Zobrazeno 1 - 10
of 137
pro vyhledávání: '"Jeehun Lee"'
Publikováno v:
Epilepsia Open, Vol 8, Iss 2, Pp 436-443 (2023)
Abstract Objective Self‐limited infantile epilepsy (SeLIE) has distinctive clinical features, and the PRRT2 gene is known to be a considerable genetic cause. There have been a few studies on PRRT2‐positive SeLIE only, and anti‐seizure medicatio
Externí odkaz:
https://doaj.org/article/cf501b6fc67549cc926ca3a4435a859b
Autor:
Jaeso Cho, Jiwon Lee, Jihye Kim, Hyunjoo Lee, Min-Jee Kim, Yun Jeong Lee, Mi-Sun Yum, Ji-Hye Byun, Chong Guk Lee, Young-Mock Lee, Jeehun Lee, Jong-Hee Chae
Publikováno v:
Frontiers in Neurology, Vol 14 (2023)
IntroductionNusinersen is the first drug approved for spinal muscular atrophy (SMA) treatment. In this study, we aimed to evaluate the long-term safety and efficacy of nusinersen, assess the therapeutic effects based on the treatment initiation timin
Externí odkaz:
https://doaj.org/article/65b462f09a114f4a939cab1a3a2cf5e4
Publikováno v:
Frontiers in Pediatrics, Vol 11 (2023)
Herein, we describe the case of a 43-month-old girl who presented with clinical manifestations of dyskinetic cerebral palsy (CP), classified as the Gross Motor Function Classification System (GMFCS) V. The patient had no family history of neurologica
Externí odkaz:
https://doaj.org/article/a42e0f77ece4463f9f823f664258298e
Publikováno v:
Annals of Child Neurology, Vol 30, Iss 3, Pp 102-110 (2022)
Purpose Frontal lobe epilepsy (FLE) has various clinical presentations depending on the anatomy involved. Seizures are brief and can mimic psychiatric conditions, and patients often cannot describe the aura. Therefore, it is difficult to characterize
Externí odkaz:
https://doaj.org/article/a448f7dd372b44e49a5b7b8ac73c8653
Autor:
So-Hee Lim, Yun-Ju Sung, Narae Jo, Na-Yoon Lee, Kyoung-Shim Kim, Da Yong Lee, Nam-Soon Kim, Jeehun Lee, Ju-Young Byun, Yong-Beom Shin, Jae-Ran Lee
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-11 (2021)
Abstract The neural circuits of the infant brain are rapidly established near 6 months of age, but neurodevelopmental disorders can be diagnosed only at the age of 2–3 years using existing diagnostic methods. Early diagnosis is very important to al
Externí odkaz:
https://doaj.org/article/c6d97dc35d924530bfecbe6899a38c80
Publikováno v:
Annals of Child Neurology, Vol 29, Iss 4, Pp 159-167 (2021)
Purpose High-resolution vessel wall-magnetic resonance imaging (VW-MRI) has been used to detect regional vessel wall pathology, significantly contributing to the diagnosis of primary angiitis of the central nervous system (PACNS) from other arteriopa
Externí odkaz:
https://doaj.org/article/a140a1d02fe2491393c4a2591975485b
Publikováno v:
Annals of Child Neurology, Vol 29, Iss 4, Pp 194-198 (2021)
Externí odkaz:
https://doaj.org/article/c27376d6879941d993d3616de5ac8566
Publikováno v:
Annals of Child Neurology, Vol 29, Iss 3, Pp 124-133 (2021)
Purpose Hypothalamic hamartoma (HH), a rare congenital disorder, can cause intractable epilepsy and requires optimal surgical treatment. This study analyzed the clinical characteristics of HH and evaluated seizure outcomes and the safety of gamma-kni
Externí odkaz:
https://doaj.org/article/18946c86c266433cb5cefeb48062541e
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 8, Iss 4, Pp 964-967 (2021)
Abstract SMA type 1 is the most severe type, characterized by early onset at
Externí odkaz:
https://doaj.org/article/7e34317d30dc46259c8bfc97a147bcb5
Publikováno v:
Annals of Child Neurology, Vol 29, Iss 1, Pp 43-46 (2021)
Externí odkaz:
https://doaj.org/article/7f37aa1748c84b7e962db4b07b1e7f26