Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Kyo Yeon Koo"'
Publikováno v:
Korean Journal of Pediatrics, Vol 53, Iss 6, Pp 694-700 (2010)
PurposeTo assess the validity of individual and combined prognostic effects of severe bronchopulmonary dysplasia (BPD), brain injury, retinopathy of prematurity (ROP), and parenteral nutrition associated cholestasis (PNAC).MethodsWe retrospectively a
Externí odkaz:
https://doaj.org/article/7fb156338cfd48c1b8dea83366008ca9
Autor:
Kyo Yeon Koo, Jun Seok Lee, Soon Min Lee, Min Soo Park, Ran Namgung, Kook In Park, Chul Lee, Choon Sik Yoon, Woo Hee Jung, Hong Shik Choi
Publikováno v:
Korean Journal of Pediatrics, Vol 53, Iss 2, Pp 258-261 (2010)
Lymphangioma is a rare benign congenital tumor of the lymphatic system, which is commonly diagnosed before 2 years of age. In the natronal report, cystic lymphangioma was usually reported as a huge translucent mass located in the head and neck area.
Externí odkaz:
https://doaj.org/article/63b1f5718949426cbbf35a791e8326f9
Publikováno v:
The Journal of Dermatology. 42:655-657
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4668f46cc6fc1e2c70b6a51d23e2ecfd
https://doi.org/10.1111/1346-8138.12856
https://doi.org/10.1111/1346-8138.12856
Publikováno v:
Journal of Genetic Medicine. 9:93-97
Kniest syndrome (OMIM #156550) is a rare autosomal dominant disorder caused by a dysfunction of type II collagen, which is encoded by the COL2A1 gene...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cefad28b4c89f731b462590ea25dd0d8
https://doi.org/10.5734/jgm.2012.9.2.93
https://doi.org/10.5734/jgm.2012.9.2.93
Publikováno v:
Korean Journal of Pediatrics, Vol 53, Iss 6, Pp 694-700 (2010)
Korean Journal of Pediatrics
Korean Journal of Pediatrics
Purpose: To assess the validity of individual and combined prognostic effects of severe bronchopulmonary dysplasia (BPD), brain injury, retinopathy of prematurity (ROP), and parenteral nutrition associated cholestasis (PNAC). Methods: We retrospectiv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::458ae87282cc4c2ad6a1a450f4613912
http://kjp.or.kr/upload/pdf/kjped-53-694.pdf
http://kjp.or.kr/upload/pdf/kjped-53-694.pdf
Autor:
Kwangsoo Jung, Kyujin Hwang, Il Shin Lee, Seokhwan Yun, Jeong Eun Shin, Miri Kim, Kyo Yeon Koo, Il Sun Kim, Haejin Lee, Kook In Park
Publikováno v:
Translational Research. 183:121-136.e9
Neonatal hypoxic-ischemic (HI) brain injury leads to high mortality and neurodevelopmental disabilities. Multipotent neural progenitor cells (NPCs) with self-renewing capacity have the potential to reduce neuronal loss and improve the compromised env
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6ba5c65f317eaa20ae1adcbdd4db6d04
https://doi.org/10.1016/j.trsl.2016.12.010
https://doi.org/10.1016/j.trsl.2016.12.010
Autor:
Ji I.n. Lee, Chul Lee, Cheol Ryong Ku, Kyu Yeon Hur, Jin Sung Lee, Myung-Shik Lee, Kyo Yeon Koo, Sena Hwang, Yumie Rhee
Publikováno v:
Journal of human genetics. 59(9)
Von Hippel-Lindau (VHL) disease is an inherited tumor syndrome caused by germline mutations in the VHL tumor suppressor gene. It is characterized by hemangioblastoma in the central nervous system and retina, renal cell carcinoma, pancreatic tumor and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a0585a9ccdb79ea1e82c880c414e5606
https://pubmed.ncbi.nlm.nih.gov/25078357
https://pubmed.ncbi.nlm.nih.gov/25078357
Autor:
Zhejiu Quan, Hyo Suk Nam, Young Mock Lee, Kyo Yeon Koo, Sang Mi Lee, Hoon Chul Kang, Joon Won Kang
Publikováno v:
Yonsei Medical Journal
X-linked adrenoleukodystrophy (X-ALD) shows a wide range of phenotypic expression, but clinical presentation as an isolated lesion of the cerebellar white matter and dentate nuclei has not been reported. We report an unusual presentation of X-ALD onl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::00ed4c70a708a87ad56aeba8ade3a926
https://doi.org/10.3349/ymj.2014.55.4.1157
https://doi.org/10.3349/ymj.2014.55.4.1157
Autor:
Jae Il Shin, Beom Jin Lim, Se Jin Park, Jin Sung Lee, Hyeon Joo Jeong, Ji Young Wang, Kyo Yeon Koo
Publikováno v:
Yonsei Medical Journal
Familial Mediterranean fever (FMF) is an auto-inflammatory disease characterized by periodic episodes of fever and recurrent polyserositis. It is caused by a dysfunction of pyrin (or marenostrin) as a result of a mutation within the MEFV gene. It occ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::125f7163b0c23d7d5e7b97fc6f16a99c
https://doi.org/10.3349/ymj.2012.53.2.454
https://doi.org/10.3349/ymj.2012.53.2.454
Autor:
Joon Soo Lee, Jin Sung Lee, Young Mock Lee, Hoon Chul Kang, Hyo Jeong Kim, Shin Hye Kim, Kyo Yeon Koo, Heung Dong Kim
Publikováno v:
Yonsei Medical Journal
Purpose Rett syndrome is a severe neurodevelopmental disorder in females. Most have mutations in the methyl-CpG-binding protein 2 (MECP2) gene (80-90%). Epilepsy is a significant commonly accompanied feature in Rett syndrome. Our study was aimed at c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e1ceb93a413b9a85ec53bc4b3f55a2c7
https://doi.org/10.3349/ymj.2012.53.3.495
https://doi.org/10.3349/ymj.2012.53.3.495