I.M.P. Gommans

A locus on chromosome 15q for a dominantly inherited nemaline myopathy with core-like lesions

I.M.P. Gommans · Brain · 2003 · 60 citations · Full text

Medicine, Genetics, Molecular Genetics +13

A new phenotype of autosomal dominant nemaline myopathy

I.M.P. Gommans, Baziel G.M. van Engelen, H. J. ter Laak et al. · Neuromuscular Disorders · 2002 · 35 citations

Life Sciences, Genetics, Neurology +11

Skeletal muscle of mice with a mutation in slow α-tropomyosin is weaker at lower lengths

A. de Haan, M.R. van der Vliet, I.M.P. Gommans et al. · Neuromuscular Disorders · 2002 · 23 citations

Life Sciences, Molecular Biology, Physiology +10

Quadriceps weakness in a family with nemaline myopathy: influence of knee angle

Karin H. L. Gerrits, I.M.P. Gommans, Baziel G.M. van Engelen et al. · Clinical Science · 2003 · 14 citations

Medicine, Neurology, Neuromuscular Disorders +16