Suchergebnisse - "Polster, Tilman"

PubPharm (127)

1

Ethosuximide lowers lamotrigine serum concentrations : Evidence for a clinically relevant interaction

enthalten in: Epilepsia | 2024

von Hagemann, A. | Herting, A. | Klimpel, D. | +2

2

Clustered de novo start-loss variants in GLUL result in a developmental and epileptic encephalopathy via stabilization of glutamine synthetase

enthalten in: American journal of human genetics | 2024

von Jones, A. | Aquilino, M. | Tinker, R. | +25

3

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

enthalten in: Human genetics | 2024

von Herbst, C. | Bothe, V. | Wegler, M. | +27

4

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

enthalten in: Human genetics | 2024

von Herbst, C. | Bothe, V. | Wegler, M. | +27

5

Critical incidents, nocturnal supervision, and caregiver knowledge on SUDEP in patients with Dravet syndrome : A prospective multicenter study in Germany

enthalten in: Epilepsia | 2024

von Maltseva, M. | Rosenow, F. | Schubert-Bast, S. | +20

6

Critical incidents, nocturnal supervision, and caregiver knowledge on SUDEP in patients with Dravet syndrome : A prospective multicenter study in Germany

enthalten in: Epilepsia | 2024

von Maltseva, M. | Rosenow, F. | Schubert‐Bast, S. | +20

7

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

enthalten in: Epilepsia | 2023

von Sullivan, J. | Lagae, L. | Cross, J. | +83

8

GABRA1-Related Disorders : From Genetic to Functional Pathways

enthalten in: Annals of neurology | 2023

von Musto, E. | Liao, V. | Johannesen, K. | +45

9

Hemispherotomy in children : A retrospective analysis of 152 surgeries at a single center and predictors for long-term seizure outcome

enthalten in: Epilepsia | 2023

von Kalbhenn, T. | Cloppenborg, T. | Woermann, F. | +6

10

Sleep quality, anxiety, symptoms of depression, and caregiver burden among those caring for patients with Dravet syndrome : a prospective multicenter study in Germany

enthalten in: Orphanet journal of rare diseases | 2023

von Maltseva, M. | Schubert-Bast, S. | Zöllner, J. | +20

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