I Hausmanowa-Pétrusewicz
Medical University of Warsaw(PL)Mossakowski Medical Research Institute, Polish Academy of Sciences(PL)Polish Academy of Sciences(PL)
Publications by Year
Research Areas
Neurogenetic and Muscular Disorders Research, Muscle Physiology and Disorders, Muscle activation and electromyography studies, Hereditary Neurological Disorders, Nuclear Structure and Function
Most-Cited Works
- → Genetic mapping of chronic childhood-onset spinal muscular atrophy to chromosome 5q1 1.2–13.3(1990)617 cited
- → Charcot-Marie-Tooth type 4B is caused by mutations in the gene encoding myotubularin-related protein-2(2000)457 cited
- → Meiotic stability and genotype – phenotype correlation of the trinucleotide repeat in X–linked spinal and bulbar muscular atrophy(1992)377 cited
- → A collaborative study on the natural history of childhood and juvenile onset proximal spinal muscular atrophy (type II and III SMA): 569 patients(1997)288 cited
- → The inner nuclear membrane protein Emerin regulates β‐catenin activity by restricting its accumulation in the nucleus(2006)236 cited
- → Mutations in the Sarcoglycan Genes in Patients with Myopathy(1997)220 cited