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Dariusz Śladowski

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Journal of Clinical Medicine|June 13, 2025
Platelet-Rich Plasma for Knee Osteoarthritis: A Comprehensive Narrative Review of the Mechanisms, Preparation Protocols, and Clinical EvidenceWojciech Michał Glinkowski, Grzegorz Gut, Dariusz Śladowski
Frontiers in Medicine|June 19, 2018
Cell and Gene Therapies: European View on Challenges in Translation and How to Address ThemCécile F Rousseau, Romaldas Mačiulaitis, Dariusz Śladowski, et al.
Methods (San Diego, Calif.)|October 18, 2017
Reconstruction method for extended depth-of-field optical diffraction tomographyWojciech Krauze, Arkadiusz Kuś, Dariusz Śladowski, et al.
Journal of Clinical Medicine|April 26, 2025
Molecular Mechanisms and Therapeutic Role of Intra-Articular Hyaluronic Acid in Osteoarthritis: A Precision Medicine PerspectiveWojciech Glinkowski, Dariusz Śladowski, Wiesław Tomaszewski, et al.
Central-European Journal of Immunology|July 9, 2015
Xenotransplantation of human cultured parathyroid progenitor cells into mouse peritoneum does not induce rejection reactionIreneusz Nawrot, Bogdan Woźniewicz, Jacek Szmidt, et al.
Pharmacological Reports : PR|February 26, 2015
Synthesis and anticancer activity of 7-hydroxycoumarinyl gallatesElżbieta Hejchman, Przemysław Taciak, Sebastian Kowalski, et al.
Science Advances|September 26, 2025
A sensory and motor neuropathy caused by a genetic variant of <i>NAMPT</i>Zhe Zhang, Jacek Pilch, Samuel Lundt, et al.
Molecular Genetics & Genomic Medicine|December 15, 2020
Variable degree of mosaicism for tetrasomy 18p in phenotypically discordant monozygotic twins-Diagnostic implicationsMałgorzata Rydzanicz, Pawel Olszewski, Darek Kedra, et al.
Human Molecular Genetics|January 31, 2021
Mosaic IL6ST variant inducing constitutive GP130 cytokine receptor signaling as a cause of neonatal onset immunodeficiency with autoinflammation and dysmorphyAnna Materna-Kiryluk, Agnieszka Pollak, Karol Gawalski, et al.
Journal of Medical Genetics|March 3, 2018
Dominant <i>ELOVL1</i> mutation causes neurological disorder with ichthyotic keratoderma, spasticity, hypomyelination and dysmorphic featuresAnna Kutkowska-Kaźmierczak, Małgorzata Rydzanicz, Aleksander Chlebowski, et al.
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Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
Journal of Clinical Medicine|June 13, 2025
Platelet-Rich Plasma for Knee Osteoarthritis: A Comprehensive Narrative Review of the Mechanisms, Preparation Protocols, and Clinical EvidenceWojciech Michał Glinkowski, Grzegorz Gut, Dariusz Śladowski
Frontiers in Medicine|June 19, 2018
Cell and Gene Therapies: European View on Challenges in Translation and How to Address ThemCécile F Rousseau, Romaldas Mačiulaitis, Dariusz Śladowski, et al.
Methods (San Diego, Calif.)|October 18, 2017
Reconstruction method for extended depth-of-field optical diffraction tomographyWojciech Krauze, Arkadiusz Kuś, Dariusz Śladowski, et al.
Journal of Clinical Medicine|April 26, 2025
Molecular Mechanisms and Therapeutic Role of Intra-Articular Hyaluronic Acid in Osteoarthritis: A Precision Medicine PerspectiveWojciech Glinkowski, Dariusz Śladowski, Wiesław Tomaszewski, et al.
Central-European Journal of Immunology|July 9, 2015
Xenotransplantation of human cultured parathyroid progenitor cells into mouse peritoneum does not induce rejection reactionIreneusz Nawrot, Bogdan Woźniewicz, Jacek Szmidt, et al.
Pharmacological Reports : PR|February 26, 2015
Synthesis and anticancer activity of 7-hydroxycoumarinyl gallatesElżbieta Hejchman, Przemysław Taciak, Sebastian Kowalski, et al.
Science Advances|September 26, 2025
A sensory and motor neuropathy caused by a genetic variant of <i>NAMPT</i>Zhe Zhang, Jacek Pilch, Samuel Lundt, et al.
Molecular Genetics & Genomic Medicine|December 15, 2020
Variable degree of mosaicism for tetrasomy 18p in phenotypically discordant monozygotic twins-Diagnostic implicationsMałgorzata Rydzanicz, Pawel Olszewski, Darek Kedra, et al.
Human Molecular Genetics|January 31, 2021
Mosaic IL6ST variant inducing constitutive GP130 cytokine receptor signaling as a cause of neonatal onset immunodeficiency with autoinflammation and dysmorphyAnna Materna-Kiryluk, Agnieszka Pollak, Karol Gawalski, et al.
Journal of Medical Genetics|March 3, 2018
Dominant <i>ELOVL1</i> mutation causes neurological disorder with ichthyotic keratoderma, spasticity, hypomyelination and dysmorphic featuresAnna Kutkowska-Kaźmierczak, Małgorzata Rydzanicz, Aleksander Chlebowski, et al.
Pageof 1