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Their epilepsy was characterized by multiple seizure types, although only 45% had more than 4 tonic clonic seizures per month on average.
Lennox-Gastaut syndrome is an epileptic encephalopathy characterized by multiple seizure types, mental retardation, and a slow spike-and-wave pattern on electroencephalography.
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The epilepsy phenotype is characterized by multiple seizures types, primarily myoclonic, and exquisite photosensitivity in most patients [ 29].
Dravet syndrome is characterized by onset of recurrent febrile and/or afebrile hemiclonic or generalized seizures, or status epilepticus, in a previously healthy infant, followed by appearance of multiple seizure types generally resistant to anti-epileptic drugs with developmental arrest or regression (Dravet et al., 2005; Jansen et al., 2006; Wolff et al., 2006).
All patients had multiple seizure types in adulthood (Table 1).
These choices were provided in a checkbox fashion so that multiple seizure types could be indicated.
All patients have had generalized seizures (although in some cases, the generalized seizures were only in febrile contexts) and 68% exhibited multiple seizure types (17/25) including partial seizures (of frontal or temporal origin) and atypical absences.
Features of Dravet syndrome in adulthood include multiple seizure types despite polytherapy, and age-dependent evolution in seizure semiology and electroencephalographic pattern.
Children with OS typically have multiple seizure types including tonic spasms and focal seizures, which are often refractory to anti-epileptic drugs (12).
These syndromes may include single or multiple seizure types, and may have a benign or a more complex course.
Patients progressively develop both physical and functional deficits including multiple seizure types, cognitive and physical decline, malnutrition and psychiatric features.
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