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
CARACTERÍSTICAS DE LA ATENCIÓN DE SALUD DE NIÑOS CON PARÁLISIS CEREBRAL EVALUADOS EN LA UNIDAD DE NEUROLOGÍA PEDIÁTRICA DEL HOSPITAL NACIONAL CAYETANO HEREDIA DURANTE EL PERIODO 2011-2012
Judith Raquel Vila

CNS Infections

CSF cultures / drug sensitivity in pediatric TBM - experience from a tertiary-care hospital in India
Vrajesh Udani, amit vatkar
Etio-patogenetic therapy of viral encephalitis in children
Natalia Skripchenko, Valentina Мalinovskaja, Galina Ivanova, Marina Ivanova, Vladimir Komantsev, Alla Vilnitz, Evgenij Gorelik, Elena Skripchenko
Neurological manifestations in childhood Baggio-Yoshinari Syndrome (Lyme Disease-like Syndrome in Brazil)
Virginia Aparecida Gelmeti Serrano Virginia, Carmen Silvia Molleis Galego Miziara Carmen, Maria Luiza Giraldes de Manreza Maysa
OPPORTUNITIES OF EMERGENCY CHEMOPROPHYLAXIS OF TICK-BORNE ENCEPHALITIS IN CHILDREN
Natalia Skripchenko, Nikolai Morgatskiy, Galina Ivanova, Marina Ivanova, Alla Vilnits, Nadejda Pulman, Evgenij Gorelik

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 IMPORTANCE OF IDENTIFYING NEUROPSYCHOMOTOR DELAYS IN THE DEVELOPMENT OF YOUNG CHILDREN
MARCIA REGINA MACHADO SANTOS VALIATI, sergio antonio antoniuk
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

USEFULNESS OF VIDEO-EEG MONITORING IN CHILDREN
Betiana G Comas, Nicolas Espinosa, Marina Aberastury, Brenda Giagante, Clarisa Maxit, Maria Vaccarezza, Guillermo Agosta, Walter Silva
Early EEG monitoring following prenatal diagnosis predicts epileptogenesis in tuberous sclerosis
Romina Moavero, Raffaella Cusmai, Federico Vigevano, Alessandra Toscano, Leonardo Caforio, Bruno Bernardi, Paolo Curatolo
Rufinamide as adjunctive drug in refractory epilepsy due to neuronal migration disorders
Giangennaro Coppola, Romina Moavero, Alberto Spalice, Raffaella Cusmai, Federico Vigevano, Alberto Verrotti, Sara MAtricardi, Dario Pruna, Domenica Battaglia, Pasquale Parisi, Paolo Curatolo
EPILEPSIA PARTIALIS CONTINUA: PRESENTING SYMPTOM OF ALPERS’ DISEASE
Angeles Schteinschnaider, María Paulina Carullo, Pablo Jorrat, Julia Vilariño
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
Three-year Follow-up on the Intavenous Immunoglobulin Therapy in Landau-Kleffner Syndrome
BULENT UNAY, Mutluay Arslan, Sebahattin Vurucu, Ridvan Akin
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
Predictors of recurrence of a first unprovoked seizure in children. A prospective study.
Dirce Fujiwara, Sergio Vranjac, Sergio Rosemberg
Effectiveness and safety of ketogenic diet in a population of drug resistant epilepsy
Maria Magdalena Vaccarezza, Marisol Toma, Alejandra Gonzalez, Guillermo Agosta
Ketogenic Diet National Consensus. Ketogenic diet Argentinian Group
Maria Vaccarezza
COMPLEX FEBRILE SEIZURES: Neuroimaging and electroencephalogram utility in emergency
Marina Aberastury, Clarisa Maxit, Maria Luz Fernandez, Pamela Romina Fernandez, Ener Villa, Nicolas Scnitzler, Guillermo Agosta
SURGICAL TREATMENT FOR SEIZURE CONTROL IN CHILDREN AND ADOLESCENTS WITH BRAIN TUMOR
Marília Rosa Abtibol Bernardino, Larissa Solange da Silva Moreira, Úrsula Thomé, Ana Paula Hamad, Vera Terra, Helio Machado, Marcelo Volpon, Antônio Carlos Santos, Christhian Castillo, Tonicarlo Velasco, Américo Sakamoto, Carolina Araújo Rodrigues Funayama
Epilepsy surgery in posterior cortex: short and long-term outcomes
nilton césar lima dos Santos, Eugênia Fialho Macedo, Maria Julia Torres Nieto, Úrsula Thome, Vera Terra, Hélio R. Machado, Marcelo Volpon, Carolina Araújo Rodrigues Funayama, Antônio Carlos Santos, Américo Ceiki Sakamoto, Ana Paula Hamad
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
REFLEX EPILEPSY IN CHILDHOOD
Mónica Ferrea, Gabriel Vazquez, Lucas Bongiorni, Pablo Jorrat, Julia Vilarino, Silvia Intruvini, Angeles Schteinschnaider
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
The use of chromosomal microarray in common clinical practice of newly diagnosed epilepsy of children in Estonia.
Klari Noormets, Kadi Veri, Kadri Väljataga, Tiia Reimand, Katrin Õunap, Tiina Talvik, Inga Talvik

Metabolic Disorders

Clinical, biochemical and Genetic Spectrum of Mitochondrial disorders in Egyptian Children: A Study of 15 cases
laila Abdel Moteleb Selim, laila Abdel Moteleb Selim, Dina Ahmed Mehany, Rudy vancoster, Sawsan Abdel hadi Hassan, iman gamal el din mahmoud, Doaa Abdo, Mariane youssry Girgis, joel smet
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
Effect Of Miglustat On Neurological Outcome In Early Infantile Niemann Pick C
Srividya Sreekantam, Evangeline Wassmer, Suresh Vijay, Saikat Santra, Louise Simmons, Anupam Chakrapani
Leukoencephalopathy is a common finding in childhood onset Mitochondrial Disease?
Srividya Sreekantam, Anupam Chakrapani, Katharine Foster, Lesley Macpherson, Louise Simmons, Saikat Santra, Suresh Vijay, Evangeline Wassmer
First case of GLUT1 deficiency syndrome in a 2-year-old Estonian girl: a case presentation
Stella Põldsepp, Kati Toom, Katrin Õunap, Ulvi Vaher, Tiina Talvik, Inga Talvik

Movement Disorders

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
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
STATUS DYSTONICUS IN CHILDREN. CASE REPORTS.
Monica Ferrea, Julia Vilariño, Pablo Jorrat, Silvia Intruvini, Angeles Schteinschnaider

Muscle and Nerve

Schwartz Jampel Syndrome: Two cases report
JOAO FRANCISCO TUSSOLINI, ISAC BRUCK, SERGIO ANTONIO ANTONIUK, LUCIA HELENA COUTINHO DOS SANTOS, DANIELLE CALDAS BUFARA RODRIGUES, ANA CRISTINA CRIPPA, PAULA VILAR, ALCIR FRANCISCO SILVA
Does Acute Motor Axonal Neuropathy hurt?
Mireya Milagros Bolo-Diaz, Jocelyn Montalvo-Ortiz, Leyda Sanchez-Ortiz, Marisel Vazquez-Correa, Maria Davila-Carlos
STIFF PERSON: PEDIATRIC CASE REPORT
Patricia Mohadeb, Eliana Cavassa, Gabriel Vazquez, Graciela Barbuzza, Pablo Jorrat, Angeles Schteinschnaider
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

EXPERIENCE WITH INDUCED HYPOTHERMIA AT A TERTIARY HOSPITAL IN A RESOURCE LIMITED SETTING: PRELIMINARY RESULTS
Firdose Lambey Nakwa, Sithembiso Christopher Velaphi
New antiepileptic drugs in newborns
Cecilia Verónica Vázquez, Marina Aberastury, Ines Denzler, Maria Magdalena Vaccarezza, Clarisa Maxit, Walter Horacio Silva, Guillermo Eduardo Agosta

Neurogenetics

AN APPROACH TO GENOTYPE-PHENOTYPE CORRELATION IN RETT SYNDROME
Paulina Carullo, Eliana Cavassa, Pablo Jorrat, Mario Massaro, Rita Valdez, Mercedes Villanueva, Angeles Schteinschnaider
Molecular characterization in children with attention deficit and hyperactivity disorder
Alberto Velez van Meerbeke, Jubby M Galvez, Claudia Talero-Gutierrez, Heidi Mateus, Dora J Fonseca
Mutation screening of FOXP2 gene in autism and Asperger syndrome
Michele Gea GUimaraes Pozzato, Patricia Maria de Carvalho Aguiar, Marcelo Rodrigues Masruha, Luiz Celso Pereira VIlanova
Tuberous Sclerosis Complex in Paraguay. Report of 8 cases.
Laura Patricia Arredondo, Zulma Irene Valenzuela, Zulma Irene Valenzuela, Carlos Franco, Carlos Franco, Néstor Waldemar Sánchez, Néstor Waldemar Sánchez, Fabiola Alarcón, Fabiola Alarcón, Marco Javier Casartelli, Marco Javier Casartelli
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
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
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
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
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

Neurocritical Care, Neurotrauma, Neuroprotection

ALTERAÇÕES AUTONÔMICAS EM EMPIEMA PLEURAL SEPTADO: RELATO DE DOIS CASOS PEDIÁTRICOS
Iara Gomes Bittencourt, Thaiza Falção, Rachel Guimarães, Cinthya Varandas, Francisco Meneses, Aialla Santos, Janeusa Leite Primo
Fatal Outcome Following First Infliximab Infusion in a Child with Inflammatory Bowel Disease
Fiona Mitchell Baumer, Niyati Mehta, Paul Rufo, Jodie Ouahed, Jay Thiagarajah, Menno Verhave, Michael Rivkin

Neuroradiology

An unusual cause of blindness: bilateral geniculate lesion.
Renata Resende Silva, Ellen Rocha Penna, Eduardo Ferracioli Fusão, Eliete Chiconelli Faria, Ricardo Silva Pinho, Luiz Celso Pereira Vilanova, Marcelo Masruha Rodrigues
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

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
Posterior Reversible Leukoencephalopathy Syndrome. Report of two cases.
Zulma Irene Valenzuela, Carlos Franco, Laura Patricia Arredondo, Nancy Garay, Jabibi Noguera, Marco Javier Casartelli
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
ANTI-GQ1B IGG ANTIBODY SYNDROME: MILLER FISHER SYNDROME AND BICKERSTAFF’S BRAINSTEM ENCEPHALITIS SUPERPOSITION
Pablo Jorrat, Gabriel Vazquez, Paulina Carullo, Angeles Schteinschnaider
Extensive unihemispheric white matter lesion as atypical presentation of X-linked adrenoleukodystrophy
Ellen Souza Siqueira, Bárbara Amorim Hackbart, Renato Nunes, Antônio Rocha, Ricardo Silva Pinho, Marcelo Masruha, Luiz Celso Vilanova
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
Mesenteric ischemia following immunoglobin infusion for treatment of anti-NMDA receptor encephalitis
Bárbara Amorim Hackbart, Ellen Souza Siqueira, Eduardo Fusão Ferracioli, Marcela Amaral Avelino, Ricardo Silva Pinho, Marcelo Masruha, Luiz Celso Vilanova
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
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

Stroke & Neurovascular Disorders

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
Epilepsy after presumed perinatal stroke
Rael Laugesaar, Anneli Kolk, Ulvi Vaher, Inga Talvik, Pilvi Ilves, Dagmar Loorits, Tiina Talvik
STURGE-WEBER: A retrospective study of 28 pacients
JOAO FRANCISCO TUSSOLINI, PAULA RUBIO VILAR, ISAC BRUCK, DANIELLE CALDAS BUFARA RODRIGUES, LUCIA HELENA COUTINHO DOS SANTOS, SERGIO ANTONIO ANTONIUK, ALCIR FRANCISCO SILVA

Headache

ACUTE HEADACHE AT THE EMERGENCY DEPARTMENT OF A PEDIATRIC HOSPITAL
Carolina Hortencia Vilte, CAROLINA HORTENCIA VILTE

Neurooncology

Gliomatosis Ceribri in childhood – case report
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
Spectrum of Neurological Complications in Childhood Malignancies-A Study from India
Lokesh Lingappa, sirisharani siddaiahgari, Darshak Makadia, Nikit Shah, Dandu Ravi Varma

Neurorehabilitation

Quality of life in children with Duchenne muscular dystrophy
TEREZA CRISTINA CARBONARI DE FARIA, Juliana Bassalobre Carvalho Borges, Gabriela de Andrade Vieira, Taciane Naressi Zambinati, Ligia Sousa, Marcelo Lourenço Silva


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