Submissions from 2012
Neurotoxicity of biologically targeted agents in pediatric cancer trials, EM Wells, AA Nageswara Rao, J Scafidi, and RJ Packer
β-Catenin signaling initiates the activation of astrocytes and its dysregulation contributes to the pathogenesis of astrocytomas, Chunzhang Yang, Rajiv R. Iyer, Albert C.H. Yu, Raymund L. Yong, Deric M. Park, Robert J. Weil, Barbara Ikejiri, Roscoe O. Brady, Russell R. Lonser, and Zhengping Zhuang
Genomic profiling reveals Pitx2 controls expression of mature extraocular muscle contraction-related genes, Yuefang Zhou, Bendi Gong, and Henry J. Kaminski
Submissions from 2011
Lovastatin as treatment for neurocognitive deficits in neurofibromatosis type 1: phase I study., MT Acosta, PG Kardel, KS Walsh, and KN Rosenbaum
CSF opening pressure in children with optic nerve head edema, R.A. Avery, D.J. Licht, S.S. Shah, and J.W. Huh
The saccadic and neurological deficits in type 3 Gaucher disease, W Benko, M Ries, EA Wiggs, and RO Brady
Research challenges in central nervous system manifestations of inborn errors of metabolism, PI Dickson, AR Pariser, SC Groft, and RW Ishihara
Novel SCN1A mutation in a proband with malignant migrating partial seizures of infancy, E.R. Freilich, J.M. Jones, W.D. Gaillard, and J.A. Conry
FMRI language dominance and FDG-PET hypometabolism, W.D. Gaillard, M.M. Berl, E.S. Duke, and E. Ritzl
Epilepsy imaging study guideline criteria: commentary on diagnostic testing study guidelines and practice parameters., WD Gaillard and JH. Cross
Epilepsy imaging study guideline criteria: Commentary on diagnostic testing study guidelines and practice parameters, W.D. Gaillard, J.H. Cross, J.S. Duncan, and H. Stefan
Racial disparities in tissue plasminogen activator treatment rate for stroke: a population-based study., AW Hsia, DF Edwards, LB Morgenstern, and JJ Wing
Re: Practice parameters in myasthenia gravis, HJ Kaminski, G Cutter, and RL Ruff
TGIF mutations in human holoprosencephaly: Correlation between genotype and phenotype, AA Keaton, BD Solomon, EF Kauvar, and KB El-Jaick
Headaches and sleep problems among adults in the United States: Findings from the National Comorbidity Survey-Replication Study, T Lateef, S Swanson, L Cui, and K Nelson
Common data elements in epilepsy research: Development and implementation of the NINDS epilepsy CDE project, DW Loring, DH Lowenstein, NM Barbaro, and BE Fureman
Histone deacetylase inhibitors prevent the degradation and restore the activity of glucocerebrosidase in Gaucher disease, J Lu, C Yang, M Chen, and DY Ye
Evidence Report: Genetic and metabolic testing on children with global developmental delay: Report of the quality standards Subcommittee of the American Academy of Neurology and the Practice Committee of the Child Neurology Society, DJ Michelson, MI Shevell, EH Sherr, and JB Moeschler
Herbs in epilepsy: evidence for efficacy, toxicity, and interactions., PL Pearl, IM Drillings, and JA Conry
Assessment of genetics knowledge and skills in medical students: Insight for a clinical neurogenetics curriculum, PL Pearl, JM Pettiford, SE Combs, and A Heffron
Epilepsy in succinic semialdehyde dehydrogenase deficiency, a disorder of GABA metabolism, P.L. Pearl, L. Shukla, W.H. Theodore, and C. Jakobs
Epilepsy in succinic semialdehyde dehydrogenase deficiency, a disorder of GABA metabolism, PL Pearl, L Shukla, WH Theodore, and C Jakobs
New frontiers in neuroimaging applications to inborn errors of metabolism., MJ Prust, AL Gropman, and N Hauser
GFAP mutations, age at onset, and clinical subtypes in Alexander disease., M Prust, J Wang, and H Morizono
Treatment of Refractory Status Epilepticus in Childhood, JM Schreiber and WD Gaillard
Cancer burden in the HIV-infected population in the United States., MS Shiels, RM Pfeiffer, MH Gail, and HI Hall
Failure of a Vagus Nerve Stimulator following a Nearby Lightning Strike, GE Terry, JA Conry, E Taranto, and A Yaun
Recessive mutations in POLR3B, encoding the second largest subunit of Pol III, cause a rare hypomyelinating leukodystrophy, M T+Otreault, K Choquet, S Orcesi, and D Tonduti
Missense mutations in the NF2 gene result in the quantitative loss of merlin protein and minimally affect protein intrinsic function, C Yang, AR Asthagiri, RR Iyer, and J Lu
Submissions from 2010
Cerebellar atrophy in human and murine succinic semialdehyde dehydrogenase deficiency, MT Acosta, J Munasinghe, PL Pearl, and M Gupta
Region-specific radiotherapy and neuropsychological outcomes in adult survivors of childhood CNS malignancies, GT Armstrong, N Jain, W Liu, and TE Merchant
Tremor-ataxia with central hypomyelination (TACH) leukodystrophy maps to chromosome 10q22.3-10q23.31, G Bernard, I Thiffault, M Tetreault, and ML Putorti
Respiratory muscle weakness in peripheral neuropathies, AZ Burakgazi
Treatment of epilepsy in children with developmental disabilities, D Depositario-Cabacar and T Zelleke
Phase I Trial of Lapatinib in Children With Refractory CNS Malignancies: A Pediatric Brain Tumor Consortium Study, M Fouladi, CF Stewart, SM Blaney, and A Onar-Thomas
Utility of functional MRI in pediatric neurology, E. R. Freilich and W. D. Gaillard
The use of Neuroimaging in the Diagnosis of Mitochondrial Disease, SD Friedman, DWW Shaw, G Ishak, and AL Gropman
A phase I and biology study of gefitinib and radiation in children with newly diagnosed brain stem gliomas or supratentorial malignant gliomas, JR Geyer, CF Stewart, M Kocak, and A Broniscer
Late-Occurring Neurologic Sequelae in Adult Survivors of Childhood Acute Lymphoblastic Leukemia: A Report From the Childhood Cancer Survivor Study, RE Goldsby, Q Liu, PC Nathan, and DC Bowers
Brain imaging in urea cycle disorders, A Gropman
Epigenetics, copy number variation, and other molecular mechanisms underlying neurodevelopmental disabilities: New insights and diagnostic approaches, AL Gropman and ML Batshaw
Diffusion tensor imaging detects areas of abnormal white matter microstructure in patients with partial ornithine transcarbamylase deficiency, A.L. Gropman, B. Gertz, K. Shattuck, and I.L. Kahn
Clinical variability and novel neurodevelopmental findings in 49, XXXXY syndrome, AL Gropman, A Rogol, I Fennoy, and T Sadeghin
Lack of Efficacy of Bevacizumab Plus Irinotecan in Children With Recurrent Malignant Glioma and Diffuse Brainstem Glioma: A Pediatric Brain Tumor Consortium Study, S Gururangan, SN Chi, TY Poussaint, and A Onar-Thomas
Carbonic Anhydrase I, II, and VI, Blood Plasma, Erythrocyte and Saliva Zinc and Copper Increase After Repetitive Transcranial Magnetic Stimulation, R. I. Henkin, S. J. Potolicchio, L. M. Levy, and R. Moharram
Carbonic anhydrase I, II, and VI, blood plasma, Erythrocyte and saliva zinc and copper increase after repetitive transcraniel magetic stimulation, R. I. Henkin, S. J. Potolicchio, L. M. Levy, and R. Moharram
New findings in the study of neuromuscular disorders, JJ Kelly
Neuropathology in Succinic Semialdehyde Dehydrogenase Deficiency, I. Kneer, K. M. Gibson, G. Murdoch, and G. S. Salomons
Uveitis and white matter abnormalities in pediatric sarcoidosis, AK Miller, Z Khademian, and PL Pearl
Elevated CSF N-acetylaspartylglutamate in patients with free sialic acid storage diseases, F. Mochel, U. F. H. Engelke, B. Yang, and N. H. McNeill
Headache and Biomarkers Predictive of Vascular Disease in a Representative Sample of US Children, KB Nelson, AK Richardson, J He, and TM Lateef
Diffusion tensor imaging in arginase deficiency reveals damage to corticospinal tracts, M.S. Oldham, J.W. vanMeter, K.F. Shattuck, and S.D. Cederbaum
Radiation therapy for pediatric low-grade gliomas: Survival and sequelae, RJ Packer
Central Nervous System Tumors, R. J. Packer, T. MacDonald, and G. Vezina
Bull's-eye Hemorrhage. A Late Complication of Gamma Knife Radiosurgery, TL Rothstein
Update on the Electrophysiologic Approach to Patients in Anoxic Coma, TL Rothstein
Magnetic resonance imaging pattern recognition in hypomyelinating disorders, ME Steenweg, A Vanderver, S Blaser, and A Bizzi
Ocular Late Effects in Childhood and Adolescent Cancer Survivors: A Report From the Childhood Cancer Survivor Study, KF Whelan, K Stratton, T Kawashima, and JW Waterbor
Linear Clinical Progression, Independent of Age of Onset, in Niemann-Pick Disease, Type C, NM Yanjanin, JI Velez, A Gropman, and K King
Submissions from 2009
Diagnostic criteria for late-onset (childhood and adult) Pompe disease, M. T. Al-Lozi, A. A. Amato, R. J. Barohn, and E. J. Cupler
Long-Term Outcomes Among Adult Survivors of Childhood Central Nervous System Malignancies in the Childhood Cancer Survivor Study, G. T. Armstrong, Q. Liu, Y. Yasui, and S. J. Huang
Development of a Pediatric Neurocritical Care Service, M. J. Bell, J. Carpenter, A. K. Au, and R. F. Keating
Bilateral and independent Broca areas confirmed by Wada test and functional magnetic resonance imaging, T. J. Biega, L. M. Levy, F. Bannout, and W. D. Gaillard
Clobazam in the treatment of Lennox-Gastaut syndrome, J. A. Conry, Y. T. Ng, J. M. Paolicchi, and L. Kernitsky
Acute and chronic magnetic resonance imaging of human hperesvirus-6 associated encephalitis, J. R. Crawford, T. Chang, B. L. Lavenstein, and B. Mariani
Medulloblastoma associated with novel PTCH mutation as primary manifestation of Gorlin syndrome, J. R. Crawford, B. R. Rood, C. T. Rossi, and G. Vezina
Primary spinal cord tumors of childhood: Effects of clinical presentation, radiographic features and pathology on survival, J. R. Crawford, A. Zaninovic, M. Santi, and E. J. Rushing
Guidelines for imaging infants and children with recent-onset epilepsy, W. D. Gaillard, C. Chiron, JH Cross, and AS Harvey
Obesity in the Pediatric Headache Population: A Multicenter Study, A. D. Hershey, S. W. Powers, T. D. Nelson, and M. A. Kabbouche
Teaching Video NeuroImages: preserved awareness in a frontal seizure with bilateral motor involvement: a psychogenic mimic, D. T. Hsieh and P. L. Pearl
Phase I Study of SU5416, a Small Molecule Inhibitor of the Vascular Endothelial Growth Factor Receptor (VEGFR) in Refractory Pediatric Central Nervous System Tumors, M. W. Kieran, J. G. Supko, D. Wallace, and R. Fruscio
Headache in Young Children in the Emergency Department: Use of Computed Tomography, T. M. Lateef, M. Grewal, W. McClintock, and J. Chamberlain
Headache in a National Sample of American Children: Prevalence and Comorbidity, T. M. Lateef, K. R. Merikangas, J. P. He, and A. Kalaydjian
Functional Connectivity of the Inferior Frontal Cortext Changes with Age in Children with Autism Spectrum Disorders: A fcMRI Study of Response Inhibition, P. S. Lee; B. E. Verys; Rosa, A. Della; and W. D. Gaillard
Limitations to plasticity of language network reorganization in localization related epilepsy, J. Mbwana, M. M. Berl, E. K. Ritzl, and L. Rosenberger
Cerebellar ataxia with elevated cerebrospinal free sialic acid (CAFSA), F. Mochel, F. Sedel, A. Vanderver, and U. F. H. Engelke
Diffusion Tensor Imaging in Arginase Deficiency Reveals Damage to Corticopinal Tracts, M. S. Oldham, J. W. vanMeter, K. F. Shattuck, and S. D. Cederbaum
Primary postoperative chemotherapy without radiotherapy for intracranial ependymoma in children.[comment], R. J. Packer
Objective response of multiply recurrent low-grade gliomas to bevacizumab and irinotecan, R. J. Packer, R. Jakacki, M. R. Horn, and G. Vezina
Neurological problems of jazz legends, P. L. Pearl
New treatment paradigms in neonatal metabolic epilepsies, P. L. Pearl
Succinic semialdehyde dehydrogenase deficiency: lessons from mice and men, P. L. Pearl, K. M. Gibson, M. A. Cortez, and Y. Wu
Succinic semialdehyde dehydrogenase deficiency: Lessons from mice and men, P.L. Pearl, K.M. Gibson, M.A. Cortez, and Y. Wu
Decreased GABA-A binding on FMZ-PET in succinic semialdehyde dehydrogenase deficiency, P. L. Pearl, K. M. Gibson, Z. Quezado, and I. Dustin
Decreased GABA-A binding on FMZ-PET in succinic semialdehyde dehydrogenase deficiency, P.L. Pearl, K.M. Gibson, Z. Quezado, and I. Dustin
Introducing a Neurogenetics Curriculum into the Neurology Medical School Clerkship, P. L. Pearl, J. M. Pettiford, A. Heffron, and S. Healton
Cerebral MRI abnormalities associated with vigabatrin therapy, P. L. Pearl, L. G. Vezina, R. l. P. Saneto, and E. Molloy-Wells
Mutations involved in Aicardi-Goutieres syndrome implicate SAMHD1 as regulator of the innate immune response, G. I. Rice, J. Bond, A. Asipu, and A. Vanderver
Interhemispheric and intrahemispheric language reorganization in complex partial epilepsy, L. R. Rosenberger, J. Zeck, M. M. Berl, and E. N. Moore
The Utility of Somatosensory Evoked Potentials in Anoxic-Ischemic Encephalopathy, TL Rothstein
Status epilepticus in children, R. K. Singh and W. D. Gaillard
Isolated Cranial Nerve Enhancement in Metachromatic Leukodystrophy, R. K. Singh, R. T. Leshner, N. Kadom, and A. L. Vanderver
Isolated cranial nerve enhancement in metachromatic leukodystrophy, R. K. Singh, R. T. Leshner, N. Kadom, and A. L. Vanderver
Correlation of cerebral Near-infrared spectroocopy (cNIRS) and neurological markers in critically ill children, A. Subbaswamy, A. A. Hsu, S. Weinstein, and M. J. Bell
Magnetic resonance imaging abnormalities associated with vigabatrin in patients with epilepsy, J. W. Wheless, L. Carmant, M. Bebin, and J. A. Conry
The fMIR success of children and adolescents: Typical development, epilepsy, attention deficit/hyperactivity disorder, and autism spectrum disorders, B. E. Yerys, K. F. Jankowski, D. Shook, and L. R. Rosenberger
Submissions from 2008
A patient with subacute onset of ophthalmoplegia, papilledema, and proptosis, A. Z. Burakgazi, C. Wang, and K. Burger
Parenting stress and childhood epilepsy: The impact of depression, learning, and seizure-related factors, S. Cushner-Weinstein, K. Dassoulas, J. A. Salpekar, and S. E. Henderson