Caroline Lund
- Consultant; PhD
Publications 2024
Pharmacokinetic variability of everolimus and impact of concomitant antiseizure medications in patients with tuberous sclerosis complex: A retrospective study of therapeutic drug monitoring data in Denmark and Norway
Medicine (Baltimore), 103 (32), e39244
DOI 10.1097/MD.0000000000039244, PubMed 39121325
Publications 2023
Effectiveness and safety of everolimus treatment in patients with tuberous sclerosis complex in real-world clinical practice
Orphanet J Rare Dis, 18 (1), 377
DOI 10.1186/s13023-023-02982-1, PubMed 38042867
Adverse life events in patients with functional seizures: Assessment in clinical practice and association with long-term outcome
Epilepsy Behav, 148, 109456
DOI 10.1016/j.yebeh.2023.109456, PubMed 37804600
Publications 2022
Genotype-phenotype correlations in SCN8A-related disorders reveal prognostic and therapeutic implications
Brain, 145 (9), 2991-3009
DOI 10.1093/brain/awab321, PubMed 34431999
The effect of attachment style on long-term outcomes in psychogenic nonepileptic seizures: Results from a prospective study
Epilepsy Behav, 135, 108890
DOI 10.1016/j.yebeh.2022.108890, PubMed 36037581
Publications 2020
A retrospective review of changes and challenges in the use of antiseizure medicines in Dravet syndrome in Norway
Epilepsia Open, 5 (3), 432-441
DOI 10.1002/epi4.12413, PubMed 32913951
Pharmacokinetic Variability During Long-Term Therapeutic Drug Monitoring of Valproate, Clobazam, and Levetiracetam in Patients With Dravet Syndrome
Ther Drug Monit, 42 (5), 744-753
DOI 10.1097/FTD.0000000000000781, PubMed 32558674
Publications 2017
Aicardi syndrome and cognitive abilities: A report of five cases
Epilepsy Behav, 73, 161-165
DOI 10.1016/j.yebeh.2017.05.002, PubMed 28641168
Publications 2016
Exome Sequencing Fails to Identify the Genetic Cause of Aicardi Syndrome
Mol Syndromol, 7 (4), 234-238
DOI 10.1159/000448367, PubMed 27781033
Publications 2014
Aicardi syndrome: an epidemiologic and clinical study in Norway
Pediatr Neurol, 52 (2), 182-6.e3
DOI 10.1016/j.pediatrneurol.2014.10.022, PubMed 25443581
CHD2 mutations in Lennox-Gastaut syndrome
Epilepsy Behav, 33, 18-21
DOI 10.1016/j.yebeh.2014.02.005, PubMed 24614520
Publications 2013
Copy number variants in adult patients with Lennox-Gastaut syndrome features
Epilepsy Res, 105 (1-2), 110-7
DOI 10.1016/j.eplepsyres.2013.01.009, PubMed 23415449
Seizures that are not epileptic
Tidsskr Nor Laegeforen, 133 (5), 537
DOI 10.4045/tidsskr.13.0010, PubMed 23463068
Publications 2012
[Dravet syndrome as a cause of epilepsy and learning disability]
Tidsskr Nor Laegeforen, 132 (1), 44-7
DOI 10.4045/tidsskr.11.0539, PubMed 22240828
Publications 2011
[Lennox-Gastaut syndrome--course and treatment]
Tidsskr Nor Laegeforen, 131 (1), 24-7
DOI 10.4045/tidsskr.09.1540, PubMed 21233883
Publications 2010
Efficacy and tolerability of long-term treatment with vagus nerve stimulation in adolescents and adults with refractory epilepsy and learning disabilities
Seizure, 20 (1), 34-7
DOI 10.1016/j.seizure.2010.10.002, PubMed 21035358
Publications 2009
[Psychogenic non-epileptic seizures]
Tidsskr Nor Laegeforen, 129 (22), 2348-51
DOI 10.4045/tidsskr.09.0300, PubMed 19935934
SCN1A mutation screening in adult patients with Lennox-Gastaut syndrome features
Epilepsy Behav, 16 (3), 555-7
DOI 10.1016/j.yebeh.2009.08.021, PubMed 19782004