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Lauxmann, Stephan
34
results:
Search for persons
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Online (34)
Mediatypes
Articles (Online) (13)
OpenAccess-fulltext (20)
Thesis (Online) (1)
Languages
german (1)
english (25)
Sorted by: Relevance
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?
1
Cenobamate: real-world data from a retrospective multicente..:
Lauxmann, Stephan
;
Heuer, David
;
Heckelmann, Jan
...
Journal of Neurology. , 2024
Link:
https://doi.org/10.1007/..
?
2
Loss or gain of function? Effects of ion channel mutations ..:
Koch, Nils A.
;
Sonnenberg, Lukas
;
Hedrich, Ulrike B. S.
..
Frontiers in Neurology. 14 (2023) - p. , 2023
Link:
https://doi.org/10.3389/..
?
3
In vitro effects of eslicarbazepine (S‐licarbazepine) as a ..:
Bayraktar, Erva
;
Liu, Yuanyuan
;
Sonnenberg, Lukas
...
British Journal of Pharmacology. 180 (2022) 8 - p. 1038-1055 , 2022
Link:
https://doi.org/10.1111/..
?
4
Genotype-phenotype correlations in SCN8A-related disorders ..:
Johannesen, Katrine M
;
Liu, Yuanyuan
;
Koko, Mahmoud
...
Brain. 145 (2021) 9 - p. 2991-3009 , 2021
Link:
https://doi.org/10.1093/..
?
5
Therapeutic Potential of Sodium Channel Blockers as a Targe..:
Lauxmann, Stephan
;
Sonnenberg, Lukas
;
Koch, Nils A.
...
Frontiers in Neurology. 12 (2021) - p. , 2021
Link:
https://doi.org/10.3389/..
?
6
Genetics of Paroxysmal Dyskinesia: Novel Variants Corrobora..:
Kegele, Josua
;
Krüger, Johanna
;
Koko, Mahmoud
...
Frontiers in Neurology. 12 (2021) - p. , 2021
Link:
https://doi.org/10.3389/..
?
7
Neuronal mechanisms of mutations in SCN8A causing epilepsy ..:
Liu, Yuanyuan
;
Schubert, Julian
;
Sonnenberg, Lukas
...
Brain. 142 (2019) 2 - p. 376-390 , 2019
Link:
https://doi.org/10.1093/..
?
8
SCN2A channelopathies: Mechanisms and models:
Hedrich, Ulrike B. S.
;
Lauxmann, Stephan
;
Lerche, Holger
Epilepsia. 60 (2019) S3 - p. , 2019
Link:
https://doi.org/10.1111/..
?
9
Relationship of electrophysiological dysfunction and clinic..:
Lauxmann, Stephan
;
Verbeek, Nienke E.
;
Liu, Yuanyuan
...
Human Mutation. 39 (2018) 12 - p. 1942-1956 , 2018
Link:
https://doi.org/10.1002/..
?
10
Thalamic transitory ischemic attacks presenting as Jacksoni..:
Schubert, Victoria
;
Lauxmann, Stephan
;
Bender, Benjamin
.
Journal of Neurology. 264 (2017) 10 - p. 2158-2161 , 2017
Link:
https://doi.org/10.1007/..
?
11
An SCN2A mutation in a family with infantile seizures from ..:
Lauxmann, Stephan
;
Boutry‐Kryza, Nadia
;
Rivier, Clotilde
...
Epilepsia. 54 (2013) 9 - p. , 2013
Link:
https://doi.org/10.1111/..
?
12
Genome-wide identification and phenotypic characterization ..:
Montanucci, Ludovica
;
Lewis-Smith, David
;
Collins, Ryan L
...
info:eu-repo/semantics/altIdentifier/doi/10.1038/s41467-023-39539-6. , 2023
Link:
https://repository.vu.lt..
?
13
Loss or gain of function? Effects of ion channel mutations ..:
Koch, Nils A
;
Sonnenberg, Lukas
;
Hedrich, Ulrike B. S
..
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10244640/. , 2023
Link:
http://www.ncbi.nlm.nih...
?
14
Genome-wide identification and phenotypic characterization ..:
Montanucci, Ludovica
;
Lewis-Smith, David
;
Collins, Ryan L
...
https://eprints.gla.ac.uk/305681/1/305681.pdf. , 2023
Link:
https://eprints.gla.ac.u..
?
15
Genotype-phenotype correlations in SCN8A-related disorders ..:
Schoonjans, An Sofie
;
Johannesen, Katrine M
;
Liu, Yuanyuan
...
boreal:278286. , 2022
Link:
http://hdl.handle.net/20..
1-15