The relationship between social anxiety and felt stigma in patients with epilepsy: a network analysis

Epilepsy, characterized by a prolonged predisposition to generate epileptic seizures, is one of the most common chronic neurologic disorders [1]. Although many differences have been found among these three categories of seizures, including generalized onset seizures, focal onset epilepsy and unknown onset epilepsy, almost 70% of patients with epilepsy (PWE) respond positively to treatment, including pharmacotherapy and nonpharmacy therapy, and become seizure free [2]. However, in addition to seizure attacks, there are many other problems faced by PWE, including social ...

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Genetic-Cellular Epilepsy: Clues to Diagnosing Newborns with Neonatal Seizures

Seizures are the most frequent sign of neurological dysfunction in newborns. They occur in an estimated 2-3 per 1,000 term newborns and in 10-15 per 1,000 in preterms [1,2]. They are mostly due to acute brain injury such as hypoxic ischaemic encephalopathy (HIE), ischaemic or haemorrhagic stroke, metabolic disorders, or infection but are sometimes the first sign of neonatal-onset epilepsy due to pathogenic genetic mutations [3].

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Brain injury markers in new-onset seizures in adults: a pilot study

There is a need for biomarkers in epilepsy, especially markers that can be used to support diagnosis and prognostication early in the disease course. In patients with a first seizure, large structural brain lesions visible on brain imaging increase the risk of seizure recurrence [1]. Whether brain pathology capturable on a biochemical level has prognostic or diagnostic value is not known.

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ANOTHER CASE OF ICONODIAGNOSIS: MISATTRIBUTION OF ALIEN HAND IN DR STRANGELOVE?

Helmstaedter and others [1-3] have interpreted the inability of the main character to control his right arm in Stanley Kubrick’s satire Dr Strangelove (1964) as an alien hand syndrome. Dr. Strangelove’s right arm has a will of its own and constantly forms a Nazi salute and, at one point, attempts to strangle him with its black-gloved right hand. But, quite frankly, Kubrick modeled this arm after the prosthesis of the evil genius scientist Dr Rotwang (Rudolf Klein-Rogge) in Fritz Lang’s ...

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Cluster analysis of a large dataset of patients with Lennox-Gastaut syndrome

Lennox-Gastaut syndrome (LGS) is a childhood epilepsy syndrome characterized by multiple seizure types (e.g., tonic, atonic, absences, etc.), a specific interictal electroencephalographic (EEG) pattern [i.e., generalized slow spike-waves (SSW) and/or generalized paroxysmal fast activity (GPFA)], and intellectual/psychosocial dysfunction.1-3 Seizures in LGS are often resistant to antiseizure medications (ASMs); reduction in the frequency of the most incapacitating seizures [i.e., Generalized tonic-clonic (GTC), tonic, and atonic] should be the major objective in their management strategy.

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Postoperative seizure and developmental outcomes of children with hemimegalencephaly and drug-resistant epilepsy

Hemimegalencephaly (HMEG) belongs to the brain overgrowth spectrum with unilateral megalencephaly involving one or almost one entire brain hemisphere [1]. Developmental delay, contralateral hemiparesis, and drug-resistant epilepsy are common in children with HMEG [2, 3]. Early epileptic seizures usually evolve into epileptic encephalopathies and lead to severe psychomotor retardation without intervention [4].

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Epilepsy and psychogenic non-epileptic seizures in forcibly displaced people: A scoping review

At the end of 2019, 79.5 million people worldwide had been forcibly displaced; 45.7 million of these were internally displaced people (IDP), while 26 million were refugees. [1] The latter are either under the mandate of the United Nations High Commissioner for Refugees (UNHCR; 20.4 million) or the mandate of the United Nations Relief and Works Agency for Palestine Refugees (UNRWA; 5.6 million Palestinian refugees). The term refugee describes people who have left their home countries and cannot return owing ...

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Exploring factors associated with interictal heart rate variability in patients with medically controlled focal epilepsy

People with epilepsy have autonomic dysfunction and a significantly higher premature mortality rate than the healthy controls. [1, 2] Heart rate variability (HRV), a marker of autonomic function, reflects the balance between sympathetic and parasympathetic activities. [3] HRV parameters are a useful objective marker of physiological stress. It measures the changes in time intervals between consecutive heartbeats. [4] Increased HRV indicates an increased parasympathetic activity, whereas decreased HRV indicates increased sympathetic activity.

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Cortical and thalamic hyper-perfusion in non-convulsive status epilepticus. Relationship between perfusion CT patterns and Salzburg EEG criteria

Status epilepticus (SE) is a common neurological emergency, with an incidence of 10-41 cases per 100 000 population [1,2] and a mortality rate of around 20% [2]. Nonconvulsive seizures, nonconvulsive status epilepticus (NCSE), and the postictal state, in particular, may masquerade as a stroke and often represent a diagnostic challenge [3] [4]. Failure in recognizing SE can have important negative consequences leading to incorrect treatment, diagnostic delay and potential treatment adverse effects [5].

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