18 results on '"Kannan, Varun"'
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2. Initial MRI, EEG, and CSF White Cell Count Are Abnormal in Children with Anti-NMDA Receptor Encephalitis with Isolated Psychiatric Symptoms (P6-14.020)
3. Biallelic variation in the choline and ethanolamine transporter FLVCR1 underlies a pleiotropic disease spectrum from adult neurodegeneration to severe developmental disorders
4. Assessing Needs and Perceptions of Research Participation in Pediatric-Onset Multiple Sclerosis: A Multistakeholder Survey
5. Pediatric Neuroinflammatory Diseases in the Intensive Care Unit
6. Anterior cervical discectomy and fusion for the treatment of pediatric Hirayama disease
7. “Fifth‐day fits” revisited: A literature review of benign idiopathic neonatal seizures and comparison with KCNQ2‐ and KCNQ3‐associated benign familial epilepsy syndromes
8. Differential responses of disease‐related GRIN variants located in pore‐forming M2 domain of N‐methyl‐D‐aspartate receptor to FDA‐approved inhibitors
9. Infectious profiles in pediatric anti-N-methyl-d-aspartate receptor encephalitis
10. Arterial Spin Labeling Changes Parallel Asymmetric Perisylvian and Perirolandic Symptoms in 3 Pediatric Cases of Anti-NMDAR Encephalitis
11. Fulminant Anti-MOG-Associated Cortical Encephalitis: Case Series of a Distinct Pediatric MOGAD Encephalitic Phenotype
12. Refractory Pediatric NMDA Receptor Encephalitis: A Case Series
13. Posterior Reversible Encephalopathy Syndrome in a Child with Sickle Cell Disease and SARS-CoV-2 Infection
14. 793: USE OF INTRA-ARTERIAL VERAPAMIL IN AN INFANT WITH CEREBRAL VASOSPASM FROM SUBARACHNOID HEMORRHAGE
15. Partial Duplication of the Lateral Semicircular Canal—A Novel Anatomical Malformation in a Child with Barakat Syndrome
16. De novoGRINvariants in NMDA receptor M2 channel pore‐forming loop are associated with neurological diseases
17. Heterogeneous clinical and functional features of GRIN2D-related developmental and epileptic encephalopathy
18. De novo mutations in GRIN1 cause extensive bilateral polymicrogyria
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