Erik A Eklund
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Explore the profile of Erik A Eklund including associated specialties, affiliations and a list of published articles.
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56
Citations
818
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Recent Articles
11.
Pearsson K, A Eklund E, Rask O, Rosen I, Sjunnesson H, Compagno-Strandberg M
Seizure
. 2023 Sep;
112:54-61.
PMID: 37757549
Purpose: This study aimed to characterize the Swedish cohort of surgically treated patients with TSC and explore differences in preoperative investigation and outcome over time. Methods: Data on patient and...
12.
Childhood tuberous sclerosis complex in southern Sweden: a paradigm shift in diagnosis and treatment
Pearsson K, Bjork Werner J, Lundgren J, Granse L, Karlsson E, Kallen K, et al.
BMC Pediatr
. 2023 Jun;
23(1):329.
PMID: 37386496
Aim: To investigate the complete clinical spectrum of individuals with paediatric tuberous sclerosis complex in southern Sweden and explore changes over time. Methods: In this retrospective observational study, 52 individuals...
13.
Vogel G, Mozer-Glassberg Y, Landau Y, Schlieben L, Prokisch H, Feichtinger R, et al.
Genet Med
. 2023 Jun;
25(6):100828.
PMID: 37272928
No abstract available.
14.
A Eklund E, Miller B, Boucher A
Mol Genet Metab
. 2023 Apr;
138(4):107562.
PMID: 37023501
Congenital disorders of glycosylation are a group of rare related disorders causing multisystem dysfunction, including ovarian failure in females that requires early estrogen replacement. Glycosylation defects also disrupt normal synthesis...
15.
Xia Z, Ng B, Jennions E, Blomqvist M, Sandqvist Wiklund A, Hedberg-Oldfors C, et al.
JIMD Rep
. 2023 Jan;
64(1):79-89.
PMID: 36636598
Here, we present the first two Swedish cases of Conserved Oligomeric Golgi complex subunit 6-congenital disorders of glycosylation (COG6-CDG). Their clinical symptoms include intellectual disability, Attention Deficit/Hyperactivity Disorder (ADHD), delayed...
16.
Ljungblad U, Lindberg M, A Eklund E, Saeves I, Sagredo C, Bjorke-Monsen A, et al.
Int J Neonatal Screen
. 2022 Dec;
8(4).
PMID: 36547383
Background: The sensitivity of newborn screening (NBS) in detecting infants that later develop symptomatic vitamin B12 deficiency is unknown. We evaluated the predictive value using NBS algorithms in detecting infants...
17.
Vogel G, Mozer-Glassberg Y, Landau Y, Schlieben L, Prokisch H, Feichtinger R, et al.
Genet Med
. 2022 Oct;
25(6):100314.
PMID: 36305855
Purpose: This study aimed to define the genotypic and phenotypic spectrum of reversible acute liver failure (ALF) of infancy resulting from biallelic pathogenic TRMU variants and determine the role of...
18.
Pearsson K, Compagno-Strandberg M, A Eklund E, Rask O, Kallen K
Seizure
. 2022 Oct;
103:39-45.
PMID: 36279595
Purpose: We conducted a cross-sectional study to evaluate long-term outcomes of epilepsy surgery in tuberous sclerosis complex (TSC) in a Swedish population. Methods: Demographic and seizure data was retrieved from...
19.
Ljungblad U, Lindberg M, A Eklund E, Saeves I, Bjorke-Monsen A, Tangeraas T
Acta Paediatr
. 2022 Aug;
111(12):2315-2321.
PMID: 36029294
Aim: Risk factors for vitamin B12 deficiency in infants are not fully understood. The aim of the study was to assess predictors of total homocysteine and methylmalonic acid analysed in...
20.
Orfanos I, Sotoca Fernandez J, Elfving K, Alfven T, A Eklund E
Acta Paediatr
. 2022 Jul;
111(10):2004-2009.
PMID: 35808896
Aim: Our aim was to evaluate the risk of bacterial meningitis, bacteremia, and urinary tract infection (UTI) in infants ≤60 days who presented to paediatric emergency departments (PEDs) after having...