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• Induction of Tolerance to Human Arysulfatase A in a Mouse Model of Metachromatic Leukodystrophy
  Ulrich Matzner, Frank Matthes, Eva Herbst, Renate Lüllmann-Rauch, Zsuzsanna Callaerts-Vegh, Rudi D' Hooge, Cecilia Weigelt, Carl Eistrup, Jens Fogh and Volkmar Gieselmann Molecular Medicine, Sept-Oct 2007, 13 (9-10): 1-9
• Enzyme replacement improves nervous system pathology and function in a mouse model for metachromatic leukodystrophy
  Ulrich Matzner, Eva Herbst, Kerstin Khalaj Hedayati, Renate Lüllmann-Rauch, Carsten Wessig, Stephan Schröder, Carl Eistrup, Christer Möller, Jens Fogh and Volkmar Gieselmann
  Human Molecular Genetics, 1 May 2005, Vol. 14, No. 9: 1139-1152
• Efficacy of Enzyme Replacement Therapy in a-Mannosidosis Mice. A Preclinical Animal Study
  Roces, D.P., Lüllmann-Rauch, R., Peng, J., Balducci, C., Andersson, C., Tollersrud, O., Fogh, J., Orlacchio, A., Beccari, T., Saftig, P. and von Figura, K.
  Human Molecular Genetics, 2004, 13, 1979 - 1988
• Characterization of Porphobilinogen Deaminase Deficient Mice During Phenobarbital Induction of Heme Synthesis and the Effect of Enzyme Replacement
  Johansson, A., Möller, C., Fogh, J. and Harper, P.
  Molecular Medicine, 2003, 9, 5/6, 193-199
• First clinical trial of I.V. rhPBGD in healthy subjects with and without diagnosed manifest Acute Intermittent Porphyria (AIP)
  Sardh E, Rejkjaer L, Harper P, Andersson D.E.H
  Dept of Internal Medicine, South General Hospital, Stockholm, Sweden, HemeBiotech A/S, Hillerød, Denmark, Porphyria Centre Sweden & Huddinge University Hospital, Stockholm, Sweden
  Porphyrins & Porphyrias 2003, Prague, September 21-24, 2003, Abstracts, Physiol. Res. 2003 Vol.52 23S
• Overt PCT in a symptomatic AIP patient on hemodialysis
  Sardh E, Harper P, Henrichson A, Möller C, Andersson D.E.H
  Dept of Internal Medicine, South General Hospital, Stockholm, Porphyria Centre Sweden, Huddinge University Hospital, Stockholm & HemeBiotech A/S, Lidingö, Sweden
  Porphyrins & Porphyrias 2003, Prague, September 21-24, 2003, Abstracts, Physiol. Res. 2003 Vol.52 22S
• Correction of the biochemical defect in porphobilinogen deaminase deficient cells by non-viral gene delivery
  Johansson A, Möller C, Harper P
  Institute for Laboratory Medicine, Porphyria Centre Sweden, Huddinge University Hospital, Stockholm & HemeBiotech A/S, Lidingö, Sweden
  Porphyrins & Porphyrias 2003, Prague, September 21-24, 2003, Abstracts, Physiol. Res. 2003 Vol.52 12S
• Correlation between plasma and urinary levels of porphobilinogen (PBG) and 5-aminolevulinic acid (ALA) in ten asymptomatic gene carriers of Acute Intermittent Porphyria (AIP) with increased porphyrin precursor excretion
  Harper P, Floderus Y, Andersson C, Möller C, Rejkjaer L, Sardh E, Andersson D.E.H
  Porphyria Centre Sweden, Huddinge University Hospital, Stockholm, Sweden, HemeBiotech A/S, Lidingö, Sweden, HemeBiotech A/S, Hillerød, Denmark & Dept Internal Medicine, South General Hospital, Stockholm, Sweden
  Porphyrins & Porphyrias 2003, Prague, September 21-24, 2003, Abstracts, Physiol. res. 2003 Vol.52 10S
• Enzyme substitution in a mouse model for metachromatic leukodystrophy, in vivo and in vitro studies
  D. Klein, C. Möller, J. Fogh, V. Gieselmann, U. Matzner
  Institut för Physiologische Chemie, Rheinische Friedrich-Wilhelms-Universität, Bonn, Germany & HemeBiotech A/S, Hillerød, Denmark
  Posters, 14th ESGLD Workshop, September 18-21, 2003, Pode brady, Czech Republic
• Correction of the biochemical defect in porphobilinogen deaminase deficient cells by non-viral gene delivery
  Johansson A, Möller C
  Porphyria Centre Sweden, Department of Medical Laboratory Sciences and Technology, Division of Clinical Chemistry, Karolinska Institute, Huddinge University Hospital, Stockholm, Sweden & HemeBiotech A/S, Lidingö, SwedeN
  Molecular and Cellular Biochemistry 250: 65-71, 2003
• Thesis - Correction of the enzymatic and biochemical defect in porphobilinogen deaminase deficient cells by non-viral mediated gene delivery
  Annika Johansson
• Thesis - Genetic Characterization of Swedish Families with Hereditary Coproporphyria, Variegate Porphyria, and Erythropoietic Protoporphyria
  Åsa Wiman
• Non-viral mediated gene transfer of porphobilinogen deaminase into mammalian cells
  A. Johansson, C. Möller, P. Gellerfors & P. Harper
  Porphyr ia Centre Sweden, Department of Medical Laboratory Sciences and Technology, Division of Clinical Chemistry, Karolinska Institute, Huddinge University Hospital, Stockholm, Sweden & HemeBiotech A/S, Lidingö, Sweden
  Scand J Clin Lab Invest 2002; 62: 105-114