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Items: 29

1.

NMR-based metabolomics in pediatric drug resistant epilepsy - preliminary results.

Boguszewicz Ł, Jamroz E, Ciszek M, Emich-Widera E, Kijonka M, Banasik T, Skorupa A, Sokół M.

Sci Rep. 2019 Oct 21;9(1):15035. doi: 10.1038/s41598-019-51337-z.

2.

Mathematical evaluation of melatonin secretion in hypoxic ischemic encephalopathy.

Paprocka J, Kijonka M, Borys D, Emich-Widera E, Wojcieszek P, Sokół M.

Neuro Endocrinol Lett. 2018 Dec;39(5):391-400.

PMID:
30664345
3.

Evidence for HNRNPH1 being another gene for Bain type syndromic mental retardation.

Pilch J, Koppolu AA, Walczak A, Murcia Pienkowski VA, Biernacka A, Skiba P, Machnik-Broncel J, Gasperowicz P, Kosińska J, Rydzanicz M, Emich-Widera E, Płoski R.

Clin Genet. 2018 Oct;94(3-4):381-385. doi: 10.1111/cge.13410. Epub 2018 Aug 2.

PMID:
29938792
4.

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

Balcerzyk A, Niemiec P, Iwanicki T, Nowak T, Kopyta I, Emich-Widera E, Pilarska E, Pienczk-Ręcławowicz K, Kaciński M, Wendorff J, Górczyńska-Kosiorz S, Grzeszczak W, Żak I.

J Stroke Cerebrovasc Dis. 2018 Jul;27(7):1885-1889. doi: 10.1016/j.jstrokecerebrovasdis.2018.02.034. Epub 2018 Mar 26.

PMID:
29598907
5.

Melatonin and Angelman Syndrome: Implications and Mathematical Model of Diurnal Secretion.

Paprocka J, Kijonka M, Wojcieszek P, Pęcka M, Emich-Widera E, Sokół M.

Int J Endocrinol. 2017;2017:5853167. doi: 10.1155/2017/5853167. Epub 2017 Dec 12.

6.

Step-Initiation Deficits in Children with Faulty Posture Diagnosed with Neurodevelopmental Disorders during Infancy.

Stania M, Sarat-Spek A, Blacha T, Kazek B, Słomka KJ, Emich-Widera E, Juras G.

Front Pediatr. 2017 Nov 3;5:239. doi: 10.3389/fped.2017.00239. eCollection 2017.

7.

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

Niemiec P, Balcerzyk A, Iwanicki T, Emich-Widera E, Kopyta I, Nowak T, Pilarska E, Pienczk-Ręcławowicz K, Kaciński M, Wendorff J, Gorczynska-Kosiorz S, Trautsolt W, Grzeszczak W, Zak I.

J Stroke Cerebrovasc Dis. 2017 Dec;26(12):2763-2768. doi: 10.1016/j.jstrokecerebrovasdis.2017.06.053. Epub 2017 Aug 1.

PMID:
28778720
8.

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

Kopyta I, Niemiec P, Balcerzyk A, Emich-Widera E, Pilarska E, Pienczk-Ręcławowicz K, Kaciński M, Wendorff J, Nowak T, Iwanicki T, Sarecka-Hujar B, Zak I.

Eur J Paediatr Neurol. 2015 Mar;19(2):176-80. doi: 10.1016/j.ejpn.2014.11.011. Epub 2014 Dec 9.

PMID:
25555432
9.

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

Balcerzyk A, Niemiec P, Kopyta I, Emich-Widera E, Pilarska E, Pienczk-Ręcławowicz K, Kaciński M, Wendorff J, Żak I.

J Stroke Cerebrovasc Dis. 2015 Jan;24(1):61-5. doi: 10.1016/j.jstrokecerebrovasdis.2014.07.034. Epub 2014 Oct 16.

PMID:
25440348
10.

Polymorphism of ABCB1/MDR1 C3435T in children and adolescents with partial epilepsy is due to different criteria for drug resistance - preliminary results.

Emich-Widera E, Likus W, Kazek B, Sieroń AL, Urbanek K.

Med Sci Monit. 2014 Sep 16;20:1654-61. doi: 10.12659/MSM.890633.

11.

CYP3A5*3 and C3435T MDR1 polymorphisms in prognostication of drug-resistant epilepsy in children and adolescents.

Emich-Widera E, Likus W, Kazek B, Niemiec P, Balcerzyk A, Sieroń AL, Zak I.

Biomed Res Int. 2013;2013:526837. doi: 10.1155/2013/526837. Epub 2013 Aug 1.

12.

Polymorphisms of genes encoding coagulation factors II, V, VII, and XIII in relation to pediatric ischemic stroke: family-based and case-control study.

Kopyta IA, Emich-Widera E, Balcerzyk A, Niemiec P, Zak I, Pilarska E, Kaciński M, Wendorff J, Nowak T, Iwanicki T, Pienczk-Ręcławowicz K, Pałatyńska K.

Neurologist. 2012 Sep;18(5):282-6. doi: 10.1097/NRL.0b013e318266f702.

PMID:
22931734
13.

Headaches as somatoform disorders in children and adolescents.

Emich-Widera E, Kazek B, Szwed-Białożyt B, Kopyta I, Kostorz A.

Ment Illn. 2012 May 28;4(1):e9. doi: 10.4081/mi.2012.e9. eCollection 2012 Jul 26.

14.

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

Balcerzyk A, Nowak M, Kopyta I, Emich-Widera E, Pilarska E, Pienczk-Ręcławowicz K, Kaciński M, Wendorff J, Zak I.

Folia Neuropathol. 2012;50(2):147-51.

15.

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.

Sarecka-Hujar B, Kopyta I, Pienczk-Reclawowicz K, Reclawowicz D, Emich-Widera E, Pilarska E.

Mol Biol Rep. 2012 Aug;39(8):7957-63. doi: 10.1007/s11033-012-1641-9. Epub 2012 May 4.

16.

The plasminogen activator inhibitor-1 gene polymorphism in determining the risk of pediatric ischemic stroke--case control and family-based study.

Balcerzyk A, Żak I, Emich-Widera E, Kopyta I, Iwanicki T, Pilarska E, Pienczk-Ręcławowicz K, Kaciński M, Wendorff J, Połatyńska K.

Neuropediatrics. 2011 Feb;42(2):67-70. doi: 10.1055/s-0031-1279785. Epub 2011 Jun 6.

PMID:
21647848
17.

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

Niemiec P, Zak I, Emich-Widera E, Balcerzyk A, Kopyta I, Nowak T, Wendorff J, Pałatyńska K, Kaciński M, Pienczk-Ręcławowicz K, Pilarska E.

Neurol Neurochir Pol. 2010 Sep-Oct;44(5):453-8.

PMID:
21082491
18.

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

Sarecka-Hujar B, Zak I, Emich-Widera E, Kopyta I, Pilarska E, Pienczk-Reclawowicz K.

Cell Biochem Funct. 2010 Oct;28(7):591-6. doi: 10.1002/cbf.1696.

PMID:
20941749
19.
20.

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

Balcerzyk A, Zak I, Niemiec P, Kopyta I, Emich-Widera E, Iwanicki T, Pilarska E, Pienczk-Recławowicz K, Kacinski M, Wendorff J, Jachowicz-Jeszka J.

Pediatr Neurol. 2010 Jul;43(1):25-8. doi: 10.1016/j.pediatrneurol.2010.02.016. Erratum in: Pediatr Neurol. 2010 Nov;43(5):374. Pilarska, Ewa [added]; Pienczk-Recławowicz, Karolina [added]; Kacinski, Marek [added]; Wendorff, Jerzy [added]; Jachowicz-Jeszka, Joanna [added].

PMID:
20682199
21.

The T allele of the 677C>T polymorphism of methylenetetrahydrofolate reductase gene is associated with an increased risk of ischemic stroke in Polish children.

Zak I, Sarecka-Hujar B, Kopyta I, Emich-Widera E, Marszal E, Wendorff J, Jachowicz-Jeszka J.

J Child Neurol. 2009 Oct;24(10):1262-7. doi: 10.1177/0883073809333527.

PMID:
19805823
22.

[Concentrations of cadmium in blood and urine and their contents in the hair of children from Katowice Murcki].

Błach-Legawiec I, Emich-Widera E, Bibrzycka A, Marszał E, Woś H.

Wiad Lek. 2002;55 Suppl 1(Pt 2):633-8. Polish.

PMID:
17474575
23.

Malformations of cortical development in children: clinical manifestation, neuroimaging and neuropathology in selected cases.

Emich-Widera E, Larysz D, Kluczewska E, Larysz P, Adamek D, Mandera M, Marszał E.

Folia Neuropathol. 2006;44(4):307-13.

24.

[The function of eye and vision system in children and youth treated with vigabatrin--our own experiences].

Pojda-Wilczek D, Emich-Widera E, Herba E, Pojda SM, Marszał E.

Klin Oczna. 2005;107(10-12):654-7. Polish.

PMID:
16619812
25.

[Tuberculosis of the central nervous system: case reports].

Kluczewska-Zygan K, Emich-Widera E, Marszał E.

Neurol Neurochir Pol. 2003;37 Suppl 2:63-70. Polish.

PMID:
14560710
26.

[Nonepileptic seizures of psychogenic origin in children: analysis and characteristics of risk factors, clinical symptoms and significance of diagnostic investigation].

Marszał E, Emich-Widera E, Szwed-Białozyt B, Bibrzycka A, Bałdys A.

Przegl Lek. 2003;60 Suppl 1:39-41. Polish.

PMID:
12945160
27.

Determination of lactic acid level in systemic liquids in children with progressive encephalopathies.

Marszał E, Wojaczyńska-Stanek K, Pietruszewski J, Emich-Widera E, Bielińska-Bujniewicz E.

Med Sci Monit. 2002 Mar;8(3):CR217-22.

PMID:
11889460
28.

[The evaluation of selected factors in the prognosis of drug-resistant epilepsy in children with brain malformations].

Marszał E, Emich-Widera E, Kluczewska E, Krawczyk R.

Neurol Neurochir Pol. 2000;34 Suppl 1:253-64. Polish.

PMID:
10768166
29.

Deletion screening and carrier detection in Duchenne muscular dystrophy in Polish population via direct analysis of DNA and RNA transcripts.

Kwiatkowska J, Lisiecka D, Sowinska J, Marszal E, Emich-Widera E, Ciesielski T, Szczególa-Przymusiak A, Nuc P, Chlebowska H, Zimowski J, Galas-Zgorzalewicz B, Slomski R.

Biochimie. 1997 Jul;79(7):439-48.

PMID:
9352094

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