Jurkiewicz E - Search Results

1

Long-term effect of everolimus on epilepsy and growth in children under 3 years of age treated for subependymal giant cell astrocytoma associated with tuberous sclerosis complex.

Kotulska K, Chmielewski D, Borkowska J, Jurkiewicz E, Kuczyński D, Kmieć T, Łojszczyk B, Dunin-Wąsowicz D, Jóźwiak S. Kotulska K, et al. Among authors: jurkiewicz e. Eur J Paediatr Neurol. 2013 Sep;17(5):479-85. doi: 10.1016/j.ejpn.2013.03.002. Epub 2013 Apr 6. Eur J Paediatr Neurol. 2013. PMID: 23567018

2

MRI of a family with leukoencephalypathy with vanishing white matter.

Jurkiewicz E, Mierzewska H, Bekiesińska-Figatowska M, Pakua-Kościesza I, Kmieć T, Scheper G, van der Knaap MS, Pronicka E. Jurkiewicz E, et al. Pediatr Radiol. 2005 Oct;35(10):1027-30. doi: 10.1007/s00247-005-1498-3. Epub 2005 May 24. Pediatr Radiol. 2005. PMID: 15912409

3

[Moyamoya disease associated with stenosis of extracranial arteries: a case report and review of the literature].

Kaczorowska M, Jóźwiak S, Litwin M, Kmieć T, Kuczyński D, Jurkiewicz E, Kościerza I. Kaczorowska M, et al. Among authors: jurkiewicz e. Neurol Neurochir Pol. 2005 May-Jun;39(3):242-6. Neurol Neurochir Pol. 2005. PMID: 15981166 Review. Polish.

4

Homozygote for mutation c.1204 + 1G > A of the ARSA gene presents with a late-infantile form of metachromatic leukodystrophy and a rare MRI white matter lesion type.

Ługowska A, Szymańska K, Kmiec T, Tarczyńska I, Czartoryska B, Tylki-Szymańska A, Jurkiewicz E. Ługowska A, et al. Among authors: jurkiewicz e. J Appl Genet. 2005;46(3):337-9. J Appl Genet. 2005. PMID: 16110195

5

Giant intracranial aneurysm in a 9-year-old boy with tuberous sclerosis.

Jurkiewicz E, Jóźwiak S. Jurkiewicz E, et al. Pediatr Radiol. 2006 May;36(5):463. doi: 10.1007/s00247-005-0092-z. Epub 2006 Mar 14. Pediatr Radiol. 2006. PMID: 16534585 No abstract available.

6

Cyst-like cortical tubers in patients with tuberous sclerosis complex: MR imaging with the FLAIR sequence.

Jurkiewicz E, Jozwiak S, Bekiesinska-Figatowska M, Pakula-Kosciesza I, Walecki J. Jurkiewicz E, et al. Pediatr Radiol. 2006 Jun;36(6):498-501. doi: 10.1007/s00247-006-0142-1. Epub 2006 Mar 28. Pediatr Radiol. 2006. PMID: 16568295

7

Acute fright induces onset of symptoms in vanishing white matter disease-case report.

Kaczorowska M, Kuczynski D, Jurkiewicz E, Scheper GC, van der Knaap MS, Jozwiak S. Kaczorowska M, et al. Among authors: jurkiewicz e. Eur J Paediatr Neurol. 2006 Jul;10(4):192-3. doi: 10.1016/j.ejpn.2006.05.008. Epub 2006 Sep 6. Eur J Paediatr Neurol. 2006. PMID: 16952472

8

[Juvenile form of Alexander's disease - a case confirmed by detection of mutation in GFAP gene].

Kmieć T, Bilska M, Mierzewska H, Jurkiewicz E, Jóźwiak S. Kmieć T, et al. Among authors: jurkiewicz e. Neurol Neurochir Pol. 2007 May-Jun;41(3):267-71. Neurol Neurochir Pol. 2007. PMID: 17629821 Polish.

9

Infantile spasms and cytomegalovirus infection: antiviral and antiepileptic treatment.

Dunin-Wasowicz D, Kasprzyk-Obara J, Jurkiewicz E, Kapusta M, Milewska-Bobula B. Dunin-Wasowicz D, et al. Among authors: jurkiewicz e. Dev Med Child Neurol. 2007 Sep;49(9):684-92. doi: 10.1111/j.1469-8749.2007.00684.x. Dev Med Child Neurol. 2007. PMID: 17718825 Free article.

10

SURF1 missense mutations promote a mild Leigh phenotype.

Piekutowska-Abramczuk D, Magner M, Popowska E, Pronicki M, Karczmarewicz E, Sykut-Cegielska J, Kmiec T, Jurkiewicz E, Szymanska-Debinska T, Bielecka L, Krajewska-Walasek M, Vesela K, Zeman J, Pronicka E. Piekutowska-Abramczuk D, et al. Among authors: jurkiewicz e. Clin Genet. 2009 Aug;76(2):195-204. doi: 10.1111/j.1399-0004.2009.01195.x. Clin Genet. 2009. PMID: 19780766

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