Zobrazeno 1 - 10
of 1 421
pro vyhledávání: '"Epileptic spasms"'
Autor:
Marília Barbosa de Matos, Paulo Breno Noronha Liberalesso, Tiago dos Santos Bara, Paula Carolina Martins Alves Gomes, Bianca Simone Zeigelboim, Jair Mendes Marques, Mara L. Cordeiro
Publikováno v:
Jornal de Pediatria, Vol 100, Iss 5, Pp 552-556 (2024)
Objective: This study aimed to investigate the prevalence of autism spectrum disorder and its possible correlations with clinical characteristics in patients with infantile epileptic spasms syndrome in a single center in Brazil. Methods: This retrosp
Externí odkaz:
https://doaj.org/article/eabb9a07cf7748ae9e785009a34a274b
Autor:
Taylor Kolosky, Andrea Goldstein Shipper, Kai Sun, Busra Tozduman, Soren Bentzen, Ahsan N. Moosa, Gozde Erdemir
Publikováno v:
Epilepsia Open, Vol 9, Iss 4, Pp 1136-1147 (2024)
Abstract To conduct a systematic review of the literature regarding rates and predictors of favorable seizure outcome after resective surgery for epileptic spasms (ES) in pediatric patients. The Preferred Reporting Items for Systematic Reviews and Me
Externí odkaz:
https://doaj.org/article/0deda1568fa94cf99b8ef1890d3004ce
Autor:
Gozde Erdemir, Ahsan N. Moosa
Publikováno v:
Annals of Indian Academy of Neurology, Vol 27, Iss 3, Pp 227-235 (2024)
Epileptic spasms are a unique, age-dependent manifestation of epilepsies in infancy and early childhood, commonly occurring as part of infantile epileptic spasms syndrome. Developmental stagnation and subsequent decline may occur in children with epi
Externí odkaz:
https://doaj.org/article/6970307aee4144d18c8b9f85b8823f95
Publikováno v:
Frontiers in Neurology, Vol 15 (2024)
PurposeInfantile epileptic spasms syndrome (IESS) is associated with abnormal neuronal networks during a critical period of synaptogenesis and brain plasticity. Hypsarrhythmia is a visual EEG biomarker used to diagnose IESS, assess response to treatm
Externí odkaz:
https://doaj.org/article/5082768c885d45039a45a6b68276be5a
Autor:
Hikaru Kobayashi, Hirofumi Inoue, Takeshi Matsushige, Madoka Hoshide, Fumitaka Kohno, Ippei Hidaka, Shunji Hasegawa
Publikováno v:
Vaccine: X, Vol 20, Iss , Pp 100558- (2024)
Adrenocorticotropic hormone (ACTH) therapy is effective for infantile epileptic spasms syndrome (IESS) but can induce immunosuppression. In Japan, Bacille Calmette-Guérin (BCG) vaccination, modified in 2013 to reduce osteitis/osteomyelitis risk, coi
Externí odkaz:
https://doaj.org/article/6d2ac75fd82f4c7c8829250231dbbb98
Autor:
Patrycja Ochman-Pasierbek, Przemysław Olczyk, Justyna Paprocka, Magdalena Machnikowska-Sokołowska, Adrianna Doman
Publikováno v:
Annales Academiae Medicae Silesiensis, Vol 78, Pp 118-126 (2024)
Aicardi syndrome (AS) is a rare congenital disorder with neurodevelopmental symptoms that in the significant majority of cases occurs in females. It is typically characterized by a classic triad of symptoms: epileptic spasms, agenesis of the corpus c
Externí odkaz:
https://doaj.org/article/b36d210668fd4d49aced87acd87efa83
Autor:
Ali Al Kaissi, Sergey Ryabykh, Farid Ben Chehida, Hamza Al Kaissi, Vasileios Dougales, Vladimir M. Kenis, Franz Grill
Publikováno v:
Pediatric Reports, Vol 16, Iss 2, Pp 410-419 (2024)
Background: Neither radiological phenotypic characteristics nor reconstruction CT scan has been used to study the early anatomical disruption of the cranial bone in children with the so-called idiopathic type of West syndrome. Material and Methods: T
Externí odkaz:
https://doaj.org/article/43259bbec7e54a17a7f5750213975033
Autor:
Balamurugan Nagarajan, Vykuntaraju K. Gowda, Sangeetha Yoganathan, Indar Kumar Sharawat, Kavita Srivastava, Nitish Vora, Rahul Badheka, Sumita Danda, Umesh Kalane, Anupriya Kaur, Priyanka Madaan, Sanjiv Mehta, Sandeep Negi, Prateek Kumar Panda, Surekha Rajadhyaksha, Arushi Gahlot Saini, Lokesh Saini, Siddharth Shah, Varunvenkat M. Srinivasan, Renu Suthar, Maya Thomas, Sameer Vyas, Naveen Sankhyan, Jitendra Kumar Sahu
Publikováno v:
Epilepsia Open, Vol 8, Iss 4, Pp 1383-1404 (2023)
Abstract Objective Literature on the genotypic spectrum of Infantile Epileptic Spasms Syndrome (IESS) in children is scarce in developing countries. This multicentre collaboration evaluated the genotypic and phenotypic landscape of genetic IESS in In
Externí odkaz:
https://doaj.org/article/2042c5f568e642f6a08dd0240ef34435
Publikováno v:
Italian Journal of Pediatrics, Vol 49, Iss 1, Pp 1-6 (2023)
Abstract Background This study aimed to investigate and analyze the risk factors for non-etiology-specific infantile spasms (IS) and unrelieved clinical symptoms after treatment. Methods Eighty-eight children with IS who were treated at our hospital
Externí odkaz:
https://doaj.org/article/3873418910964df9bfbc04ed73764643
Autor:
Jithangi Wanigasinghe, Gemunu Hewawitharana, Pyara Ratnayake, Saraji Wijesekera, Chathurika Weeraratne, Ashan Jayawickrama, Jayasanka Jayawardena
Publikováno v:
Annals of the Child Neurology Society, Vol 1, Iss 2, Pp 137-143 (2023)
Abstract Objectives Infantile epileptic spasm syndrome (IESS) is an epileptic encephalopathy with often devastating developmental consequences. Most children with IESS have a known etiology, although differing in proportion by geographical settings.
Externí odkaz:
https://doaj.org/article/9338f2ad4dc74e339ada2a031723ee02