Cargando…

Time course of serum cytokine level changes within 72 h after onset in children with acute encephalopathy and febrile seizures

BACKGROUND: Cytokine levels have been measured in acute encephalopathy (AE) to determine its pathology or as a diagnostic biomarker to distinguish it from febrile seizures (FS); however, the dynamics of cytokine level changes have not yet been fully captured in these two neurological manifestations....

Descripción completa

Detalles Bibliográficos
Autores principales:	Tomioka, Kazumi, Nishiyama, Masahiro, Tokumoto, Shoichi, Yamaguchi, Hiroshi, Aoki, Kazunori, Seino, Yusuke, Toyoshima, Daisaku, Kurosawa, Hiroshi, Tada, Hiroko, Sakuma, Hiroshi, Nozu, Kandai, Maruyama, Azusa, Tanaka, Ryojiro, Iijima, Kazumoto, Nagase, Hiroaki
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2023
Materias:	Research
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9824967/ https://www.ncbi.nlm.nih.gov/pubmed/36609211 http://dx.doi.org/10.1186/s12883-022-03048-8

Ejemplares similares

Prognostic effects of treatment protocols for febrile convulsive status epilepticus in children
por: Tokumoto, Shoichi, et al.
Publicado: (2022)

Early steroid pulse therapy for children with suspected acute encephalopathy: An observational study
por: Ishida, Yusuke, et al.
Publicado: (2021)

Clinical and laboratory characteristics of complex febrile seizures in the acute phase: a case-series study in Japan
por: Tanaka, Tsukasa, et al.
Publicado: (2023)

Timing of therapeutic interventions against infection-triggered encephalopathy syndrome: a scoping review of the pediatric literature
por: Nagase, Hiroaki, et al.
Publicado: (2023)

Association of early bedtime at 3 years of age with higher academic performance and better non-cognitive skills in elementary school
por: Nishiyama, Masahiro, et al.
Publicado: (2023)

Seizure prevalence in children aged up to 3 years: a longitudinal population-based cohort study in Japan
por: Nishiyama, Masahiro, et al.
Publicado: (2020)

The association between prehospital vital signs of children and their critical clinical outcomes at hospitals
por: Kurosawa, Hiroshi, et al.
Publicado: (2022)

Improved renal survival in Japanese children with IgA nephropathy
por: Yata, Nahoko, et al.
Publicado: (2008)

Clinical features predicting group A streptococcal pharyngitis in a Japanese paediatric primary emergency medical centre
por: Nishiyama, Masahiro, et al.
Publicado: (2018)

Rituximab Treatment for Nephrotic Syndrome in Children
por: Iijima, Kazumoto, et al.
Publicado: (2014)

Rituximab for nephrotic syndrome in children
por: Iijima, Kazumoto, et al.
Publicado: (2016)

An updated view of the pathogenesis of steroid-sensitive nephrotic syndrome
por: Horinouchi, Tomoko, et al.
Publicado: (2022)

Alport syndrome caused by a COL4A5 deletion and exonization of an adjacent AluY
por: Nozu, Kandai, et al.
Publicado: (2014)

Rituximab in steroid-sensitive nephrotic syndrome: lessons from clinical trials
por: Iijima, Kazumoto, et al.
Publicado: (2017)

Yersinia pseudotuberculosis infection in Kawasaki disease and its clinical characteristics
por: Horinouchi, Tomoko, et al.
Publicado: (2015)

Multivariate analysis of the impact of weather and air pollution on emergency department visits for night-time headaches among children: retrospective, clinical observational study
por: Yamaguchi, Hiroshi, et al.
Publicado: (2021)

Autosomal dominant pseudohypoaldosteronism type 1 with a novel splice site mutation in MR gene
por: Kanda, Kyoko, et al.
Publicado: (2009)

Impact of the State of Emergency during the COVID-19 Pandemic in 2020 on Asthma Exacerbations among Children in Kobe City, Japan
por: Yamaguchi, Hiroshi, et al.
Publicado: (2021)

Glomerular galactose-deficient IgA1 expression analysis in pediatric patients with glomerular diseases
por: Ishiko, Shinya, et al.
Publicado: (2020)

Contradiction between genetic analysis and diuretic loading test in type I Bartter syndrome: a case report
por: Kuroda, Jumpei, et al.
Publicado: (2021)

Comparison of neurological manifestation in children with and without coronavirus 2019 experiencing seizures with fever
por: Hongo, Hiroto, et al.
Publicado: (2023)

Preliminary Effectiveness and Safety of High Frequency Oscillation in Addition to Mechanical Insufflation and Exsufflation for Intratracheal Mucus Removal in Patients With Neuromuscular Disease: Protocol for a Prospective Study
por: Awano, Hiroyuki, et al.
Publicado: (2019)

A Case of Transforming Growth Factor-β-Induced Gene-Related Oculorenal Syndrome: Granular Corneal Dystrophy Type II with a Unique Nephropathy
por: Iwafuchi, Yoichi, et al.
Publicado: (2016)

Establishment of X-linked Alport syndrome model mice with a Col4a5 R471X mutation
por: Hashikami, Kentarou, et al.
Publicado: (2018)

Extranodal natural killer/T‐cell lymphoma in an 11‐year‐old child
por: Ninchoji, Takeshi, et al.
Publicado: (2020)

Clinical and Genetic Characteristics in Patients With Gitelman Syndrome
por: Fujimura, Junya, et al.
Publicado: (2018)

A birth of bipartite exon by intragenic deletion
por: Nozu, Kandai, et al.
Publicado: (2017)

Changes in the numbers of patients with acute gastroenteritis after voluntary introduction of the rotavirus vaccine in a Japanese children’s primary emergency medical center
por: Morioka, Ichiro, et al.
Publicado: (2017)

The utility of urinary CD80 as a diagnostic marker in patients with renal diseases
por: Minamikawa, Shogo, et al.
Publicado: (2018)

Comprehensive genetic diagnosis of Japanese patients with severe proteinuria
por: Nagano, China, et al.
Publicado: (2020)

Comparison between conventional and comprehensive sequencing approaches for genetic diagnosis of Alport syndrome
por: Yamamura, Tomohiko, et al.
Publicado: (2019)

An Orofaciodigital Syndrome 1 Patient and Her Mother Carry the Same OFD1 Mutation but Have Different X Chromosome Inactivation Patterns
por: Iijima, Takashi, et al.
Publicado: (2019)

Three Severe Cases of Viral Infections with Post-Kidney Transplantation Successfully Confirmed by Polymerase Chain Reaction and Flow Cytometry
por: Nakanishi, Keita, et al.
Publicado: (2018)

Determination of the pathogenicity of known COL4A5 intronic variants by in vitro splicing assay
por: Horinouchi, Tomoko, et al.
Publicado: (2019)

Medullary Cystic Kidney Disease and Focal Segmental Glomerulosclerosis Caused by a Compound Heterozygous Mutation in TTC21B
por: Hibino, Satoshi, et al.
Publicado: (2020)

A Japanese boy with NAA10-related syndrome and hypertrophic cardiomyopathy
por: Shishido, Ayumi, et al.
Publicado: (2020)

A pediatric case of hypomagnesemia 1 (HOMG1) caused by novel compound heterozygous mutations in TRPM6
por: Goda, Takeshi, et al.
Publicado: (2019)

An infantile case of pseudohypoaldosteronism type 1 (PHA1) caused by a novel mutation of NR3C2
por: Goda, Takeshi, et al.
Publicado: (2020)

Pathogenic evaluation of synonymous COL4A5 variants in X‐linked Alport syndrome using a minigene assay
por: Horinouchi, Tomoko, et al.
Publicado: (2020)

Septic Encephalopathy Characterized by Acute Encephalopathy with Biphasic Seizures and Late Reduced Diffusion and Early Nonconvulsive Status Epilepticus
por: Yamaguchi, Hiroshi, et al.
Publicado: (2016)

Cannot write session to /tmp/vufind_sessions/sess_asoumldb6f2a49eooecojt9ss1