K. Pienczk‐Reclawowicz

发表

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.

The C242T polymorphism of the gene encoding cytochrome b-245 alpha is not associated with paediatric ischaemic stroke: family-based and case-control study.

E. Emich-Widera, I. Kopyta, A. Balcerzyk, 2010, Neurologia i neurochirurgia polska.

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.

The TT genotype of methylenetetrahydrofolate reductase 677C>T polymorphism increases the susceptibility to pediatric ischemic stroke: meta-analysis of the 822 cases and 1,552 controls

E. Emich-Widera, B. Sarecka-Hujar, I. Kopyta, 2012, Molecular Biology Reports.

The rs10757278 Polymorphism of the 9p21.3 Locus in Children with Arterial Ischemic Stroke: A Family-Based and Case-Control Study.

W. Grzeszczak, S. Górczyńska-Kosiorz, W. Trautsolt, 2017, Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association.

Association analysis of the E‐selectin 98G > T polymorphism and the risk of childhood ischemic stroke

E. Emich-Widera, B. Sarecka-Hujar, I. Kopyta, 2010, Cell biochemistry and function.

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.

Tolosa-Hunt syndrome preceded by facial palsy in a child.

E. Pilarska, K. Pienczk‐Reclawowicz, 2011, Pediatric 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.

Cessation of sporadic hemiplegic migraine attacks after patent foramen ovale closure

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

Methylenetetrahydrofolate reductase gene A1298C polymorphism in pediatric stroke--case-control and family-based study.

E. Emich-Widera, I. Kopyta, A. Balcerzyk, 2015, Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association.

APOE gene epsilon polymorphism does not determine predisposition to ischemic stroke in children.

E. Emich-Widera, I. Kopyta, A. Balcerzyk, 2010, Pediatric neurology.

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

J. Sławek, E. Pilarska, A. Olszewska, 2021, Sleep medicine.

Restless legs syndrome in children.

J. Sławek, E. Pilarska, K. Pienczk‐Reclawowicz, 2020, Sleep medicine.

Upstream Stimulating Factor 1 (USF-1) Gene Polymorphisms and the Risk, Symptoms, and Outcome of Pediatric Ischemic Stroke.

W. Grzeszczak, S. Górczyńska-Kosiorz, E. Emich-Widera, 2018, Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association.

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

E. Emich-Widera, I. Kopyta, A. Balcerzyk, 2012, Folia neuropathologica.

The TT genotype of methylenetetrahydrofolate reductase 677C>T polymorphism increases the susceptibility to pediatric ischemic stroke: meta-analysis of the 822 cases and 1,552 controls

E. Emich-Widera, B. Sarecka-Hujar, I. Kopyta, 2012, Molecular Biology Reports.

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

K. Połatyńska, E. Emich-Widera, I. Kopyta, 2011, Neuropediatrics.

Long-Term Follow-Up with Video of a Patient with Deafness-Dystonia Syndrome Treated with DBS-GPi

J. Sławek, T. Mandat, J. Dulski, 2016, Stereotactic and Functional Neurosurgery.