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Profil bibliographique

Shelagh Smith

Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.

28Publications signalées
1269Citations signalées
0Affiliations récentes

Les domaines associés

Epilepsy research and treatmentPharmacological Effects and Toxicity StudiesNeuroscience and Neuropharmacology ResearchEEG and Brain-Computer InterfacesAutoimmune Neurological Disorders and Treatments

Les publications récentes

2013 article OpenAlex

Faciobrachial dystonic seizures: the influence of immunotherapy on seizure control and prevention of cognitive impairment in a broadening phenotype

Sarosh R. Irani, Charlotte J. Stagg, Jonathan M. Schott, Clive R. Rosenthal et autres

Voltage-gated potassium channel complex antibodies, particularly those directed against leucine-rich glioma inactivated 1, are associated with a common form of limbic encephalitis that presents with cognitive impairment and seizures. Faciobrachial dystonic seizures have recently been reported as immunotherapy-responsive, brief, frequent events that …

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439 citations Brain
Accès ouvert 2011 article OpenAlex

Epilepsy causing pupillary hippus: an unusual semiology

María Centeno, M Feldmann, Neil A. Harrison, Fergus Rugg‐Gunn et autres

Altered pupillary behavior is commonly present during and following epileptic seizures, but symptomatic pupillary hippus as the main feature of a seizure has not been reported in the modern literature. We present the case of a woman with epileptic seizures consisting of …

gb, es (code pays fourni par la source)

25 citations Epilepsia
Accès ouvert 2010 article OpenAlex

Mosaicism of a missenseSCN1Amutation and Dravet syndrome in a Roma/Gypsy family

Dimitar N. Azmanov, Sashka Zhelyazkova, P. Dimova, Melania Radionova et autres

SCN1A mutations account for a large proportion of Dravet syndrome patients, and are reported in other cases of epilepsy, such as some families with genetic epilepsy with febrile seizures plus (GEFS+). While most Dravet syndrome cases are caused by de novo mutations, …

au, bg, gb, nl (code pays fourni par la source)

19 citations Epileptic Disorders
2009 article OpenAlex

Partial epilepsy syndrome in a Gypsy family linked to 5q31.3‐q32

Dora Angelicheva, Ivailo Tournev, Velina Guergueltcheva, Violeta Mihaylova et autres

PURPOSE: The restricted genetic diversity and homogeneous molecular basis of Mendelian disorders in isolated founder populations have rarely been explored in epilepsy research. Our long-term goal is to explore the genetic basis of epilepsies in one such population, the Gypsies. The aim …

au, bg, gb, nl (code pays fourni par la source)

16 citations Epilepsia
2009 article OpenAlex

Acute, localised paroxysmal pain as the initial manifestation of focal seizures: A case report and a brief review of the literature

Gavin Charlesworth, Imad Soryal, Shelagh Smith, Sanjay M. Sisodiya

Pain is a rare manifestation of epileptic seizures. Yet, despite its rarity as a clinical entity, the pain associated with such seizures can be both severe and disabling. It thus remains important to consider epilepsy in the differential diagnosis of unexplained paroxysmal …

gb, us, ie (code pays fourni par la source)

15 citations Pain
Accès ouvert 2008 article OpenAlex

Extratemporal ictal clinical features in hippocampal sclerosis: Their relationship to the degree of hippocampal volume loss and to the outcome of temporal lobectomy

Paolo Borelli, Simon Shorvon, John Stevens, Shelagh Smith et autres

PURPOSE: Since extratemporal clinical features in patients with unilateral hippocampal sclerosis (HS) are likely to indicate aberrant ictal spread or a more extensive epileptogenic zone, we asked whether such features are associated with more severe HS and a worse outcome following temporal …

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12 citations Epilepsia

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