Zobrazeno 1 - 10
of 521
pro vyhledávání: '"Youn Jung Kim"'
Autor:
Yun Jung Jung, Ji Eun Park, Ji Won Park, Keu Sung Lee, Wou Young Chung, Joo Hun Park, Seung Soo Sheen, Seulgi You, Joo Sung Sun, Kyung Joo Park, Youn Jung Kim, Kwang Joo Park
Publikováno v:
Respiratory Research, Vol 24, Iss 1, Pp 1-11 (2023)
Abstract Purpose To address the limited utility of the interferon (IFN)-γ release assay (IGRA) caused by its variability and inconsistency. Methods This retrospective cohort study was based on data obtained between 2011 and 2019. QuantiFERON-TB Gold
Externí odkaz:
https://doaj.org/article/7c54ca2f779f4bfc960c81e96bfd7c35
Publikováno v:
Journal of Personalized Medicine, Vol 14, Iss 2, p 191 (2024)
Hypodontia, i.e., missing one or more teeth, is a relatively common human disease; however, oligodontia, i.e., missing six or more teeth, excluding the third molars, is a rare congenital disorder. Many genes have been shown to cause oligodontia in no
Externí odkaz:
https://doaj.org/article/5e73c4896777415496c8d784736128a1
Publikováno v:
Journal of Personalized Medicine, Vol 13, Iss 10, p 1494 (2023)
Hereditary conditions that affect tooth enamel in quantity and/or quality are called amelogenesis imperfecta (AI). AI can occur as an isolated condition or as a symptom of a syndrome. An OMIM search with the term “AI” yielded 79 result entries. M
Externí odkaz:
https://doaj.org/article/d68d7c9668c041638196e45d3464f697
Autor:
Youn Jung Kim, Hong Zhang, Yejin Lee, Figen Seymen, Mine Koruyucu, Yelda Kasimoglu, James P. Simmer, Jan C.-C. Hu, Jung-Wook Kim
Publikováno v:
Journal of Personalized Medicine, Vol 13, Iss 2, p 326 (2023)
Amelogenesis imperfecta (AI) is a heterogeneous collection of hereditary enamel defects. The affected enamel can be classified as hypoplastic, hypomaturation, or hypocalcified in form. A better understanding of normal amelogenesis and improvements in
Externí odkaz:
https://doaj.org/article/e260c2489f714da1ab7191a3b0d6252d
Autor:
Sung Min Jung, Youn Jung Kim, Seung Mok Ryoo, Chang Hwan Sohn, Dong Woo Seo, Kyoung Soo Lim, Won Young Kim
Publikováno v:
The Korean Journal of Internal Medicine, Vol 35, Iss 4, Pp 979-987 (2020)
Background/Aims Among patients with febrile neutropenia that developed after chemotherapy, high-risk patients, such as those having clinical instability or Multinational Association of Supportive Care in Cancer score of < 21, require hospitalization
Externí odkaz:
https://doaj.org/article/91284d65e1eb4aa58c45fb2ff4a673f5
Publikováno v:
Journal of Personalized Medicine, Vol 12, Iss 9, p 1401 (2022)
The process of tooth formation is a series of reciprocal interactions between the ectoderm and mesoderm, and it is believed that many genetic factors are involved in this complex process. More than a dozen genes have been identified in non-syndromic
Externí odkaz:
https://doaj.org/article/006f15883bf14fcdaf15f207c272b769
Autor:
Youn Jung Kim, Yejin Lee, Hong Zhang, Figen Seymen, Mine Koruyucu, Sule Bayrak, Nuray Tuloglu, James P. Simmer, Jan C.-C. Hu, Jung-Wook Kim
Publikováno v:
Journal of Personalized Medicine, Vol 12, Iss 6, p 1002 (2022)
Hereditary dentin defects are conventionally classified into three types of dentinogenesis imperfecta (DGI) and two types of dentin dysplasia (DD). Mutations in the dentin sialophosphoprotein (DSPP) gene have been identified to cause DGI type II and
Externí odkaz:
https://doaj.org/article/ef404692779247ca9bedeaa237f28907
Autor:
Yejin Lee, Hong Zhang, Figen Seymen, Youn Jung Kim, Yelda Kasimoglu, Mine Koruyucu, James P. Simmer, Jan C.-C. Hu, Jung-Wook Kim
Publikováno v:
Journal of Personalized Medicine, Vol 12, Iss 2, p 150 (2022)
Amelogenesis imperfecta (AI) is a group of rare genetic diseases affecting the tooth enamel. AI is characterized by an inadequate quantity and/or quality of tooth enamel and can be divided into three major categories: hypoplastic, hypocalcified and h
Externí odkaz:
https://doaj.org/article/eb7a2e9d2c584931b4b654d35243ba29
Publikováno v:
Journal of Personalized Medicine, Vol 11, Iss 6, p 526 (2021)
Hereditary dentin defects can be categorized as a syndromic form predominantly related to osteogenesis imperfecta (OI) or isolated forms without other non-oral phenotypes. Mutations in the gene encoding dentin sialophosphoprotein (DSPP) have been ide
Externí odkaz:
https://doaj.org/article/42457e7afebb49c0948a8ddf3cb89465
Autor:
Youn Jung Kim, Yejin Lee, Hong Zhang, John Timothy Wright, James P. Simmer, Jan C.-C. Hu, Jung-Wook Kim
Publikováno v:
Biomedicines, Vol 9, Iss 5, p 456 (2021)
Amelogenesis imperfecta (AI) is a collection of rare genetic conditions affecting tooth enamel. The affected enamel can be of insufficient quantity and/or altered quality, impacting structural content, surface integrity and coloration. Heterozygous m
Externí odkaz:
https://doaj.org/article/7a1a096f10c64968b1cd59135204150e