about
Emergence of the primary pediatric stroke center: impact of the thrombolysis in pediatric stroke trial.Compound heterozygous mutations in glycyl-tRNA synthetase are a proposed cause of systemic mitochondrial disease.Subdural haemorrhage and severe coagulopathy resulting in transtentorial uncal herniation in a neonate undergoing therapeutic hypothermia.Autoimmune neuromuscular disorders in childhoodLumbar puncture simulation in pediatric residency training: improving procedural competence and decreasing anxiety.Childhood chronic inflammatory demyelinating polyradiculoneuropathy: combined analysis of a large cohort and eleven published series.Medical students' perception of lesbian, gay, bisexual, and transgender (LGBT) discrimination in their learning environment and their self-reported comfort level for caring for LGBT patients: a survey study.Hereditary neuropathy with liability to pressure palsies in childhood: Case series and literature update.Association Between Chronic Aspiration and Chronic Airway Infection with Pseudomonas aeruginosa and Other Gram-Negative Bacteria in Children with Cerebral Palsy.Autosomal recessive axonal polyneuropathy in a sibling pair due to a novel homozygous mutation in IGHMBP2.Congenital Trismus From Brainstem Dysgenesis: Case Report and Review of Literature.The time to and determinants of first fractures in boys with Duchenne muscular dystrophy.Histomorphometry and Bone Matrix Mineralization Before and After Bisphosphonate Treatment in Boys With Duchenne Muscular Dystrophy: A Paired Transiliac Biopsy Study.Novel MPZ mutations and congenital hypomyelinating neuropathyCongenital Visual Impairment and Progressive Microcephaly Due to Lysyl-Transfer Ribonucleic Acid (RNA) Synthetase (KARS) Mutations: The Expanding Phenotype of Aminoacyl-Transfer RNA Synthetase Mutations in Human Disease.Specific combination of compound heterozygous mutations in 17β-hydroxysteroid dehydrogenase type 4 (HSD17B4) defines a new subtype of D-bifunctional protein deficiency.Adolescent onset cognitive regression and neuropsychiatric symptoms associated with the A140V MECP2 mutation.Pediatric monomelic amyotrophy: evidence for poliomyelitis in vulnerable populations.Evidence for clinical, genetic and biochemical variability in spinal muscular atrophy with progressive myoclonic epilepsy.Developing standardized corticosteroid treatment for Duchenne muscular dystrophy.Brainstem compression: a predictor of postoperative cerebellar mutism.Serum transaminase levels in boys with Duchenne and Becker muscular dystrophy.Pediatric sciatic neuropathy associated with neoplasms.Debunking Occam's razor: Diagnosing multiple genetic diseases in families by whole-exome sequencing.Congenital Nemaline Myopathy: The Value of Magnetic Resonance Imaging of Muscle.Myostatin inhibitor ACE-031 treatment of ambulatory boys with Duchenne muscular dystrophy: Results of a randomized, placebo-controlled clinical trial.Homozygous contiguous gene deletion of 13q12 causing LGMD2C and ARSACS in the same patient.Diagnosis and outcome of childhood perineurioma.Disability, Quality of Life, and Pain Coping in Pediatric Migraine: An Observational StudyCanadian Paediatric Neurology Workforce Survey and Consensus StatementCase 2: Gross Motor Regression in an 18-month-old GirlMononeuritis multiplex associated with minocycline in an adolescentCongenital muscular dystrophies: New evidence-based guidelines for the diagnosis and management of this evolving group of muscle disordersAcute asymmetrical spinal infarct secondary to fibrocartilaginous embolismChiari 1 malformation and holocord syringomyelia presenting as abrupt onset foot dropAchalasia, chronic sensory neuropathy, and N-type calcium channel autoantibodies: beneficial response to IVIGBrachial Plexopathy and Nonaccidental Injury: Role of the NeurologistCranial nerve hypertrophy in pediatric chronic inflammatory demyelinating polyradiculoneuropathyElectrophysiologic Evidence for Anterior Horn Cell Disease in AmyoplasiaWATERSHED INFARCTION DUE TO ACUTE HYPEREOSINOPHILIA
P50
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P50
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Hugh J. McMillan
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P106
P1153
6603383437
P21
P31
P496
0000-0001-8927-2018