Zobrazeno 1 - 10
of 82
pro vyhledávání: '"Su-Jeong You"'
Autor:
Su-Jeong You
Publikováno v:
Annals of Child Neurology, Vol 32, Iss 3, Pp 176-180 (2024)
Purpose Febrile seizures (FSs) are neurological events associated with fever, typically occurring in children between 6 months and 5 years of age in the absence of central nervous system infection. Growing evidence suggests that coronavirus disease 2
Externí odkaz:
https://doaj.org/article/e0e946129b22470d902cd34ecb147083
Autor:
Kyu Un Cho, Su Jeong You
Publikováno v:
Annals of Child Neurology, Vol 29, Iss 2, Pp 83-90 (2021)
Purpose This study evaluated the clinical and laboratory characteristics of infants ≤90 days old with meningitis who presented to the hospital with a fever. We also investigated whether initial C-reactive protein levels and white blood cell counts
Externí odkaz:
https://doaj.org/article/82894dc8015e496683cd56eb630c9f90
Publikováno v:
Annals of Child Neurology, Vol 27, Iss 4, Pp 128-134 (2019)
Purpose Prenatal diagnosis of cardiac rhabdomyoma is suggestive of the presence of tuberous sclerosis complex (TSC), which is commonly associated with epilepsy. This study investigated the diagnostic rate of TSC, the incidence and treatment outcomes
Externí odkaz:
https://doaj.org/article/30ffb548dbb74cd0a69baaa60e3e4570
Autor:
Gu Hyun Jung, Su Jeong You
Publikováno v:
Korean Journal of Pediatrics, Vol 62, Iss 8, Pp 312-316 (2019)
Purpose The major side effects of treatment with oxcarbazepine (OXC) are skin rash and hyponatremia. Hematologic side effects are reported rarely. The aim of this study was to investigate the rate and types of the hematologic side effects of OXC. Met
Externí odkaz:
https://doaj.org/article/264566278e554d518cf192d82af4e3c0
Publikováno v:
Korean Journal of Pediatrics, Vol 62, Iss 3, Pp 108-112 (2019)
Subacute sclerosing panencephalitis (SSPE) is a rare, progressive, and fatal central nervous system disorder resulting from persistent measles virus infection. Long-term data are scarce, with a maximum follow-up period of 10 years. Interferon-alpha (
Externí odkaz:
https://doaj.org/article/e0fae78398634b48b953258eb90bfb51
Prognostic factors of neurological outcomes in late-preterm and term infants with perinatal asphyxia
Publikováno v:
Korean Journal of Pediatrics, Vol 59, Iss 11, Pp 440-445 (2016)
PurposeThis study aimed to identify prognostic factors of neurological outcomes, including developmental delay, cerebral palsy and epilepsy in late-preterm and term infants with perinatal asphyxia.MethodsAll late-preterm and term infants with perinat
Externí odkaz:
https://doaj.org/article/700ecb7ee2764919be6248f1cf5af472
Publikováno v:
Korean Journal of Pediatrics, Vol 58, Iss 2, Pp 60-63 (2015)
PurposeMany patients presenting with headache also complain of constipation; the relationship between these two symptoms has not been explored in detail. The aim of this study was to investigate the association between primary headache and constipati
Externí odkaz:
https://doaj.org/article/226eff62f8db47e08008e07c5a5f3b59
Autor:
Sun Young Seo, Su Jeong You
Publikováno v:
Korean Journal of Pediatrics, Vol 59, Iss Suppl 1, Pp S157-S160 (2016)
Coexistence of paroxysmal kinesigenic dyskinesia (PKD) with benign infantile convulsion (BIC) and centrotemporal spikes (CTS) is very rare. A 10-year-old girl presented with a 3-year history of frequent attacks of staggering while laughing and of sud
Externí odkaz:
https://doaj.org/article/8f9a4f91733a43baa8dce454daa1438c
Autor:
Su Jeong You
Publikováno v:
Neuropediatrics. 51:354-358
Purpose Benign convulsions with mild gastroenteritis (CwG) is a condition that does not usually require treatment. However, when the patient experiences multiple seizures or prolonged seizures, anticonvulsant treatment may be required. We investigate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e1b485ec12302163778a2f335e1f35b9
https://doi.org/10.1055/s-0040-1701442
https://doi.org/10.1055/s-0040-1701442
Publikováno v:
Korean Journal of Pediatrics, Vol 55, Iss 10, Pp 397-402 (2012)
Pelizaeus-Merzbacher disease (PMD) is a rare, X-linked recessive disorder characterized by dysmyelination in the central nervous system. PMD results from deletion, mutation, or duplication of the proteolipid protein gene (PLP1) located at Xq22, leadi
Externí odkaz:
https://doaj.org/article/c78728415b0943e1bfc34320ff19f308