340 results on '"Polster, Tilman"'
Search Results
2. Sleep quality, anxiety, symptoms of depression, and caregiver burden among those caring for patients with Dravet syndrome: a prospective multicenter study in Germany
3. Clustered de novo start-loss variants in GLUL result in a developmental and epileptic encephalopathy via stabilization of glutamine synthetase
4. 6/w – verträumt, nervös, Schulschwierigkeiten: Vorbereitung auf die Facharztprüfung: Fall 118
5. Biophysical characterization and modelling of SCN1A gain-of-function predicts interneuron hyperexcitability and a predisposition to network instability through homeostatic plasticity
6. Genome Sequencing for Diagnosing Rare Diseases
7. Exploring the relationships between composite scores of disease severity, seizure-freedom and quality of life in Dravet syndrome
8. Hypochondroplasia and temporal lobe epilepsy – A series of 4 cases
9. DNA methylation-based classification of malformations of cortical development in the human brain
10. Ethosuximide lowers lamotrigine serum concentrations: Evidence for a clinically relevant interaction
11. Reading and the visual word form area (VWFA) – Management and clinical experience at one epilepsy surgery center
12. Treatment with fenfluramine in patients with Dravet syndrome has no long-term effects on weight and growth
13. Epilepsy associated with tuberous sclerosis complex in childhood: Long-term outcome in children after epilepsy surgery and children non-eligible for epilepsy surgery
14. Improved everyday executive functioning following profound reduction in seizure frequency with fenfluramine: Analysis from a phase 3 long-term extension study in children/young adults with Dravet syndrome
15. Stereotactic depth electrode placement surgery in paediatric and adult patients with the Neuromate robotic device: Accuracy, complications and epileptological results
16. Variants in GNAI1 cause a syndrome associated with variable features including developmental delay, seizures, and hypotonia
17. GABRA1-related disorders:from genetic to functional pathways
18. Seizure outcome and use of antiepileptic drugs after epilepsy surgery according to histopathological diagnosis: a retrospective multicentre cohort study
19. Genotype-phenotype correlation on 45 individuals with West syndrome
20. Heterozygous loss-of function variants in DOCK4 cause neurodevelopmental delay and microcephaly
21. Mosaic trisomy of chromosome 1q in human brain tissue associates with unilateral polymicrogyria, very early-onset focal epilepsy, and severe developmental delay
22. Klinische Charakteristika, Ressourcenverbrauch, Lebensqualität und Versorgungssituation beim Dravet-Syndrom in Deutschland
23. Development and Validation of Prediction Models for Developmental and Intellectual Outcome Following Pediatric Epilepsy Surgery
24. Burden-of-illness and cost-driving factors in Dravet syndrome patients and carers: A prospective, multicenter study from Germany
25. GABRA1‐Related Disorders: From Genetic to Functional Pathways
26. Critical incidents, nocturnal supervision, and caregiver knowledge on SUDEP in patients with Dravet syndrome: A prospective multicenter study in Germany
27. Epilepsiechirurgie
28. Effects of Levetiracetam and Sulthiame on EEG in benign epilepsy with centrotemporal spikes: A randomized controlled trial
29. CASPR2 autoimmunity in children expanding to mild encephalopathy with hypertension
30. The landscape of epilepsy-related GATOR1 variants
31. Critical incidents, nocturnal supervision, and caregiver knowledge on SUDEP in patients with Dravet syndrome: A prospective multicenter study in Germany.
32. Neue Antiepileptika für Kinder mit Epilepsie.
33. Biophysical characterization and modeling ofSCN1Again-of-function predicts interneuron hyperexcitability and a predisposition to network instability through homeostatic plasticity
34. Adjunctive everolimus therapy for treatment-resistant focal-onset seizures associated with tuberous sclerosis (EXIST-3): a phase 3, randomised, double-blind, placebo-controlled study
35. Fenfluramine in the treatment of Dravet syndrome: Results of a third randomized, placebo‐controlled clinical trial.
36. Thermoablation bei nodulären Heterotopien: 2 Fallberichte mit Verlauf über mehr als 5 Jahre
37. An examination of the efficacy and safety of fenfluramine in adults, children, and adolescents with Dravet syndrome in a real‐world practice setting: A report from the Fenfluramine European Early Access Program
38. Everolimus for treatment-refractory seizures in TSC: Extension of a randomized controlled trial
39. Hemispherotomy in children: A retrospective analysis of 152 surgeries at a single center and predictors for long‐term seizure outcome.
40. Epilepsy surgery in Neurofibromatosis Type 1
41. Development and Validation of Prediction Models for Developmental and Intellectual Outcome Following Pediatric Epilepsy Surgery
42. Neurodevelopmental Disorders Caused by De Novo Variants in KCNB1 Genotypes and Phenotypes
43. Delineating SPTAN1 associated phenotypes: from isolated epilepsy to encephalopathy with progressive brain atrophy
44. CAD mutations and uridine-responsive epileptic encephalopathy
45. Mild Malformation of Cortical Development with Oligodendroglial Hyperplasia in Frontal Lobe Epilepsy: A New Clinico‐Pathological Entity
46. Timing of antiepileptic drug withdrawal and long-term seizure outcome after paediatric epilepsy surgery (TimeToStop): a retrospective observational study
47. Correction: The landscape of epilepsy-related GATOR1 variants
48. Correction to: The landscape of epilepsy-related GATOR1 variants
49. Fenfluramine hydrochloride for the treatment of seizures in Dravet syndrome: a randomised, double-blind, placebo-controlled trial
50. DNA methylation-based classification of malformations of cortical development in the human brain
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