Results 261 to 270 of about 639,655 (303)
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Brain and Development, 2001
Zonisamide (ZNS), a new antiepileptic drug developed in Japan, is being used as the initial treatment of West syndrome in some Japanese institutes. The reported response rate varied from 20 to 38%. The cryptogenic patients showed a better response than the symptomatic patients.
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Zonisamide (ZNS), a new antiepileptic drug developed in Japan, is being used as the initial treatment of West syndrome in some Japanese institutes. The reported response rate varied from 20 to 38%. The cryptogenic patients showed a better response than the symptomatic patients.
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Revista de neurologia, 2000
The author presents a review and actualization of West syndrome related knowledges, ethiological issues, clinics, and the EEG tracings. It is also include a literature review about different therapeutic treatments emphasizing the use of vigabatrin.
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The author presents a review and actualization of West syndrome related knowledges, ethiological issues, clinics, and the EEG tracings. It is also include a literature review about different therapeutic treatments emphasizing the use of vigabatrin.
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West syndrome with cerebellar porencephalus
Journal of Intellectual Disability Research, 1993ABSTRACTThe authors report six very low birth weight newborn infants who had RDS, IVH and cerebellar porencephalus and later suffered from West syndrome. Four of them have been followed up to the present time and have had MRI scans performed. Their present clinico‐neurological features and MRI findings are described.
H, Koide, H, Shime
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Induced microseizures in West syndrome
Brain and Development, 1991Induced microseizures (IMS) were observed in a 5-month-old girl with symptomatic West syndrome. The seizures occurred following the suppression of infantile spasms with adrenocorticotropic hormone therapy and disappeared following the cessation of clonazepam administration.
K, Otani +4 more
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2018
UVOD: West sindrom (WS) je epileptička encefalopatija čija je incidencija 2-5/10 000. U 94% slučajeva javlja se u prvih 12 mjeseci života, a karakteriziran je epileptičkim spazmima, tipičnim nalazom hipsaritmije u elektroencefalografskom zapisu i psihomotoričkim zaostajanjem oboljele djece.
Đuranović, Vlasta +2 more
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UVOD: West sindrom (WS) je epileptička encefalopatija čija je incidencija 2-5/10 000. U 94% slučajeva javlja se u prvih 12 mjeseci života, a karakteriziran je epileptičkim spazmima, tipičnim nalazom hipsaritmije u elektroencefalografskom zapisu i psihomotoričkim zaostajanjem oboljele djece.
Đuranović, Vlasta +2 more
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The West Syndrome: Developmental Aspects
Pediatrics International, 1987AbstractThe electro‐clinical characteristics of childhood epilepsy are known to appear during the development of the brain and to change their features with age. Accordingly, developmental viewpoints are indispensable to researches on childhood epilepsy.Age‐dependent epileptic encephalopathy has the most remarkable developmental characteristics among ...
S, Ohtahara, Y, Ohtsuka, Y, Yamatogi
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2002
Many cases of West's syndrome are inoperable, because there is no clear epileptic focus. In some cases, however, there is a structural abnormality which can be surgically removed. Dr. Hoffman discusses his experience with surgery for cortical dysplasia in West's syndrome.
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Many cases of West's syndrome are inoperable, because there is no clear epileptic focus. In some cases, however, there is a structural abnormality which can be surgically removed. Dr. Hoffman discusses his experience with surgery for cortical dysplasia in West's syndrome.
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West syndrome associated with hyperlexia
Pediatric Neurology, 1990Two patients are reported with West syndrome associated with hyperlexia. They had peculiar linguistic and psychosocial development and autistic behavior, yet began to read Japanese and Chinese characters, numbers, Roman alphabet letters, and trademark letters at 3 years of age.
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