Results 111 to 120 of about 1,226,813 (207)
Ketogenic diet for infantile epileptic spasms
Abstract Approximately half of all cases of Infantile Epileptic Spasms Syndrome (IESS) do not respond to vigabatrin and hormonal therapies. There is no clear consensus as to the second‐line therapy for IESS. Ketogenic diet (KD) has emerged as an effective treatment for certain drug‐resistant epilepsies and in many cases of IESS.
Morris H. Scantlebury +3 more
wiley +1 more source
Ketogenic diet in infantile spasms: time for new perspectives
Evaluation of: Hong A, Turner Z, Hamdy RF, Kossoff EH: Infantile spasms treated with the ketogenic diet: Prospective single-center experience in 104 consecutive infants. Epilepsia DOI: 10.1111/j.1528–1167.2010.02586.x (2010) (Epub ahead of print).
Stéphane Auvin
core +1 more source
Abstract Objective Epileptic spasms (ES) in children carry a high risk of neurodevelopmental delay, yet predictors of long‐term surgical outcome remain incompletely defined. This study aimed to evaluate seizure outcomes following epilepsy surgery and to identify independent prognostic factors for postoperative recurrence.
Hua Li +7 more
wiley +1 more source
Infantile Spasms in Down Syndrome
The clinical characteristics, EEG abnormalities, response to therapy, and outcome of 14 patients with infantile spasms and Down syndrome were studied at the Hopital Saint Vincent de Paul, Paris (9 cases); Universita Degli Studi de Pisa, Italy (2 cases ...
J Gordon Millichap
core +1 more source
Genetic analysis of human absence epilepsy [PDF]
Idiopathic Mendelian epilepsies have been typically identified as channelopathies. Evidence suggests that mutations in genes encoding GABAA receptors, GABAB receptors or voltage-dependent calcium channels (VDCCs) may underlie childhood absence epilepsy ...
Robinson, R.A.
core
Background: Early-onset infantile epileptic spasm syndrome is a known feature of phosphatase and actin regulator 1 (PHACTR1) gene mutation. However, its association with whole-cell pertussis vaccination is unknown.
Sreejana Sharma +3 more
doaj +1 more source
The genetic architecture of epilepsy across molecular mechanisms and clinical heterogeneity
Abstract Epilepsy comprises a highly heterogeneous group of neurological disorders unified by a persistent predisposition to recurrent seizures, yet driven by remarkably diverse genetic, molecular, and network‐level mechanisms. Advances in genomic technologies have revealed that epilepsy arises from a multilayered genetic architecture encompassing rare
Mohammad Reza Seyedtaghia +4 more
wiley +1 more source
Infantile Spasms in Children with Down Syndrome [PDF]
Down syndrome (DS) is the most common genetic cause of mental retardation. It is estimated that 5–13% of persons affected by DS have seizures. Infantile spasms are the most common type of seizures and usually are well controlled with steroids and ...
Lucija Lujić +9 more
core +1 more source
Infantile Spams is an epilepsy syndrome that usually appears in children between the ages of four and eight months. The spasms generally occur upon waking or right after feeding, and can occur in clusters of a hundred or more at a time (Go et al., 2012).
Cash, Ashley
core
Linear Nevus Sebaceum Syndrome and Infantile Spasms
Two infants with linear nevus sebaceum syndrome and infantile spasms are reported from Safra Childrens Hospital, Sheba Medical Center, Tel Hashomer, Israel; and Hospital for Sick Children, Toronto ...
J Gordon Millichap
core +1 more source

