K. Pienczk-Ręcławowicz

The syndrome of deafness‐dystonia: Clinical and genetic heterogeneity

I. Parees, M. Edwards, K. Bhatia, 2013, Movement disorders : official journal of the Movement Disorder Society.

Polymorphisms of Genes Encoding Coagulation Factors II, V, VII, and XIII in Relation to Pediatric Ischemic Stroke: Family-based and Case-Control Study

E. Emich-Widera, I. Kopyta, A. Balcerzyk, 2012, The neurologist.

Cessation of sporadic hemiplegic migraine attacks after patent foramen ovale closure

M. Szmuda, E. Pilarska, K. Pienczk-Ręcławowicz, 2009, Developmental medicine and child neurology.

Paediatric Tolosa‐Hunt syndrome: the need for treatment guidelines and renewed criteria

E. Pilarska, K. Pienczk-Ręcławowicz, M. Lemka, 2010, Developmental medicine and child neurology.

Fibrinogen alpha and beta gene polymorphisms in pediatric stroke--case-control and family based study.

E. Emich-Widera, B. Sarecka-Hujar, I. Kopyta, 2015, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.