Erik Eklund
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- 2022
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Mark
Breastfed Infants With Spells, Tremor, or Irritability : Rule Out Vitamin B12 Deficiency
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- Contribution to journal › Article
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Mark
Novel imaging findings in pyruvate dehydrogenase complex (PDHc) deficiency—Results from a nationwide population-based study
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- Contribution to journal › Article
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Mark
A Retrospective Evaluation of the Predictive Value of Newborn Screening for Vitamin B12 Deficiency in Symptomatic Infants Below 1 Year of Age
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- Contribution to journal › Article
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Mark
Management and Outcome of Febrile Infants ≤60 days, With Emphasis on Infants ≤21 Days Old, in Swedish Pediatric Emergency Departments
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- Contribution to journal › Article
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Mark
Paediatric emergency departments should manage young febrile and afebrile infants the same if they have a fever before presenting
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- Contribution to journal › Article
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Mark
Satisfaction and seizure outcomes of epilepsy surgery in tuberous sclerosis : A Swedish population-based long-term follow-up study
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- Contribution to journal › Article
- 2021
-
Mark
Age- and sex-specific prevalence of serious bacterial infections in febrile infants ≤60 days, in Sweden
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- Contribution to journal › Article
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Mark
Abnormal glucose tolerance and lung function in children with cystic fibrosis. Comparing oral glucose tolerance test and continuous glucose monitoring
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- Contribution to journal › Article
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Mark
The prevalence and clinical relevance of hyperhomocysteinemia suggesting vitamin B12 deficiency in presumed healthy infants
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- Contribution to journal › Article
- 2020
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Mark
Fasting reveals largely intact systemic lipid mobilization mechanisms in respiratory chain complex III deficient mice
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- Contribution to journal › Article
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Mark
Predominant and novel de novo variants in 29 individuals with ALG13 deficiency: Clinical description, biomarker status, biochemical analysis, and treatment suggestions
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- Contribution to journal › Article
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Mark
Early infantile epileptic encephalopathy due to biallelic pathogenic variants in PIGQ : Report of seven new subjects and review of the literature
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- Contribution to journal › Article
- 2019
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Mark
TANGO2 deficiency as a cause of neurodevelopmental delay with indirect effects on mitochondrial energy metabolism
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- Contribution to journal › Article
- 2018
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Mark
Three unreported cases of TMEM199-CDG, a rare genetic liver disease with abnormal glycosylation
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- Contribution to journal › Article
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Mark
DPAGT1 deficiency with encephalopathy (DPAGT1-CDG) : Clinical and genetic description of 11 new patients
(
- Chapter in Book/Report/Conference proceeding › Book chapter