4141. Vitamin D3 Supplementation Along With Topiramate in Pediatric Migraine Prophylaxis: Is it Effective?. (February 2023) Authors: Panda, Prateek Kumar; Ramachandran, Aparna; Sharawat, Indar Kumar Journal: Journal of child neurology Issue: Volume 38:Number 1/2(2023) Page Start: 103 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4142. Volpe's Neurology of the newborn. (2017) Authors: Volpe, Joseph J; Inder, Terrie E; Darras, Basil T; Vries, Linda S de; Plessis, Adre J du; Neil, Jeffrey; Perlman, Jeffrey M Record Type: Book Extent: 1 online resource, illustrations View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4143. Walker-Warburg syndrome and tectocerebellar dysraphia: A novel association caused by a homozygous DAG1 mutation. (May 2018) Authors: Leibovitz, Zvi; Mandel, Hanna; Falik-Zaccai, Tzipora C.; Ben Harouch, Shani; Savitzki, David; Krajden-Haratz, Karina; Gindes, Liat; Tamarkin, Mordechai; Lev, Dorit; Dobyns, William B.; Lerman-Sagie, Tally Journal: European journal of paediatric neurology Issue: Volume 22:Number 3(2018:May) Page Start: 525 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4144. WDR81 mutations cause microlissencephaly and microcephaly and impair mitotic progression in neural progenitors. (June 2017) Authors: Cavallin, M.; Rujano, Maria A.; Bednarek, N.; Medina-Cano, D.; Bernabe Gelot, A.; Drunat, S.; Maillard, C.; Nitschké, P.; Beneteau, C.; Poirier, K.; Rio, M.; Boddaert, N.; Passemard, S.; Baffet, A.; Thomas, S.; Bahi-Buisson, N. Journal: European journal of paediatric neurology Issue: Volume 21(2017)Supplement 1 Page Start: e84 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4145. Weakness and Fatigue in Diverse Neuromuscular Diseases. (October 2013) Authors: Montes, Jacqueline; Blumenschine, Michelle; Dunaway, Sally; Alter, Aliza S.; Engelstad, Kristin; Rao, Ashwini K.; Chiriboga, Claudia A.; Sproule, Douglas M.; Vivo, Darryl C. De Journal: Journal of child neurology Issue: Volume 28:Number 10(2013) Page Start: 1277 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4146. Wechsler Intelligence Scale for Children-V: Test Review. Issue 2 (2nd April 2016) Authors: Na, Sabrina D.; Burns, Thomas G. Journal: Applied neuropsychology Issue: Volume 5:Issue 2(2016) Page Start: 156 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4147. Wechsler profiles in referred children with intellectual giftedness: Associations with trait-anxiety, emotional dysregulation, and heterogeneity of Piaget-like reasoning processes. (July 2015) Authors: Guénolé, Fabian; Speranza, Mario; Louis, Jacqueline; Fourneret, Pierre; Revol, Olivier; Baleyte, Jean-Marc Journal: European journal of paediatric neurology Issue: Volume 19:Number 4(2015:Jul.) Page Start: 402 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4148. Wernicke Encephalopathy in Pediatric Neuro-oncology: Presentation of 2 Cases and Review of Literature. (December 2014) Authors: Cefalo, Maria Giuseppina; De Ioris, Maria Antonietta; Cacchione, Antonella; Longo, Daniela; Staccioli, Susanna; Arcioni, Francesco; Bernardi, Bruno; Mastronuzzi, Angela Journal: Journal of child neurology Issue: Volume 29:Number 12(2014:Dec.) Page Start: NP181 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4149. WES in nonprogressive congenital ataxia: Diagnostic yield and identification of novel loci. (June 2017) Authors: Macaya, A.; Drechsel, O.; Álvarez-Molinero, M.; Marcé-Grau, A.; Ferrer-Aparicio, S.; Gómez-Andrés, D.; Flotats-Bastardas, M.; Pons, M.R.; Raspall-Chaure, M.; Bezdan, D.; Bossio, M.; Munell, F.; Ossowski, S. Journal: European journal of paediatric neurology Issue: Volume 21(2017)Supplement 1 Page Start: e219 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4150. West syndrome due to compound heterozygous QARS mutations. (June 2017) Authors: Poulat, A.L.; Lesca, G.; Chatron, N.; Labalme, A.; Des Portes, V.; Sanlaville, D.; De Bellescize, J.; Ville, D. Journal: European journal of paediatric neurology Issue: Volume 21(2017)Supplement 1 Page Start: e99 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗