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Scheduled Conference Title
 
ICNC 2018 The Landscape of Genetic causes of basal ganglia and thalamus involvement in children based on the first 5000 MRI studies Abstract
SAAD ALSHAHWAN
 
ICNC 2018 The latest finding of genetic testing in Chinese patients with unexplained Epileptic encephalopathy(EE) Abstract
Sun Dan
 
ICNC 2018 The latest finding of genetic testing in Chinese patients with unexplained Epileptic encephalopathy(EE). Abstract
Liu Zhi Sheng
 
ICNC 2018 The mosaicism and incomplete penetrance of PCDH19 mutations Abstract
Aijie Liu, Xiaoxu Yang, Xiaoling Yang, Qixi Wu, Jing Zhang, Dan Sun, Zhixian Yang, Yuwu Jiang, Xiru Wu, Liping Wei, Yuehua Zhang
 
ICNC 2018 The neurological manifestations of lympho-haematopoietic malignancies Abstract
Dr Sonam Rameshchandra Kothari, Dr Shilpa Kulkarni, Dr Meghana Nadiger, Dr Anaita Udwadia Hegde, Dr K N Shah
 
ICNC 2018 The Perception and Performance of Headache Management among School Health Teachers Abstract
Young-Il Rho, Shin-Young Park, Mi-Sun Jang
 
ICNC 2018 The Perturbance of Microbiome and Gut Brain Axis in Autism Spectrum Disorders Abstract
Sue Xue Ming
 
ICNC 2018 The prevalence of parental ADHD in children newly diagnosed with ADHD in urban India Abstract
shriganesh patil, Abhinav Neela, Arpita Thakker, Smita Patil, Nandkishor Jadhav, Mona Gajre
 
ICNC 2018 The prevalence of parental ADHD in children newly diagnosed with ADHD in urban India Abstract
shriganesh patil
 
ICNC 2018 The prevalence of parental ADHD in children newly diagnosed with ADHD in urban India Abstract
shriganesh patil, Abhinav Neela, Arpita Thakker
 
ICNC 2018 The prevalence of parental ADHD in children newly diagnosed with ADHD in urban India Abstract
shriganesh patil, Abhinav Neela, Arpita Thakker, Smita Patil, Nandkishor Jadhav, Mona Gajre
 
ICNC 2018 The Quality of Life (QoL) in Indian Children with Learning Disorders – a case control study Abstract
lekha mishra
 
ICNC 2018 The Quality of Life (QoL) in Indian Children with Learning Disorders – a case control study Abstract
lekha mishra, jagruti bawa, smita patil, arpita thakker, manikantan r, mona gajre
 
ICNC 2018 The role of sleep and awake EEGs in detection of epileptiform discharges in pediatric population. Abstract
Nupur Sinha, Shilpa Kulkarni, Suresh Birajdar, Tushar Maniar
 
ICNC 2018 The sensory processing patterns of children with Autism Spectrum Disorder: Impact on behavior problems and adaptive behavior Abstract
MUTHUVEL RAJANGAM
 
ICNC 2018 The spectrum of clinical findings, radiological profile and genetics of Vanishing White Matter Disease from tertiary care center of Southern India. Abstract
Syed Shah Naseeruddin Sarmast
 
ICNC 2018 The spectrum of leukodystrophies in children: Experience at a tertiary care centre from North India Abstract
Biswaroop Chakrabarty, Priyanka Madaan, Puneet Jain, Sachendra Badal, Prashant Jauhari, Atin Kumar, Manisha Jana, Neerja Gupta, Madhulika Kabra, Sheffali Gulati
 
ICNC 2018 The Study of Genotype-phenotype Correlation in Patients with Alternating Hemiplegia of Childhood Abstract
Shupin Li,, Xiaoling Yang, Jiaoyang Chen, Qi Zeng, Jing Zhang, Yuehua Zhang
 
ICNC 2018 The Tonic Labyrinthine Response (TLR) also known as “Scissoring” is a hallmark of Dystonia Abstract
Federica Graziola
 
ICNC 2018 The Unified Batten Disease Rating Scale (UBDRS): Validation and Reliability in an Independent Sample Abstract
Jonathan W Mink, Miriam Nickel, Eva Wibbeler, Christoff Schwering, Angela Schulz
 
ICNC 2018 The value of mobile phone videos in increasing the diagnosis accuracy and saving cost of consultation for infant paroxysmal events: a prospective study in China Abstract
Lu-Lu Huang, Yang-Yang Wang, Li-Ying Liu, Hong-Ping Tang, Meng-Na Zhang, Shu-Fang Ma, Li-Ping Zou
 
ICNC 2018 THE СLINICAL CASE OF TOXIC CRANIAL NEUROPATHY IN A CHILD WITH NEUROBLASTOMA Abstract
Akmal Asatullayevic Mukhamedov
 
ICNC 2018 Therapeutic Antisense Oligonucleotides based Exon Skipping Gene Editing Strategies in Duchenne Muscular Dystrophy Abstract
Arun Shastry
 
ICNC 2018 Therapeutic plasma exchange in inflammatory demyelinating CNS syndromes in paediatric patients Abstract
Silvia Noemi Tenembaum, Andrea Savransky, Marina Huaman Rios, Silvana Liz Vergel, Mabel Castro Velasquez, Sara Perez Sierra, Gabriela Marcarian, Romina Alba, Ana Maria Pugliese
 
ICNC 2018 Three Cases Of Creatine Deficiency Syndromes Caused By GAMT Gene Mutation Abstract
Lei Yang, Fang Fang
 
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