Zobrazeno 1 - 10
of 144
pro vyhledávání: '"refractory seizure"'
Publikováno v:
National Board of Examinations Journal of Medical Sciences, Vol Volume 2, Iss Issue 8, Pp 819-824 (2024)
Background: A Wu type X-linked syndromic intellectual developmental disorder is caused by mutations in the GRIA3 gene This disorder is characterised by autistic features, hyporeflexia, intellectual disability and facial dysmorphism. Case report: The
Externí odkaz:
https://doaj.org/article/3caaabecb221408db8da11ef1f55d71e
Autor:
Suraj Sharma, MBBS, Prakash Dhakal, MBBS, Sajiva Aryal, MBBS, Seema Bhandari, MBBS, Abhishek Sharma, MBBS
Publikováno v:
Radiology Case Reports, Vol 17, Iss 10, Pp 3587-3590 (2022)
Rasmussen's encephalitis (RE) is a relatively rare chronic inflammatory neurological disease that usually only affects one hemisphere of the brain. It primarily affects children under the age of 10, although it can also affect teens and adults, causi
Externí odkaz:
https://doaj.org/article/cd71f77ce6dc4326bc2256db54dab62b
Autor:
Ja Un Moon, Sook Kyung Yum
Publikováno v:
Children, Vol 10, Iss 9, p 1461 (2023)
Partial deletion of the long arm (q) in chromosome 21 is an extremely rare condition with various phenotypes, including microcephaly, neurodevelopmental delay, dysmorphic features, and epileptic seizures. Neonatal hypoxic-ischemic encephalopathy (HIE
Externí odkaz:
https://doaj.org/article/938a6e9d00a042cbab4d6580a53f7983
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 6, p 5491 (2023)
Tandem of P domains in a weak inwardly rectifying K+ channel (TWIK)-related acid sensitive K+-1 channel (TASK-1) is activated under extracellular alkaline conditions (pH 7.2–8.2), which are upregulated in astrocytes (particularly in the CA1 region)
Externí odkaz:
https://doaj.org/article/bd7b7c5e32fd40f69ceaee37ae3a93cc
Autor:
Meng-Ying Hsieh, Jainn-Jim Lin, Shao-Hsuan Hsia, Jing-Long Huang, Kuo-Wei Yeh, Kuei-Wen Chang, Wen-I. Lee
Publikováno v:
Biomedical Journal, Vol 43, Iss 3, Pp 293-304 (2020)
Background: Defective human TLR3 signaling causes recurrent and refractory herpes simplex encephalitis/encephalopathy. Children with febrile infection-related epilepsy syndrome with refractory seizures may have defective TLR responses. Methods: Child
Externí odkaz:
https://doaj.org/article/cdbf42a69620400eb7a389bf4eb6211a
Autor:
Mehdi Valipour, Hamid Irannejad
Publikováno v:
Journal of Mazandaran University of Medical Sciences, Vol 29, Iss 172, Pp 188-206 (2019)
Epilepsy is a neurological condition characterized by recurrent seizures influencing about 1% of the worldwide population. Despite much progress in understanding the pathogenesis of epilepsy, the molecular basis of human epilepsy still remains unclea
Externí odkaz:
https://doaj.org/article/df433be6273849faaddff7fa2ba1a75a
Autor:
Shaghayegh Omrani, Mohammad Taheri, Mir Davood Omrani, Shahram Arsang-Jang, Soudeh Ghafouri-Fard
Publikováno v:
Clinical and Translational Medicine, Vol 8, Iss 1, Pp 1-6 (2019)
Abstract Long chain omega-3 fatty acids (omega-3 FAs) supplements have been shown to exert beneficial effects in patients with epilepsy through elevation of seizure thresholds and dampening of inflammatory responses. In this triple blind randomized,
Externí odkaz:
https://doaj.org/article/50b7c2eaf8a24e10855264c94efca31c
Autor:
Ji-Eun Kim, Tae-Cheon Kang
Publikováno v:
Biomedicines, Vol 10, Iss 4, p 787 (2022)
Tandem of P domains in a weak inwardly rectifying K+ channel (TWIK)-related acid sensitive K+-1 channel (TASK-1) is an outwardly rectifying K+ channel that acts in response to extracellular pH. TASK-1 is upregulated in the astrocytes (particularly in
Externí odkaz:
https://doaj.org/article/3d11803814b747789e336a789d87ffb5
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Akademický článek
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