Zobrazeno 1 - 10
of 77
pro vyhledávání: '"Yun Jung Hur"'
Autor:
Soyoung Park, Hye Eun Kwon, Chung Mo Koo, Yun Jung Hur, Hoon-Chul Kang, Joon Soo Lee, Heung Dong Kim
Publikováno v:
Annals of Child Neurology, Vol 32, Iss 1, Pp 13-20 (2024)
Purpose This study examined the characteristics and outcomes of resective epilepsy surgery following corpus callosotomy (CC) in children with Lennox-Gastaut syndrome (LGS). Methods We retrospectively analyzed 17 children with LGS who underwent resect
Externí odkaz:
https://doaj.org/article/3d103029c19242229177680e3e4c018f
Publikováno v:
Annals of Child Neurology, Vol 30, Iss 1, Pp 31-34 (2022)
Externí odkaz:
https://doaj.org/article/040801041d6d4913aa27b4b46a6dd037
Autor:
Zhi Ji Wang, Byoung Ho Noh, Eun Seong Kim, Donghwa Yang, Shan Yang, Nam Young Kim, Yun Jung Hur, Heung Dong Kim
Publikováno v:
Frontiers in Neurology, Vol 13 (2022)
ObjectiveFor patients with drug–resistant focal epilepsy, intracranial monitoring remains the gold standard for surgical intervention. Focal cortical dysplasia (FCD) is the most common cause of pharmacoresistant focal epilepsy in pediatric patients
Externí odkaz:
https://doaj.org/article/e03e8077a7524d169f84217f688fcbce
Publikováno v:
Annals of Child Neurology, Vol 29, Iss 2, Pp 101-104 (2021)
Externí odkaz:
https://doaj.org/article/c6babf949cd94c12a71421e479c4fb9f
Publikováno v:
International Journal of Infectious Diseases, Vol 104, Iss , Pp 551-555 (2021)
Objectives: We estimated the impact of universal hepatitis B immunization using 18-year data of women who are of childbearing age in South Korea. Methods: We used hepatitis B surface antigen (HBsAg) and antibody (anti-HBs) data of 145,993 women aged
Externí odkaz:
https://doaj.org/article/2a01edaea36b4138b97143c5f28ca67c
Autor:
Yun Jung Hur
Publikováno v:
Clinical and Experimental Pediatrics, Vol 63, Iss 3, Pp 100-101 (2020)
Externí odkaz:
https://doaj.org/article/d4226be178e946409c0d9cf6a5d2eb56
Publikováno v:
Annals of Indian Academy of Neurology, Vol 19, Iss 4, Pp 518-522 (2016)
Background: There have been a few reports of patients who developed Lennox-Gastaut syndrome (LGS) in the second decades of their life. Objectives: The aim of this study was to investigate electroclinical presentation in patients with late-onset LGS.
Externí odkaz:
https://doaj.org/article/1e0ebb3748264631b3eab3ff980c169a
Autor:
Hyun Hee Lee, Yun Jung Hur
Publikováno v:
Korean Journal of Pediatrics, Vol 59, Iss Suppl 1, Pp S29-S31 (2016)
Glucose transport 1 (GLUT-1) deficiency is a rare syndrome caused by mutations in the glucose transporter 1 gene (SLC2A1) and is characterized by early-onset intractable epilepsy, delayed development, and movement disorder. De novo mutations and seve
Externí odkaz:
https://doaj.org/article/7ba825919a6c4774b4e30bd210261b6f
Autor:
Yun Jung Hur, Taegyu Hwang
Publikováno v:
Korean Journal of Pediatrics, Vol 55, Iss 10, Pp 393-396 (2012)
Trisomy 14 mosaicism is a rare chromosome disorder characterized by delayed development, failure to thrive, and facial dysmorphism. Only approximately 30 trisomy 14 mosaicism cases have been reported in the literature because trisomy 14 is associated
Externí odkaz:
https://doaj.org/article/0d617b12cb47475aac0f0d9bddccdd87
Autor:
Yun Jung Hur, Taegyu Hwang
Publikováno v:
Korean Journal of Pediatrics, Vol 56, Iss 1, Pp 42-44 (2013)
Neurological complications associated with 2009 H1N1 infection in children have been reported and recognized worldwide. The most commonly reported neurological complications are seizures and encephalopathy. Secondary movement disorders are also assoc
Externí odkaz:
https://doaj.org/article/60fc986ca2104039ac10b7b7d0224658