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Atherosclerosis|February 1, 1991
Molecular basis of lipoprotein lipase deficiency in two Austrian families with type I hyperlipoproteinemiaB Paulweber, H Wiebusch, G Miesenboeck, et al.
Nutrition, Metabolism, and Cardiovascular Diseases : NMCD|July 17, 2012
Heterozygosity for lysosomal acid lipase E8SJM mutation and serum lipid concentrationsSa Muntoni, H Wiebusch, M Jansen-Rust, et al.
Zeitschrift Fur Kardiologie|July 23, 2002
[Clinical aspects and molecular genetics of the Jervell- and Lange-Nielsen Syndrome]G Mönnig, E Schulze-Bahr, H Wedekind, et al.
Pacing and Clinical Electrophysiology : PACE|May 9, 2001
Clinical value of electrocardiographic parameters in genotyped individuals with familial long QT syndromeG Moennig, E Schulze-Bahr, H Wedekind, et al.
International Journal of Rehabilitation Research. Internationale Zeitschrift Fur Rehabilitationsforschung. Revue Internationale De Recherches De Readaptation|January 1, 1985
[Opinions of normal citizens on asocial behavior--various aspects, its dimensions and stability]E H Funke
Atherosclerosis|February 10, 1997
Heterozygous hepatic lipase deficiency, due to two missense mutations R186H and L334F, in the HL geneP Knudsen, M Antikainen, M Uusi-Oukari, et al.
Neuroscience Letters|March 6, 1998
Absence of mutations in peripheral myelin protein-22, myelin protein zero, and connexin 32 in autosomal recessive Dejerine-Sottas syndromeF Stögbauer, P Young, H Wiebusch, et al.
The Journal of Clinical Investigation|December 1, 1995
A unique genetic and biochemical presentation of fish-eye diseaseJ A Kuivenhoven, E J van Voorst tot Voorst, H Wiebusch, et al.
Nature Genetics|August 4, 1999
Tangier disease is caused by mutations in the gene encoding ATP-binding cassette transporter 1S Rust, M Rosier, H Funke, et al.
The Netherlands Journal of Medicine|November 1, 1996
Compound heterozygosity for a known and a novel defect in the lipoprotein lipase gene (Asp250-->Asn; Ser251-->Cys) resulting in lipoprotein lipase (LPL) deficiencyS M Bijvoet, H Wiebusch, Y Ma, et al.
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