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The Idiopathic Form of West Syndrome
Epilepsia, 1993Summary: The clinical and electroencephalographic data of 31 children with cryptogenic West syndrome (WS), selected from a series of 103 WS patients, with a follow‐up between 4 and 12 years, were studied retrospectively to verify whether this group included patients who fulfilled the criteria for an idiopathic etiology.
F, Vigevano +5 more
openaire +2 more sources
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 +3 more
openaire
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 +3 more
openaire
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.
openaire +1 more source
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.
openaire +1 more source
Monatsschrift Kinderheilkunde : Organ der Deutschen Gesellschaft fur Kinderheilkunde, 1992
West-Syndrome is an age-dependent early epileptic encephalopathy manifesting during the first year of life. It carries a high risk for an unfavourable longterm prognosis, especially for the prevailing group of patients with the symptomatic form. Etiologically associated factors are heterogeneous.
openaire +1 more source
West-Syndrome is an age-dependent early epileptic encephalopathy manifesting during the first year of life. It carries a high risk for an unfavourable longterm prognosis, especially for the prevailing group of patients with the symptomatic form. Etiologically associated factors are heterogeneous.
openaire +1 more source
Genotype-phenotype correlation on 45 individuals with West syndrome
European Journal of Paediatric Neurology, 2020Johannes R Lemke +2 more
exaly
West syndrome: A study of 26 patients receiving short-term therapy
Epilepsy and Behavior, 2021Roberto H Caraballo
exaly