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Journal of Korean Medical Science|February 6, 2009
Clinico-genetic study of nail-patella syndromeBeom Hee Lee, Tae-Joon Cho, Hyun Jin Choi, et al.Clinical Genetics|November 21, 2014
Setleis syndrome: clinical, molecular and structural studies of the first TWIST2 missense mutationR Ozgur Rosti, Z Oya Uyguner, Irina Nazarenko, et al.Molecular Genetics and Metabolism Reports|August 19, 2016
MPV17 mutations in patients with hepatocerebral mitochondrial DNA depletion syndromeJoonil Kim, Eungu Kang, Yoonmyung Kim, et al.Journal of Human Genetics|December 15, 2010
Low prevalence of classical galactosemia in Korean populationBeom Hee Lee, Chong Kun Cheon, Jae-Min Kim, et al.Pediatric Nephrology (Berlin, Germany)|July 7, 2009
Decreased renal uptake of (99m)Tc-DMSA in patients with tubular proteinuriaBeom Hee Lee, So Hee Lee, Hyun Jin Choi, et al.Pediatrics International : Official Journal of the Japan Pediatric Society|February 14, 2015
Clinical features, outcomes, and genetic analysis in Korean children with Alagille syndromeJin Min Cho, Seak Hee Oh, Hyun Jin Kim, et al.Integrative Medicine Research|July 1, 2017
Pu-18-<i>N</i>-butylimide-NMGA-GNP conjugate is effective against hepatocellular carcinomaJin-Geun Kwon, In-Sung Song, Min-Soo Kim, et al.BMC Cancer|March 29, 2025
Factors that predict progression of von Hippel-Lindau disease-related malignancy: a longitudinal cohort studyJae Ho Lee, Hyun Young Lee, Ji Eun Park, et al.BMC Medical Genomics|May 16, 2026
Long-term safety and efficacy of triheptanoin in Korean patients with long-chain fatty acid oxidation disorders: a prospective, open-label, single-center, phase II clinical studyJi-Hee Yoon, Jun-Hong Park, Dohyung Kim, et al.International Journal of Molecular Sciences|November 26, 2022
Aberrant Cortical Layer Development of Brain Organoids Derived from Noonan Syndrome-iPSCsBumsoo Kim, Yongjun Koh, Hyunsu Do, et al.Pageof 20