E. Pilarska

发表

Early intervention and its short-term effect on the temporal organization of fidgety movements.

L. Adde, C. Einspieler, Michał Sokołów, 2020, Early human development.

SPEECH AND LANGUAGE DYSFUNCTION IN CHILDREN WITH EPILEPSY

M. Mazurkiewicz-Bełdzińska, M. Szmuda, E. Pilarska, 2015 .

Laryngological causes of headaches with special emphasis on the pediatric population

E. Pilarska, przyczyny laryngologiczne bólów, populacji dziecięcej, 2016 .

Prothrombotic risk factors in ischemic stroke and migraine in children

E. Pilarska, A. Bąkowska, M. Lemka, 2006, Acta neurologica Scandinavica.

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.

Peri-ictal headaches in the paediatric population – prospective study

M. Mazurkiewicz-Bełdzińska, M. Szmuda, M. Zawadzka, 2020, Cephalalgia : an international journal of headache.

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.

Re: Field testing of ICHD-3 beta criteria of periictal headache in patients with focal epilepsy – a prospective diary study

M. Mazurkiewicz-Bełdzińska, M. Szmuda, M. Zawadzka, 2018, Cephalalgia : an international journal of headache.

Lateral petrosectomy with obliteration cavity for spontaneous cerebrospinal otorrhea in children.

K. Niemczyk, E. Szurowska, E. Pilarska, 2014, American journal of otolaryngology.

Headaches in selected systemic diseases in children

E. Pilarska, Patrycja Harat-Smętek, 2015 .

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.

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.

[Antiphospholipid antibodies in children with migraine].

E. Pilarska, A. Bąkowska, M. Lemka, 2006, Neurologia i neurochirurgia polska.

[Epileptic seizures in the vascular malformations in children].

E. Pilarska, M. Lemka, 2006, Przeglad lekarski.

The impact of hippotherapy on the quality of trunk stabilisation, evaluated by EMG biofeedback, in children with infantile cerebral palsy

K. Górska, R. Hansdorfer-Korzon, E. Pilarska, 2017 .

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

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

Temperament traits of children with episodic tension-type headaches.

E. Pilarska, A. Olszewska, 2009, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

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.

Polish recommendations for diagnosis and therapy of paediatric stroke.

N. Irga-Jaworska, E. Emich-Widera, E. Szurowska, 2023, Neurologia i neurochirurgia polska.

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.