Zobrazeno 1 - 10
of 93
pro vyhledávání: '"Jung Hye Byeon"'
Autor:
Go Hun Seo, Hane Lee, Jungsul Lee, Heonjong Han, You Kyung Cho, Minji Kim, Yunha Choi, Jeongmin Choi, In Hee Choi, Seonkyeong Rhie, Kyu Young Chae, Yoo-Mi Kim, Chong Kun Cheon, Su Jin Kim, Jieun Lee, Eungu Kang, Jung Hye Byeon, Hee Joon Yu, Young-Lim Shin, Arum Oh, Woo Jin Kim, Mi-Sun Yum, Beom Hee Lee, Baik-Lin Eun
Publikováno v:
Molecular Medicine, Vol 28, Iss 1, Pp 1-15 (2022)
Abstract Background The diagnostic yield of whole-exome sequencing (WES) varies from 30%–50% among patients with mild to severe neurodevelopmental delay (NDD)/intellectual disability (ID). Routine retrospective reanalysis of undiagnosed patients ha
Externí odkaz:
https://doaj.org/article/4cf814bc387f4a96a50b40323f14c258
Publikováno v:
Annals of Child Neurology, Vol 29, Iss 1, Pp 15-21 (2021)
Purpose The aim of the treatment of epileptic seizures is to achieve a seizure-free state without adverse effects. The mainstays of seizure treatment are anticonvulsant medication, diet therapy, and surgery. Antiepileptic drugs and a ketogenic diet a
Externí odkaz:
https://doaj.org/article/0efcb0f177d342c8908d6ae8c8d0e3ce
Publikováno v:
Neonatal Medicine, Vol 27, Iss 4, Pp 159-166 (2020)
Purpose Preterm infants are known to be at a risk of neurodevelopmental delay; however, limited data are available on the outcomes of moderate-to-late preterm (MLPT) infants (born at 32 to 36 weeks’ gestation). The Korean Developmental Screening Te
Externí odkaz:
https://doaj.org/article/ef4735d38a684facb8d7f3127aaa3c78
Publikováno v:
Annals of Child Neurology, Vol 29, Iss 1, Pp 51-53 (2021)
Externí odkaz:
https://doaj.org/article/d8631c9769a042a7aca87739aae40477
Publikováno v:
BMC Pediatrics, Vol 18, Iss 1, Pp 1-6 (2018)
Abstract Background Suboptimal intake of magnesium become prevalent due to the modern diet of processed food low in magnesium. Magnesium may modulate seizure activity by antagonizing excitatory calcium influx through the N-methyl-D-aspartate receptor
Externí odkaz:
https://doaj.org/article/cdfdd3a7272b41108c136141313e3b65
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 31, Iss , Pp 23-25 (2018)
Lymphatic malformation is a rare congenital lesion caused by lymphatic abnormality. Herein is a case of extensive pediatric lymphatic malformation involving almost entire neck from skull base to mouth floor. Surgical excision of the huge mass was per
Externí odkaz:
https://doaj.org/article/6e007c05cb5e4182a072cb008e2b7c29
Publikováno v:
Korean Journal of Pediatrics, Vol 59, Iss 2, Pp 74-79 (2016)
PurposeFebrile seizure, the most common type of pediatric convulsive disorder, is a benign seizure syndrome distinct from epilepsy. However, as epilepsy is also common during childhood, we aimed to identify the prognostic factors that can predict epi
Externí odkaz:
https://doaj.org/article/5e981107d52849b69014fd144b73c1e5
Publikováno v:
Korean Journal of Pediatrics, Vol 58, Iss 11, Pp 446-450 (2015)
PurposeMeningitis is among the most common infections affecting the central nervous system. It can be difficult to determine the exact pathogen responsible for the infection and patients are often treated with empiric antibiotics. This study was cond
Externí odkaz:
https://doaj.org/article/b8c0c33abc744c45aa7820db107e4641
Publikováno v:
Korean Journal of Pediatrics, Vol 59, Iss Suppl 1, Pp S10-S13 (2016)
Chromosome 11q13 deletion syndrome has been previously reported as either otodental syndrome or oculo-oto-dental syndrome. The otodental syndrome is characterized by dental abnormalities and high-frequency sensorineural hearing loss, and by ocular co
Externí odkaz:
https://doaj.org/article/69a9936f7dd0441b97de9de795b68c1c
Publikováno v:
Korean Journal of Pediatrics, Vol 59, Iss Suppl 1, Pp S129-S132 (2016)
Ictal tachycardia and bradycardia are common arrhythmias; however, ictal sinus pause and asystole are rare. Ictal arrhythmia is mostly reported in adults with temporal lobe epilepsy. Recently, ictal arrhythmia was recognized as a major warning sign o
Externí odkaz:
https://doaj.org/article/d7d446af4de54e16816d97e3907908d0