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Analytical Biochemistry|December 10, 2002
Measurement of ATP production and respiratory chain enzyme activities in mitochondria isolated from small muscle biopsy samplesRolf Wibom, Lars Hagenfeldt, Ulrika von DöbelnCurrent Opinion in Hematology|October 31, 2012
Guidelines for newborn screening of primary immunodeficiency diseasesStephan Borte, Ulrika von Döbeln, Lennart HammarströmJIMD Reports|February 23, 2013
Galactosemia screening with low false-positive recall rate: the Swedish experienceAnnika Ohlsson, Claes Guthenberg, Ulrika von DöbelnInternational Journal of Neonatal Screening|February 4, 2021
Gunnar Jungner and the Principles and Practice of Screening for DiseaseLars Jungner, Ingmar Jungner, Martin Engvall, et al.Journal of Inherited Metabolic Disease|June 14, 2019
Heterogeneity of disease-causing variants in the Swedish galactosemia population: Identification of 16 novel GALT variantsAnnika Ohlsson, Mary Hunt, Anna Wedell, et al.Journal of Inherited Metabolic Disease|March 13, 2010
Profound biotinidase deficiency: a rare disease among native SwedesAnnika Ohlsson, Claes Guthenberg, Elisabeth Holme, et al.International Journal of Neonatal Screening|October 19, 2020
Incidence of Glucose-6-Phosphate Dehydrogenase Deficiency among Swedish Newborn InfantsAnnika Ohlsson, Katarina Rehnholm, Kumar Shubham, et al.Acta Paediatrica (Oslo, Norway : 1992)|October 3, 2014
Epidemiology of lysosomal storage diseases in SwedenMalin Hult, Niklas Darin, Ulrika von Döbeln, et al.European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|June 24, 2026
Peroxisomal disorders - incidences in SwedenMaria Blomqvist, Karin Naess, Jan-Eric Månsson, et al.Annals of the New York Academy of Sciences|January 13, 2012
Newborn screening for primary immunodeficiencies: beyond SCID and XLAStephan Borte, Ning Wang, Sólveig Oskarsdóttir, et al.Pageof 6