79 results on '"Grinton BE"'
Search Results
2. Long term follow up of patients with MNV3 treated with intra-vitreal Aflibercept
3. Identifying individuals with rare disease variants by inferring shared ancestral haplotypes from SNP array data
4. Real-world outcomes of treatment resistant neovascular-age related macular degeneration switched from Aflibercept to Faricimab
5. Familial mesial temporal lobe epilepsy: clinical spectrum and genetic evidence for a polygenic architecture
6. The Toronto Tele-Retinal Screening Program for the Elderly in Long-Term Care: A Pilot Project (Preprint)
7. School-Based Telemedicine and Reduced Avoidable Emergency Care Among Rural Pediatric Patients
8. Recognition and Epileptology of Protracted CLN3 Disease
9. Genes4Epilepsy : An epilepsy gene resource
10. The effect of COVID-19 on referral patterns for clinical electrophysiological testing
11. A founder event causing a dominant childhood epilepsy survives 800 years through weak selective pressure
12. Review on Gilbert’s Syndrome
13. Keeping Our Heads above Water: An Exploratory Study on the Equity Opportunities of Coastal Virginia Wireless Emergency Alerts
14. An Investigation of Anticonvulsant Activity of Aqueous Extract of Ficus carica Linn Fruits in Experimental Animal Models
15. Nephroprotective Properties of Natural Herbs: A Systemic Review
16. Non-Traditional Safety Messages Elicit Different Brain Connectivity Patterns Among Drivers
17. Patient with Diabetes Mellitus and Ocular Complications: A Brief review
18. Delayed follow-up of medical retina patients due to COVID-19: impact on disease activity and visual acuity
19. Association of SLC32A1 Missense Variants With Genetic Epilepsy With Febrile Seizures Plus
20. Contribution of rare genetic variants to drug response in absence epilepsy
21. Desferrioxamine-Related Pseudo-Vitelliform Dystrophy and the Effect of Anti-Vascular Endothelial Growth Factor
22. A Brief Review on Sechium edule
23. Determinants of vitreomacular traction width: associations with foveal floor width and vitreoretinal interface changes
24. The Association between Foveal Floor Measurements and Macular Hole Size
25. Novel Missense CACNA1G Mutations Associated with Infantile-Onset Developmental and Epileptic Encephalopathy
26. Comment on: “Seeking a practical definition of stable glaucoma: a Delphi consensus survey of UK glaucoma consultants”
27. Acute Macular Neuroretinopathy Associated with Acute Influenza Virus Infection
28. Asthma
29. Epidemiology and etiology of infantile developmental and epileptic encephalopathies in Tasmania
30. Splice variant in ARX leading to loss of C‐terminal region in a boy with intellectual disability and infantile onset developmental and epileptic encephalopathy
31. Cochrane Corner: Ocriplasmin—why isn’t it being used more?
32. Randomized Controlled Trial of Melatonin for Sleep Disturbance in Dravet Syndrome: The DREAMS Study
33. The polarity sensitivity factor of some fluorescent probe molecules used for studying supramolecular systems and other heterogeneous environments
34. Genetic epilepsy with febrile seizures plus
35. Photoreceptor Outer Segment on Internal Limiting Membrane after Macular Hole Surgery: Implications for Pathogenesis
36. Familial neonatal seizures in 36 families: Clinical and genetic features correlate with outcome
37. A variant of KCC 2 from patients with febrile seizures impairs neuronal Cl − extrusion and dendritic spine formation
38. Epilepsy health consumer groups and charities; How representative of patients are they?
39. The Association Between Retinal Vessel Morphology and Retinal Nerve Fiber Layer Thickness in an Elderly Population
40. PRRT2 phenotypic spectrum includes sporadic and fever-related infantile seizures
41. In vivo loss of slow potassium channel activity in individuals with benign familial neonatal epilepsy in remission
42. Clinical genetic studies in benign childhood epilepsy with centrotemporal spikes
43. PRRT2 Mutations Cause Benign Familial Infantile Epilepsy and Infantile Convulsions with Choreoathetosis Syndrome
44. Investigation of the 15q13.3 CNV as a genetic modifier for familial epilepsies with variable phenotypes
45. 35. Peripheral nerve excitability testing shows distinctive ion channel dysfunction in patients with KCNQ2 mutations and epilepsy
46. Familial mesial temporal lobe epilepsy: a benign epilepsy syndrome showing complex inheritance
47. Familial neonatal seizures with intellectual disability caused by a microduplication of chromosome 2q24.3
48. Multicentre search for genetic susceptibility loci in sporadic epilepsy syndrome and seizure types: a case-control study
49. Deletions or duplications in KCNQ2 can cause benign familial neonatal seizures
50. ELO01 Phenotypic characterisation of a large family with benign familial neonatal seizures associated with an exon duplication of the KCNQ2 gene
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