Cerebral Palsy and Neurodisability
Go for the Cause: Significant Genomic Rearrangements in Cryptogenic Cerebral Palsy | |
Hilla Ben-Pazi, Reeval Segal, Efrat Levy-Lahad |
Hemiplegic Cerebral Palsy- Etiology , clinical features and outcome | |
ELI LAHAT, NATANEL ZELNIK, MITCHEL SCHERTZ, AVIVA FATAL-VALEVSKI |
Adapting the Sniffin' Sticks smell identification test for the pediatric population | |
Laís Orrico Donnabella Bastos, Marilisa Mantovani Guerreiro, Andrew John Lees, Thomas Warner, Laura Silveira-Moriyama |
A case of Korean infant with clinically diagnosed Cerebro-Oculo-Facio-Skeletal Syndrome | |
Jun Hwa Lee |
CNS Infections
Exogenous BDNF Improves Endogenous Neurogenesis Following Experimental Streptococcus Pneumoniae Meningitis | |
Di Lian, Dake He, Xiaoqing Song, Mingjie Zhu, Jiaming Sun, Ling Li |
Clinical Presentation and Prognosis of Pediatric Encephalitis : Experience of a Korean Single Tertiary Center | |
Jun-Sung Park, Mi-Sun Yum, Eun-Hee Kim, Ree-Nar Yoo, Hye-Jin Lee, Tae-Sung Ko |
Predictors of Neuropsychiatric Manifestations among children with Dengue infection | |
Loudella Valdon Calotes-Castillo, Marilyn Tan, Marissa Lukban, Aida Salonga, Benilda Sanchez-Gan, martha Lu-Bolanos |
Forma infanto-juvenil da Mielopatia associada ao HTLV-1/ paraparesia espástica tropical (HAM / TSP): Seguimento clínico em uma coorte de 10 ano | |
Janeusa Rita Chagas, Mariana Azevedo Bastos, Maria Fátima de Oliveira, José Lucas Sena da Silva, Maria Lourdes Farré, Achiléa Cândida Lisboa Bittencourt |
Development, Cognition and Psychiatry
Cognitive profile, neuropsychological disorders and concerns in patients with neurofibromatosis Type 1 | |
Esteban Vaucheret, Maria Celeste Puga, Maria José García Basalo, Mariana Leist, Florencia Baliarda, Christy Ann Ekonen, Magdalena Reichart, Agustina López Ballent, Mariela Corleto, Victoria Madariaga, Guillermo Agosta |
SCHOOLING OF EPILEPTIC CHILDREN. FACTORS ASSOCIATED WITH THE NEED FOR SCHOOL SUPPORT. | |
María José García Basalo, Mariana Leist, María Celeste Puga, Mariela Corleto, María Florencia Baliarda, Isabel María Lascombes, Esteban Vaucheret Paz, Christy Ann Ekonen, Marina Aberastury, Guillermo Agosta |
Conners´ Continuous Performance Test profile in children with Attention Deficit Hyperactivity Disorder in relation to their intellectual performance | |
Maria Celeste Puga, Esteban Vaucheret, María José García Basalo, Mariana Leist, Florencia Baliarda, Isabel María Lascombes, Victoria Madariaga, Mariela Corleto, Guillermo Agosta |
The first European studies of lisdexamfetamine dimesylate in children with attention deficit/hyperactivity disorder | |
Claudia Gasparian, Tobias Banaschewski, Michel Lecendreux, César Soutullo, Mats Johnson, Alessandro Zuddas, Colleen Anderson, Matthew Dauphin, Andrew Lyne, Maria Gasior, Liza A Squires, Richard Civil, David R Coghill |
FMR1 intron 1 methylation analysis: an epigenetic biomarker for the neurodevelopmental phenotype of children with Fragile X. | |
Marta Arpone, Xin Li, Howard Slater, Yoshimi Inaba, Cheryl Dissanayake, David Amor, Laura Rodwell, Lesley Bretherton, David Godler |
Analysis of motor performance in infants with congenital hypothyroidism who began treatment in the first month of life | |
Môyra Romero Patresi, Maura Mikie Fukujima Goto, Michelle P. C. Ouro, Maria Cecília M. P. Lima, Vivian Freitas, Carolina Taddeo Mendes Santos, Denise Castilho Cabrera Santos |
Epileptiform discharges in children with attention deficit/hyperactivity disorder | |
Sajun Chung, Eun Hye Lee, Geon Ho Bahn |
Influence of congenital hypothyroidism on psychomotor performance in infants | |
Michelle Prado Cabral do Ouro, Maura Mikie Fukujima Goto, Maria Cecilia Marconi Pinheiro Lima, Môyra Romero Patresi, Vivian Dutra, Sofia Helena Valente Lemos-Marini, Denise Castilho Cabrera Santos, Maria Francisca Colella-Santos |
Repetitive transcranial magnetic stimulation of dorsolateral prefrontal cortex in adolescent depression: Clinical and neurochemical effects. | |
Adam Kirton, Xiao-Ru Yang, Chris Wilkes, Glenda MacQueen, Sarah Pradhan, Irene Liu, Natalia Jaworska, Omar Damji, Jamie Keess, Lisa Marie Langevin, Thilinie Rajapakse, Marc Lebel, Mariko Sembo, Marilyn Fife, Frank MacMaster |
Assessment of working memory and its relationship to the general intellectual performance in patients with Tuberous Sclerosis assessed by the Wechsler Intelligence Scale | |
sergio antonio antoniuk, Laís Faria Masulk, Regina Teixeira, Bruna Lacava, Daiane Álex Seccon de Azevedo, Daniele Fajardo Nascimento, Mara Lúcia Santos, Isac Bruck, Ana Paula Almeida de Pereira |
Atention Deficit Hyperactivity Disorder and Videogames: Which games do they play when they play? | |
Esteban Vaucheret, Celeste Puga, Mariana Leist, Clarisa Maxit, Marisol Toma, Fernanda Rios Pistoia, Florencia Corleto, Christy Ekonen, Maria Jose Garcia Basalo, Vctoria Madariaga, Florencia Baliarda, Isabel Lascombes, Guillermo Agosta |
Epilepsy
Bone Health Screening Practices Amongst Boston Children’s Hospital Neurologists in Pediatric Epilepsy Patients: Follow Up on a Quality Improvement Project | |
Kristina Julich, Archana Patel, Mark Schomer, Christopher Elitt, Jamie Heath, Christelle Moufawad El Achkar, Karen Spencer, Melissa Putman, Elizabeth Hart, Nina Ma, Tobias Loddenkemper |
Successful use of Fenfluramine as add-on treatment in Dravet syndrome: A three years prospective follow-up | |
Lieven Lagae, Berten Ceulemans |
Clinico etiological profile of infantile onset epilepsy at a tertiary care center in India | |
Sirish Bhartiya, Lokesh Lingappa, Ramesh Konanki |
Relation to Cortical blood flow and electrographic activity in Childhood-onset Seizures: Correlation Between MRI-SWI and EEG | |
Yun-Jin Lee, Yong Woo Kim, Jae Yeon Hwang, Young Mi Kim, Sang Ook Nam |
EPISTOP – INTERNATIONAL, LONG-TERM, PROSPECTIVE STUDY EVALUATING CLINICAL AND MOLECULAR BIOMARKERS OF EPILEPTOGENESIS IN A GENETIC MODEL OF EPILEPSY – TUBEROUS SCLEROSIS COMPLEX | |
Sergiusz Jozwiak, Eleonora Aronica, Paolo Curatolo, Martha Feucht, Christoph Hertzberg, Anna Jansen, Floor Jansen, Barth Jansen, Jacek Jaworski, Katarzyna Kotulska, Pavel Krsek, David Kwiatkowski, Lieven Lagae, Karola Lehmann, Rima Nabbout, Bernhard Weschke |
Attention impairments in Benign Childhood Epilepsy with Centrotemporal spikes and Childhood Absence Epilepsy | |
Elisa D'Agati, Caterina Cerminara, Livia Casarelli, Ivo Kaunzinger, Klaus W. Lange, Oliver Tucha, Paolo Curatolo |
EEG study in Myanmar children with complex febrile seizures | |
aye mu saan, kyaw linn |
Designing a Clinical Study of Clobazam for Dravet Syndrome Using Pharmacokinetic/Pharmacodynamic Modeling | |
Deborah Lee, Rachel Omasta, Colleen Canavan, Mahlaqa Patel, Thomas Stothoff, Guangbin Peng, Dwain Tolbert |
Febrile seizure recurrence reduced by intermittent oral levetiracetam | |
Lin-Yan Hu, Li-Ping Zou, Jian-Min Zhong, Lei Gao, Jian-Bo Zhao, Nong Xiao, Hong Zhou, Meng Zhao, Xiu-Yu Shi, Yu-Jie Liu, Jun Ju, Wei-Na Zhang, Xiao-Fan Yang, Patrick Kwan |
Early epileptic encephalopathy with suppression-burst revealing RFT1-CDG syndrome: report of two new cases. | |
Alec Aeby, Cynthia Prigogine, Catheline Vilain, Geneviève Malfilatre, Jaak Jaeken, Damien Lederer, Patrick Van Bogaert |
Status epilepticus in infants and children | |
Hsiu-Fen Lee |
Comparative study of Febrile seizures Vs Generalised epilepsy with febrile seizure plus syndrome | |
Lokesh Lingappa, Darshak Makadia, Ramesh Konanki |
An easy to use diagnostic tool for pediatric epilepsy in low-resource regions | |
Archana A Patel, Adrian Njau, Francis Frederick, Ann Marie Bergin, Tobias Loddenkemper, Chellamani Harini, Masanori Takeoka, Edward Kija, Jurriaan Peters |
Hot executive functionm in children with epilepsy | |
Luciane Lorencetti Lunardi, Daniel Fuentes, Mirela Boscariol, Catarina Abraão, Marilisa Mantovani Guerreiro |
Seizures not related to hypoglycemia in type 1 diabetic patients (DM1) | |
Alejandra Hernández Gómez, Verónica Isabel Sáez Galaz, Scarlet Witting Enríquez, Carla Rojas Henríquez, María Francisca López Avaria, Mónica Troncoso Schifferli, Karla Henríquez Guaita |
CLINICAL SPECTRUM AND HANDLING IN 13 CHILDREN WITH ELECTRIC SLEEP STATUS | |
Maria Francisca Lopez, Daniela Muñoz, Patricia Parra, Erika De los Angeles Márquez Félix, Carla Rojas, Alejandra Hernandez, Scarlet Witting, Ledia Troncoso, Mónica Troncoso |
ELECTROENCEPHALOGRAPHIC CHARACTERIZATION OF PATIENTS WITH PERVASIVE DISORDER DEVELOPMENT | |
Claudia Lopez, Maria Orellana, Alejandra Mendez, Ledia Troncoso |
EPILEPSY ASSOCIATED TO INBORN ERRORS OF METABOLISM, STUDY AND EVOLUTION OF 68 PATIENTS | |
Scarlett Vitting, Mónica Troncoso, Karla Henriquez, Susana Del Pilar Araya Ramirez, Paola Santander, Ledia Troncoso, Carla Rojas, Andres Barrios, Francisca López, Rodrigo Diaz |
DRAVET SYNDROME: DESCRIPTION OF 4 PATIENTS WITH GENETIC CONFIRMATION | |
Scarlet Witting, Monica Troncoso, Carla Rojas, Daniela Salvo, Claudia Lopez, Guillermo Fariña |
Mutational analysis of TSC1 and TSC2 in Korean patients with tuberous sclerosis complex: genotype and epilepsy | |
JIN SOOK LEE, Yong Seoung Hwang, Byung Chan Lim, Moon-Woo Seong, Sung Sup Park, Jong-Hee Chae, Ki Joong Kim |
Metabolic Disorders
SUBACUTE COMBINED SCLEROSIS OF THE SPINAL CORD AND NECROTIZING ENTEROCOLITIS AFTER ILEAL RESECTION: A FORGOTTEN LINK | |
GUSTAVO NOGUEIRA DE HOLANDA, KALYNE MEDEIROS LACERDA, MARIA EUNICE XAVIER COELHO, MARIA DURCE COSTA GOMES, VANESSA VAN DER LINDEN MOTA |
WHITE MATTER DISORDERS IN A SERIE OF 150 PATIENTS WITH METABOLIC DISEASE | |
Lucy Monica Troncoso, Paola Santander, Carlos Alberto Jaque, Rodrigo Díaz, María Francisca López, Scarlet Amalia Witting, Salvador Camelio, Ledia Troncoso, Andres Barrios |
CONGENITAL METABOLISM DISEASES OF NEUROTRANSMITTERS IN PEDIATRIC NEUROLOGY: CLINICAL DESCRIPTION AND NEUROLOGICAL TRACING OF A GROUP OF PATIENTS. | |
monica troncoso, paola santander, carla rubilar, valentina micolich, carla rojas, rodrigo diaz, doris leon, francisca faure, ledia troncoso |
“Mucopolysaccharidosis type IV A: Evidence of Primary and Secondary Central Nervous System Involvement” | |
Felippe Borlot, Paula R Arantes, Caio R Quaio, José FS Franco, Charles M Lourenço, Israel Gomy, Debora R Bertola, Chong Ae Kim |
EPILEPSY AS A FORM OF PRESENTATION OF HYPERPROLINEMIA TYPE I: A PURPOSE OF TWO CASES | |
Ana Isabel Maraña-Pérez, Teresa Escobar-Delgado, Inmaculada Carreras-Sáez, Verónica Puertas-Martín, Jana Domínguez-Carral, Laura López-Marín |
"NEW INSIGHTS IN MUCOPOLYSACCHARIDOSIS TYPE VI: NEUROLOGICAL PERSPECTIVE" | |
Felippe Borlot, Paula Ricci Arantes, Caio Robledo Quaio, José Francisco da Silva Franco, Charles Marques Lourenço, Debora Romeo Bertola, Chong Ae Kim |
PROFILE OF IEM CASES (SMALL MOLECULE TYPE) IN A TERTIARY CARE REFERRAL CENTRE FROM INDIA | |
Lokesh Lingappa, lokesh lingappa, Nitin nayak, Akkela radharama devi, Ramesh Konanki, Alpa Dherai |
Differential diagnosis of the chronic encephalopathies: the importance of following the psychomotor development marks | |
Tania Saad, DENISE SANTANA, Ana Paula Rodrigues Lazzari Amâncio, Lúcio José Santa-Ignêz, Dafne Horowitz, Carmelo Conti, Fernanda Veiga Góes, Flávia Nardes, Ana Carolina Esposito, Sheila Lucena |
Association of dermal Melanocytosis with GM1-Gangliosidosis Type 1 | |
Lucia Cibils, Francisco Espinel, Conrado Medici, Mariela Alvarez, Natalia Dorado, Andrea Rey, Aida Lemes, Gabriel Gonzalez |
TAY-SACHS DISEASE B1 VARIANT: CASE REPORT | |
Cristina Nogueira Marques Alencar, Juliana Oliveira Ferreira, Avessandra Costa Cardoso Oliveira, Juliana de Castro Naves Peixoto, Paulo Roberto Alves Seixas, Janaina Monteiro Chaves, Renata Brasileiro Reis Pereira, Cristiane Sales Low, Marisa Vale Cavalcante, Maria Angélica Cavalcante Barbosa Viana, Christian Muller |
BIOPTERIN DISORDER CAUSING HIPERPHENYLALANINEMIA: TWO DIFFERENT CASES | |
Cristina Nogueira Marques Alencar, Avessandra Costa Cardoso Oliveira, Juliana de Castro Naves Peixoto, Paulo Roberto Alves Seixas, Janaína Monteiro Chaves, Renata Brasileiro Reis Pereira, Cristiane Sales Low, Marisa Vale Cavalcante, Maria Angélica Cavalcante Barbosa Viana, Christian Muller, Juliana Oliveira Ferreira |
Chondrodysplasia Punctata or Conradi-Hünnermann Syndrome. The first Guatemalan case | |
Christian D. López, Elie De Leon, Hugo H Galvez |
Mutation spectrum of Glutaryl-CoA Dehydrogenase Deficiency in South Indian population with Glutaric Aciduria Type I | |
Lokesh Lingappa, Akella Radharama Devi, Jayanthi Undamatla, Satish s |
Movement Disorders
Coprophenomena are Associated with High Clinical Impact in Tourette Syndrome | |
Erika F Augustine, Kathleen D Black, Heather Adams, Adam Lewin, Alyssa Thatcher, Tanya Murphy, Jonathan W Mink |
Phenotypical and Molecular Characterization of Patients with Neurodegeneration with Brain Iron Accumulation (NBIA) due to PKAN2 gene mutations | |
Navin Mishra, Felippe Borlot, Krutika Joshi, Saadet Mahmutoglu, Jane McCabe, William Logan, Teesta Soman |
An open label clinical pilot study of resveratrol as a treatment for Friedreich ataxia | |
Eppie Yiu, Tai Geneieve, Peverill Roger, Katherine Lee, Kevin Croft, Trevor Mori, Barbara Scheiber-Mojdehkar, Brigitte Sturm, Monika Praschberger, Adam Vogel, Gary Rance, Sarah Stephenson, Paul Lockhart, Joseph Sarsero, Chung-Yung Lee, Andrew Churchyard, Marguerite Evans-Galea, Monique Ryan, Louise Corben, Martin Delatycki |
Movement Disorder in Three Filipino Adolescents with Anti NMDA Receptor Encephalitis: A case series | |
Philomine Daphne Patricio Obligar, Lillian Villaruz Lee |
Redefining the clinical phenotype of psychomotor disabilities with X-Linked MCT8 Disease: Implications for improved therapies. | |
Rebecca Lehman, Leonardo Bonilha, Maria Gisele Matheus, Kenton R Holden |
Paroxysmal Dyskinesias in childhood | |
Monica Troncoso Schifferli, karla Gemita Henriquez Guaita, Andrés Barrios, Scarlet Witting Enrique, Claudia Lopez, Veronica Saez Galaz, Guillermo Guzman, Carolina Coria, carolina Diaz, Ana Flandes |
Muscle and Nerve
Peripheral nerve ultrasound in paediatric Charcot-Marie-Tooth disease Type 1A | |
Eppie Yiu, Cain Brockley, Katherine Lee, Kate Carroll, Katy De Valle, Rachel Kennedy, Padma Rao, Monique Ryan |
The Investigation of Genetics, Serum Biochemistry and Pathology in Duchenne Muscular Dystrophy | |
Jianxiang Liao, Chunxi Han |
RELIABILITY OF THE EK SCALE VERSUS HAND GRIP DYNAMOMETER TESTING IN NON-AMBULANT DUCHENNE MUSCULAR DYSTROPHY PATIENTS | |
Stacey KH Tay, Sarah JC Tapawan, Jeremy BY Lin, Furene SJ Wang, Yanrong Guo, Michael TC Lim, Hian-Tat Ong |
Limb Girdle Myasthenia: An uncommon, treatable cause of proximal muscle weakness in children | |
Ramesh Konanki, Lokesh Lingappa, Nikit Shah |
Polysomnographic abnormalities in children with Duchenne muscular dystrophy | |
Carla Rojas, Alejandra Hernández, Jocelyn Gutiérrez, Daniela Castillo, Mónica Troncoso, Susana Lara, Carola Peña, Verónica Sáez |
Chronic Inflammatory Demyelinating Polyneuropathy Secondary (CIDP) to Inflammatory Bowel Disease (IBD) and Associated to Vitamin B12 Deficiency | |
FERNANDA Veiga de GOES, Gabriela Rochedo Villela, Rita Farias Oliveira, Julia Valeriano de Almeida, Andre Felipe Pinto Duarte, Eugenia Figueredo Costa de Lacerda |
Prepubertal Myasthenia Gravis-Is infection a trigger or the cause? | |
Sandya Tirupathi, Clare Loughran, Lyndsey Thompson |
Poliomielitis Aguda Pos Vacunal en el Perú Reporte de cinco casos y análisis del impacto social y sanitario entre los años 2009 y 2011 | |
Inés Caro-Kahn, Luis Suárez-Ognio, Rene Leiva-Rosado, María Ticona, Jorge Uchuya, Washington Toledo, Brenda Cáceres-Mejía, Reneé Pereyra-Elías, Mario Martinez |
Atypical clinical and histological presentations in patients with mutations on the RYR1 gene | |
Cristiane Araújo Martins, Osorio Abath Neto, Marco Antonio Veloso Albuquerque, Jocelyn Laporte, Umbertina Conte Reed, Anne Rutkowski, Carsten Bönnemann, Edmar Zanoteli |
Neonatal & Fetal Neurology
Rotavirus infection can cause seizures accompanied by diffuse cerebral white matter injury in full-term newborns | |
Kyung Yeon Lee |
Fetal ventriculomegaly investigations and outcomes - 5 year experience | |
Prakash Satodia, Lauren Lacey, Hiten Mehta, Soma Mukherjee |
Effect of severe perinatal asphyxia on pituitary and thyroid functions in neonates | |
Reetika Saini, Pramod Lali, Siddarth Ramji, Vedika Bhat, Sudhesna Mohapatra, Bidhan Chandra Koner |
Neurogenetics
De Novo DiGenic Heterozygous Mutations in EZR and NR2E3 revealed by Exome Sequencing in a patient with Cataract, Retinal Degeneration, Epilepsy and Leukodystrophy | |
Majed J. Dasouki, Yiran Guo, Jinlong Liang, Xuanzhu Liu, Fengxiang Wang, Brendan J. Keating, Jianguo Zhang, Jun Wang, Jennifer Roberts, Atul Kakrana, Victor Chang, Irfan Saadi, Salil Lachke, Hakon Hakonarson |
Proteolipid protein 1 and gap junction α12 gene mutations in 72 Chinese patients with Pelizaeus-Merzbacher disease/ Pelizaeus-Merzbacher like disease and prenatal diagnosis of 15 fetuses in twelve Chinese families with PMD probands | |
Jingmin Wang, Dongxiao Li, Dongxiao Li, Ye Wu, Ye Wu, Jiangxi Xiao, Jiangxi Xiao, Xinhua Bao, Xinhua Bao, Hui Xiong, Hui Xiong, Jiong Qin, Jiong Qin, Xiru Wu, Xiru Wu, Yuwu Jiang, Yuwu Jiang |
The 9p13 Deletion Syndrome: Confirmation and Expansion of the Phenotype | |
MAJED J. Dasouki, Jennifer Roberts, Angela Santiago Lennon, Karine Hovanes |
Neuropsychiatric Manifestations in Children with 22q11.2 microdeletion syndrome : Single Center Study | |
Eunhee Kim, Mi-Sun Yum, Beom-Hee Lee, Han-Wook Yoo, Tae-Sung Ko |
The Relationship between Academic Performance and Academic-related Boredom: the 5-HTTLPR Gene Polymorphism as a Moderator | |
Yangyang Liu |
Pontocerebellar hypoplasia in the differential diagnosis of floppy infant syndrome | |
Tania Saad, Fernanda Veiga Góes, Alessandra Augusta Penna e Costa, Flávia Nardes, Ana Paula Rodrigues Lazzari Amâncio, Denise Santana, Carla Quero Cunha, Alexandre Lucidi, Lúcio José Santa-Ignêz |
Torsion dystonia (DYT 1) caused by mutation in TOR 1A presenting with Myoclonic dystonia | |
André Luiz Santos Pessoa, Danielle Pessoa Lima, Alexandre Bastos Lima, Fernando Kok |
Aicardi syndrome in a genotypic male. Case report | |
Marzhan Lepessova, Bakhytkul Myrzaliyeva, Gyuzel Khudayberdiyeva, Sholpan Tankayeva, Aidana Berdaliyeva |
INFANTILE POMPE'S DISEASE: A CASE REPORT | |
Juliana de Castro Naves Peixoto, Avessandra Costa Cardoso Oliveira, Cristina Nogueira Marques Alencar, Paulo Roberto Alves Seixas, Janaína Monteiro Chaves, Renata Brasileiro Reis Pereira, Cristiane Sales Low, Marisa Vale Cavalcante, Maria Angélica Cavalcante Barbosa Viana, Christian Muller, Gerson da Silva Carvalho, Maria Teresinha de Oliveira Cardoso, Cristina Touguinha Neves Medina |
Brown-Vialetto-van Laere syndrome: a case report | |
Aline Cupertino Lemos, Igor Dórea Bandeira, João Gabriel Jagersbacher Passos Oliveira, Fernanda Costa de Queirós, Rita de Cássia Saldanha de Lucena |
A case of GLUT1 deficiency syndrome with developmental delay and absence of seizures and movement disorder | |
André Luiz Santos Pessoa, Danielle Pessoa Lima, Alexandre Bastos Lima, Fernando Kok |
GM2 synthase deficiency: a New Inborn Error of Metabolism presenting as Hereditary Spastic Paraplegia with Infantile Onset | |
CHARLES MARQUES LOURENCO, Giovanni Stevanin, Stephan Zuchner, Wilson Marques Junior |
Neurocritical Care, Neurotrauma, Neuroprotection
Protective effect of Niuhuang Qingxin Powders on experimental seizure in developing rats | |
Xiaolu Chen, Wenjuan Li, Li Jiang |
Protective effect of Niuhuang Qingxin Powders on hyperthermia induced seizure in developing rats | |
Xiaolu Chen, Wenjuan Li, Hengsheng Chen, Li Jiang |
Neuroprotective effect of mild hypoxia in organotypic hippocampal slice cultures of rat | |
Soo Ahn Chae, Na Mi Lee, Seh Hyun Kim, Woo Soon Lee |
CLINICAL FEATURES OF ENCEPHALOPATHY IN CHILDREN WITH BURNS | |
Olga Lvova, Olga Kovtun, Anna Orlova, Elena Orlova, Fedor Brezgin, Aleksey Shtukaturov |
Neuroradiology
Microstructural abnormalities of the supratentorial white matter tracts on brain MRI in X-Linked MCT8 Deficiency: Implications for earlier diagnosis and treatments. | |
Maia Gisele Matheus, Leonardo Bonilha, Rebecca Lehman, Kenton R. Holden |
N-methyl D-aspartate receptor (NMDAR) antibodies associated with distinct clinico-radiological white matter syndromes: clinical evidence for an anti-NMDAR leukoencephalopathy? | |
yael hacohen, Michael Absoud, Cheryl Hemingway, Leslie Jacobson, Jean-Pierre Lin, Mike Pike, Sunil Pullaperuma, Ata Siddiqui, Evangeline Wassmer, Patrick Waters, Sarosh Irani, Camilla Buckley, Angela Vincent, Ming Lim |
Neuroimmunology
Utility and Safety of Rituximab in pediatric autoimmune and inflammatory CNS disease | |
Russell Dale, Fabienne Brilot, Lisa Duffy, Marinka Twilt, Amy Waldman, Sona Narula, Amber Stocco, Kumaran Deiva, Erik Anderson, Michael Eyre, Despina Eleftheriou, Paul Brogan, Rachel Kneen, Gulay Alper, Banu Anlar, Evangeline Wassmer, Kirsten Hineman, Cheryl Hemingway, Catherine Riney, Andrew Kornberg, Marc Tardieu, Eyal Muscal, Brenda Banwell, Mark Gormon, Sussanne Benseler, Ming Lim |
Voltage Gated Potassium Channel (VGKC)-complex antibodies in children: what do they mean? | |
Yael Hacohen, Rahul Singh, Meghan Rossi, Cheryl Hemmingway, Ming Lim, Angela Vincent |
Spectrum of MOG autoantibody-associated demyelinating diseases in pediatric patients | |
Silvia Noemi Tenembaum, Patrick Waters, Maria Isabel Leite, Mark R. Woodhall, Juan P. Princich, Martin Jose Segura, María Elena Talarico, Marina Szlago, Angela Vincent |
Myelin oligodendrocyte glycoprotein (MOG) antibodies in children without oligoclonal bands predict a non-MS course of acquired demyelination syndrome (ADS). | |
yael hacohen, Michael Absoud, Kumaran Deiva, Cheryl Hemingway, Jacqueline Palace, Evangeline Wassmer, Patrick Waters, Marc Tardieu, Ming Lim, Angela Vincent |
Therapeutic plasma exchange in paediatric neurology: indications, side effects and outcomes from four UK tertiary centres | |
Michael Eyre, Kate Lamb, Michael Absoud, Shakti Agrawal, Jonathan Gadian, Rajat Gupta, Rachel Kneen, Ming Lim, David Milford, Sunny Philip, Katie Rose, Martin Smith, Stefan Spinty, Evangeline Wassmer, Cheryl Hemingway |
Clinical characteristics of Irish narcolepsy patients following H1N1 influenza epidemic and vaccination in 2009/2010 | |
Elaine Catherine Reade, Bryan Lynch, Mary King |
The clinical natural course after a first episode of central nerve systems demyelination in children | |
Cha Gon Lee, Jeehun Lee, Munhyang Lee |
Anti-N-methyl-D-aspartate Receptor Encephalitis in Taiwan | |
Kuang-Lin Lin, Jainn-Jim Lin, Shao-Hsuan Hsia, Huei-Shyong Wang |
Screening autoimmune synaptic antibodies in pediatric patients suspecting autoimmune encephalitis | |
ByungChan Lim |
Striving for the best treatment for Pediatric Acute demyelinating syndromes: results from cohort analysis | |
Tania Regina Dias Saad, Alessandra augusta penna e costa alessandra penna e costa, Leonardo Costa de Azevedo Leonardo de Azevedo, Mirian Calheiros Mirian Calheiros Monterio, Carla Marcia Marcia Carvalho Carla Marcia Carvalho Vieira, Fernanda Tovar Fernanda Moll, Elisabeth Soares Magalhães Elisabeth Magalhães |
Variable manifestations of Anti-NMDA receptor encephalitis in children: Case series from tertiary care centre in India | |
Ramesh Konanki, Lokesh Lingappa, Vivek Jain, Nikit Shah |
Optic neuritis in juvenile idiopathic arthritis patient | |
fernanda castro monti, Daniela Mencaroni Rodrigues Lourenço, Izabel Mantovani Buscatti, Benito Lourenço, José Albino Paz, Clovis Artur Almeida Silva, Umbertina Conti Reed |
RECURRENT ACUTE DISSEMINATED ENCEPHALOMYELITIS (ADEM): A CASE REPORT | |
AVESSANDRA COSTA CARDOSO OLIVEIRA, CRISTINA NOGUEIRA MARQUES ALENCAR, JULIANA DE CASTRO NAVES PEIXOTO, RENATA BRASILEIRO PEREIRA, CRISTIANE SALES LOW, JANAÍNA CHAVES MONTEIRO, CHRISTIAN MULLER, MARIA ANGÉLICA CAVALCANTE BARBOSA VIANA, MARISA VALE CAVALCANTE, LUCIANO TALMO |
Hemiconvulsion-Hemiplegia-Epilepsy (HHE) syndrome presenting with no apparent hemiconvulsion: A case report. | |
Rahul Raman Singh, Ata Siddiqui, Ming Lim, Tammy Hedderly |
Electrophysiological features of childhood autoimmune encephalitis | |
Rahul Raman Singh, Claudia Palmer, Yael Hacohen, Sushma Goyal, Ming Lim |
Stroke & Neurovascular Disorders
Social competence following pediatric stroke: Contributions of brain insult and family environment | |
Vicki Anne Anderson, Alison Gomes, Mardee Greenham, Stephen Hearps, Anne Gordon, Nicole Rinehart, Linda Gonzalez, Keith Owen Yeates, Chrissie Hajek, Warren Lo, Mark Mackay |
Is D-dimer measurement useful in pediatric cerebral sinovenous thrombosis? | |
Ana-Marissa Lagman-Bartolome, leonardo brandao, ann-marie pontigon, gabrielle deveber, daune macgregor, rand askalan, ivanna yau, mahendranath moharir |
Role of prothrombotic risk factors (thrombophilia) in neonatal arterial ischemic stroke | |
veerle labarque, leonardo brandao, gabrielle deveber, daune macgregor, rand askalan, ivanna yau, mahendranath moharir |
Shingles of the Brain - recurrent Herpes Zoster Ophthalmicus Causing Arteriopathy and Basal Ganglia Infarction | |
Nomazulu Dlamini, Luis Amaya, Ata Siddiqui, Jean-Pierre Lin |
Neurological Involvement in Children with E. coli O104:H4-induced Haemolytic Uraemic Syndrome | |
Angela Bauer, Sebastian Loos, Dirk Horstmann, Frank Donnerstag, Lars Pape, Dieter Haffner, Thurid Ahlenstiel, Markus Kemper, Carola Wehrmann, Ulrike Loebel, Johanna Lemke, Georg Hillebrand, Anette Melk, Jun Oh, Hans Hartmann |
Are methylenetetrahydrofolate reductase polymorphisms A1298C and C677T genetic risk factors for pediatric stroke and is there difference between boys and girls? | |
Anneli Kolk, Anna-Liisa Lorenz, Eno-Martin Lotman, Tiina Kahre, Rael Laugesaar, Tiit Nikopensius, Evelin Mihailov |
Epilepsy after presumed perinatal stroke | |
Rael Laugesaar, Anneli Kolk, Ulvi Vaher, Inga Talvik, Pilvi Ilves, Dagmar Loorits, Tiina Talvik |
Risk Factors for Perinatal Arterial Ischaemic Stroke: a Case-control Study | |
Monica Troncoso, Daniela Muñoz, Maria Jose Hidalgo, Susana Lara, Patricia Parra, Andres Barrios, Cesar Mateluna, Fernanda Balut, Rodrigo Diaz |
Transient cerebral arteriopathy in a child associated with cytomegalovirus infection | |
Tai-Heng Chen, Wei - Chen Lin, Yung-Hao Tseng, San-Nan Yang |
Pediatric arterial ischemic stroke in a serie of 63 patients: Clinical profile, risk factors and severity | |
Monica Troncoso, Maria Jose Hidalgo, Daniela Muñoz, Susana Lara, Patricia Parra, Cesar Mateluna, Fernanda Balut, Andrés Barrios, Rodrigo Díaz |
Evolution and prognosis in pediatric arterial ischemic stroke in a serie of 64 patients | |
Mónica Troncoso, César Mateluna, Patricia Parra, Susana Lara, María Jose Hidalgo, Daniela Muñoz, José Zamora, Fernanda Balut |
Headache
Significance of Head-up Tilt Test in the Intractable Pediatric Migraine with Dizziness | |
KON-HEE LEE |
A possible relation of methylenetetrahydrofolate reductase (MTHFR) gene polymorphisms 677T/1298C to migraine in boys and girls. | |
Anna-Liisa Lorenz, Eno-Martin Lotman, Tiina Kahre, Anneli Kolk |
Chronic and Recurrent Vertigo and Dizziness in Children and Adolescents | |
Thyra Langhagen, A. Sebastian Schroeder, Nicole Lehrer, Florian Heinen, Klaus Jahn |
Pediatric migraine: use of ICHD II. criteria and treatment efficacy | |
Zvonka Rener-Primec, Simona Legisa, Simona Legisa, klara krvavica, klara krvavica, mihael Rogac, mihael Rogac |
Neurosurgery
Childhood Cavernomas. A 12-year experience | |
monica troncoso, susana lara, daniela muñoz, kay gittermann |
Neurooncology
Spectrum of Neurological Complications in Childhood Malignancies-A Study from India | |
Lokesh Lingappa, sirisharani siddaiahgari, Darshak Makadia, Nikit Shah, Dandu Ravi Varma |
Neurophthalmology
The utility of a semi-quantitative scoring of orbital imaging following the first episode of optic neuritis: A pilot study. | |
Rahul Raman Singh, Claudia Palmer, Ata Siddiqui, Jean Marie U-kim, Michael Absoud, Ming Lim |
Neurorehabilitation
Repetitive transcranial magnetic stimulation effects on motor learning in perinatal stroke: Short-term outcomes from the PLASTIC CHAMPS trial. | |
Adam Kirton, John Andersen, Mia Herrero, Lisa Carsolio, Aleksandra Mineyko, Colleen Lane, Jamie Keess, Omar Damji, Jacquie Hodge, Alberto Nettel-Aguirre, Michael Hill |
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