Zobrazeno 1 - 10
of 103
pro vyhledávání: '"Inn‐Chi Lee"'
Autor:
Yen-Ju Chu, Lee-Chin Wong, Che-Sheng Ho, Jia-Yun Huang, I-Chun Lee, Hsin-Pei Wang, Cheng-Hsien Huang, Chia-Jui Hsu, Wen-Hsin Hsu, Yu-Chia Kao, Bi-Chun Duan, Inn-Chi Lee, Yung-Ting Kuo, Fu-Man Chang, Su-Ching Hu, Chang-Chun Wu, Lung-Chang Lin, Wan-Ling Hsiao, Chuan-Yu Wang, Kun-Long Hung, Hsiao-Ju Chi, Shi-Bing Wong, Wang-Tso Lee
Publikováno v:
Journal of the Formosan Medical Association, Vol 123, Iss 7, Pp 811-817 (2024)
Background: The SARS-CoV-2 virus has been a global public health threat since December 2019. This study aims to investigate the neurological characteristics and risk factors of coronavirus disease 2019 (COVID-19) in Taiwanese children, using data fro
Externí odkaz:
https://doaj.org/article/344f9beb9a47440b8c19073390d715f6
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-10 (2023)
Abstract Unconjugated bilirubin (UB) levels during the first week after birth are related to outcomes in neonatal hypoxic-ischemic encephalopathy (HIE). Clinical Sarnat staging of HIE, brain magnetic resonance imaging (MRI), hearing outcomes, and neu
Externí odkaz:
https://doaj.org/article/6017a728720a479f917aad5e6ac18f69
Autor:
Chia-Hsuan Huang, Pi-Lien Hung, Pi-Chuan Fan, Kuang-Lin Lin, Ting-Rong Hsu, I-Jun Chou, Che-Sheng Ho, I-Ching Chou, Wei-Sheng Lin, Inn-Chi Lee, Hueng-Chuen Fan, Shyi-Jou Chen, Jao-Shwann Liang, Yi-Fang Tu, Tung-Ming Chang, Su-Ching Hu, Lee-Chin Wong, Kun-Long Hung, Wang-Tso Lee
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-9 (2021)
Abstract Dravet syndrome (DS) is an uncommon epilepsy syndrome that may negatively affect the patients and their caregivers. However, reliable and valid measures of its impact on caregivers and the characteristics of patients with DS in Taiwan are la
Externí odkaz:
https://doaj.org/article/d12a8820811846fabf0c479b27cba1ec
Publikováno v:
Frontiers in Endocrinology, Vol 13 (2022)
BackgroundThe diagnosis of neonatal hypocalcemic seizures (HS) in newborns is made based on clinical signs and serum calcium level. Their etiology is broad and diverse, and timely detection and initiation of treatment is essential.MethodsWe retrospec
Externí odkaz:
https://doaj.org/article/4cd73b43ce79427da00953756063a96b
Publikováno v:
Journal of the Formosan Medical Association, Vol 120, Iss 1, Pp 744-754 (2021)
Background: KCNQ2-associated epilepsy is most common in neonatal genetic epilepsy. A prompt diagnosis to initialize early treatment is important. Methods: We studied the electroencephalographic (EEG) changes including automated EEGs and conventional
Externí odkaz:
https://doaj.org/article/a8e3c64635524192b328d564ed5f11f9
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2021)
Background: To evaluate seizure diagnosis in sick infants in the neonatal intensive care unit (NICU) based on electroencephalography (EEG) monitoring combined with amplitude integrated electroencephalography (aEEG).Methods: We retrospectively reviewe
Externí odkaz:
https://doaj.org/article/31bd015dd86842388724682c2530face
Publikováno v:
BMC Pediatrics, Vol 19, Iss 1, Pp 1-8 (2019)
Abstract Background Kawasaki disease (KD) is a common vasculitis of childhood in East Asia. The complications of KD ascribed to long-term cardiovascular sequelae are considerably diverse. Although studies have investigated neurodevelopmental problems
Externí odkaz:
https://doaj.org/article/28b75b16e5f14b63b54c3e0c447b9fb9
Autor:
Chien-Heng Lin, Jung-Nien Lai, Inn-Chi Lee, I-Ching Chou, Wei-De Lin, Mei-Chen Lin, Syuan-Yu Hong
Publikováno v:
Frontiers in Neurology, Vol 12 (2021)
Background: Kawasaki disease is a common vasculitis of childhood in East Asia. The complications following Kawasaki disease mostly included cardiovascular sequelae; non-cardiac complications have been reported but less studied. This study investigate
Externí odkaz:
https://doaj.org/article/ef89859e36f1481ea082965fa61d36d4
Publikováno v:
Cells, Vol 11, Iss 5, p 894 (2022)
KCNQ2 mutations can cause benign familial neonatal convulsions (BFNCs), epileptic encephalopathy (EE), and mild-to-profound neurodevelopmental disabilities. Mutations in the KCNQ2 selectivity filter (SF) are critical to neurodevelopmental outcomes. T
Externí odkaz:
https://doaj.org/article/05ecdea7263a4e3897d01e8bf15aff11
Publikováno v:
BMC Neurology, Vol 18, Iss 1, Pp 1-6 (2018)
Abstract Background Noonan syndrome-like disorder with loose anagen hair-2 (NSLH2) is an extremely rare disease caused by a heterozygous mutation in the PPP1CB gene on chromosome 2p23. The syndrome causes not only numerous dysmorphic features but als
Externí odkaz:
https://doaj.org/article/ca2f1d1ef7df4b62b1efb727cc22debd