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Stödberg, Tommy
41
results:
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Online (41)
Mediatypes
Articles (Online) (15)
OpenAccess-fulltext (26)
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1
Unraveling GRIA1 neurodevelopmental disorders: Lessons lear..:
Tvergaard, Nicolai Kohring
;
Tkemaladze, Tinatin
;
Stödberg, Tommy
...
Clinical Genetics. , 2024
Link:
https://doi.org/10.1111/..
?
2
Individualised human phenotype ontology gene panels improve..:
Henry, Olivia J.
;
Stödberg, Tommy
;
Båtelson, Sofia
...
Molecular Genetics & Genomic Medicine. 11 (2023) 7 - p. , 2023
Link:
https://doi.org/10.1002/..
?
3
Case report: Fatal outcome of pyridoxine-dependent epilepsy..:
Aquilano, Giulia
;
Linnér, Agnes
;
Ygberg, Sofia
..
Frontiers in Pediatrics. 10 (2022) - p. , 2022
Link:
https://doi.org/10.3389/..
?
4
Outcome at age 7 of epilepsy presenting in the first 2 year..:
Stödberg, Tommy
;
Tomson, Torbjörn
;
Anderlid, Britt‐Marie
...
Epilepsia. 63 (2022) 8 - p. 2096-2107 , 2022
Link:
https://doi.org/10.1111/..
?
5
Epilepsy syndromes, etiologies, and the use of next‐generat..:
Stödberg, Tommy
;
Tomson, Torbjörn
;
Barbaro, Michela
...
Epilepsia. 61 (2020) 11 - p. 2486-2499 , 2020
Link:
https://doi.org/10.1111/..
?
6
MEG and navigated TMS jointly enable spatially accurate app..:
Islam, Mominul
;
Westin, Karin
;
Carvalho, Ana
...
Brain Stimulation. 12 (2019) 5 - p. 1312-1314 , 2019
Link:
https://doi.org/10.1016/..
?
7
Diagnostic pitfalls in vitamin B6‐dependent epilepsy caused..:
Jensen, Kristian Vestergaard
;
Frid, Maria
;
Stödberg, Tommy
...
JIMD Reports. 50 (2019) 1 - p. 1-8 , 2019
Link:
https://doi.org/10.1002/..
?
8
Benign paroxysmal torticollis of infancy does not lead to n..:
Danielsson, Annika
;
Anderlid, Britt‐Marie
;
Stödberg, Tommy
...
Developmental Medicine & Child Neurology. 60 (2018) 12 - p. 1251-1255 , 2018
Link:
https://doi.org/10.1111/..
?
9
An LC–MS/MS-Based Method for the Quantification of Pyridox(..:
Wilson, Matthew P.
;
Footitt, Emma J.
;
Papandreou, Apostolos
...
Analytical Chemistry. 89 (2017) 17 - p. 8892-8900 , 2017
Link:
https://doi.org/10.1021/..
?
10
Mutations in SLC12A5 in epilepsy of infancy with migrating ..:
Stödberg, Tommy
;
McTague, Amy
;
Ruiz, Arnaud J.
...
Nature Communications. 6 (2015) 1 - p. , 2015
Link:
https://doi.org/10.1038/..
?
11
A de novo gain-of-function mutation in SCN11A causes loss o..:
Leipold, Enrico
;
Liebmann, Lutz
;
Korenke, G Christoph
...
Nature Genetics. 45 (2013) 11 - p. 1399-1404 , 2013
Link:
https://doi.org/10.1038/..
?
12
SLC25A22is a novel gene for migrating partial seizures in i..:
Poduri, Annapurna
;
Heinzen, Erin L.
;
Chitsazzadeh, Vida
...
Annals of Neurology. 74 (2013) 6 - p. 873-882 , 2013
Link:
https://doi.org/10.1002/..
?
13
Dolichol kinase deficiency (DOLK-CDG) with a purely neurolo..:
Helander, Anders
;
Stödberg, Tommy
;
Jaeken, Jaak
...
Molecular Genetics and Metabolism. 110 (2013) 3 - p. 342-344 , 2013
Link:
https://doi.org/10.1016/..
?
14
Homozygous PLCB1 deletion associated with malignant migrati..:
Poduri, Annapurna
;
Chopra, Sameer S.
;
Neilan, Edward G.
...
Epilepsia. 53 (2012) 8 - p. , 2012
Link:
https://doi.org/10.1111/..
?
15
Late Onset Bradyarrhythmia during Vagus Nerve Stimulation:
Åmark, Per
;
Stödberg, Tommy
;
Wallstedt, Lars
Epilepsia. 48 (2007) 5 - p. 1023-1024 , 2007
Link:
https://doi.org/10.1111/..
1-15