O Eeg-Olofsson
Overview
Explore the profile of O Eeg-Olofsson including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
92
Citations
744
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
11.
Eeg-Olofsson O, Lundberg S, Raininko R
Epileptic Disord
. 2001 Mar;
2 Suppl 1:S51-3.
PMID: 11231225
Hippocampal and/or white matter abnormalities have been found on the MRIs in 10/18 children with typical rolandic epilepsy. The etiology of the first-mentioned is not evident, whereas the latter may...
12.
Eeg-Olofsson O, Zhang W, Olsson Y, Jagell S, Hagenfeldt L
J Child Neurol
. 2000 Aug;
15(7):488-92.
PMID: 10921524
D-2-Hydroxyglutaric Aciduria is a rare metabolic disorder that can cause injury to the brain and other organs. This case report concerns a 14-year-old boy showing irritability and typical signs of...
13.
Croona C, Kihlgren M, Lundberg S, Eeg-Olofsson O, Eeg-Olofsson K
Dev Med Child Neurol
. 2000 Jan;
41(12):813-8.
PMID: 10619279
Benign childhood epilepsy with centrotemporal spikes (BCECTS) is a well-known idiopathic age- and localization-related epileptic syndrome with characteristic clinical and EEG manifestations. Due to the reported benign evolution of this...
14.
Lundberg S, Eeg-Olofsson O, Raininko R, Eeg-Olofsson K
Epilepsia
. 1999 Dec;
40(12):1808-15.
PMID: 10612349
Purpose: To look for brain abnormalities by using magnetic resonance imaging (MRI) in patients with benign childhood epilepsy with centrotemporal spikes (BCECTS), which is the most common epilepsy syndrome in...
15.
16.
Trenite D, Binnie C, HARDING G, Wilkins A, Covanis T, Eeg-Olofsson O, et al.
Neurophysiol Clin
. 1999 Nov;
29(4):318-24.
PMID: 10546250
Rationale: In many EEG laboratories in Europe, intermittent photic stimulation (IPS) is not performed routinely, and consequently, great variation exists in the type of photo stimulator used, the methodology employed,...
17.
van der Knaap M, Jakobs C, Hoffmann G, Duran M, Muntau A, Schweitzer S, et al.
J Inherit Metab Dis
. 1999 Jul;
22(4):404-13.
PMID: 10407777
It has recently been recognized that D-2-hydroxyglutaric aciduria is a distinct neurometabolic disorder with a severe and a mild phenotype. Whereas the clinical and neuroimaging findings of the severe phenotype...
18.
Neubauer B, Fiedler B, Himmelein B, Kampfer F, Lassker U, Schwabe G, et al.
Neurology
. 1998 Dec;
51(6):1608-12.
PMID: 9855510
Objective: To localize a gene predisposing to benign epilepsy of childhood with centrotemporal spikes (BECTS). Background: BECTS, or rolandic epilepsy, is the most prevalent idiopathic epilepsy syndrome in childhood. Functional...
19.
Phillips H, Scheffer I, Crossland K, Bhatia K, Fish D, Marsden C, et al.
Am J Hum Genet
. 1998 Oct;
63(4):1108-16.
PMID: 9758605
Autosomal dominant nocturnal frontal-lobe epilepsy (ADNFLE) is a recently identified partial epilepsy in which two different mutations have been described in the alpha4 subunit of the neuronal nicotinic acetylcholine receptor...
20.
Larsen K, Herder G, Prytz J, Henriksen O, Eeg-Olofsson O, Eeg-Olofsson K, et al.
Tidsskr Nor Laegeforen
. 1997 Jan;
117(2):195-9.
PMID: 9064832
Moyamoya disease is a rare cerebrovascular disease with a wide variety of clinical outcomes. The main signs of the disease are progressive occlusion of the main intracerebral arteries and development...