Erik Eklund

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2024
Mark Newborn screening in metachromatic leukodystrophy – European consensus-based recommendations on clinical management
Laugwitz, Lucia ; Schoenmakers, Daphne H. ; Adang, Laura A. ; Beck-Woedl, Stefanie ; Bergner, Caroline ; Bernard, Geneviève ; Bley, Annette ; Boyer, Audrey ; Calbi, Valeria and Dekker, Hanka , et al. (2024) In European Journal of Paediatric Neurology 49. p.141-154
- Contribution to journal › Article
Mark Clinical Characteristics Suggestive of a Genetic Cause in Cerebral Palsy : A Systematic Review
Janzing, Anna M ; Eklund, Erik ^LU ; De Koning, Tom J ^LU and Eggink, Hendriekje (2024) In Pediatric Neurology 153. p.144-151
- Contribution to journal › Scientific review
Mark Cost Effectiveness of Adding Fenfluramine to Standard of Care for Patients with Dravet Syndrome in Sweden
Malmberg, Chiara ; Värendh, Magnus ; Berling, Patric ; Charokopou, Mata and Eklund, Erik ^LU (2024) In Applied Health Economics and Health Policy 22(4). p.543-554
- Contribution to journal › Article
Mark Overuse of EEG and ECG in children with breath-holding spells and its implication for the management of the spells
Hellström Schmidt, Sanna ^LU ; Smedenmark, Julia ; Jeremiasen, Ida ^LU ; Sigurdsson, Björn ^LU ; Eklund, Erik A ^LU and Pronk, Cornelis Jan ^LU (2024) In Acta Pædiatrica 113(2). p.317-326
- Contribution to journal › Article
Mark Physician's conceptions of the decision-making process when managing febrile infants ≤ 60 days old : a phenomenographic qualitative study
Orfanos, Ioannis ^LU ; Lindkvist, Rose-Marie ^LU ; Eklund, Erik G A ^LU ; Elfving, Kristina ^LU ; Alfvén, Tobias ^LU ; de Koning, Tom J ^LU and Castor, Charlotte ^LU (2024) In BMC Pediatrics 24.
- Contribution to journal › Article
Mark Coagulation abnormalities and vascular complications are common in PGM1-CDG
Radenkovic, Silvia ; Bleukx, Sofie ; Engelhardt, Nicole ; Eklund, Erik ^LU ; Mercimek-Andrews, Saadet ; Edmondson, Andrew C. and Morava, Eva (2024) In Molecular Genetics and Metabolism 142(4).
- Contribution to journal › Article
Mark Frontiers in congenital disorders of glycosylation consortium, a cross-sectional study report at year 5 of 280 individuals in the natural history cohort
Lam, Christina ; Eklund, E.A. ^LU and Morava, E. (2024) In Molecular Genetics and Metabolism 142(4).
- Contribution to journal › Article
2023
Mark Childhood tuberous sclerosis complex in southern Sweden: A paradigm shift in diagnosis and treatment.
Pearson, Kevin ^LU ; Björk Werner, Josefin ^LU ; Lundgren, Johan ^LU ; Gränse, Lotta ^LU ; Karlsson, Emma ; Källen, Kristina ^LU ; Eklund, Erik A ^LU and Bekassy, Zivile ^LU (2023) In BMC Pediatrics 23(1).
- Contribution to journal › Article
Mark Genotypic and phenotypic spectrum of infantile liver failure due to pathogenic TRMU variants
Vogel, G.F. ; Eklund, E.A. ^LU and Wortmann, S. (2023) In Genetics in Medicine 25(6).
- Contribution to journal › Article
Mark The evolution of epilepsy surgery in tuberous sclerosis in Sweden: A national registry study
Pearson, Kevin ^LU ; Eklund, Erik ^LU ; Rask, Olof ^LU ; Rosén, Ingmar ^LU ; Sjunnesson, Håkan ^LU and COMPAGNO STRANDBERG, MARIA ^LU (2023) In Seizure 112. p.54-61
- Contribution to journal › Article

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