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1. Neurodevelopmental and Epilepsy Phenotypes in Individuals With Missense Variants in the Voltage-Sensing and Pore Domains of KCNH5.

2. Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders

3. Damaging de novo missense variants in EEF1A2 lead to a developmental and degenerative epileptic-dyskinetic encephalopathy

5. Improving Treatment Trial Outcomes for Rett Syndrome

7. Damaging de novo missense variants in EEF1A2lead to a developmental and degenerative epileptic-dyskinetic encephalopathy

8. Development of Consensus-Based Best Practice Guidelines for the Perioperative and Postoperative Care of Pediatric Patients With Spinal Deformity and Programmable Implanted Devices.

9. Clinical Features and Disease Progression in Older Individuals with Rett Syndrome.

10. Hyperkinetic Movement Disorder Caused by the Recurrent c.892C>T NACC1 Variant.

11. Parental perspectives of episodic irritability in an ultra-rare genetic disorder associated with NACC1.

12. GABRA1-Related Disorders: From Genetic to Functional Pathways.

13. Chronic striatal cholinergic interneuron excitation induces clinically-relevant dystonic behavior in mice.

14. Anodal Contralesional tDCS Enhances CST Excitability Bilaterally in an Adolescent with Hemiparetic Cerebral Palsy: A Brief Report.

15. Safety and feasibility of transcranial direct current stimulation stratified by corticospinal organization in children with hemiparesis.

16. Neurodevelopmental and Epilepsy Phenotypes in Individuals With Missense Variants in the Voltage-Sensing and Pore Domains of KCNH5 .

17. Analysis of X-inactivation status in a Rett syndrome natural history study cohort.

18. Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders.

19. Author Correction: Mutations disrupting neuritogenesis genes confer risk for cerebral palsy.

20. Phenotypic features in MECP2 duplication syndrome: Effects of age.

21. Mutations disrupting neuritogenesis genes confer risk for cerebral palsy.

22. Associations Among Diurnal Salivary Cortisol Patterns, Medication Use, and Behavioral Phenotype Features in a Community Sample of Rett Syndrome.

23. Damaging de novo missense variants in EEF1A2 lead to a developmental and degenerative epileptic-dyskinetic encephalopathy.

24. Ipsilateral Corticospinal Tract Excitability Contributes to the Severity of Mirror Movements in Unilateral Cerebral Palsy: A Case Series.

25. EMG breakthrough during cortical silent period in congenital hemiparesis: a descriptive case series.

26. Microvascular decompression with partial occipital condylectomy in a case of pediatric spasmodic torticollis.

27. Characterizing the phenotypic effect of Xq28 duplication size in MECP2 duplication syndrome.

28. The array of clinical phenotypes of males with mutations in Methyl-CpG binding protein 2.

29. Transcranial Direct Current Stimulation (tDCS) Paired with Occupation-Centered Bimanual Training in Children with Unilateral Cerebral Palsy: A Preliminary Study.

30. Transcranial direct current stimulation and constraint-induced therapy in cerebral palsy: A randomized, blinded, sham-controlled clinical trial.

31. Non-Invasive Brain Stimulation in Children With Unilateral Cerebral Palsy: A Protocol and Risk Mitigation Guide.

33. Quality improvement in neurology: Child neurology quality measure set: Executive summary.

34. A Double-Blind, Randomized, Placebo-Controlled Clinical Study of Trofinetide in the Treatment of Rett Syndrome.

35. Determining Electrode Placement for Transcranial Direct Current Stimulation: A Comparison of EEG- Versus TMS-Guided Methods.

36. Less-Affected Hand Function in Children With Hemiparetic Unilateral Cerebral Palsy: A Comparison Study With Typically Developing Peers.

37. A case-controlled comparison of postoperative analgesic dosing between girls with Rett syndrome and girls with and without developmental disability undergoing spinal fusion surgery.

38. Dystonia in ATP2B3-associated X-linked spinocerebellar ataxia.

39. Repetitive Transcranial Magnetic Stimulation/Behavioral Intervention Clinical Trial: Long-Term Follow-Up of Outcomes in Congenital Hemiparesis.

40. Solid organ transplantation in primary mitochondrial disease: Proceed with caution.

41. Ipsilesional motor-evoked potential absence in pediatric hemiparesis impacts tracking accuracy of the less affected hand.

42. Synergistic effect of combined transcranial direct current stimulation/constraint-induced movement therapy in children and young adults with hemiparesis: study protocol.

43. Improving Treatment Trial Outcomes for Rett Syndrome: The Development of Rett-specific Anchors for the Clinical Global Impression Scale.

44. Pain experience and expression in Rett syndrome: Subjective and objective measurement approaches.

45. Infrared Thermal Analysis and Individual Differences in Skin Temperature Asymmetry in Rett Syndrome.

46. Safety of primed repetitive transcranial magnetic stimulation and modified constraint-induced movement therapy in a randomized controlled trial in pediatric hemiparesis.

47. Safety and feasibility of transcranial direct current stimulation in pediatric hemiparesis: randomized controlled preliminary study.

48. Primed low-frequency repetitive transcranial magnetic stimulation and constraint-induced movement therapy in pediatric hemiparesis: a randomized controlled trial.

49. Myotonic dystrophy type 1 coexisting with myasthenia gravis and thymoma.

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