K. Skworc

Phenotypic variability in fatal familial insomnia (D178N-129M) genotype

A. Giese, W. Schulz-Schaeffer, H. Kretzschmar, 1998, Neurology.

Familial Creutzfeldt‐Jakob disease with a novel 120‐bp insertion in the prion protein gene

A. Giese, W. Schulz-Schaeffer, H. Kretzschmar, 1999, Annals of neurology.

Molecular genetics of human prion diseases in Germany

A. Giese, H. Kretzschmar, W. Schulz-Schaeffer, 1999, Human Genetics.

The German FFI Cases

A. Giese, H. Kretzschmar, W. Schulz-Schaeffer, 1998, Brain pathology.

Familial Creutzfeldt-Jakob disease with a novel 120-bp insertion in the prion protein gene.

A. Giese, W. Schulz-Schaeffer, H. Kretzschmar, 1999, Annals of neurology.