Erik Eklund
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- 2025
-
Mark
Gene therapy in advanced metachromatic leukodystrophy : tempering expectations
- Contribution to journal › Debate/Note/Editorial
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Mark
The effect of elexacaftor-tezacaftor-ivacaftor on liver stiffness in children with cystic fibrosis
- 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
-
Mark
Autosomal dominant HK1-related neurodevelopmental disorder with visual defects and brain anomalies (NEDVIBA) : An emerging mitochondrial disorder
- Contribution to journal › Article
-
Mark
Key lessons from the first international treatment eligibility committee : the case of metachromatic leukodystrophy
- Contribution to journal › Article
- 2024
-
Mark
Overuse of EEG and ECG in children with breath-holding spells and its implication for the management of the spells
- Contribution to journal › Article
-
Mark
Biallelic variants in RINT1 present as early-onset pure hereditary spastic paraplegia
- Contribution to journal › Letter
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Mark
Newborn screening in metachromatic leukodystrophy – European consensus-based recommendations on clinical management
- Contribution to journal › Article
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Mark
Manifestations of X-linked pyruvate dehydrogenase complex deficiency in female PDHA1 carriers
- Contribution to journal › Article
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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
