491 results on '"Gulati, Sheffali"'
Search Results
2. Rare paediatric disorders in Indian healthcare settings with focus on neuromuscular disorders: Diagnostic and management challenges
3. A randomised controlled trial of clinical and cost-effectiveness of the PASS Plus intervention for young children with autism spectrum disorder in New Delhi, India: study protocol for the COMPASS trial
4. Global leadership is needed to optimize early childhood development for children with disabilities
5. Congenital Myasthenia Syndrome Due to a Novel DPAGT1 Gene Mutation - An Error of Glycosylation Masquerading as a Congenital Myopathy
6. Novel SLC16A2 Gene Mutation: A Rare Case of Delayed Myelination with Dysthyroidism,v Allan-Herndon-Dudley Syndrome
7. Teaching Neuroimage - Aicardi Syndrome: A Triad of Epileptic Spasms, Agenesis of Corpus Callosum, and Chorio-Retinal Lacunae
8. Teaching Neuroimage: A Rare Case of Encephalocraniocutaneous Lipomatosis: A Clinico-Radiological Diagnosis
9. Teaching Neuroimage: Juvenile Krabbe - A MRI Pattern Recognition in Leukodystrophy
10. Locked down-locked in: experiences of families of young children with autism spectrum disorders in Delhi, India
11. Development of a cost of illness inventory questionnaire for children with autism spectrum disorder in South Asia
12. Early childhood development strategy for the world's children with disabilities.
13. A Genetically Confirmed Case of Laminopathy: Clues from the Clinical Picture and Muscle Biopsy
14. Electrographic pattern recognition: A simple tool to predict clinical outcome in children with lissencephaly
15. Telephone-based follow-up of children with epilepsy: Comparison of accuracy between a specialty nurse and a pediatric neurology fellow
16. SLEEP ABNORMALITIES AND POLYSOMNOGRAPHIC PROFILE IN CHILDREN WITH DRUG-RESISTANT EPILEPSY
17. Craniosynostosis: A pediatric neurologist's perspective
18. Brain Stimulation and Constraint Induced Movement Therapy in Children With Unilateral Cerebral Palsy: A Randomized Controlled Trial
19. Hyperekplexia: A Frequent Near Miss in Infants and Young Children
20. Clinical spectrum of psychogenic non epileptic seizures in children; an observational study
21. Using mobile health technology to assess childhood autism in low-resource community settings in India: an innovation to address the detection gap
22. Postnatal Maturation of Amplitude Integrated Electroencephalography (aEEG) in Preterm Small for Gestational Age Neonates
23. Tuberous Sclerosis Complex: Are We Prepared For The Paradigm Shift?
24. Caregiver Perceptions of Autism and Neurodevelopmental Disabilities in New Delhi, India
25. Optic nerve glioma in neurofibromatosis: Radiological clues to diagnosis in a young child
26. Cerebral Venous Sinus Thrombosis in a Child with Lesch-Nyhan Syndrome
27. Decoding of novel missense TSC2 gene variants using in-silico methods
28. Teaching Neuroimage – Aicardi Syndrome: A Triad of Epileptic Spasms, Agenesis of Corpus Callosum, and Chorio-Retinal Lacunae
29. Teaching Neuroimage: A Rare Case of Encephalocraniocutaneous Lipomatosis: A Clinico-Radiological Diagnosis
30. sj-docx-1-nnr-10.1177_15459683231174222 – Supplemental material for Brain Stimulation and Constraint Induced Movement Therapy in Children With Unilateral Cerebral Palsy: A Randomized Controlled Trial
31. Solving the Riddle of Developmental Delay with Hair Microscopy: Trichothiodystrophy (MPLKIP Mutation in an Indian Child)
32. Bilateral facial palsy in lymphomatous meningitis
33. Bilateral pallidotomy for acquired or heredodegenerative generalized dystonia in children
34. Cerebral palsy and developmental intellectual disability in children younger than 5 years: Findings from the GBD-WHO Rehabilitation Database 2019
35. Orbital apex syndrome: a clinico-anatomical diagnosis
36. Prescription pattern of antiepileptic drugs in a tertiary care center of India
37. COVID-19 and Child Neurology Care
38. The Development and Validation of DSM 5-Based AIIMS-Modified INDT ADHD Tool for Diagnosis of ADHD: A Diagnostic Test Evaluation Study
39. Stroke as an initial manifestation of thiamine-responsive megaloblastic anemia
40. A novel homozygous mutation in POLR3A gene causing 4H syndrome: a case report
41. Peripheral neuropathy in cystic fibrosis: A prevalence study
42. Submandibular Duct Re-routing for Drooling in Neurologically Impaired Children
43. Additional file 1 of Development of a cost of illness inventory questionnaire for children with autism spectrum disorder in South Asia
44. Chronic meningitis with persistent hypoglycorrhachia: An unusual presentation of Lyme's disease
45. Intravenous immunoglobulin for severe protracted pediatric Guillain-Barre syndrome: Is single dose adequate?
46. X-linked Myopathy with Excessive Autophagy - A Rare Cause of Vacuolar Myopathy in Children
47. Serum Trace Elements in Children with Well-Controlled and Drug Refractory Epilepsy Compared to Controls: An Observational Study
48. Classical Clinical and Radiological Findings in Fucosidosis
49. Acute Isolated External Ophthalmoplegia: Think of Anti-GQ1b Antibody Syndrome
50. Craniosynostosis: A pediatric neurologist’s perspective
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