Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Tamara Herrera Fortin"'
Publikováno v:
Epileptic Disorders. 22:349-352
Porphyrias are rare genetic disorders which cause a deficiency in the enzymes involved in the biosynthesis of heme. The treatment of epilepsy in patients with acute intermittent porphyria can be difficult since many anticonvulsants can increase heme
Autor:
Laura Gagliano, Mohamad Sawan, Tamara Herrera-Fortin, Elie Bou Assi, Frédéric Lesage, Dang Khoa Nguyen
Publikováno v:
The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques.
Objective:Uncontrolled epilepsy creates a constant source of worry for patients and puts them at a high risk of injury. Identifying recurrent “premonitory” symptoms of seizures and using them to recalibrate seizure prediction algorithms may impro
Autor:
Marie-Pierre Gagnon, Elie Bou Assi, Dang Khoa Nguyen, Elisabeth Beauchamp-Chalifour, Tamara Herrera Fortin
BackgroundEpilepsy is a chronic neurological disease characterized by recurrent seizures due to excessive neuronal discharges and abnormal neuronal discharges. 30-40% of them are pharmaco-resistant, which is associated with cognitive impairment. seiz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e40ce9cde72dd0c747039fc572ee01c0
https://doi.org/10.21203/rs.3.rs-66216/v2
https://doi.org/10.21203/rs.3.rs-66216/v2
Autor:
Elisabeth Beauchamp-Chalifour, Marie-Pierre Gagnon, Tamara Herrera Fortin, Elie Bou Assi, Dang Khoa Nguyen
BackgroundEpilepsy is a chronic neurological disease characterized by recurrent seizures due to excessive neuronal discharges and abnormal neuronal discharges. 30-40% of them are pharmaco-resistant, which is associated with cognitive impairement. sei
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::125d997786873f8e537783763a0a7400
https://doi.org/10.21203/rs.3.rs-66216/v1
https://doi.org/10.21203/rs.3.rs-66216/v1