Search

Your search keyword '"Polster, Tilman"' showing total 340 results

Search Constraints

Start Over You searched for: Author "Polster, Tilman" Remove constraint Author: "Polster, Tilman"
340 results on '"Polster, Tilman"'

Search Results

1. Heterozygous loss-of-function variants in DOCK4 cause neurodevelopmental delay and microcephaly

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

6. Genome Sequencing for Diagnosing Rare Diseases

9. DNA methylation-based classification of malformations of cortical development in the human brain

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

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

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

28. Effects of Levetiracetam and Sulthiame on EEG in benign epilepsy with centrotemporal spikes: A randomized controlled trial

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.

35. Fenfluramine in the treatment of Dravet syndrome: Results of a third randomized, placebo‐controlled clinical trial.

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

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

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

Catalog

Books, media, physical & digital resources