32 results on '"Iype, Mary"'
Search Results
2. Long-term survival and factors associated with mortality among children with infantile epileptic spasms syndrome – A retrospective cohort study
3. Congenital muscular dystrophy due to POMGNT1 mutation presenting as cardioembolic stroke
4. Hypomethylation of Wnt signaling regulator genes in developmental language disorder
5. The genetic landscape of polymicrogyria
6. MECP2 Mutations in the Rett Syndrome Patients from South India
7. Short term outcome of ADEM: Results from a retrospective cohort study from South India
8. Dravet syndrome presenting with extrapyramidal features, ataxia and basal ganglia hyperintensity on brain magnetic resonance imaging
9. Mitochondrial dysfunction in cognitive neurodevelopmental disorders: Cause or effect?
10. Knowledge, Attitude, and Practices of Primary and Secondary School Teachers on Specific Learning Disorder
11. Epileptic Syndromes
12. The genetic landscape of polymicrogyria
13. Baller-Gerold syndrome: Further evidence for association with prenatal exposure to valproate
14. Viral Encephalitis
15. Vitamins and Cognition: A Nutrigenomics Perspective
16. Mutations in the Rett Syndrome Patients from South India.
17. IMPACT OF A SHORT TERM AWARENESS TEACHING PROGRAMME ON PRIMARY AND MIDDLE SCHOOL TEACHERS ABOUT THE NEUROLOGICAL FACTORS THAT AFFECT LEARNING DISABILITY
18. Management of Infantile Spasms: An Updated Review
19. The early electroclinical manifestations of infantile spasms: A video EEG study
20. Factors Related to Long Term Motor, Behavioral, and Scholastic Outcome in Children with Acute Disseminated Encephalomyelitis
21. Hypomelanosis of Ito with cerebral malformation
22. Callosal agenesis and open lip schizencephaly
23. An uncommon presentation of hexosaminidase deficiency
24. Additional file 1: of A large Indian family with rearrangement of chromosome 4p16 and 3p26.3 and divergent clinical presentations
25. Infantile spasms: A prognostic evaluation
26. A large Indian family with rearrangement of chromosome 4p16 and 3p26.3 and divergent clinical presentations
27. Acute encephalopathy with a lesion of the splenium of the corpus callosum – A report of two cases
28. A Mild Variant of Pontocerebellar Hypoplasia Type 1 in a 12-Year-Old Indian Boy
29. The Newborn with Seizures -- A Follow-up Study.
30. A pilot study to assess the pattern of reading writing and mathematical errors in nine to eleven year old children identified to have specific learning disability.
31. Understanding of Autism.
32. Comprehensive Genetic Study of a Monozygotic Triplet Discordant for Autism Spectrum Disorder.
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.