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Autor:
Lesko N.
Publikováno v:
Науково-інформаційний вісник Івано-Франківського університету права імені Короля Данила Галицького, Vol 2, Iss 15(27), Pp 106-111 (2023)
Purpose. The purpose of the study is to develop theoretical provisions on ensuring the reliability of information by state information systems. Method. The methodology includes a comprehensive analysis and generalization of the available scientific a
Externí odkaz:
https://doaj.org/article/156824917fa74be6ad17319599089f7b
Autor:
Lesko N.
Publikováno v:
Науково-інформаційний вісник Івано-Франківського університету права імені Короля Данила Галицького, Iss 13(25), Pp 98-105 (2022)
Purpose. The aim of the article is to analyze the legal basis for preventing media violence against children. Method. The methodology includes a comprehensive analysis and generalization of existing scientific and theoretical material and the formula
Externí odkaz:
https://doaj.org/article/0f5f65dae1cb4fd39ec3b496b0b6a5a0
Autor:
Correia SP; Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.; Centre for Inherited Metabolic Diseases, Karolinska University Hospital, Stockholm, Sweden., Moedas MF; Centre for Inherited Metabolic Diseases, Karolinska University Hospital, Stockholm, Sweden.; Department of Medical Biochemistry and Biophysics, Karolinska Institutet, Stockholm, Sweden., Taylor LS; Mitochondrial Research Group, Translational and Clinical Research Institute, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, United Kingdom.; NHS Highly Specialised Service for Rare Mitochondrial Disorders, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, United Kingdom., Naess K; Centre for Inherited Metabolic Diseases, Karolinska University Hospital, Stockholm, Sweden.; Department of Medical Biochemistry and Biophysics, Karolinska Institutet, Stockholm, Sweden., Lim AZ; Mitochondrial Research Group, Translational and Clinical Research Institute, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, United Kingdom.; NHS Highly Specialised Service for Rare Mitochondrial Disorders, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, United Kingdom., McFarland R; Mitochondrial Research Group, Translational and Clinical Research Institute, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, United Kingdom.; NHS Highly Specialised Service for Rare Mitochondrial Disorders, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, United Kingdom., Kazior Z; Centre for Inherited Metabolic Diseases, Karolinska University Hospital, Stockholm, Sweden., Rumyantseva A; Department of Medical Biochemistry and Biophysics, Karolinska Institutet, Stockholm, Sweden., Wibom R; Centre for Inherited Metabolic Diseases, Karolinska University Hospital, Stockholm, Sweden.; Department of Medical Biochemistry and Biophysics, Karolinska Institutet, Stockholm, Sweden., Engvall M; Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.; Centre for Inherited Metabolic Diseases, Karolinska University Hospital, Stockholm, Sweden., Bruhn H; Centre for Inherited Metabolic Diseases, Karolinska University Hospital, Stockholm, Sweden.; Department of Medical Biochemistry and Biophysics, Karolinska Institutet, Stockholm, Sweden., Lesko N; Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.; Centre for Inherited Metabolic Diseases, Karolinska University Hospital, Stockholm, Sweden.; Department of Medical Biochemistry and Biophysics, Karolinska Institutet, Stockholm, Sweden., Végvári Á; Department of Medical Biochemistry and Biophysics, Karolinska Institutet, Stockholm, Sweden., Käll L; Science for Life Laboratory, School of Engineering Sciences in Chemistry, Biotechnology and Health, KTH-Royal Institute of Technology, Solna, Sweden., Trost M; Mitochondrial Research Group, Translational and Clinical Research Institute, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, United Kingdom.; Laboratory for Biomedical Mass Spectrometry, Biosciences Institute, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, United Kingdom., Alston CL; Mitochondrial Research Group, Translational and Clinical Research Institute, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, United Kingdom.; NHS Highly Specialised Service for Rare Mitochondrial Disorders, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, United Kingdom., Freyer C; Centre for Inherited Metabolic Diseases, Karolinska University Hospital, Stockholm, Sweden.; Department of Medical Biochemistry and Biophysics, Karolinska Institutet, Stockholm, Sweden., Taylor RW; Mitochondrial Research Group, Translational and Clinical Research Institute, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, United Kingdom.; NHS Highly Specialised Service for Rare Mitochondrial Disorders, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, United Kingdom., Wedell A; Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.; Centre for Inherited Metabolic Diseases, Karolinska University Hospital, Stockholm, Sweden., Wredenberg A; Centre for Inherited Metabolic Diseases, Karolinska University Hospital, Stockholm, Sweden.; Department of Medical Biochemistry and Biophysics, Karolinska Institutet, Stockholm, Sweden.
Publikováno v:
JCI insight [JCI Insight] 2024 Oct 22; Vol. 9 (20). Date of Electronic Publication: 2024 Oct 22.
Akademický článek
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The disease-causing mutation p.F907I reveals a novel pathogenic mechanism for POLγ-related diseases.
Autor:
Erdinc D; Department of Medical Biochemistry and Cell Biology, University of Gothenburg, Gothenburg SE-40530, Sweden., Macao B; Department of Medical Biochemistry and Cell Biology, University of Gothenburg, Gothenburg SE-40530, Sweden., Valenzuela S; Department of Medical Biochemistry and Cell Biology, University of Gothenburg, Gothenburg SE-40530, Sweden., Lesko N; Department of Medical Biochemistry and Biophysics, Karolinska Institute, Stockholm SE-17177, Sweden; Centre for Inherited Metabolic Diseases, Karolinska University Hospital, Stockholm, Sweden., Naess K; Department of Medical Biochemistry and Biophysics, Karolinska Institute, Stockholm SE-17177, Sweden; Centre for Inherited Metabolic Diseases, Karolinska University Hospital, Stockholm, Sweden., Peter B; Department of Medical Biochemistry and Cell Biology, University of Gothenburg, Gothenburg SE-40530, Sweden., Bruhn H; Department of Medical Biochemistry and Biophysics, Karolinska Institute, Stockholm SE-17177, Sweden; Centre for Inherited Metabolic Diseases, Karolinska University Hospital, Stockholm, Sweden., Wedell A; Department of Molecular Medicine and Surgery, Karolinska Institute, Stockholm, Sweden; Centre for Inherited Metabolic Diseases, Karolinska University Hospital, Stockholm, Sweden., Wredenberg A; Department of Medical Biochemistry and Biophysics, Karolinska Institute, Stockholm SE-17177, Sweden; Department of Molecular Medicine and Surgery, Karolinska Institute, Stockholm, Sweden. Electronic address: anna.wredenberg@ki.se., Falkenberg M; Department of Medical Biochemistry and Cell Biology, University of Gothenburg, Gothenburg SE-40530, Sweden. Electronic address: maria.falkenberg@medkem.gu.se.
Publikováno v:
Biochimica et biophysica acta. Molecular basis of disease [Biochim Biophys Acta Mol Basis Dis] 2023 Oct; Vol. 1869 (7), pp. 166786. Date of Electronic Publication: 2023 Jun 10.
Autor:
Engvall M., Kawasaki A., Carelli V., Wibom R., Bruhn H., Lesko N., Schober F. A., Wredenberg A., Wedell A., Traisk F.
Publikováno v:
Frontiers in Neurology
Frontiers in neurology, vol. 12, pp. 652590
Frontiers in neurology, vol. 12, pp. 652590
Leber hereditary optic neuropathy (LHON) is a mitochondrial disease causing severe bilateral visual loss, typically in young adults. The disorder is commonly caused by one of three primary point mutations in mitochondrial DNA, but a number of other r
Akademický článek
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Autor:
Schwarz G; Department of Neurology and Stroke Unit, ASST Grande Ospedale Metropolitano Niguarda, Milan, Italy (G.S., A.C.R., G.G., E.C.A.).; Stroke Research Centre, University College London, Institute of Neurology, UK (G.S.)., Cascio Rizzo A; Department of Neurology and Stroke Unit, ASST Grande Ospedale Metropolitano Niguarda, Milan, Italy (G.S., A.C.R., G.G., E.C.A.)., Matusevicius M; Department of Neurology, Karolinska University Hospital, Stockholm, Sweden (M.M., N.A.).; Department of Clinical Neuroscience, Karolinska Institutet, Stockholm, Sweden (M.M., N.A.)., Giussani G; Department of Neurology and Stroke Unit, ASST Grande Ospedale Metropolitano Niguarda, Milan, Italy (G.S., A.C.R., G.G., E.C.A.).; Department of Neurology - Stroke Unit, Ospedale San Giuseppe MultiMedica IRCCS, Milano, Italy (G.G.)., Invernizzi P; Neuroradiology and Neurology Units, Istituto Ospedaliero Fondazione Poliambulanza, Brescia, Italy (P.I.)., Melis F; S.S. Neurovascolare, ASL Città di Torino, Ospedale Maria Vittoria, Italia (F.M.)., Lesko N; Department of Neurology, P.J. Safarik University, Kosice, Slovakia (N.L.)., Toni D; Emergency Department Stroke Unit, Department of Human Neurosciences, Sapienza University of Rome, Italy (D.T.)., Agostoni EC; Department of Neurology and Stroke Unit, ASST Grande Ospedale Metropolitano Niguarda, Milan, Italy (G.S., A.C.R., G.G., E.C.A.)., Ahmed N; Department of Neurology, Karolinska University Hospital, Stockholm, Sweden (M.M., N.A.).; Department of Clinical Neuroscience, Karolinska Institutet, Stockholm, Sweden (M.M., N.A.).
Publikováno v:
Stroke [Stroke] 2023 Mar; Vol. 54 (3), pp. 743-750. Date of Electronic Publication: 2023 Feb 27.