A. Havelaar

发表

A new gene, encoding an anion transporter, is mutated in sialic acid storage diseases

Peter J. van der Spek, Leena Peltonen, Pertti Aula, 1999, Nature Genetics.

Lysosomal transport disorders

G. Mancini, F. Verheijen, A. Havelaar, 2000, Journal of Inherited Metabolic Disease.

NPT4, a new microsomal phosphate transporter: Mutation analysis in glycogen storage disease type Ic

G. Mancini, A. Benedetti, D. Melis, 2004, Journal of Inherited Metabolic Disease.

Transport of organic anions by the lysosomal sialic acid transporter: a functional approach towards the gene for sialic acid storage disease

G. Mancini, F. Verheijen, C. Beerens, 1999, FEBS letters.

Interindividual and intraindividual variability in plasma fibrinogen, TPA antigen, PAI activity, and CRP in healthy, young volunteers and patients with angina pectoris.

C. Kluft, M. D. de Maat, P. Meijer, 1996, Arteriosclerosis, thrombosis, and vascular biology.

Characterization of a heavy metal ion transporter in the lysosomal membrane

G. Mancini, F. Verheijen, C. Beerens, 1998, FEBS letters.

Variability in information from a single venapuncture in healthy volunteers: Analysis of the haemostatic variables fibrinogen, Plasminogen Activator Inhibitor (PAI) activity and histidine-rich glycoprotein (HRG)

A. Havelaar, B. C. Hennis, A. Bart, 1992 .

Purification of the Lysosomal Sialic Acid Transporter

F. Verheijen, C. Beerens, A. Havelaar, 1998, The Journal of Biological Chemistry.

A role for the transient increase of cytoplasmic free calcium in cell rescue after photodynamic treatment.

L. Penning, J. van der Zee, T. Dubbelman, 1992, Biochimica et biophysica acta.

Fibroblast silver loading for the diagnosis of Menkes disease.

G. Mancini, W. Kleijer, F. Verheijen, 1998, Journal of Medical Genetics.