Erik Eklund
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        - 2025
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        Autosomal dominant HK1-related neurodevelopmental disorder with visual defects and brain anomalies (NEDVIBA) : An emerging mitochondrial disorder
    
    - Contribution to journal › Article
 
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                        Mark
        Validating the PECARN rule to identify febrile infants at low risk of serious bacterial infections : an international validation study
    (2025) In Archives of Disease in Childhood- Contribution to journal › Article
 
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                        Mark
        Gene therapy in advanced metachromatic leukodystrophy : tempering expectations
    
    - Contribution to journal › Debate/Note/Editorial
 
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        The effect of elexacaftor-tezacaftor-ivacaftor on liver stiffness in children with cystic fibrosis
    
    - Contribution to journal › Article
 
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                        Mark
        Key lessons from the first international treatment eligibility committee : the case of metachromatic leukodystrophy
    
    - Contribution to journal › Article
 
- 2024
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                        Mark
        Coagulation abnormalities and vascular complications are common in PGM1-CDG
    
    - Contribution to journal › Article
 
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                        Mark
        Frontiers in congenital disorders of glycosylation consortium, a cross-sectional study report at year 5 of 280 individuals in the natural history cohort
    
    - Contribution to journal › Article
 
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        Newborn screening in metachromatic leukodystrophy – European consensus-based recommendations on clinical management
    
    - Contribution to journal › Article
 
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        ALG13-Congenital Disorder of Glycosylation (ALG13-CDG) : Updated clinical and molecular review and clinical management guidelines
    
    - Contribution to journal › Scientific review
 
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                        Mark
        Clinical characteristics of children with Borrelia-related peripheral facial palsy and utility of cerebrospinal fluid testing
    
    - Contribution to journal › Article
 
