Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Wung Joo Song"'
Autor:
Woo Jin Hwang, Han Hyuk Lim, Yoo-Mi Kim, Mea Young Chang, Hong Ryang Kil, Jae Young Kim, Wung Joo Song, Harvey L. Levy, Sook-Za Kim
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-9 (2021)
Abstract Background Repeated inflammation of the pancreas can cause pancreatitis or diabetes. It is well recognized that the organic acidemias may be complicated by pancreatitis but less recognized are other metabolic disorders in which pancreatitis
Externí odkaz:
https://doaj.org/article/d6c6f12b9e9948ccbb408ed2d9e61ffd
Autor:
Sun Ho Lee, Wung Joo Song
Publikováno v:
Genomics & Informatics, Vol 15, Iss 3, Pp 82-86 (2017)
Chromosomal microarray (CMA) is a high-resolution, high-throughput method of identifying submicroscopic genomic copy number variations (CNVs). CMA has been established as the first-line diagnostic test for individuals with developmental delay (DD), i
Externí odkaz:
https://doaj.org/article/35e8d111a5e648a2864d6801281c3649
Autor:
Mea Young Chang, Wung Joo Song, Joon Won Kang, Kyu Sang Song, Dae Young Kang, Sook Kim, Yoon Jin Lee
Publikováno v:
Journal of Genetic Medicine. 16:31-38
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::243a82192f06c8334ca8d9033a21bfb2
https://doi.org/10.5734/jgm.2019.16.1.31
https://doi.org/10.5734/jgm.2019.16.1.31
Autor:
Yoo-Mi Kim, Wung Joo Song, Han Hyuk Lim, Sook-Za Kim, Jae Young Kim, Harvey L. Levy, Mea Young Chang, Woo Jin Hwang, Hong Ryang Kil
Publikováno v:
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-9 (2021)
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-9 (2021)
BackgroundRepeated inflammation of the pancreas can cause pancreatitis or diabetes. It is well recognized that the organic acidemias may be complicated by pancreatitis but less recognized are other metabolic disorders in which pancreatitis can occur.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::14a8d252d274227e5a7d127cb099c898
https://doi.org/10.1186/s13023-021-01685-9
https://doi.org/10.1186/s13023-021-01685-9
Publikováno v:
Clinica Chimica Acta. 413:1151-1155
Background In hyperornithinemia–hyperammonemia–homocitrullinemia (HHH) syndrome, impaired ornithine transport across the mitochondrial membrane causes ornithine accumulation in cytoplasm. The resulting mitochondrial ornithine deficiency leads to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6f694bcf6bebef62fd0c72f30ebacc92
https://doi.org/10.1016/j.cca.2012.03.015
https://doi.org/10.1016/j.cca.2012.03.015