Submissions from 2012
Biologically targeted therapeutics in pediatric brain tumors, Amulya A. Nageswara Rao, Joseph Scafidi, Elizabeth M. Wells, and Roger J. Packer
Temozolomide for pediatric high-grade gliomas, RJ Packer
Neuro-oncology: Understanding the molecular complexity of medulloblastoma., RJ Packer and EP Hoffman
Temozolomide for pediatric high-grade gliomas, Roger J. Packer
Neuro-oncology: Understanding the molecular complexity of medulloblastoma, Roger J. Packer and Eric P. Hoffman
Medulloblastoma and primitive neuroectodermal tumors, Roger J. Packer, Tobey Macdonald, Gilbert Vezina, Robert F. Keating, and Mariarita Santa
Inherited Metabolic Epilepsies, Phillip Pearl
Does therapeutic hypothermia alter the role of SSEP in predicting outcome after cardiac arrest?, Ted L. Rothstein
Therapeutic hypothermia and reliability of somatosensory evoked potentials in predicting outcome after cardiopulmonary arrest, Ted L. Rothstein
Does therapeutic hypothermia alter the role of SSEP in Predicting Outcome after Cardiac Arrest?, TL Rothstein
Medulloblastoma/Primitive Neuroectodermal Tumor and Germ Cell Tumors: The Uncommon but Potentially Curable Primary Brain Tumors, A Samkari, E Hwang, and RJ Packer
Medulloblastoma/primitive neuroectodermal tumor and germ cell tumors: the uncommon but potentially curable primary brain tumors, Ayman Samkari, Eugene Hwang, and Roger J. Packer
Insights into pediatric diffuse intrinsic pontine glioma through proteomic analysis of cerebrospinal fluid, Amanda M. Saratsis, Sridevi Yadavilli, Suresh N. Magge, Brian R. Rood, Jennifer Perez, D. Ashley Hill, Eugene Hwang, Lindsay Kilburn, Roger J. Packer, and Javad Nazarian
Insights into pediatric diffuse intrinsic pontine glioma through proteomic analysis of cerebrospinal fluid., AM Saratsis, S Yadavilli, S Magge, and BR Rood
Neurologic considerations in propionic acidemia, J Schreiber, KA Chapman, ML Summar, and N Ah Mew
Continuous video EEG for patients with acute encephalopathy in a pediatric intensive care unit, JM Schreiber, T Zelleke, WD Gaillard, and H Kaulas
Neurologic considerations in propionic acidemia., John M. Schreiber, Kimberly A. Chapman, Marshall Summar, Nicholas Ah Mew, V. R. Sutton, Erin MacLeod, Kathy Stagni, Keiko Ueda, Jill Franks, Eddie Island, Dietrich Matern, Loren Pena, Brittany Smith, Tiina Urv, Charles P. Venditti, Anupam Chakarapani, and Andrea L. Gropman
Continuous video EEG for patients with acute encephalopathy in a pediatric intensive care unit, John M. Schreiber, Tesfaye Zelleke, William D. Gaillard, Himanshu Kaulas, Nathan Dean, and Jessica L. Carpenter
Seizures in acute childhood stroke, Rani K. Singh, Nassim Zecavati, Jarnail Singh, Himanshu Kaulas, Karin B. Nelson, Nathan P. Dean, William D. Gaillard, and Jessica Carpenter
Seizures in acute childhood stroke, RK Singh, N Zecavati, J Singh, and H Kaulas
High intellectual function in individuals with mutation-positive microform holoprosencephaly, BD Solomon, DE Pineda-Alvarez, AL Gropman, and MJ Willis
High intellectual function in individuals with mutation-positive microform holoprosencephaly, B. D. Solomon, D. E. Pineda-Alvarez, Andrea L. Gropman, M. J. Willis, D. W. Hadley, and M. Muenke
Protective effect of scFv-DAF fusion protein on the complement attack to acetylcholine receptor: a possible option for treatment of myasthenia gravis, Chen Song, Zhikai Xu, Jianting Miao, Jiang Xu, Xingan Wu, Fanglin Zhu, Hong Lin, Zhuyi Li, and Henry J. Kaminski
Protective effect of scFv-DAF fusion protein on the complement attack to acetylcholine receptor: A possible option for treatment of myasthenia gravis, C Song, Z Xu, J Miao, and J Xu
Placental weight and neurologic outcome in the infant: A review, J Teng, T Chang, C Reyes, and KB Nelson
Placental weight and neurologic outcome in the infant: A review, Jennifer Teng, Taeun Chang, Christine Reyes, and Karin B. Nelson
The quick motor function test: A new tool to rate clinical severity and motor function in Pompe patients, Carine I. van Capelle, Nadine A.M.E. van der Beek, Juna M. de Vries, Pieter A. van Doorn, Hugo J. Duivenvoorden, Robert T. Leshner, Marloes L.C. Hagemans, and Ans T. van der Ploeg
The quick motor function test: A new tool to rate clinical severity and motor function in Pompe patients, CI Van Capelle, N Van Der Beek, JM De Vries, and PA Van Doorn
A prognostic gene expression signature in infratentorial ependymoma, Khalida Wani, Terri S. Armstrong, Elizabeth Vera-Bolanos, Aditya Raghunathan, David Ellison, Richard Gilbertson, Brian Vaillant, Stewart Goldman, Roger J. Packer, and +11 additional authors
Sirolimus for non-progressive NF1-associated plexiform neurofibromas: An NF clinical trials consortium phase II study, Brian Weiss, Brigitte C. Widemann, Pamela Wolters, Eva Dombi, Alexander A. Vinks, Alan Cantor, Bruce Korf, John Perentesis, David H. Gutmann, Elizabeth Schorry, Roger J. Packer, and Michael J. Fisher
Pediatric brain tumors and epilepsy, Elizabeth M. Wells, William D. Gaillard, and Roger J. Packer
Neurotoxicity of biologically targeted agents in pediatric cancer trials, Elizabeth M. Wells, Amulya A. Nageswara Rao, Joseph Scafidi, and Roger J. Packer
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