Zobrazeno 1 - 10
of 169
pro vyhledávání: '"Tomasz, Litwin"'
Autor:
Tomasz Litwin, Barbara Rędzia-Ogrodnik, Agnieszka Antos, Adam Przybyłkowski, Anna Członkowska, Jan Paweł Bembenek
Publikováno v:
Brain Sciences, Vol 14, Iss 7, p 727 (2024)
Wilson’s disease (WD) is a genetic disorder of copper metabolism with pathological copper accumulation in many organs, resulting in clinical symptoms, mostly hepatic and neuropsychiatric. As copper accumulates in the brain during WD, and almost 50%
Externí odkaz:
https://doaj.org/article/eff437774aa849c2a9034efdd27ca3f4
Publikováno v:
Magna Scientia UCEVA, Vol 3, Iss 1 (2023)
La EW es causada por las variantes de ATP7B que alteran el eflujo de cobre y provocan una acumulación excesiva de cobre, principalmente en el hígado y el cerebro. El diagnóstico de la EW se ve dificultado por su evolución clínica variable, su ap
Externí odkaz:
https://doaj.org/article/7806f284186c4509bb4b01e82fe7003a
Autor:
Magdalena Antczak‐Kowalska, Anna Członkowska, Ceren Eyileten, Anna Palejko, Agnieszka Cudna, Marta Wolska, Agnieszka Piechal, Tomasz Litwin
Publikováno v:
JIMD Reports, Vol 63, Iss 5, Pp 508-517 (2022)
Abstract Symptoms of Wilson disease (WD) vary and additional factors such as autoimmunity may play an important role in WD pathogenesis. The presence of antinuclear antibodies (ANA), anti‐neutrophil cytoplasmic antibodies, neuronal surface antibodi
Externí odkaz:
https://doaj.org/article/0ec3302178da401dbe181613131750ca
Autor:
Tomasz Litwin
Publikováno v:
Politeja, Vol 19, Iss 5(80) (2022)
POLITICAL LEADERSHIP AND THE RULES OF THE CONSTITUTION OF REPUBLIC OF POLAND FROM 1997 The main aim of this article is the analysis of how “political leadership” – a theoretical category from the political science – could be used in the leg
Externí odkaz:
https://doaj.org/article/dbed2da13ac74bae920172ec31407174
Publikováno v:
Life, Vol 13, Iss 8, p 1715 (2023)
Wilson’s disease (WD) is a genetic disorder with copper accumulation in various tissues leading to related clinical symptoms (mainly hepatic and neuropsychiatric) which can be in 85% of patients successfully treated with anti-copper agents. However
Externí odkaz:
https://doaj.org/article/01deb82b23724c898808a11a088e8f95
Autor:
Tomasz Litwin, Agnieszka Antos, Jan Bembenek, Adam Przybyłkowski, Iwona Kurkowska-Jastrzębska, Marta Skowrońska, Anna Członkowska
Publikováno v:
Diagnostics, Vol 13, Iss 14, p 2424 (2023)
Background: Treatment of Wilson’s disease (WD), an inherited disease characterized by copper overload, is lifelong and there is the possibility that copper deficiency (CD) may occur. We systematically reviewed the literature to describe treatment p
Externí odkaz:
https://doaj.org/article/ae42020f8ab94645bccc1caf7fc41bc4
Autor:
Agnieszka Antos, Anna Członkowska, Jan Bembenek, Marta Skowronska, Iwona Kurkowska-Jastrzębska, Tomasz Litwin
Publikováno v:
Diagnostics, Vol 13, Iss 9, p 1554 (2023)
Wilson’s disease (WD) is an inherited disorder of copper metabolism with clinical symptoms related to pathological copper accumulation, which are mainly hepatic and/or neuropsychiatric. The disease is potentially treatable with pharmacological agen
Externí odkaz:
https://doaj.org/article/0a8e43e16eb142f4933feb4077117244
Publikováno v:
BMC Neurology, Vol 19, Iss 1, Pp 1-6 (2019)
Abstract Background Wilson disease (WD) is genetically induced failure of copper metabolism which can be successfully treated with pharmacological agents. The prognosis for survival in most WD patients is favorable if diagnosis and anti-copper treatm
Externí odkaz:
https://doaj.org/article/42216c2589984116be112821382d3bc4
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-7 (2019)
Abstract Background Wilson disease (WD) is a genetic disorder involving impaired copper metabolism, which presents with hepatic, neurological, and/or psychiatric manifestations. WD requires lifelong pharmacotherapy and treatment persistence may be pr
Externí odkaz:
https://doaj.org/article/949fadc9a80943ac941d0669c66bb847
Autor:
Charles E. Mordaunt, Dorothy A. Kieffer, Noreene M. Shibata, Anna Członkowska, Tomasz Litwin, Karl-Heinz Weiss, Yihui Zhu, Christopher L. Bowlus, Souvik Sarkar, Stewart Cooper, Yu-Jui Yvonne Wan, Mohamed R. Ali, Janine M. LaSalle, Valentina Medici
Publikováno v:
Epigenetics & Chromatin, Vol 12, Iss 1, Pp 1-16 (2019)
Abstract Background Wilson disease (WD) is an autosomal recessive disease caused by mutations in ATP7B encoding a copper transporter. Consequent copper accumulation results in a variable WD clinical phenotype involving hepatic, neurologic, and psychi
Externí odkaz:
https://doaj.org/article/521022df0db14cdea7bc6260ed7768fa