Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Young Hye Ryu"'
Autor:
Uisook Song, Young Hye Ryu, Kiteak Hong, So-Yeon Shim, Seongyeol Park, Jeong Seok Lee, Young Seok Ju, Seung Han Shin, Soyoung Lee
Publikováno v:
BMC Pediatrics, Vol 21, Iss 1, Pp 1-6 (2021)
Abstract Background Severe protein C deficiency is a rare and inherited cause of thrombophilia in neonates. Protein C acts as an anticoagulant, and its deficiency results in vascular thrombosis. Herein, we report a case of protein C deficiency with a
Externí odkaz:
https://doaj.org/article/01effd51216f465a8f7afe5d08761da8
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 8, Iss 10, Pp n/a-n/a (2020)
Abstract Background Lacrimo‐auriculo‐dento‐digital (LADD) syndrome is a rare autosomal dominant disorder caused by mutations in one of the three genes: fibroblast growth factor receptor 2 (FGFR2), FGFR3, or FGF10. Affected patients have hypopla
Externí odkaz:
https://doaj.org/article/944a8daaddcf4965ac3e1fe74de90ce8
Autor:
HyungJin Chin1,2, Young Hye Ryu1,2, Da Yun Kang1,2, Hyun Jin Park3, Kyung Taek Hong3, Jung Yoon Choi3, Ki Wook Yun1,2, Bongjin Lee1, Hyoung Jin Kang3, Eun Hwa Choi1,2 eunchoi@snu.ac.kr
Publikováno v:
Pediatric Infection & Vaccine. Dec2023, Vol. 30 Issue 3, p173-179. 7p.
Autor:
Soyoung Lee, Seung Han Shin, Seongyeol Park, Uisook Song, Kiteak Hong, Young Hye Ryu, Young Seok Ju, Jeong Seok Lee, So Yeon Shim
Publikováno v:
BMC Pediatrics, Vol 21, Iss 1, Pp 1-6 (2021)
BMC Pediatrics
BMC Pediatrics
Background Severe protein C deficiency is a rare and inherited cause of thrombophilia in neonates. Protein C acts as an anticoagulant, and its deficiency results in vascular thrombosis. Herein, we report a case of protein C deficiency with a homozygo
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 8, Iss 10, Pp n/a-n/a (2020)
Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine
Background Lacrimo‐auriculo‐dento‐digital (LADD) syndrome is a rare autosomal dominant disorder caused by mutations in one of the three genes: fibroblast growth factor receptor 2 (FGFR2), FGFR3, or FGF10. Affected patients have hypoplasia/aplas
Publikováno v:
Neonatology. 116(4)
Introduction: This study aimed to assess the association between antenatal corticosteroid (ACS) and in-hospital outcomes of preterm singleton appropriate for gestational age (AGA) infants according to the presence of maternal histologic chorioamnioni