| Scheduled Conference | Title | |
| ICNC 2018 | Tics in a child with Hashimoto encephalopathy | Abstract |
| Padma Balaji, Vasanthi Thiruvengadam, Ashish Badaya | ||
| ICNC 2018 | TITLE: PAROXYSMAL NON-EPILEPTIC EVENTS IN A PEDIATRIC EPILEPSY CLINIC: A PROSPECTIVE STUDY | Abstract |
| Neelu desai | ||
| ICNC 2018 | TITLE: Spectrum of Neurocutaneous Disorders in Pediatric Neurology Clinic in Western Rajasthan | Abstract |
| Ankit Manoj Panday | ||
| ICNC 2018 | TITLE: Status of Genetic Counselling in Hereditary Neurogenetic disorders: A clinic-epidemiologic study in Western Rajasthan | Abstract |
| Ankit Manoj Panday | ||
| ICNC 2018 | To address the issue comprehensively by measuring various neurobiological parameters exclusively in children and adolescents and an effort to bridge the gap between childhood and adult aggressive behavior. | Abstract |
| P K Maheshwari, Sagar Lavania, Vishwas K | ||
| ICNC 2018 | To study correlation of social emotional and communication scores based on Development profile 3 test and the Childhood Autism Rating Scale ( CARS) scores in children fulfilling the DSM V criteria for Autism Spectrum disorder. | Abstract |
| Shambhavi Seth, Satinder Walia, Zeba Parveen | ||
| ICNC 2018 | To test if separation anxiety(SA) is absent/attenuated in autistic children | Abstract |
| Nisreen Hussain Bohra | ||
| ICNC 2018 | Tolerance to cannabidiol in children and adults with treatment-resistant epilepsy | Abstract |
| Shimrit Uliel-Sibony, Moran Hausman-Kedem, Uri Kramer | ||
| ICNC 2018 | Top 15 research priorities in tuberous sclerosis complex | Abstract |
| Anna Jansen, Eva Schoeters, Alain Wouters, Peter Raeymaekers | ||
| ICNC 2018 | Tourette syndrome -a developmental dopamine disorder | Abstract |
| Yoshiko Nomura | ||
| ICNC 2018 | Transcranial magnetic stimulation in the treatment of Tourette's syndrome in children: A pilot study | Abstract |
| Cynthia K Kahl, Adam Kirton, Tamara Pringsheim, Paul Croarkin, Rose Swansburg, Ephrem Zewdie, Frank P MacMaster | ||
| ICNC 2018 | Transition to adult medical care for adolescents with epilepsy-identifying care gaps in current models: Perspectives from a UK neurology tertiary centre | Abstract |
| Thomas Robb | ||
| ICNC 2018 | Treatable Leigh syndrome involving mitochondrial cofactor metabolism | Abstract |
| Zhimei Liu, Fang Fang | ||
| ICNC 2018 | Treatment approach for neonates with acute symptomatic seizures influences length of hospital stay | Abstract |
| Hannah C. Glass | ||
| ICNC 2018 | Treatment outcome of children with Congenital CMV infection at ICH and Dr. MR Khan Shishu(Children) Hospital | Abstract |
| MASHAYA ZAMAN KOLI, SELINA HUSNA BANU, RAWNAK ARA | ||
| ICNC 2018 | TRPM6 gene mutation resulted in primary hypomagnesemia with secondary hypocalcemia（HSH） in 3 cases | Abstract |
| xiaohui wang, shen zhang, weihua zhang, jiuwei li, changhong ding, fang fang | ||
| ICNC 2018 | Tuberous Sclerosis Complex (TSC) - Associated Epilepsy: Final Results from the TOSCA Study | Abstract |
| Rima Nabbout, Elena Belousova, Mirjana P Benedik, Tom Carter, Vincent Cottin, Paolo Curatolo, Maria Dahlin, Lisa D´Amato, Guillaume B d'Augères, Petrus J De Vries, José C Ferreira, Martha Feucht, Carla Fladrowski, Christoph Hertzberg, Sergiusz Jozwiak, John A Lawson, Alfons Macaya, Ruben Marques, Finbar O’Callaghan, Jiong Qin, Valentin Sander, Matthias Sauter, Seema Shah, Yukitoshi Takahashi, Renaud Touraine, Sotiris Youroukos, Bernard Zonnenberg, Anna C Jansen, John C Kingswood | ||
| ICNC 2018 | Tuberous Sclerosis Complex (TSC)-Associated Neuropsychiatric Disorders (TAND): New Findings on Age, Gender and Genotype in Relation to Intellectual Phenotype | Abstract |
| Petrus J De Vries, Elena Belousova, Mirjana P Benedik, Tom Carter, Vincent Cottin, Paolo Curatolo, Maria Dahlin, Lisa D´Amato, Guillaume B d'Augères, José C Ferreira, Martha Feucht, Carla Fladrowski, Christoph Hertzberg, Sergiusz Jozwiak, John A Lawson, Alfons Macaya, Ruben Marques, Rima Nabbout, Finbar O’Callaghan, Jiong Qin, Valentin Sander, Matthias Sauter, Seema Shah, Yukitoshi Takahashi, Renaud Touraine, Sotiris Youroukos, Bernard Zonnenberg, John C Kingswood, Anna C Jansen | ||
| ICNC 2018 | Two Different Phenotypes of Tyrosine Hydroxylase Deficiency Syndrome | Abstract |
| Punita Chandra Segaran, Tajudin Tajul Ariffin | ||
| ICNC 2018 | Two distinct phenotypes caused by the same mutation in the SAMHD1 gene | Abstract |
| Serdal Gungor, Derya Okur, Elmasnur Yilmaz, Ana Topf, Rita Horvath, Hanns Lochmuller, Bilge Ozgor, Ece Sonmezler, Uluc Yis, Ahmet Yaramis, Yavuz Oktay, Semra Hiz | ||
| ICNC 2018 | Two novel PCDH19 missense mutations in a mosaic male and a female epilepsy patients | Abstract |
| Qian Peng, Haiming Yuan | ||
| ICNC 2018 | Two Siblings with Congenital Myotonia carrying a New Mutation in the CLCN 1 Gene | Abstract |
| Nezir Özgün | ||
| ICNC 2018 | UK initiative to speed up diagnosis of Duchenne muscular dystrophy worldwide | Abstract |
| Henriette van Ruiten, Mayhew Anna, Helen Aspey, Robert Muni Lofra, Volker Straub, Michela Guglieri | ||
| ICNC 2018 | Unsolved mystery:11-year-old patient with antibody negative immune-mediated necrotizing myopathy | Abstract |
| Cemal Karakas, Jeetendra Sah, Yaacov Anziska, Yoshimi Hisamoto, Radha Giridharan, Joan Cracco, Alexandra Reznikov, Geetha Chari | ||
| ICNC 2018 | Unusual Presentation of 4H Syndrome as Post Varicella Ataxia | Abstract |
| Ridhimaa Jain, Aman Elwadhi, Suvasini Sharma, Nicole Wolf, Resie M van Spaendonk, Bijoy Patra | ||
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