artikel
|
| 8 |
Editorial Board
|
|
|
2019
|
23 |
2 |
p. i
|
artikel
|
| 9 |
Epilepsy in children with type 1 diabetes mellitus: Pathophysiological basis and clinical hallmarks
|
Mastrangelo, Mario
|
|
2019
|
23 |
2 |
p. 240-247
|
artikel
|
| 10 |
Functional outcome after traumatic cervical spinal cord injury: Can adolescents be truly compared to adults?
|
Wirtz, Mirja M.
|
|
2019
|
23 |
2 |
p. 229-230
|
artikel
|
| 11 |
Functional outcome after traumatic cervical spinal cord injury is superior in adolescents compared to adults
|
Geuther, Martina
|
|
2019
|
23 |
2 |
p. 248-253
|
artikel
|
| 12 |
GLUT1 deficiency and pediatric-onset hereditary spastic paraplegia: A new association
|
Verrotti, Alberto
|
|
2019
|
23 |
2 |
p. 233-234
|
artikel
|
| 13 |
Motor function in survivors of pediatric acute lymphoblastic leukemia treated with chemotherapy-only
|
Goebel, Anna-Maria
|
|
2019
|
23 |
2 |
p. 304-316
|
artikel
|
| 14 |
Nesprinopathy: A multi-faceted genetic disorder
|
Bektaş, Hatice
|
|
2019
|
23 |
2 |
p. 231
|
artikel
|
| 15 |
Predictive factors and prognostic value for status epilepticus in newborns
|
Gokce-Samar, Zeynep
|
|
2019
|
23 |
2 |
p. 270-279
|
artikel
|
| 16 |
Punctate white-matter lesions in the full-term newborn: Underlying aetiology and outcome
|
Hayman, Michael
|
|
2019
|
23 |
2 |
p. 280-287
|
artikel
|
| 17 |
Re-emergence of SSPE: Consequence of the decline of adherence to vaccination programmes?
|
Masnada, Silvia
|
|
2019
|
23 |
2 |
p. 338-340
|
artikel
|
| 18 |
Risk of Developmental Coordination Disorder in Italian very preterm children at school age compared to general population controls
|
Caravale, Barbara
|
|
2019
|
23 |
2 |
p. 296-303
|
artikel
|
| 19 |
SLC2A1 mutations are a rare cause of pediatric-onset hereditary spastic paraplegia
|
Nicita, Francesco
|
|
2019
|
23 |
2 |
p. 329-332
|
artikel
|
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