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
Prevalence & Risk Factors for neurological disorders in children aged 9-15 years in northern India
Rashmi Kumar, Anupama Bhave, Roli Bhargava, Girdhar Agarwal
My Special Case: A Rare Storm In Pediatrics
Mahmoud Ibrahim Abeidah
EVALUATION NUTRITIONAL AND GASTROINTESTINAL DISORDERS IN HEALTHY AND CEREBRAL PALSY PATIENTS
DANIELLE CALDAS BUFARA RODRIGUES, LUCIA HELENA COUTINHO SANTOS, ISAC BRUCK, SERGIO ANTONIO ANTONIUK, ANA CRISTINA CRIPPA, ALCIR FRANCISCO SILVA

CNS Infections

Herpes-simplex encephalitis in patients with onco-hematological disease
Mariana González Suarez, Lorena Ornella, Maria Belen Ramirez, Carlos Rugilo, Hugo Arroyo
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

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
Pharmacokinetics and pharmacodynamics of the prodrug stimulant lisdexamfetamine dimesylate in children and adolescents with ADHD
Claudia Gasparian, David R Coghill, Shaw Sorooshian, James Ermer, Ben Adeyi, Liza A Squires, Richard Civil
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
THE IMPORTANCE OF IDENTIFYING NEUROPSYCHOMOTOR DELAYS IN THE DEVELOPMENT OF YOUNG CHILDREN
MARCIA REGINA MACHADO SANTOS VALIATI, sergio antonio antoniuk
The Influence of Fish Oil on Neurological Development and Function
Noran M Abu-Ouf, Mohammed M Jan
Intuitive physics in high functioning autists
Cristina Maria Pozzi, Francisco B Assumpção Jr
Twin-twin transfusion syndrome: follow up of infants treated with laser surgery
Marilisa M Guerreiro, Amabile V. Arias, Denise Campos, Thatiane C. Zanelli, Daniela S. Souza, Orlando G. Santos Neto, Cleisson F. Peralta
STUDY OF AUDITORY PROCESSING IN CHILDREN WITH AUTISTIC DISORDER
hesham saad kozou, rania mohamed abdou, hanan galal azouz, mona mohamed khalil
Adaptation of the Vineland Adaptive Behavior Scale and its use in 3-9 year old Indian Children
Rashmi Kumar, Kaushaki Shanker, Vima Kush, Chandrakanta Kumar, Anupama Bhave, Vivek Agarwal
PANDAS Diagnosis in the Ultimate Context of Pediatric Neurology
Carolina Carvalho, Iaciara Souza, Daniella Nazzetta, Anna Silva, Aline Domingues, Adriana Santos, Liubiana Araujo
Evaluation of adaptive profiles of Indian children aged 2 – 9 years with Autism Spectrum Disorder
Sharmila Banerjee Mukherjee, Manoj Malhotra, Satinder Aneja
Diagnostic accuracy of 'Indian Scale of Assessment of Autism (ISAA)' in 2 – 9 year old Indian children with Autism Spectrum Disorder
Sharmila Banerjee Mukherjee, Manoj Kumar Malhotra, Satinder Aneja
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
"Is Autism a Curable Disease: The Successful OSHA Program From Alex"
hussein hosny abdeldayem, omayma abdelhamid Selim
Autism Spectrum Disorders in a Brazilian Developmental Disorders Project
Cristina Maria Pozzi, Alessandra Freitas Russo, Milena Rossetti, Francisco Baptista Assumpção Jr
Effects of stimulant medications for Attention Deficit/ Hyperactivity Disorder: study of 452 Brazilian patients
sergio antonio antoniuk, Mariane Wehmuth, Mariana Richartz
Unexpected Subclinical Spikes: Clinical and Neuropsychological Correlations
Mark Mintz, Maliheh Mohamadpour, Jeffrey Keating, Madeline Chadehumbe, Greg Alberts, Sarah Woldoff, Laura Szklarski

Epilepsy

Clinical, EEG and imaging characteristics of children with Sturge-Weber syndrome: A prospective, longitudinal study
Csaba Juhasz, Eishi Asano, Michael E. Behen, William C. Guy, Otto Muzik, Harry T. Chugani
USEFULNESS OF VIDEO-EEG MONITORING IN CHILDREN
Betiana G Comas, Nicolas Espinosa, Marina Aberastury, Brenda Giagante, Clarisa Maxit, Maria Vaccarezza, Guillermo Agosta, Walter Silva
Efficacy and Tolerability of the Modified Atkins Diet in young children with refractory epilepsy
Ranju Mehta, Suvasini Sharma, Puneet Jain, Satinder Aneja, Anju Seth
Parent's Knowledge and Attitudes toward Children with Epilepsy
Lama E Zainy, Daniah M Atteyah, Walaa M Aldisi, Hanadi A Abdulkarim, Rawia F Alhelo, Haneen A Alhelali, Mohammed M Jan
Autoimmune Encephalitis with Anti-VGKC Antibodies Mimicking HSV Encephalitis in a Teenage Boy
Huiyuan Jiang, Cresha Davis, Addulradha Alqallaf
Quantification of connectivity strength between epileptogenic cortex and remote FDG PET abnormalities in children with ETL epilepsy
Otto Muzik, Csaba Juhasz, Eishi Asano, Harry Chugani
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
Ketogenic Diet Efficacy in the Treatment of Intractable Epileptic Spasms
Ahmed Tawfik Abdelmoity, Husam Kayyali, Megan Gustafson
The simultaneous use of Ketogenic diet and Vagus Nerve Stimulator in patients with pharmacologically refractory epilepsy
Ahmed Tawfik Abdelmoity, Kamie Mceachran, Megan Gustafson, Tara Myers, Erin Fecske
Primary School Teacher's knowledge and attitudes toward children with epilepsy
Albaraa S Abulhamail, Fahad E Al-Sulami, Mouneeb A Alnouri, Najeeb M Mahrous, Dima G Joharji, Maha M Albogami, Mohammed M Jan
Assessment of the Implementation of the Epilepsy Quality Measures in the Commission for Children with Special Health Care Needs (CCSHCN)
Alejandra Maria Stewart, Muhammad Affan, Heather Mckee, Gulam Khan, Robert Baumann, Meriem Bensalem-Owen
Nodding syndrome patients improve with symptomatic treatment
Richard Idro, Brian Byamah Mutamba, Hanifa Namusoke, Robert Opika Opoka, Angelina Kakooza-Mwesige, Catherine Abbo, Abdu Musubire, Bernard Toilva Opar
Clinical profile of children with late onset spasms - A report of 24 cases
Satinder Aneja, Puneet Jain, Suvasini Sharma, Bijoy Patra, Jayashankar Kaushik, Prabaharan Chellamuthu, Vedavathi Kunnanayaka
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
MULTIMODAL INTRAOPERATIVE MONITORING IN SPINAL SURGERY: RETROSPECTIVE MULTICENTRIC ANALYSIS AND RECOMENDATIONS BASED IN 1890 CASES.
Guillermo Agosta, Javier Muntadas, Mariana Bendersky, Adrian Albajari, Silvana Claigaris
Infantile spasms: Ictal video-EEG classification based on the Delphi West Group proposal
Marina Aberastury, Betiana Comas, Nicolas Espinosa, Fernanda Rios Pistoia, Guillermo Agosta, Walter Silva
Effectiveness and safety of ketogenic diet in a population of drug resistant epilepsy
Maria Magdalena Vaccarezza, Marisol Toma, Alejandra Gonzalez, Guillermo Agosta
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 of status epilepticus
Marina Aberastury, Betiana Comas, Maria del Carmen Garcia, Ana Gabriela Besocke, Carlos Ciraolo, Guillermo Agosta, Walter Silva
SAFETY, FEASIBILITY AND EFFECTIVENESS OF ORAL ZONISAMIDE MONOTHERAPY IN COMPARISON WITH INTRAMUSCULAR ADRENOCORTICOTROPIC HORMONE IN INFANTS WITH WEST SYNDROME
Dhanalakshmi A, Jitendra Kumar Sahu, Pratibha Singhi
“Epilepsy Transition: challenges of caring for adults with childhood-onset seizures”
Felippe Borlot, Jose Francisco Tellez-Zenteno, Anita Allen, Anfal Ali, O Carter Snead III, Danielle M Andrade
Head-to-Head Comparison of Ketogenic Diet and Vagus Nerve Stimulation in Paediatric Population with Pharamacoresistant Epilepsies
Ramalakshmi Ramiah, Nikil Sudarsan, Sunny Philip, Vanessa Hopkins, Shakti Agrawal
Surgical treatment of status epilepticus
Betiana G Comas, Marina Aberastury, Maria Garcia, Gabriela Besocke, Carlos Ciraolo, Guillermo Agosta, Walter Silva
Morbidity in epilepsy surgery using grids or depth electrodes or combined implantations
Betiana G Comas, Marina Aberastury, Daniela Benech, Gabriela Besoke, Carina Maineri, Carlos Ciraolo, Maria Garcia, Guillermo Agosta, Walter Silva
PREVALENCE OF FEBRILE SEIZURE – A POPULATION-BASED STUDY
Juliane Sauter Dalbem, Heloise Helena Siqueira, Regina Papais Alvarenga
Hot executive functionm in children with epilepsy
Luciane Lorencetti Lunardi, Daniel Fuentes, Mirela Boscariol, Catarina Abraão, Marilisa Mantovani Guerreiro
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
Sustained short term spasm control with intramuscular ACTH or oral prednisolone: Randamised, single blind clinical trial – preliminary report
Jithangi Wanigasinghe, Carukshi Arambepola, Shalini SriRanganathan, Samanmali Sumanasena, Eindrini Muhandirum, Gangani Attanepola
Seizure and Developmental Outcome of Infantile (epileptic) Spasms Starting as FE in Early Infancy
Siddharth Jain, Sunny Philip, Leslie Notghi, Shakti Agrawal
The Knock in mouse model of Alternating Hemiplegia of Childhood
Ute Hochgeschwender, Amanda Swearingen, Stacy Forbes, Arsen Hunanyan, Eric Arehart, Mohamad A Mikati

Metabolic Disorders

COENZYME Q10 DEFICIENCY: CLINICAL AND BIOCHEMICAL CHARACTERIZATION
Juliana Harumi Arita, José Luiz Pedroso, Priscila Bezerra Bacetti, Priscila Meira Oliveira, Mario Henrique Barros, Marcelo Rodrigues Masruha, Orlando Graziani Povoas Barsottini, Claudia Cristina Ferreiro Barros
Clinical profile of children with biotinidase deficiency and response to oral biotin therapy: Experience from a developing country
Pratibha Singhi, Arushi Gahlot Saini, Puneet Jain, Savita Attri, Renu Suthar, Jitendra Kumar Sahu, Naveen Sankhyan, N Khandelwal
2-HydroxyGlutaric Aciduria in Saudi Arabia
Majed J. Dasouki, Lujane Yousef, Minnie Jacob, Asmahan Ahmad, Ekhlass Quraan, Basma AlRasheed, Ali Odaib, Mohamed Alamoodi
“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
“Remote Spinal Cord Injury in Mucopolysaccharidosis type IVA after Cervical Decompression”
Felippe Borlot, Paula R Arantes, Alberto Capel Cardoso, Chong Ae Kim
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
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
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
"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
An experience of childhood neurometabolic diseases registry in Iran,2010-2012
Mahmoud Reza Ashrafi, Alireza Tavasoli
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
Characterization of behavioral and seizure related manifestations of guanidinoacetate-methyltransferase deficiency.
Gulcin Akinci, Unsal Yilmaz, Orkide Guzel, Gajja S Salomons
Management of patients with adrenoleukodystrophy
Gabriela Del Pilar Reyes Valenzuela, Carlos Figueroa, Raquel Staciuk, Hernan Eiroa, Carlos Rugilo, Hugo A. Arroyo

Movement Disorders

Movement Disorders in the Neuronal Ceroid Lipofusinoses
Jonathan W Mink, Erika F Augustine, The Batten Study Group
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
METHODOLOGY OF APPROACHES TO CHILDHOOD HEREDITARY ATAXIAS
Elif Acar Arslan, Rahşan Gocmen, Kader K. Oguz, Gokcen Duzgun, Haluk Topaloglu, Meral Topcu
Botulinum toxin- A in pediatric stiff hips
Tamer Rizk, Yasser Awaad
Primary myoclonus-dystonia – Often underdiagnosed entity: Report of four affected families
Puneet Jain, Suvasini Sharma, Satinder Aneja

Muscle and Nerve

Enterovirus 71 associated lower motor neuron disease in infants and children
T Kandula, HL Teoh, I Andrews, A Bye, MA Farrar
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
Sibling-pair with Mitofusin 2 mutation
Siddharth Jain, Tracy Willis, Evangeline Wassmer, Shakti Agrawal
Psychosocial intervention programme for families of patients with Duchenne Muscular Dystrophy
Priya Treesa Thomas, Prakashi Rajaram, Nalini A
ARRAY-CGH TECHNOLOGY IN THE DISCOVERY OF X-CHROMOSOME COPY NUMBER VARIANTS IN MALE PATIENTS WITH MENTAL RETARDATION SYNDROMES
Arif Anwar, Malinee Thambyayah, Eldarina Azfar Wijaya, Farah Liyana Abdul Aziz, Farhanah Abdul Aziz, Nurul Shielawati Mohamed Rosli, Nur Aaina Mohd Mohayadi, Lock-Hock Ngu, Rozaimi Mohamad Razali
Infantile Axonal Neuropathy -a case series
Nikil Sudarsan, Evangeline Wassmer, Sunny Philip, Shakti Agrawal
Triplication of PMP22 gene region associated with Charcot-Marie-Tooth disease-1A
Manjeet Singh Raina, Shakti Agrawal
A child with anti-GQ1b syndrome presenting with complete ophthalmoplegia and unilateral facial palsy.
Puneet Jain, Suvasini Sharma, Satinder Aneja, Hina Kausar
Unusual neuroimaging findings in two families with giant axonal neuropathy
Suvasini Sharma, Puneet Jain, Mahesh Kamate, Virupaxi Hattiholi, Anita Mahadevan, Bijoy Patra, Satinder Aneja
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
CMTPedS.br: Brazilian version of the Charcot-Marie-Tooth Pediatric scale
Anita Saporta, Mario Saporta, Marcia Ribeiro, Alexandra Araujo
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

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
Altered expression of non-neuronal cells in normal and Down syndrome developing brain
takeshi kanaumi, Ivan Milenkovic, Homa Adle-Biassette, Eleonora Aronica, Atsushi Ogawa, Gabor Geza Kovacs
New antiepileptic drugs in newborns
Cecilia Verónica Vázquez, Marina Aberastury, Ines Denzler, Maria Magdalena Vaccarezza, Clarisa Maxit, Walter Horacio Silva, Guillermo Eduardo Agosta
EEG Monitoring in preterm neonates using a new portable EEG device – microEEG®
Geetha Chari, Zachary Ibrahim, Roger Kim, Samah Abdul Baki, Joan B Cracco, Jacob Aranda
HYPOMELANOSIS OF ITO ASSOCIATED WITH MULTIPLE BRAIN MALFORMATIONS
Bosanka Jocic-Jakubi, MARINA JOVANOVIC, IVANA MARKOVIC, RIMA AL SAWAN

Neurogenetics

Identification of genes for autosomal recessive microcephaly by whole-exome sequencing
Ganeshwaran H. Mochida, Timothy W. Yu, R. Sean Hill, Anna Rajab, Samir Khalil, Klaus Schmitz-Abe, Sarah Servattalab, Malak El-Quessny, Almundher Al-Maawali, Jennifer N. Partlow, Brenda J. Barry, Muna Al-Saffar, Christopher A. Walsh
Outcome of Hematopoietic Stem Cell Tranplant (HCT) in childhood cerebral Adrenoleukodystrophy (CCALD): a Multi-Institutional Study
Asif M Paker, Patrick Aubourg, Maria L Escolar, Joanne Kurtzberg, Susan Paadre, John J Balser, Paul Orchard, Gerald V Raymond
Episodic weakness, cerebellar ataxia, deafness and optic atrophy - a new phenotype of a novel ATP1A3 mutation
Bruria Ben-Zeev, Gali Heimer, Lorri Israelian, Yair Zadaka, Alessandra Ruggieri, Christian Marshall, Stephen Walter Scherer, Yair Anikster, Andreea Nissenkorn, Berge A. Minassian
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
Pellagra-like Syndrome Proves to be a Variant of Xeroderma Pigmentosum-Cockayne Syndrome and Niacin Confers Clinical Benefit
Mustafa Abdalla Salih, Hadia Hijazi, Muddathir H Hamad, Hamdy H. Hassan, Shifa B Salih, Khalid A Mohamed, Maowia M Mukhtar, Zein A Karrar, Shinu Ansari, Fowzan S Alkuraya
Case Report: Joubert Syndrome
GIULIANA FRANZAGO SALMAZO, RUBENS WAJNSZTEJN, PAULO BREINIS, ROBERTA CARAMICO PINTO, DANIELA FONTES BEZERRA, FLAVIO GERALDES ALVES, CAMILA EXPOSTO ALVES, RAFAEL GUERRA CINTRA, DEBORA ALMEIDA, REGIA GASPARETTO, PRISCILA PASSARELI, BRUNA DA CRUZ BEYRUTH BORGES, PATRICIA OLIVEIRA MEIRELES MARIANO COSTA
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
Prevalence of LIS1 and related genes mutations in a population sample of 109 patients with structural CNS abnormalities.
Francisco Carratalá-Marco, Patricia Andreo-Lillo, Teresa Escamez, Arancha Botella, Salvador Martínez
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

Neurocritical Care, Neurotrauma, Neuroprotection

A CASE WİTH DİFFUSE AXONAL İNJURY PRESENTED RİGHT HEMİPARESİS
Meltem Uzun, meltem uzun, öykü şerife öztürk, murat serhat aygün

Neuroradiology

EVALUATION OF THE NERVE CONDUCTION STUDIES AND AUTONOMIC FUNCTIONS IN PATIENTS WITH AGENESIS OF CORPUS CALLOSUM
Erhan Bayram, Ozlem Akdogan, yasemin topcu, pakize karaoglu, uluc yis, ibrahim oztura, semra hiz kurul
Inherited manganism: typical clinical and neuroimaging features
Marcela Amaral Avelino
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
Neurofibromatosis Type 1 (NF1) in children and Unidentified Bright Objects (UBOs) on Magnetic Resonance imaging (MRI).
Rita Ilari, Maria Luz Fernandez, Celeste Puga, Vaucheret Esteban, Maria Fernanda Rios Pistoia, Micaela Pauni, Guillermo Agosta

Neuroimmunology

Clinical outcomes in children younger than 12 years with multiple sclerosis treated with subcutaneous interferon beta-1a: subgroup analysis of a retrospective study (REPLAY)
Silvia Noemi Tenembaum, Lauren B Krupp, Daniela Pohl, Alexey Boyko, Brenda Banwell, Ernesto Aycardi, Liang Chen, Angelo Ghezzi
NON-TRAUMATIC ACUTE MYELOPHATY: A SERIES OF 76 CASES
andrea savransky, natalia cejas bestard, maria belen ramirez, mauricio zapata, carlos rugilo, Silvia Tenembaum, Hugo Arroyo
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).
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