Presentations and Authors


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Cerebral Palsy and Neurodisability

Development of a portable electronic goniodynamometer for the evaluation of equinus foot in cerebral palsy.
Eduardo Ferracioli Fusão, Priscila Cunha Santos, Ricardo Silva Pinho, Marília Santos Andrade, Antônio Carlos da Silva, Luiz Celso Pereira Vilanova, Marcelo Rodrigues Masruha
Neurological manifestations of Incontinentia Pigmenti
Inmaculada Carreras-Sáez, Verónica Puerta-Martín, Jana Domínguez-Carral, Ana Maraña-Pérez, Teresa Escobar-Delgado, Juan-Jose García-Peñas
Long term follow-up of hemiplegic cerebral palsy treated with botulinum toxin type A: epilepsy impact
Lucia Helena Coutinho dos Santos, Arnolfo de Carvalho Neto, Marise Bueno Zonta, Sandra Regina Baggio Muzzolon, Danielle Caldas Bufara Rodrigues, Isac Bruck
Long term follow-up of hemiplegic cerebral palsy treated with botulinum toxin type A: neuroimage influence
Lucia Helena Coutinho dos Santos, Arnolfo de Carvalho Neto, Marise Bueno Zonta, Sandra Regina Baggio Muzzolon, Isac Bruck

CNS Infections

Clinicoradiological outcomes in children with solitary neurocysticercosis with and without albendazole therapy: a retrospective case record analysis.
Sheffali Gulati, Puneet Jain, Deepak Sachan, Biswaroop Chakrabarty, Arun Kumar Gupta, Atin Kumar, Ajay Kumar, Ravindra Mohan Pandey, Manoj Singh, Rachana Dubey
Meningitis in childrens, in Quetzaltenango, Guatemala. Factor of Prognosis.
Henry Hugo Galvez, Paulina Bixcul, Elie De Leon
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
DENGUE WITH NEUROLOGICAL COMPLICATIONS OF DIFFICULT DIAGNOSIS IN PEDIATRIC PATIENT- A CASE REPORT
Francisco Manoel Guedes Nobre, TALITA DE LIMA AQUINO NOGUEIRA, REGINA COELI CARVALHO PORTO CARNEIRO, ANA NEYLA MARTINS DA MOTA, VIRGIANNE ALVES FERREIRA

Development, Cognition and Psychiatry

CHILDREN WITH AUTSIM AND EPILEPSY:A DESCRIPTIVE CLINICAL COHORT STUDY FROM SOUTH AFRICA
Nerica Ramsundhar, Jo M Wilmshurst, Kirsten Ann Donald
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
Modulation of the TMS-evoked N100 during a go/nogo task in children with ADHD
Elisa D'Agati, Thomas Hoegl, Gabriel Dippel, Paolo Curatolo, Stephan Bender, Oliver Kratz, Gunther H. Moll, Hartmut Heinrich
Correlation with urinary nonylphenol levels and clinical symptoms in children with attention-deficit hyperactivity disorder
Jung-Chieh Du, Ching-Jung Yu, Mei-Lien Chen, Winnie Yang
Early white matter effects of alcohol exposure on the infant brain
Kirsty Ann Donald, Annerine Roos, Jeanne Pierre Fouche, Fleur Howells, Nastassja Koen, Woods Roger, Heather Zar, Katherine Narr, Dan Stein
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
THE ROLE OF EPILEPSY IN AUTISTIC REGRESSION
Jana Domínguez-Carral, Ana Isabel Maraña-Pérez, Teresa Escobar-Delgado, Inmaculada Carreras-Sáez, Veronica Puertas-Martín, Juan-José García-Peñas
Functional neurological disorder in the pediatric emergency room: characteristics, outcome and diagnostic accuracy
Claudio Melo de Gusmão
Adaptive Behavior and Developmental Level in Preschool Children Referred for Possible Autism Spectrum Disorder
Paulina Carullo, Flavia Dorrego, Nicolas Cataldo, Silvia Intruvini, Angeles Schteinschnaider
PANDAS Diagnosis in the Ultimate Context of Pediatric Neurology
Carolina Carvalho, Iaciara Souza, Daniella Nazzetta, Anna Silva, Aline Domingues, Adriana Santos, Liubiana Araujo
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
Delivery and breastfeeding in autism.
Alexandra Prufer de Q. C. Araujo, Giuseppe Mario Carmine Pastura, Lais de Carvalho Pires, Marlos Melo Martins, Aline Chacon Pereira, Sheyla Ribeiro Magalhães, Katiane Sayão Souza Cabral, Gilca Maria Soares Gonzaga, Roberta da Silva Mendonça Thurler, Viviane Barreto Serour, Alessandra Maria Rocha Rodrigues, Rita Farias Oliveira, Karen Grazielle Capuano de Sant'Anna, Andreia de Santana Silva Moreira, Viviane Romão Soares da Rocha
Learning difficulty in risk children Is it possible to prevent?
Maria Gabriela Delucchi Bottaro, Margarita Isola, Marisa Burgueño, Maria Isabel Grajales, Virginia Marichal, Kessler Pamela

Epilepsy

Clinical markers of Postictal Generalized EEG Suppression (PGES) in children
Elizabeth Kouzmitcheva, Kazuo Okanari, Hiroshi Otsubo, Elizabeth J Donner
Autoimmune Encephalitis with Anti-VGKC Antibodies Mimicking HSV Encephalitis in a Teenage Boy
Huiyuan Jiang, Cresha Davis, Addulradha Alqallaf
Topiramate use and the risk of glaucoma development in children.
SANJAYA SHANTHIPUTHRA FERNANDO, Nilal Ratnayake, T.H.A.R Diloshini, Jithangi Wanigasinghe, Dharma Irugalbandara, Pyara Ratnayake
ATOMOXETINE TREATMENT IN PATIENTS WITH ATTENTION DEFICIT HYPERACTIVITY DISORDER AND EPILEPSY
Inmaculada Carreras-Sáez, Teresa Escobar-Delgado, Ana Maraña-Pérez, Jana Domínguez-Carral, Verónica Puertas-Martín, Juan-José García-Peñas
Does vigabatrin treatment for infantile spasms cause visual field defects ? An international multicenter study
Raili Riikonen, Lionel Carmant, Marina Yuryevna Dorofeyeva, Katalin Hollody, Branka Stirn Kranjc, Rener Primec Zvonka, Ilona Szabo, Gabriele Wohirab, Iiris Sorri
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
Simultaneous ACTH and antiviral therapy in West syndrome
Dorota Dunin-Wasowicz, Dorota Dunin-Wasowicz, Dorota Domanska-Pakiela, Jolanta Kasprzyk-Obara, Dariusz Chmielewski, Katarzyna Tomaszek
Lack of efficacy of monotherapy in epilepsy of the 1st year of life- possible correlation with etiology?
Dorota Dunin-Wasowicz, Dariusz Kuczynski, Dariusz Chmielewski, Julita Borkowska, Katarzyna Tomaszek, Dorota Domanska-Pakiela
Using Self-Regulation concepts to predict sleep problems in adolescents with epilepsy.
Ioanna Rizou, Antigone Papavasiliou, Veronique de Gucht, Stan Maes
Attention Deficit Hyperactivity Disorder in children with epilepsy
Anita Choudhary, Sheffali Gulati, Rajesh Sagar, Savita Sapra, Madhulika Kabra, Naveen Sankhyan, Rachna Dubey
Treatment with modified Atkins diet type in nine patients with drug-resistant epilepsy
Maria Magdalena Vaccarezza, Marisol Vanesa Toma, Cecilia Griselda Diez, Guillermo Agosta
EPILEPSY DUE TO PROTOCADHERIN 19 GENE MUTATION: report of the first Argentinean case.
Cecilia Vazquez, Noelia Deltetto, Walter Silva, Maria Magdalena Vaccarezza, Marina Aberastury, Guillermo Agosta
Using a self-regulation frame of reference for the prediction of quality of life in adolescents with epilepsy
Ioanna Rizou, Stan Maes, Veronique de Gucht, Antigone Papavasiliou
Long term outcome of children with West syndrome: A retrospective case record analysis
Sheffali Gulati, Puneet Jain, Lakhsminarayanan Kannan, Rachna Sehgal, Biswaroop Chakrabarty, Rachana Dubey
Epilepsy in Tuberous Sclerosis Complex.
Katarzyna Kotulska, Dorota Domańska-Pakieła, Julita Borkowska, Dariusz Chmielewski, Jolanta Kasprzyk-Obara, Sergiusz Jóźwiak
Hemispheric surgery for epilepsy in children: outcome regarding seizures and language
JOCELI RODRIGUES DA SILVA
Epileptic encephalopathy with STXBP1 mutations - expanding the eletroclinical phenotype
Cláudia Melo, Inês Carrilho, Rui Chorão, Sara Domingues, Catarina Magalhães, Pedro Guimarães, Mafalda Barbosa, Patricia Maciel, Teresa Temudo
Epilepsy surgery in the first 3 years of life: clinical outcome and risk-benefits
Marcela Lopes de Almeida, Vera Terra, Helio R Machado, Marcelo Volpon, Antonio Carlos Santos, Americo C Sakamoto, Úrsula Thome, Ana Paula Hamad, Reinaldo Regis Silva
Dispersion durations of P-wave and QT interval in children treated with ketogenic diet
onder doksoz, orkide guzel, Unsal Yilmaz, Rana İşgüder, Kübra Çeleğen, Timur Mese
PREVALENCE OF FEBRILE SEIZURE – A POPULATION-BASED STUDY
Juliane Sauter Dalbem, Heloise Helena Siqueira, Regina Papais Alvarenga
SCN1A mutations in Indian patients with SCN1A-related epileptic disorders
Vrajesh Udani, Sarbani Raha, Shinichi Hirose, Dhanjit Kumar Das, Pradnya Gadgil
Vagus nerve stimulation in children with drug-resistant epilepsy: two case reports.
Luciane Silveira Baratelli, Stella de Aparecida Elderli Pintos dos Santos, Fernanda Cristina Guedes Morgado, Carla Quero Cunha, Heloisa Viscaino Fernandes Souza Pereira
Absence status epilepticus in children as their first presentation of absence epilepsy: a report of 4 cases.
Helene Dubreuil
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
Doose Syndrome: review and evolution-related factors in 20 cases
Teresa Escobar-Delgado, Inmaculada Carreras-Saez, Jana Domínguez-Carral, Verónica Puertas, Ana Maraña, Juan-José García-Peñas

Metabolic Disorders

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
MITOCHONDRIAL DNA DISEASE: CLINICAL SPECTRUM FROM THE GENOTYPE TO THE PHENOTYPE
Paola Santander, Monica Troncoso, César Mateluna, Andrés Barrios, Patricio Guerra, Ana Flandes, Rodrigo Diaz, Ledia Troncoso, Francisca Millán
GLUTARIC ACIDURIA TYPE I (GA1), CLINICAL CARACTERIZATION AND GENETIC STUDY OF 11 CHILEAN CHILDREN.
Mónica Troncoso, Paola Santander, Carolina Yáñez, Javiera Tello, Rodrigo Diaz, Ledia Troncoso, Andrés Barrios, Francisca Faure
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
2-HydroxyGlutaric Aciduria in Saudi Arabia
Majed J. Dasouki, Lujane Yousef, Minnie Jacob, Asmahan Ahmad, Ekhlass Quraan, Basma AlRasheed, Ali Odaib, Mohamed Alamoodi
Clinical and radiologic features in 12 patients with juvenile and adult GM1 Gangliosidosis.
João Stein Kannebley, Laura Siveira Moryama, Laís Orrico Donnabella Bstos, Marilisa Mantovani Guerreiro, Augusto Amato, Li Li Min, Carlos Eduardo Steiner
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
Novel PEX3 mutations identified as the cause of a peroxisomal biogenesis disorder with moderate clinical phenotype
Clarisa Maxit, Ines Denzler, Delfina Marchione, Guillermo Agosta, J Koster, Ronald Wanders, S Ferdinandusse, Hans Waterham
Multiple carboxylase deficiency presenting as acute encephalopathy
harshuti biren shah, Sunali desai
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
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
Chondrodysplasia Punctata or Conradi-Hünnermann Syndrome. The first Guatemalan case
Christian D. López, Elie De Leon, Hugo H Galvez
Tetrahydrobiopterin (BH4) Deficiency: A Case Report
Priscila Souza Soares, Leticia Leal Miranda, Fernanda de Castro Monti, Mauricio Rangel Zamboni, Camila Almeida Santos, Ana Carolina de Melo Cyrino, Patricia Gushiken Takahashi, Juliana Barbosa de Pádua Pinheiro, Pollyanna Barbosa Lima Cerqueira, Clarissa Bueno, Fernando Kok, José Albino da Paz, Leticia Pereira Brito Sampaio, Erasmo Barbante Casella, Maria Joaquina Marques-Dias, Umbertina Conti Reed

Movement Disorders

METHODOLOGY OF APPROACHES TO CHILDHOOD HEREDITARY ATAXIAS
Elif Acar Arslan, Rahşan Gocmen, Kader K. Oguz, Gokcen Duzgun, Haluk Topaloglu, Meral Topcu
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 phenomenology helps differentiate NMDAR encephalitis from autoimmune basal ganglia encephalitis
Shekeeb S Mohammad, Sudarshini Ramanathan, Victor S. C. Fung, Padraic Grattan-Smith, Fabienne Brilot, Russell C Dale
Clinical and genetic analysis of eight idiopathic cases of paroxysmal dyskinesia
ShuiZhen Zhou, YiFeng Ding
Chorea as a Manifestation of CNS Vasculitis in a 6-Year-Old Boy with Systemic Lupus Erythematosus
Jocelyn Montalvo-Ortiz, Leyda Sánchez-Ortiz, Mireya Bolo-Díaz, Marisel Vázquez-Correa, María Dávila-Carlos
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

Spinal Muscular Atrophy life span
Alexandra Prufer de Q. C. Araujo, Giuseppe Mario Carmine Carmine Pastura, Marlos Melo Martins, Aline Chacon Pereira, Roberta da Silva Mendonça Thurler, Sheyla Ribeiro Magalhães, Alessandra Maria Rocha Rodrigues, Rita Farias de Oliveira, Karen Grazielle Capuano de Sant'Anna, Viviane Romão Soares da Rocha
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
Does Acute Motor Axonal Neuropathy hurt?
Mireya Milagros Bolo-Diaz, Jocelyn Montalvo-Ortiz, Leyda Sanchez-Ortiz, Marisel Vazquez-Correa, Maria Davila-Carlos
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

Neonatal & Fetal Neurology

Emergence and evolution of neurological deficits following acute neonatal arterial ischemic stroke
aly aziz, gabrielle deveber, ann-marie pontigon, daune macgregor, rand askalan, ivanna yau, mahendranath moharir
New antiepileptic drugs in newborns
Cecilia Verónica Vázquez, Marina Aberastury, Ines Denzler, Maria Magdalena Vaccarezza, Clarisa Maxit, Walter Horacio Silva, Guillermo Eduardo Agosta
An Unusual Cause of Brachial Plexus Palsy in Neonatal Period: Retropharyngeal Abscess
Pinar Gencpinar, Yalciner Erdogan, Ozgur Duman
Neonatal seizures and metabolic disorders in a tertiary NICU
Prakash Satodia, Richard deBoer

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
Follow up study of 34 Chinese patients with vanishing white matter disease and role of UPR and autophagy in the pathogenesis
Ye Wu, Na Chen, Haihua Zhang, Lifang Dai, Lili Zang, Jingmin Wang, Yuwu Jiang, Xiru Wu
The 9p13 Deletion Syndrome: Confirmation and Expansion of the Phenotype
MAJED J. Dasouki, Jennifer Roberts, Angela Santiago Lennon, Karine Hovanes
Hotfoot mutant in human characterized by cerebellar ataxia and early-onset retinal dystrophy caused by homozygous GRID2 deletion
nicolas deconinck, Kristof Van Schil, Francois Meire, Miriam Bauwens, Hannah Verdin, Frauke Coppieters, Elfride De Baere
Novel mitochondrial mutation in an Indian family causing autosomal recessive neurodegenerative disorder
Biswaroop Chakrabarty, Sheffali Gulati, Rajeshwari R Moganty, Dantham Subrahamanyum, Rachana Dubey
CLINICAL AND RADIOLOGICAL FINDINGS IN MALFORMATIONS OF CORTICAL DEVELOPMENT: CLUES FOR GENETIC TESTING
Paulina Carullo, Mercedes Villanueva, Rita Valdez, Gabriel Vazquez, Lucas Bongiorni, Cecilia Perandones, Paulina Yañez, Soma Das, Mario Massaro, Angeles Schteinschnaider
RETT SYNDROME: CLINICAL PHENOTYPES ASSOCIATED TO MUTATIONS IN MECP2 GENE
Paola Santander, Mónica Troncoso, Ledia Troncoso, Sebastián Silva, Andrés Barrios, Patricia Parra, Rodrigo Díaz
Treatment of facial myotonia with botulinum toxin type A (BTX-A) in the Schwartz-Jampel syndrome (SJS): report of two cases
Igor Dórea Bandeira, João Gabriel Jagersbacher Passos Oliveira, Camilo Vieira Santos, Fernanda Costa de Queirós, Rita de Cássia Saldanha de Lucena
DEFECTS IN THE SYNTHESIS OF PROTEOLIPID PROTEIN, DIFFERENT FORMS OF PRESENTATION FOR DEFECTS IN THE SAME GENE.
Daniela Muñoz, Mónica Troncoso, Paola Santander, Carolina Quintana, Ledia Troncoso, Patricio Guerra, María José Hidalgo, Rodrigo Diaz, Ana Flandes, Andrés Barrios
VANISHING WHITE MATTER DISEASE (VWM): CLINICAL FEATURES, GENETIC STUDY AND EVOLUTION IN 10 CHILEAN PATIENTS.
Mónica Troncoso, Paola Santander, Andrés Barrios, Diane Vergara, Ledia Troncoso, Rodrigo Diaz, María Soledad Rojas, Christian Galleguillos
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
Use of cyclodextrin in two Brazilian girls with Niemann-Pick disease type C
Camilo Vieira Santos, João Gabriel Jagersbacher Passos Oliveira, Igor Dórea Bandeira, Fernanda Costa de Queirós, Rita de Cássia Saldanha de Lucena
Protein C deficiency in children and adolescents with sickle cell anemia post-stroke
João Gabriel Jagersbacher Passos Oliveira, Igor Dórea Bandeira, Camilo Vieira Santos, Fernanda Costa de Queirós, Rita de Cássia Saldanha de Lucena
Congenital fibrosis of extra ocular muscles (CFEOM) resulting from mutations in tubulin 3 (TUBB3) can mimic Moebius syndrome
Kosmapatabendige Chryshanth Saminda Dalpatadu, Peta Sharples, Sarah Smithson, Anirban Majumdar, Kayal Vijayakumar
Lisdexanfetamine as a treatment option for narcholepsia
Fernanda Guedes Morgado, Stella Pinto dos Santos, Roseane Beker, Marcella Vieira, Heloisa Pereira

Neuroimmunology

Diagnosing childhood small vessel CNS vasculitis: A proposed histological tool.
Maryam Nabavi Nouri, Marinka Twilt, Brett Danielson, Susanne Benseler, Anastasia Dropol, Cynthia Hawkins
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
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
Autoimmune encephalitis in children: experience of a tertiary care teaching hospital in North India
Sheffali Gulati, Biswaroop Chakrabarty, Rachana Dubey, Harsh Patel, Anil Israni, Lokesh Saini, Sangeetha Yoganathan, Manjari Tripathi, Aditi Sinha
The clinical and predictive factors for relapse after an initial event of acute disseminated encephalomyelitis in children.
Marie Bernadine Hidalgo, Maria E Davila
Acute Necrotizing Encephalopathy of Childhood in a Non-Asian 4-Year-Old Child after Varicella Immunization
Leyda Gisselle Sanchez-Ortiz, Jocelyn Montalvo-Ortiz, Mireya Bolo-Diaz, Marisel Vazquez-Correa, Maria Davila-Carlos
Kleine-Levin syndrome with rapid cycling – case report and review of the literature
Claudio Melo de Gusmão
Spinal cord involvement in children and adolescents with multiple sclerosis
Katarzyna Kotulska, Elżbieta Jurkiewicz, Katarzyna Nowak, Katarzyna Malczyk, Chmielewski Dariusz, Małgorzata Bilska, Sergiusz Jozwiak
A pediatric cohort of recurrent central nervous system demyelination; experience of a tertiary centre from north India
Sheffali Gulati, Biswaroop Chakrabarty, Atin Kumar, Rachana Dubey, Jayashankar Kaushik, Akbar Mohamed CH, Ankush Singh, Puneet Jain
Hemorrhagic Acute Diffuse Encephalomyelitis associated with Bordetella pertussis
Marcela Matos Monteiro Gonçalves, Rafaela Vasconcelos Viana, Josemar Marchezan, Manuela Graef Da Rosa, Gabriela Casagrande Dagostim, Leticia Machado Rosa Da Silva, Michele Michelin Becker, Josiane Ranzan, Maria Isabel Bragatti Winckler, Lygia Ohlweiler, Rudimar Dos Santos Riesgo
Association between acute disseminated encephalomyelitis and Guillain-Barré syndrome in a child
Rafaela Vasconcelos Viana, Josemar Marchezan, Marcela Matos Monteiro Gonçalves, Leticia Machado Rosa da Silva, Manuela Graef da Rosa, Gabriela Casagrande Dagostim, Michele Michelin Becker, Josiane Ranzan, Maria Isabel Bragatti Winckler, Lygia Ohlweiler, Rudimar dos Santos Riesgo
CASE REPORT: SUBACUTE SCLEROSING PANENCEPHALITIS
Patricia Oliveira Meirelles Mariano da Costa, Rubens Wajnsztejn, Paulo Breinis, Daniela Fontes Bezerra, Roberta Caramico Pinto, Flávio Geraldes Alves, Camila Exposto Alves, Débora Pereira Almeida, Rafael Guerra Cintra, Régia Gasparetto, Giuliana Franzago Salmazo, Bruna da Cruz Beyruth Borges, Camila Domingues
The aetiology, outcome and MRI of acute childhood encephalitis in a retrospective Australian cohort; emerging antibody-mediated encephalitides
Sekhar Cyril Pillai, Esther Tantsis, Alison Kesson, Kristina Prelog, Nicholas Davies, Yael Hacohen, Fabienne Brilot, Angela Vincent, Russell Dale
LONGITUDINALLY EXTENSIVE TRANSVERSE MYELITIS IN A-17-MONTH OLD GİRL PATİENT WİTH RECURRENT HYPOTONİA ATTACKS TREATED WITH INTRAVENOUS IMMUNGLOBULIN
Pinar Gencpinar, Kamil Karaali, Senay Haspolat, Ozgur Duman

Stroke & Neurovascular Disorders

Perinatal stroke risk factors: Syndrome-controlled analysis in the Canadian Cerebral Palsy Registry
Elizabeth Williams, Maryam Oskoui, Lynn Dagenias, Michael Shevell, Adam Kirton
Profile of Childhood Cerebrovascular Outpatient Clinic at Hospital in the South of Brazil
Josemar Marchezan, Marcela Matos Monteiro Gonçalves, Josiane Ranzan, Leticia Machado da Rosa da Silva, Rafaela Vasconcelos Viana, Manuela Graef da Rosa, Gabriela Casagrande Dagostim, Michele Michelin Becker, Maria Isabel Bragatti Winckler, Lygia Ohlweiler, Rudimar dos Santos Riesgo
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
Robotic quantification of proprioceptive dysfunction in children with perinatal stroke
Andrea Kuczynski, Sean Dukelow, Janice Yajure, Jamie Roe, Steve Scott, Adam Kirton
Malignant Middle Cerebral Artery Infarction in Children
Andrea V Andrade, Ivanna Yau, Mahendra Moharir, Gabrielle deVeber
Shingles of the Brain - recurrent Herpes Zoster Ophthalmicus Causing Arteriopathy and Basal Ganglia Infarction
Nomazulu Dlamini, Luis Amaya, Ata Siddiqui, Jean-Pierre Lin
Long-term Neuropsychological Outcome after Childhood Cerebral Sinovenous Thrombosis
aly aziz, robyn westmacott, gabrielle deveber, daune macgregor, rand askalan, ivanna yau, mahendranath moharir
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