Per Bengtson
Malmoe, M, Sweden
Last Updated: 09/26/2026
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Found 18 publications
A non-affinity-dependent high-resolution mass spectrometry method for detecting and typing monoclonal free light immunoglobulin chains.
Journal: Journal of mass spectrometry and advances in the clinical lab
Published: May 10, 2025
Three unreported cases of TMEM199-CDG, a rare genetic liver disease with abnormal glycosylation.
Journal: Orphanet journal of rare diseases
Published: November 12, 2017
Mineral surface-reactive metabolites secreted during fungal decomposition contribute to the formation of soil organic matter.
Journal: Environmental microbiology
Published: August 10, 2017
Phenotyping of α-1-Antitrypsin by liquid chromatography-high resolution mass spectrometry.
Journal: Clinical mass spectrometry (Del Mar, Calif.)
Published: November 28, 2016
Decoupling of soil carbon and nitrogen turnover partly explains increased net ecosystem production in response to nitrogen fertilization.
Journal: Scientific reports
Published: February 14, 2016
Comparative Toxicities of Salts on Microbial Processes in Soil.
Journal: Applied and environmental microbiology
Published: December 20, 2015
A novel mutation on the transferrin gene abolishes one N-glycosylation site and alters the pattern of transferrin isoforms, mimicking that observed after excessive alcohol consumption.
Journal: Clinical biochemistry
Published: October 26, 2015
Archaeal Ammonia Oxidizers Dominate in Numbers, but Bacteria Drive Gross Nitrification in N-amended Grassland Soil.
Journal: Frontiers in microbiology
Published: September 14, 2015
Serum transferrin carrying the xeno-tetrasaccharide NeuAc-Gal-GlcNAc2 is a biomarker of ALG1-CDG.
Journal: Journal of inherited metabolic disease
Published: March 23, 2015
A fast semi-quantitative LC-MS method for measurement of intact apolipoprotein A-I reveals novel proteoforms in serum.
Journal: Clinica chimica acta; international journal of clinical chemistry
Published: December 03, 2014
A novel phenotype in N-glycosylation disorders: Gillessen-Kaesbach-Nishimura skeletal dysplasia due to pathogenic variants in ALG9.
Journal: European journal of human genetics : EJHG
Published: November 29, 2014
Last Updated: 09/26/2026