K. Handschug

Genetic and functional characteristics of the human in vivo LRP1/A2MR receptor suggested as a risk marker for Alzheimer’s disease and other complex (degenerative) diseases

K. Huse, G. Birkenmeier, S. Schulz, 2004, Neuroscience Research.

Chromosomal fragility in patients with triple A syndrome

S. Gollin, D. Finegold, A. Huebner, 2003, American journal of medical genetics. Part A.

Triple A syndrome is caused by mutations in AAAS, a new WD-repeat protein gene.

S. Hennig, S. Sperling, A. Huebner, 2001, Human molecular genetics.

Triple A syndrome: genotype–phenotype assessment

A. Huebner, I. Prpić, M. Peršić, 2003, Clinical genetics.

Triple a Syndrome—Clinical Aspects and Molecular Genetics

A. Huebner, F. Ozkinay, A. Huebner, 2000, Endocrine research.

NEW INSIGHTS INTO THE MOLECULAR BASIS OF THE TRIPLE A SYNDROME

A. Huebner, A. Kaindl, K. Handschug, 2002, Endocrine research.

Different expression of the α2-macroglobulin receptor/low-density lipoprotein receptor-related protein in human keratinocytes and fibroblasts

G. Birkenmeier, E. Fabricius, K. Handschug, 1998, Archives of Dermatological Research.

Low-density lipoprotein receptor-related protein in atherosclerosis development: up-regulation of gene expression in patients with coronary obstruction

S. Schulz, C. Gläser, W. Teichmann, 1998, Journal of Molecular Medicine.