High incidence of electrocardiogram abnormalities in young patients with duchenne muscular dystrophyWhite-matter injury is associated with impaired gaze in premature infantsThe neuropharmacology of the ketogenic dietApplying the Lessons of Tuberous Sclerosis: The 2015 Hower Award LectureDelay in Diagnosis of Spinal Muscular Atrophy: A Systematic Literature ReviewAlpers-Huttenlocher syndromePathophysiology and neuroprotection of global and focal perinatal brain injury: lessons from animal modelsEpilepsy in Muenke syndrome: FGFR3-related craniosynostosisBrain Injury in the Preterm Infant: New Horizons for Pathogenesis and PreventionPrevention of epileptogenesis--a new goal for epilepsy therapyGlucose Transporter Type I Deficiency (G1D) at 25 (1990-2015): Presumptions, Facts, and the Lives of Persons With This Rare DiseaseNoonan syndrome, moyamoya-like vascular changes, and antiphospholipid syndromeBiotinidase deficiency: clinical and MRI findings consistent with myelopathyMoyamoya syndrome with spherocytosis: effect of splenectomy on strokesTransient nonketotic hyperglycinemia: two case reports and literature reviewPediatric migraine equivalents: occurrence and clinical features in practiceIdentification of MeCP2 mutations in a series of females with autistic disorderRelationship between clinical and genetic features in "inverted duplicated chromosome 15" patientsMeningitis and shunt infection caused by anaerobic bacteria in childrenDevelopment of GABAergic neurons and their transporter in human temporal cortexThree novel SURF-1 mutations in Japanese patients with Leigh syndromeTrials in sickle cell diseaseRisk factors for pediatric stroke: consequences for therapy and quality of lifeA new mutation of IGHMBP2 gene in spinal muscular atrophy with respiratory distress type 1MRI abnormalities in Behr syndromeNormal serum beta-galactosidase in juvenile GM1 gangliosidosisAnti-brain antibodies in PANDAS versus uncomplicated streptococcal infectionCloxazolam treatment for patients with intractable epilepsyIn memoriam: Manuel Rodriguez Gomez, MD July 4, 1928 - January 21, 2006Central neurogenic hyperventilation in a conscious child associated with glioblastoma multiformeNovel mutations in three patients with LGMD2C with phenotypic differencesNeurofibromatosis: novel and recurrent mutations in Turkish patientsMevalonic aciduria in 3 siblings: a new recognizable metabolic encephalopathyPCR diagnosis of primary herpesvirus type I in poliomyelitis-like paralysis and respiratory tract diseaseClinical efficacy of piracetam in treatment of breath-holding spellsNovel de novo mutation in the KCNJ2 gene in a patient with Andersen-Tawil syndromeHopkins syndrome: T2-weighted high intensity of anterior horn on spinal MR imagingSequence analysis of the PLEXIN-D1 gene in Möbius syndrome patientsBreath-holding spellsSCN2A mutation is associated with infantile spasms and bitemporal glucose hypometabolism
P1433
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P1433
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wetenschappelijk tijdschrift van Elsevier
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wissenschaftliche Fachzeitschrift
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Pediatric Neurology
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Pediatric Neurology
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Pediatric Neurology
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Pediatric Neurology
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Pediatric Neurology
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Pediatric Neurology
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Pediatric Neurology
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Pediatric Neurology
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Pediatric Neurology
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Pediatric Neurology
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Pediatric Neurology
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Pediatric Neurology
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Pediatric Neurology
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Pediatric Neurology
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Pediatric Neurology
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Pediatric Neurology
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Pediatric Neurology
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Pediatric Neurology
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Pediatric Neurology
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Pediatric Neurology
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Pediatric Neurology
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Pediatric Neurology
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Pediatric Neurology
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Pediatric Neurology
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P236
P243
P3181
P3417
Pediatric-Neurology
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P571
1985-01-01T00:00:00Z
P6180
P6366
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