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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 Evidence
Wojciech 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 Them
Cécile F Rousseau, Romaldas Mačiulaitis, Dariusz Śladowski, et al.
Methods (San Diego, Calif.)
|
October 18, 2017
Reconstruction method for extended depth-of-field optical diffraction tomography
Wojciech 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 Perspective
Wojciech 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 reaction
Ireneusz Nawrot, Bogdan Woźniewicz, Jacek Szmidt, et al.
Pharmacological Reports : PR
|
February 26, 2015
Synthesis and anticancer activity of 7-hydroxycoumarinyl gallates
Elżbieta 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 implications
Małgorzata 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 dysmorphy
Anna 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 features
Anna Kutkowska-Kaźmierczak, Małgorzata Rydzanicz, Aleksander Chlebowski, et al.
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Search research articles
Search
Showing results (1-10 of 10) with videos related to
Sort By:
Page
of 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 Evidence
Wojciech 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 Them
Cécile F Rousseau, Romaldas Mačiulaitis, Dariusz Śladowski, et al.
Methods (San Diego, Calif.)
|
October 18, 2017
Reconstruction method for extended depth-of-field optical diffraction tomography
Wojciech 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 Perspective
Wojciech 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 reaction
Ireneusz Nawrot, Bogdan Woźniewicz, Jacek Szmidt, et al.
Pharmacological Reports : PR
|
February 26, 2015
Synthesis and anticancer activity of 7-hydroxycoumarinyl gallates
Elżbieta 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 implications
Małgorzata 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 dysmorphy
Anna 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 features
Anna Kutkowska-Kaźmierczak, Małgorzata Rydzanicz, Aleksander Chlebowski, et al.
Page
of 1