J. Wendorff

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 assessment of comorbid disorders in ADHD children and adolescents.

B. Wiśniewska, J. Wendorff, W. Baranowska, 2007, Advances in medical sciences.

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 state of diagnostication of neurodevelopmental disorders coexisting with ADHD in children and adolescents – own studies

B. Wiśniewska, J. Wendorff, 2011 .

Associations between MDR1 C3435T polymorphism and drug-resistant epilepsy in the Polish population

Andrzej Marchel, H. Romanowicz, B. Smolarz, 2017, Acta Neurologica Belgica.

The unusually large striae distensae all over the body.

H. Rotsztejn, B. Kamer, J. Wendorff, 2010, Advances in medical sciences.

The effect of seizures on functional status of people with spastic forms of cerebral palsy

A. Michalska, J. Wendorff, 2015 .

Skuteczność kwasu walproinowego w zespołach neurologicznych przebiegających z ruchami mimowolnymi u dzieci The effectiveness of sodium valproate in neurological syndromes with involuntary movements in children

J. Wendorff, J. Wendorff, 2006 .

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.

[Allergy effect on migraine course in older children and adolescents].

O. Hofman, B. Kamer, J. Wendorff, 1999, Neurologia i neurochirurgia polska.

[The diagnostic and therapeutic management in the first cerebral attack in childhood].

J. Wendorff, 2007, Przeglad lekarski.

Botulinum toxin treatment of spasticity in diplegic cerebral palsy: a randomized, double-blind, placebo-controlled, dose-ranging study.

T. Theologis, A. Cosgrove, Jean-Pierre Lin, 2002 .

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.

Botulinum toxin treatment of spasticity in diplegic cerebral palsy: a randomized, double‐blind, placebo‐controlled, dose‐ranging study

T. Theologis, A. Cosgrove, L. Carr, 2002, Developmental medicine and child neurology.

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 T Allele of the 677C>T Polymorphism of Methylenetetrahydrofolate Reductase Gene is Associated With an Increased Risk of Ischemic Stroke in Polish Children

E. Marszał, E. Emich-Widera, B. Sarecka-Hujar, 2009, Journal of child neurology.

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.

Nicolaides-Baraitser syndrome in the assessment of an interdisciplinary team

A. Michalska, A. Baran, J. Wendorff, 2013 .

[Photosensitivity in children with idiopathic headaches].

J. Wendorff, B. Juchniewicz, 2005, Neurologia i neurochirurgia polska.