about
Ectopic virilising adrenocortical tumour in the spinal region in an 8 year-old boy: a case report and review of the literatureIn vitro anti-HIV-1 activity of chondroitin polysulphateAttenuated adenylosuccinate lyase deficiency: a report of one case and a review of the literature.Basal ganglia lesions in children and adults.Apparent diffusion coefficient is increased in children with tuberous sclerosis complex personal experience and review of the literature.Giant cerebellar cavernous malformation in 4-month-old boy. Case report and review of the literature.Long-term MRI cell tracking after intraventricular delivery in a patient with global cerebral ischemia and prospects for magnetic navigation of stem cells within the CSFEpilepsy in newborns with tuberous sclerosis complex.MR imaging, apparent diffusion coefficient and histopathological features of desmoplastic infantile tumors-own experience and review of the literature.[Moyamoya disease associated with stenosis of extracranial arteries: a case report and review of the literature]."Drop attacks" as first clinical symptoms in a child carrying MTTK m.8344A>G mutation.MRI findings in the young infant with brainstem disconnection and extracerebral features. Report of one case and review of the literature.Trilateral retinoblastoma: an institutional experience and review of the literature.Magnetic resonance imaging in the evaluation of the fetal spinal canal contents.Recessive Mutations in POLR3B Encoding RNA Polymerase III Subunit Causing Diffuse Hypomyelination in Patients with 4H Leukodystrophy with Polymicrogyria and Cataracts.[Neuroimaging of multiple sclerosis in children].Magnetic resonance imaging of the brain in adenylosuccinate lyase deficiency: a report of seven cases and a review of the literature.Congenital subependymal giant cell astrocytomas in patients with tuberous sclerosis complex.New perspective in diagnostics of mitochondrial disorders: two years' experience with whole-exome sequencing at a national paediatric centre.Absence of an orphan mitochondrial protein, c19orf12, causes a distinct clinical subtype of neurodegeneration with brain iron accumulation.Contrast enhancement pattern predicts poor survival for patients with non-WNT/SHH medulloblastoma tumours.Severe central and peripheral paraneoplastic demyelination associated with tumours of the ovaries.Intracerebroventricular Transplantation of Cord Blood-Derived Neural Progenitors in a Child With Severe Global Brain Ischemic Injury.Bioimpedance Analysis as a Method to Evaluate the Proportion of Fatty and Muscle Tissues in Progressive Myopathy in Pompe DiseaseSpinal cord compression in Maroteaux-Lamy syndrome: case report and review of the literature with effects of enzyme replacement therapy.Clinical and radiological pictures of two newborn babies with manifestations of chondrodysplasia punctata and review of available literature.Brain Metastases from Ewing's Sarcoma. A Report of Two Cases and Review of the Literature.Naturally occurring V1-env region variants mediate simian immunodeficiency virus SIVmac escape from high-titer neutralizing antibodies induced by a protective subunit vaccine.Congenital disorder of glycosylphosphatidylinositol (GPI)-anchor biosynthesis--The phenotype of two patients with novel mutations in the PIGN and PGAP2 genes.Magnetic resonance imaging of brain abnormalities in patients with the Nijmegen breakage syndrome.Infratentorial tumors in children - value of ADC in prediction of grade of neoplasms.Usefulness of magnetic resonance imaging with SWI sequence (susceptibility-weighted imaging) in diagnosing cerebral hemosiderosis - case reportRhombencephalosynapsis - isolated anomaly or complex malformation?SURF1 missense mutations promote a mild Leigh phenotype.Severe encephalopathy with brain atrophy and hypomyelination due to adenylosuccinate lyase deficiency--MRI, clinical, biochemical and neuropathological findings of Polish patients.Arterial hypertension with brachydactyly in a 15-year-old boy.[MRI in the diagnosis of congenital white matter diseases and other neurodegenerative diseases].Blood pressure rhythmicity and visceral fat in children with hypertension.EEG abnormalities preceding the epilepsy onset in tuberous sclerosis complex patients - a prospective study of 5 patients.LG-35LOW GRADE GLIOMAS (LGG) IN INFANTS - ONE INSTITUTION EXPERIENCE.
P50
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P50
description
Polish radiologist and medical imaging specialist
@en
Pools onderzoekster
@nl
investigadora polaca
@gl
polska lekarka, radiolog i specjalistka metod obrazowych w medycynie
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name
Elzbieta Jurkiewicz
@ast
Elzbieta Jurkiewicz
@es
Elzbieta Jurkiewicz
@nl
Elżbieta Jurkiewicz
@ca
Elżbieta Jurkiewicz
@cs
Elżbieta Jurkiewicz
@en
Elżbieta Jurkiewicz
@ga
Elżbieta Jurkiewicz
@gl
Elżbieta Jurkiewicz
@it
Elżbieta Jurkiewicz
@pl
type
label
Elzbieta Jurkiewicz
@ast
Elzbieta Jurkiewicz
@es
Elzbieta Jurkiewicz
@nl
Elżbieta Jurkiewicz
@ca
Elżbieta Jurkiewicz
@cs
Elżbieta Jurkiewicz
@en
Elżbieta Jurkiewicz
@ga
Elżbieta Jurkiewicz
@gl
Elżbieta Jurkiewicz
@it
Elżbieta Jurkiewicz
@pl
altLabel
Elzbieta Jurkiewicz
@en
prefLabel
Elzbieta Jurkiewicz
@ast
Elzbieta Jurkiewicz
@es
Elzbieta Jurkiewicz
@nl
Elżbieta Jurkiewicz
@ca
Elżbieta Jurkiewicz
@cs
Elżbieta Jurkiewicz
@en
Elżbieta Jurkiewicz
@ga
Elżbieta Jurkiewicz
@gl
Elżbieta Jurkiewicz
@it
Elżbieta Jurkiewicz
@pl
P214
P101
P106
P1153
12801083900
P1412
P1559
Elżbieta Jurkiewicz
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P21
P214
P27
P31
P3124
P496
0000-0003-4505-8815
P734
P735
P7859
viaf-164106120