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European Journal of Paediatric Neurology
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Volume 23, Issue 3
Pages 341-540 (May 2019)
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1. Commentary on gait deviations in patients with Dravet syndrome: A systematic review
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Tác giả
Jill Rodda.
Nội dung
Page 341
2. Neurological complications in nephrotic syndrome – Could they be prevented?
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Tác giả
Zvonka Rener-Primec.
Nội dung
Pages 342-343
3. Dravet syndrome – Time to consider the burden beyond the disease
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Tác giả
Andreas Brunklaus.
Nội dung
Page 344
4. The expanding spectrum of ATP1A3 related disease
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Tác giả
Cecilia Fernandes, Mohamad A. Mikati.
Nội dung
Pages 345-346
5. Quality of life of patients with spinal muscular atrophy: A systematic review
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Tác giả
Erik Landfeldt, Josefin Edström, Thomas Sejersen, Már Tulinius, Janbernd Kirschner.
Nội dung
Pages 347-356
6. Gait deviations in patients with dravet syndrome: A systematic review Pages 357-367
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Tác giả
Lore Wyers, Patricia Van de Walle, Aurélie Hoornweg, Ionela Tepes Bobescu, Ann Hallemans.
7. Perinatal stroke syndromes: Similarities and diversities in aetiology, outcome and management
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Tác giả
Joel Fluss, Mickaël Dinomais, Stéphane Chabrier.
Nội dung
Pages 368-383
8. Neurological complications in childhood nephrotic syndrome: A systematic review
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Tác giả
Stella Stabouli, Katerina Chrysaidou, Juan C. Kupferman, Dimitrios I. Zafeiriou.
Nội dung
Pages 384-391
9. Burden-of-illness and cost-driving factors in Dravet syndrome patients and carers: A prospective, multicenter study from Germany
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Tác giả
Adam Strzelczyk, Malin Kalski, Thomas Bast, Adelheid Wiemer-Kruel, Susanne Schubert-Bast.
Nội dung
Pages 392-403
10. Failure of ketogenic diet therapy in GLUT1 deficiency syndrome
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Tác giả
Yvonne A.C. Bekker, Danielle A. Lambrechts, Judith S. Verhoeven, Jessy van Boxtel, Hilde M.H. Braakman.
Nội dung
Pages 404-409
11. Cortical malformations and COL4A1 mutation: Three new cases
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Tác giả
G. Vitale, A. Pichiecchio, F. Ormitti, D. Tonduti, O. Zuffardi.
Nội dung
Pages 410-417
12. Novel WWOX deleterious variants cause early infantile epileptic encephalopathy, severe developmental delay and dysmorphism among
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Tác giả
Yemenite Jews M. Weisz-Hubshman, H. Meirson, R. Michaelson-Cohen, R. Beeri, G. Heimer.
Nội dung
Pages 418-426
13. The genetic etiology in cerebral palsy mimics: The results from a Greek tertiary care center
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Tác giả
Vasiliki Zouvelou, Delia Yubero, Loukia Apostolakopoulou, Eleftheria Kokkinou, Roser Pons.
Nội dung
Pages 427-437
14. Clinical and genetic spectrum of SCN2A-associated episodic ataxia
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Tác giả
N. Schwarz, T. Bast, E. Gaily, G. Golla, W. Fazeli.
Nội dung
Pages 438-447
15. Relapsing encephalopathy with cerebellar ataxia are caused by variants involving p.Arg756 in ATP1A3
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Tác giả
Pascal Sabouraud, Audrey Riquet, Marie-Aude Spitz, Kumaran Deiva, Vincent Laugel.
Nội dung
Pages 448-455
16. Evolution of pediatric epilepsy surgery program over 2000–2017: Improvement of care?
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Tác giả
Anezka Belohlavkova, Petr Jezdik, Alena Jahodova, Martin Kudr, Pavel Krsek.
Nội dung
Pages 456-465
17. Spectrum of the neurologic manifestations in childhood-onset cryopyrin-associated periodic syndrome
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Tác giả
Huseyin Kilic, Sezgin Sahin, Cisem Duman, Amra Adrovic, Sema Saltik
Nội dung
Pages 466-472
18. Gross motor function outcomes following deep brain stimulation for childhood-onset dystonia: A descriptive report
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Tác giả
Kylee Tustin, Markus C. Elze, Daniel E. Lumsden, Hortensia Gimeno, Jean-Pierre Lin.
Nội dung
Pages 473-483
19. Maternal chorioamnionitis & long term neurological morbidity in the offspring
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Tác giả
Amir Freud, Tamar Wainstock, Eyal Sheiner, Ron Beloosesky, Asnat Walfisch.
Nội dung
Pages 484-490
20. Language development in children with congenital heart disease aged 12–24 months
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Tác giả
Solène Fourdain, Ariane St-Denis, Julien Harvey, Ala Birca, Natacha Trudeau.
Nội dung
Pages 491-499
21. Incidence and mortality of moderate and severe traumatic brain injury in children: A ten year population-based cohort study in Norway
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Tác giả
Mari Olsen, Anne Vik, Tom Ivar Lund Nilsen, Oddvar Uleberg, Toril Skandsen.
Nội dung
Pages 500-506
22. Cerebral palsy among children of immigrants in Denmark and the role of socioeconomic status
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Tác giả
Tanja Gram Petersen, Ingeborg Forthun, Theis Lange, Sarah Fredsted Villadsen, Katrine Strandberg-Larsen.
Nội dung
Pages 507-516
23. Modalities of reading acquisition in three siblings with infantile-onset saccade initiation delay (Cogan congenital ocular motor apraxia): A longitudinal study
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Tác giả
Marjolaine Cohen, Pascal Zesiger, Laura Merlini, Raoul de Haller, Joel Fluss.
Nội dung
Pages 517-524
24. Is diffuse axonal injury on susceptibility weighted imaging a biomarker for executive functioning in adolescents with traumatic brain injury?
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Tác giả
Catharine Vander Linden, Helena Verhelst, Eva Genbrugge, Ellen Deschepper, Karel Deblaere.
Nội dung
Pages 525-536
25. Expanding phenotype of mitochondrial depletion syndrome in association with TWNK mutations
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Tác giả
Biayna Sukhudyan, Ani Gevorgyan, Ashot Sarkissian, Eugen Boltshauser.
Nội dung
Pages 537-540
