Find link

language:

Find link is a tool written by Edward Betts.

searching for Epilepsy syndromes 23 found (28 total)

Reflex seizure (2,193 words) [view diff] exact match in snippet view article find links to article

(simple or complex), generalized, myoclonic, or absence seizures. Epilepsy syndromes characterized by repeated reflex seizures are known as reflex epilepsies

Epilepsy surgery (1,671 words) [view diff] exact match in snippet view article find links to article

epilepsy (0.4% of the population of industrialized countries) have focal epilepsy syndromes. In 15% to 20% of these patients, the condition is not adequately

Neonatal seizure (4,791 words) [view diff] exact match in snippet view article find links to article

neonatal period when the secondary cause is treated. Neonates with epilepsy syndromes often have seizures later in life. It has been estimated that approximately

Ingrid Scheffer (471 words) [view diff] exact match in snippet view article find links to article

the aetiology of epilepsy, Ingrid has worked to characterise new epilepsy syndromes, from infancy to adulthood, which have permitted appropriate treatment

Early myoclonic encephalopathy (294 words) [view diff] exact match in snippet view article find links to article

Cross, J. Helen (June 2022). "ILAE classification and definition of epilepsy syndromes with onset in neonates and infants: Position statement by the ILAE

Ring chromosome 20 syndrome (1,409 words) [view diff] exact match in snippet view article find links to article

telomeric region includes two genes that are related to other distinct epilepsy syndromes, autosomal dominant nocturnal frontal lobe epilepsy and benign familial

Childhood absence epilepsy (857 words) [view diff] case mismatch in snippet view article find links to article

Ernest (June 2022). "ILAE definition of the Idiopathic Generalized Epilepsy Syndromes: Position statement by the ILAE Task Force on Nosology and Definitions"

KCNJ10 (1,324 words) [view diff] exact match in snippet view article find links to article

associated with seizure susceptibility of common idiopathic generalized epilepsy syndromes. Humans with mutations in the KCNJ10 gene that cause loss of function

Hypsarrhythmia (444 words) [view diff] case mismatch in snippet view article find links to article

(2): 100–4. doi:10.1055/s-2002-32371. PMID 12075493. "EEG in Common Epilepsy Syndromes: eMedicine Neurology". 2019-07-08. {{cite journal}}: Cite journal

Seizure (7,089 words) [view diff] exact match in snippet view article find links to article

ages of six months and five years. During childhood, well-defined epilepsy syndromes are generally seen. In adolescence and young adulthood, non-compliance

Lamotrigine (6,511 words) [view diff] exact match in snippet view article find links to article

protective against generalised absence epilepsy and other generalised epilepsy syndromes, including primary generalised tonic–clonic seizures, juvenile myoclonic

SLC6A1 epileptic encephalopathy (912 words) [view diff] exact match in snippet view article find links to article

treatment is guided by existing strategies for the specific clinical epilepsy syndromes, rather than underlying genetic etiology, using broad-spectrum anti-seizure

GABRD (2,694 words) [view diff] case mismatch in snippet view article find links to article

MP, et al. (June 2018). "Association of GABAA Receptor Gene with Epilepsy Syndromes". Journal of Molecular Neuroscience. 65 (2): 141–153. doi:10.1007/s12031-018-1081-7

Rochester Epidemiology Project (1,612 words) [view diff] exact match in snippet view article find links to article

(2011). "Incidence and classification of new-onset epilepsy and epilepsy syndromes in children in Olmsted County, Minnesota from 1980 to 2004: a population-based

Benign familial neonatal seizures (2,574 words) [view diff] exact match in snippet view article find links to article

seizures and comparison with KCNQ2- and KCNQ3-associated benign familial epilepsy syndromes". Annals of the Child Neurology Society. 1 (3): 202–208. doi:10.1002/cns3

Lennox–Gastaut syndrome (3,434 words) [view diff] exact match in snippet view article find links to article

"International League Against Epilepsy classification and definition of epilepsy syndromes with onset in childhood: Position paper by the ILAE Task Force on

Myoclonus (3,575 words) [view diff] exact match in snippet view article find links to article

Minassian, BA. (Jul 2009). "Treatment options for epileptic myoclonus and epilepsy syndromes associated with myoclonus". Expert Opin Pharmacother. 10 (10): 1549–60

Causes of seizures (3,840 words) [view diff] case mismatch in snippet view article find links to article

"Electroencephalography in the Diagnosis of Genetic Generalized Epilepsy Syndromes". Frontiers in Neurology. 8: 499. doi:10.3389/fneur.2017.00499. PMC 5622315

University of Virginia School of Medicine (2,595 words) [view diff] exact match in snippet view article find links to article

Was instrumental in the classification of epileptic seizures and epilepsy syndromes. Was one of the leaders in promotion of Child Neurology as a specific

CDKL5 deficiency disorder (2,202 words) [view diff] case mismatch in snippet view article find links to article

Francophone. Retrieved 21 June 2021. "LAE Classification & Definition of Epilepsy Syndromes in the Neonate and Infant: Position Statement by the ILAE Task Force

Vagus nerve stimulation (6,011 words) [view diff] exact match in snippet view article find links to article

be good candidates for VNS. VNS may provide benefit for particular epilepsy syndromes and seizure types such as Lennox-Gastaut syndrome, tuberous sclerosis

Panayiotopoulos syndrome (5,827 words) [view diff] exact match in snippet view article find links to article

is now based includes over 800 cases of all races; there are few epilepsy syndromes which are better characterised."What emerges are a remarkably uniform

2014 Queen's Birthday Honours (Australia) (11,455 words) [view diff] exact match in snippet view article

academic and mentor, and to research into the identification of epilepsy syndromes and genes. Winifred Schubert – For distinguished service to the community