Monotherapy or polytherapy for childhood epilepsies? [PDF]
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Impact of Bacille Calmette-Guérin vaccination on the therapeutic schedule of infantile epileptic spasms syndrome: A 25-year Japanese single-center survey. [PDF]
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Infantile epileptic spasms syndrome in a child with lissencephaly associated with de novo PAFAH1B1 variant and coincidental CMV infection. [PDF]
Ying Eng N, Nie DA.
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Initial combination versus early sequential standard therapies for Infantile Epileptic Spasms Syndrome-Feedback from stakeholders. [PDF]
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Adrenocorticotropic hormone combined with magnesium sulfate therapy for infantile epileptic spasms syndrome: a real-world study. [PDF]
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Genetics of infantile epileptic spasms syndrome in China.
Developmental Medicine & Child NeurologyAIM To construct a genetic landscape of infantile epileptic spasms syndrome (IESS) and explore the pathogenic mechanisms of IESS-associated genes. METHOD We conducted a nationwide, multicentre, retrospective study across six centres in China, enrolling
Zhao Xu +9 more
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Identification and treatment of surgically-remediable causes of infantile epileptic spasms syndrome
Expert Review of NeurotherapeuticsIntroduction Infantile epileptic spasms syndrome (IESS) is a common developmental and epileptic encephalopathy with poor long-term outcomes. A substantial proportion of patients with IESS have a potentially surgically remediable etiology.
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Infantile Epileptic Spasms Syndrome
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Infantile epileptic spasm syndrome as a new NR2F1 gene phenotype
International Journal of Developmental Neuroscience, 2023AbstractIntroductionNR2F1 pathogenetic variants are associated with the Bosch–Boonstra–Schaaf optic atrophy syndrome (BBSOAS). Recent studies indicate that BBSOAS patients not only have visual impairments but may also have developmental delays, hypotonia, thin corpus callosum and epileptic seizures.
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