Search Results - "Rong, Shiwen"
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Trio-whole exome sequencing reveals the importance of de novo variants in children with intellectual disability and developmental delay
Published in Scientific reports (11-11-2024)“…Understanding the genetic basis of developmental delay (DD) and intellectual disability (ID) remains a considerable clinical challenge. This study evaluated…”
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Ketogenic Diet Attenuates Refractory Epilepsy of Harel-Yoon Syndrome With ATAD3A Variants: A Case Report and Review of Literature
Published in Pediatric neurology (01-06-2023)“…Harel-Yoon syndrome is a disease caused by variants in the ATAD3A gene, which manifest as global developmental delay, hypotonia, intellectual disability, and…”
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Cytotoxicity in vitro, cellular uptake, localization and apoptotic mechanism studies induced by ruthenium(II) complex
Published in Journal of biological inorganic chemistry (01-03-2018)“…Ruthenium-based complexes have been regarded as one of the most potential metal-based candidates for anticancer therapy. Herein, two ruthenium (II)…”
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