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                             19 results found
no title author magazine year volume issue page(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
article
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
article
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
article
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
article
5 Characteristic clinical and ultrastructural findings in nesprinopathies Kölbel, Heike
2019
23 2 p. 254-261
article
6 Clinical deterioration despite syringomyelia resolution after successful foramen magnum decompression for Chiari malformation - Case series Shetty, J.
2019
23 2 p. 333-337
article
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
article
8 Editorial Board 2019
23 2 p. i
article
9 Epilepsy in children with type 1 diabetes mellitus: Pathophysiological basis and clinical hallmarks Mastrangelo, Mario
2019
23 2 p. 240-247
article
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
article
11 Functional outcome after traumatic cervical spinal cord injury is superior in adolescents compared to adults Geuther, Martina
2019
23 2 p. 248-253
article
12 GLUT1 deficiency and pediatric-onset hereditary spastic paraplegia: A new association Verrotti, Alberto
2019
23 2 p. 233-234
article
13 Motor function in survivors of pediatric acute lymphoblastic leukemia treated with chemotherapy-only Goebel, Anna-Maria
2019
23 2 p. 304-316
article
14 Nesprinopathy: A multi-faceted genetic disorder Bektaş, Hatice
2019
23 2 p. 231
article
15 Predictive factors and prognostic value for status epilepticus in newborns Gokce-Samar, Zeynep
2019
23 2 p. 270-279
article
16 Punctate white-matter lesions in the full-term newborn: Underlying aetiology and outcome Hayman, Michael
2019
23 2 p. 280-287
article
17 Re-emergence of SSPE: Consequence of the decline of adherence to vaccination programmes? Masnada, Silvia
2019
23 2 p. 338-340
article
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
article
19 SLC2A1 mutations are a rare cause of pediatric-onset hereditary spastic paraplegia Nicita, Francesco
2019
23 2 p. 329-332
article
                             19 results found
 
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