Erik Eklund
31 – 40 of 64
- show: 10
- |
- sort: year (new to old)
Close
Embed this list
<iframe src=" "
width=" "
height=" "
allowtransparency="true"
frameborder="0">
</iframe>
- 2017
-
Mark
Respiratory chain complex III deficiency due to mutated BCS1L : A novel phenotype with encephalomyopathy, partially phenocopied in a Bcs1l mutant mouse model
(
- Contribution to journal › Article
- 2016
-
Mark
Serum transferrin carrying the xeno-tetrasaccharide NeuAc-Gal-GlcNAc2 is a biomarker of ALG1-CDG.
(
- Contribution to journal › Article
-
Mark
ALG1-CDG: Clinical and Molecular Characterization of 39 Unreported Patients.
2016) In Human Mutation(
- Contribution to journal › Article
- 2015
-
Mark
Neurological Aspects of Human Glycosylation Disorders
(
- Contribution to journal › Scientific review
- 2014
-
Mark
Dermatan sulfate epimerase 1 deficient mice as a model for human abdominal wall defects.
(
- Contribution to journal › Article
- 2012
-
Mark
Neurology of inherited glycosylation disorders
(
- Contribution to journal › Scientific review
- 2011
-
Mark
A novel treatment approach for paediatric Gorham-Stout syndrome with chylothorax
(
- Contribution to journal › Article
- 2010
-
Mark
Neonatal invasiv grupp B-streptokockinfektion. Förhastat av Socialstyrelsen att avfärda allmän screening.
(
- Contribution to journal › Article
- 2009
-
Mark
Reduced production of sulfated glycosaminoglycans occurs in Zambian children with kwashiorkor but not marasmus
(
- Contribution to journal › Article
- 2007
-
Mark
The importance of fibroblasts in remodelling of the human uterine cervix during pregnancy and parturition.
(
- Contribution to journal › Article