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101. The ENIGMA-Epilepsy working group: Mapping disease from large data sets.

102. Lacosamide in patients with epilepsy of cerebrovascular etiology

106. Artificial intelligence for classification of temporal lobe epilepsy with ROI-level MRI data: A worldwide ENIGMA-Epilepsy study

110. KOMET: an unblinded, randomised, two parallel-group, stratified trial comparing the effectiveness of levetiracetam with controlled-release carbamazepine and extended-release sodium valproate as monotherapy in patients with newly diagnosed epilepsy

111. Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A

120. Seizure outcome and use of antiepileptic drugs after epilepsy surgery according to histopathological diagnosis: a retrospective multicentre cohort study

121. Network-based atrophy modelling in the common epilepsies: a worldwide ENIGMA study

126. Common genetic variation and susceptibility to partial epilepsies: a genome-wide association study

129. Analysis of shared heritability in common disorders of the brain

135. Adult onset epilepsy incidence in Finland over 34 years: A nationwide registry study.

142. Recalling Biobank Participants to Clinical Study of Alzheimer's Disease – FinnGen Pilot Study.

148. Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals

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