24 results on '"Sival, Deborah A"'
Search Results
2. Moving across disorders: A cross-sectional study of cognition in early onset ataxia and dystonia
3. Early onset ataxia with comorbid myoclonus and epilepsy: A disease spectrum with shared molecular pathways and cortico-thalamo-cerebellar network involvement
4. Developmental neurobiology of cerebellar and Basal Ganglia connections
5. Applicability of quantitative oculomotor and SARA assessment in children
6. Clinical phenotypes of infantile onset CACNA1A-related disorder
7. A detailed description of the phenotypic spectrum of North Sea Progressive Myoclonus Epilepsy in a large cohort of seventeen patients
8. Motor function in survivors of pediatric acute lymphoblastic leukemia treated with chemotherapy-only
9. Motor and non-motor determinants of health-related quality of life in young dystonia patients
10. Fever-Induced Paroxysmal Weakness and Encephalopathy (FIPWE)—Part of a Phenotypic Continuum in Patients With ATP1A3 Mutations?
11. Osteogenic transdifferentiation as ideal in vivo model for inherited hypomyelination with spondylometaphyseal dysplasia (H-SMD)
12. Long-term impact of lead poisoning on neurologic function in children and adolescents
13. De Novo Coding Variants Are Strongly Associated with Tourette Disorder
14. Automatic classification of gait in children with early-onset ataxia or developmental coordination disorder and controls using inertial sensors
15. Pre- and perinatal complications in relation to Tourette syndrome and co-occurring obsessive-compulsive disorder and attention-deficit/hyperactivity disorder
16. Patience is the key: Contraceptive induced chorea in a girl with Down Syndrome
17. Riluzole in patients with hereditary cerebellar ataxia
18. Muscle Ultrasound in Patients with Glycogen Storage Disease Types I and III
19. Myoclonus in childhood-onset neurogenetic disorders: The importance of early identification and treatment
20. Visual Screening of Muscle Ultrasound Images in Children
21. Muscle Ultrasound Quantifies Segmental Neuromuscular Outcome in Pediatric Myelomeningocele
22. Visual Assessment of Segmental Muscle Ultrasound Images in Spina Bifida Aperta
23. Bilateral polymicrogyria as the indicative feature in a child with a 22q11.2 deletion
24. Shah-Waardenburg syndrome and PCWH associated with SOX10 mutations: A case report and review of the literature
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