Karolina Pienczk-Ręcławowicz

The syndrome of deafness‐dystonia: Clinical and genetic heterogeneity

Maja Kojović, Isabel Pareés, Tânia Lampreia et al. · Movement Disorders · 2013 · 31 citations

Life Sciences, Genetics, Neurology +15

The prevalence of the restless legs Syndrome/Willis-Ekbom disease among teenagers, its clinical characteristics and impact on everyday functioning

Karolina Pienczk-Ręcławowicz, Ewa Pilarska, Anna Olszewska et al. · Sleep Medicine · 2021 · 16 citations

Medicine, Neurology, Pediatrics +6

Polymorphisms of Genes Encoding Coagulation Factors II, V, VII, and XIII in Relation to Pediatric Ischemic Stroke

Ilona Kopyta, Ewa Emich‐Widera, Anna Balcerzyk et al. · The Neurologist · 2012 · 15 citations

Life Sciences, Genetics, Molecular Genetics +16

Impact of the -174G/C interleukin-6 (IL-6) gene polymorphism on the risk of paediatric ischemic stroke, its symptoms and outcome.

Anna Balcerzyk, Marta Nowak, Ilona Kopyta et al. · PubMed · 2012 · 14 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

The Plasminogen Activator Inhibitor-1 Gene Polymorphism in Determining the Risk of Pediatric Ischemic Stroke − Case Control and Family-Based Study

Anna Balcerzyk, Iwona Żak, Ewa Emich‐Widera et al. · Neuropediatrics · 2011 · 12 citations

Life Sciences, Genetics, Molecular Genetics +16