Browse Title Index


 
Scheduled Conference Title
 
ICNC 2018 Cerebral Sinovenous Thrombosis in Children: Single Center Experience Abstract
İpek Dokurel Cetin, Hepsen Mine SERIN, Cenk Eraslan, Erdem Simsek, Seda Kanmaz, Sanem Yilmaz, Gul Aktan, Hasan Tekgul, Sarenur Gokben
 
ICNC 2018 Cerebral Sinus Venous Thrombosis as the Initial Presentation in a Child with Homocystinuria : Case Report . Abstract
Amal Yousef Kentab, Amal Y. Kentab, Hamdy H. Hassan
 
ICNC 2018 Cerebral vision impairment in children: How much of it is preventable? Abstract
Ramesh Konanki, Sravanthi Kuruva, Lokesh Lingappa, Nikit Milind Shah, Srikanth Domala
 
ICNC 2018 CHALLENGES IN CLINICAL INTERPRETATION OF NEW MUTATIONS IN RARE CONDITIONS Abstract
Diana Gabriela Barca, Sorina Mihaela Papuc, Carmen Burloiu, Aurora Arghir, Magdalena Budisteanu
 
ICNC 2018 Challenges in diagnosis and management of Acute Necrotising Encephalitis in a large South African family with RANBP2 mutation Abstract
Gillian Tracy Riordan, Alvin Ndondo, Sara Seneca, Karen Fieggen, Jo Wilmshurst
 
ICNC 2018 Changing face of Pediatric Neurotuberculosis. Abstract
Kritika Tiwari, Purva Keni Karnavat, Anaita Udwadia Hegde
 
ICNC 2018 Characteristics of exosomes in the cerebrospinal fluid of preterm infants Abstract
Robert Spaull, Bryony McPherson, Andriana Gialeli, Aled Clayton, James Uney, Oscar Cordero-Llana, Axel Heep
 
ICNC 2018 Chikungunya infection and Horner Syndrome: a case report Abstract
Lucas Victor Alves, Filipe Marinho Pinheiro Câmara, Mayara Batista Granhara, Alfredo Meneses Neto, João Guilherme Bezerra Alves
 
ICNC 2018 CHILDHOOD ONSET CHRONIC ATAXIA: A CLINICAL, ETIOPATHOLOGICAL, RADIOLOGIC AND GENETIC AUDIT. Abstract
Pallavi Shriram Todase, shilpa kulkarni, sonam kothari, anaita hegde, krishankumar shah
 
ICNC 2018 Childhood Onset Limb Girdle Muscular Dystrophies in Aegean Part of Turkey Abstract
Uluç Yiş, Gülden Diniz, Filiz Hazan, hülya sevcan daimagüler, bahar toklu baysal, figen baydan, gülçin akıncı, aycan ünalp, gül aktan, erhan bayram, semra hız, cem paketçi, derya okur, erdener özer, ayça ersen danyeli, gökhan uyanık, sebahattin çırak
 
ICNC 2018 Children's Pathology Leading to Disruption of Object Relations Abstract
Umesh Jain
 
ICNC 2018 Chronic Lymphocytic Inflammation With Pontine Perivascular Enhancement Responsive To Steroids (CLIPPERS) Abstract
Manish Prasad
 
ICNC 2018 Classifying Electroencephalographic Diagnoses of Epilepsy without Epileptiform Discharges and Nonepileptic Paroxysmal Events Using Deep Convolutional Neural Networks Abstract
Lung-Chang Lin, Chen-Sen Ouyang, Ching-Tai Chiang, Rong-Ching Wu, Hui-Chuan Wu, Rei-Cheng Yang
 
ICNC 2018 Clinical and Genetic Spectrum of Disorders with Cerebellar Atrophy Abstract
Ramya Bandi, lokesh lingappa, Prasanthi Aripirala, Rini Kothari, Ramesh Konanki, Nikit Milind Shah, Smilu Mohanlal, Thenral SG, Ramprasad VL
 
ICNC 2018 Clinical & Neuro-Imaging Changes of Subacute sclerosing panencephalitis- Experience 30 Cases in Tertiary Care Center in Bangladesh Abstract
Gopen Kumar Kundu
 
ICNC 2018 Clinical & Neuro-Imaging Changes of Subacute sclerosing panencephalitis- Experience 30 Cases in Tertiary Care Center in Bangladesh Abstract
Gopen Kumar Kundu
 
ICNC 2018 Clinical and EEG characteristics of epilepsy of infancy with migrating focal seizures Abstract
Shuqian Zhang, Ruopeng Sun, Baomin Li
 
ICNC 2018 Clinical and genetic analysis in three Chinese patients with congenital disorder of glycosylation Abstract
Changhong Ren, Fang Fang, Changhong Ding
 
ICNC 2018 Clinical and genetic analysis of progressive cavitating leukoencephalopathy in China Abstract
Ren Changhong, Fang Fang, Zhimei Liu
 
ICNC 2018 Clinical and genetic characteristics of congenital myasthenia syndrome with episodic apnea caused by CHAT gene mutation in China Abstract
Zhimei Liu, Fang Fang
 
ICNC 2018 Clinical and genetic characteristics of GDAP1 gene mutation in Charcot Marie Tooth disease Abstract
JUN LAN LU, JUN LAN LU
 
ICNC 2018 Clinical and Genetic Correlation in Childhood Onset Pharmacoresistant Epilepsy Abstract
Ami Shah, Neeta Naik, Abhinav Sahu, Abhinav Tiwari Tiwari
 
ICNC 2018 Clinical and genetic studies on fifteen patients with tyrosine hydroxylase deficiency Abstract
Yao Zhang
 
ICNC 2018 Clinical and hereditary characteristics of MECP2 duplication syndrome in Chinese patients Abstract
zhanwen he, Xiangyang Luo, Liyang Liang
 
ICNC 2018 Clinical and Imaging Characteristics of Subependymal Giant Cell Astrocytoma in Patients with Tuberous Sclerosis Complex included in TOSCA – TuberOus SClerosis Registry to IncreAse Disease Awareness Abstract
Anna C Jansen, 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, Rima Nabbout, Finbar O’Callaghan, Jiong Qin, Valentin Sander, Matthias Sauter, Seema Shah, Yukitoshi Takahashi, Renaud Touraine, Sotiris Youroukos, Bernard Zonnenberg, John C Kingswood
 
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