Justyna Zielińska-Turek

Dr. Justyna Zielińska-Turek

Central Clinical Hospital of Ministry of Internal Affairs and Administration
orcid

Research Focus & Metrics

Academic Career Length

15Years (2012-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 December 2018 in The Lancet Neurology
Verified
Journal Article
Closed access
SKScott E Kasner
Scott E Kasner
BSBalakumar Swaminathan
Balakumar Swaminathan
PLPablo Lavados
Pablo Lavados
MSMukul Sharma
Mukul Sharma
KMKeith Muir
Keith Muir
JZJ Zwiernik
J Zwiernik

27 February 2019 in Neural Plasticity
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Journal Article
Open access
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JDJan Dąbrowski
Jan Dąbrowski
ACAnna Czajka
Anna Czajka
JZJustyna Zielińska-Turek
Justyna Zielińska-Turek
JJJanusz Jaroszyński
Janusz Jaroszyński
MFMarzena Furtak-Niczyporuk
Marzena Furtak-Niczyporuk
AZAndrzej Ziemba
Andrzej Ziemba
Stroke is the second cause of death and more importantly first cause of disability in people over 40 years of age. Current therapeutic management of ischemic stroke does not provide fully satisfactory outcomes. Stroke management has significantly changed since the time when there were opened modern stroke units with early motor and speech rehabilitation in hospitals. In recent decades, researchers searched for biomarkers of ischemic stroke and neuroplasticity in order to determine effective diagnostics, prognostic assessment, and therapy. Complex background of events following ischemic episode hinders successful design of effective therapeutic strategies. So far, studies have proven that regeneration after stroke and recovery of lost functions may be assigned to neuronal plasticity understood as ability of brain to reorganize and rebuild as an effect of changed environmental conditions. As many neuronal processes influencing neuroplasticity depend on expression of particular genes and genetic diversity possibly influencing its effectiveness, knowledge on their mechanisms is necessary to understand this process. Epigenetic mechanisms occurring after stroke was briefly discussed in this paper including several mechanisms such as synaptic plasticity; neuro-, glio-, and angiogenesis processes; and growth of axon.

Verified
Journal Article
Open access
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ZZZuzanna Ząbek
Zuzanna Ząbek
AWAleksandra Wyczałkowska-Tomasik
Aleksandra Wyczałkowska-Tomasik
KPKamil Poboży
Kamil Poboży
Jakub Piotr AdamusJakub Piotr Adamus
Jakub Piotr Adamus
GTGrzegorz Turek
Grzegorz Turek
LPLeszek Pączek
Leszek Pączek
Intervertebral disc degeneration is a leading contributor to chronic back pain and disability worldwide. This review comprehensively explores the complex interplay of cellular, molecular, and biomechanical alterations within the disc microenvironment that underlie intervertebral disc degeneration pathophysiology. Emphasis is placed on extracellular matrix degradation, cellular senescence, inflammation, oxidative stress, angiogenesis, and multiple forms of programmed cell death including apoptosis, pyroptosis, and ferroptosis. An in-depth analysis of key signaling pathways and regulatory molecules illustrates how these processes disrupt homeostasis and drive disease progression. Additionally, the review highlights emerging therapeutic approaches aimed at modifying the disc microenvironment, including mesenchymal and notochordal cell-based therapies, senolytics, ferroptosis inhibitors, gene therapy, and biomaterial innovations such as hydrogels, scaffolds, and nanocarriers. These strategies target degenerative cascades at the molecular level and represent a shift toward regenerative and disease-modifying interventions. While several approaches show promise in preclinical and early clinical studies, challenges related to safety, delivery, and long-term efficacy remain. This review underscores the importance of integrating molecular insights with translational innovations to develop targeted therapies for intervertebral disc degeneration and guide future research efforts.

10 January 2020 in Acta Neurologica Scandinavica
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Journal Article
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SDSebastian M. Dzierzecki
Sebastian M. Dzierzecki
GTGrzegorz Turek
Grzegorz Turek
BCBartosz Czapski
Bartosz Czapski
KDKatarzyna Dyttus‐Cebulok
Katarzyna Dyttus‐Cebulok
RTRyszard Tomasiuk
Ryszard Tomasiuk
MZMirosław Ząbek
Mirosław Ząbek

1 October 2015 in Journal of Neurosurgery
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Journal Article
Closed access
GTGrzegorz Turek
Grzegorz Turek
JKJan Kochanowicz
Jan Kochanowicz
ALAndrzej Lewszuk
Andrzej Lewszuk
TLTomasz Lyson
Tomasz Lyson
JZJustyna Zielińska-Turek
Justyna Zielińska-Turek
ZMZenon Mariak
Zenon Mariak
OBJECT: Distal coil or stent migration is a rare, but potentially morbid complication of intracranial aneurysm embolization. At present, there is no established standard of surgical evacuation of displaced material—in particular, there is no consensus on the optimum time for such intervention. The authors report their positive experiences with an ultra-early surgical evacuation of 2 migrated coils and a flow-diverter stent. METHODS: Uncontrolled coil or stent migration occurred in 3 (0.75%) of approximately 400 patients treated between 1999 and 2012 in the authors' institution. In all 3 cases, the materials moved from their intended position to the middle cerebral artery (MCA). Surgical evacuation was started immediately (within half an hour) after a futile attempt of removing them via intraarterial route, under the same anesthesia and with no active reversal of heparinization. RESULTS: No excessive bleeding was observed. Displaced coils were extracted through an incision of a branch of MCA—the anterior temporal artery, the stent was removed through a direct incision of MCA. Recombinant tissue plasminogen activator (rtPA) was injected to the stem of the internal carotid artery toward the end of the procedure, with no discernible adverse effects. Two patients were discharged with no deficit (Glasgow Outcome Scale [GOS] Score 5); the other patient was conscious with mild hemiparesis (GOS Score 4) at discharge. CONCLUSIONS: The experiences of these 3 cases suggest that immediate removal of a migrated stent/coil is feasible and may be effective. Indirect access to the MCA through its branch helps to shorten the time of temporary clipping of the artery to a minimum. Maintaining active heparinization and direct intraarterial injection of rtPA are helpful in promoting blood flow in the MCA.

1 September 2017 in Neurologia i Neurochirurgia Polska
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Journal Article
Closed access
ASAgnieszka Słowik
Agnieszka Słowik
MWMarcin Wnuk
Marcin Wnuk
PBPaweł Brzegowy
Paweł Brzegowy
JCJoanna Chrzanowska-Waśko
Joanna Chrzanowska-Waśko
AGAleksandra Golenia
Aleksandra Golenia
TPTadeusz J. Popiela
Tadeusz J. Popiela
Mechanical thrombectomy (MT) is not reimbursed by the Polish public health system. We present a description of 5 years of experience with MT in acute stroke in Comprehensive Stroke Centers (CSCs) in Poland. We retrospectively analyzed the results of a structured questionnaire from 23 out of 25 identified CSCs and 22 data sets that include 61 clinical, radiological and outcome measures. Most of the CSCs (74%) were founded at University Hospitals and most (65.2%) work round the clock. In 78.3% of them, the working teams are composed of neurologists and neuro-radiologists. All CSCs perform CT and angio-CT before MT. In total 586 patients were subjected to MT and data from 531 of them were analyzed. Mean time laps from stroke onset to groin puncture was 250±99min. 90.3% of the studied patients had MT within 6h from stroke onset; 59.3% of them were treated with IV rt-PA prior to MT; 15.1% had IA rt-PA during MT and 4.7% - emergent stenting of a large vessel. M1 of MCA was occluded in 47.8% of cases. The Solitaire device was used in 53% of cases. Successful recanalization (TICI2b-TICI3) was achieved in 64.6% of cases and 53.4% of patients did not experience hemorrhagic transformation. Clinical improvement on discharge was noticed in 53.7% of cases, futile recanalization - in 30.7%, mRS of 0-2 - in 31.4% and mRS of 6 in 22% of cases. Our results can help harmonize standards for MT in Poland according to international guidelines.