I. Willers

Anderson–Fabry disease: Clinical manifestations of disease in female heterozygotes

Catharina Whybra, C. Kampmann, I. Willers et al. · Journal of Inherited Metabolic Disease · 2001 · 274 citations

The early clinical phenotype of Fabry disease: a study on 35 European children and adolescents

Markus Ries, Uma Ramaswami, Rossella Parini et al. · European Journal of Pediatrics · 2003 · 214 citations

Early Clinical Phenotype, Fabry Disease, Mendelian Disorder +3

A Co-operative Numerical Analysis of Nonscoto- and Nonphotochromogenic Slowly Growing Mycobacteria

K. H. Schröder, G Amadío, W. Anz et al. · Journal of General Microbiology · 1974 · 80 citations

Pathogenic Microbiology, Bacteriology, Bacterial Pathogens +19

Two-dimensional electrophoresis of soluble and structure-bound proteins from cultured human fibroblasts and hair root cells: Qualitative and quantitative variation

J. Klose, I. Willers, Surjit Singh et al. · Human Genetics · 1983 · 27 citations

Quantitative Variation, Structure-bound Proteins, Capillary Electrophoresis +13

5-Ethyl-2?-deoxyuridine: Absence of effects on the chromosomes of human lymphocytes and fibroblasts in culture

Surjit Singh, I. Willers, H. W. Goedde et al. · Human Genetics · 1974 · 20 citations

Human Lymphocytes, Cell Division, Cytogenetics +5