Zobrazeno 1 - 10
of 48
pro vyhledávání: '"Amina Chentouf"'
Publikováno v:
The Egyptian Journal of Neurology, Psychiatry and Neurosurgery, Vol 60, Iss 1, Pp 1-7 (2024)
Abstract Background Epilepsy is one of the most common neurological diseases that affects people of different ages, ethnicities, and geographical locations. The objective of the present study was to determine the demographic and clinical characterist
Externí odkaz:
https://doaj.org/article/1bef510cbcd74fa482a991565761558a
Autor:
Amina Chentouf, Rand Talhi, Aicha Dahdouh, Soumia Benilha, Mohand Laid Oubaiche, Malika Chaouch
Publikováno v:
Journal de la Faculté de Médecine d'Oran, Vol 1, Iss 3 (2024)
Résumé Introduction - L’épilepsie est une maladie neurologique chronique dont les facteurs de risque sont très hétérogènes d’une population à une autre. Le rôle important attribué à la consanguinité dans le développement de maladies
Externí odkaz:
https://doaj.org/article/06b25834bd5049f5b37a3f2ff38b2de1
Publikováno v:
Journal de la Faculté de Médecine d'Oran, Vol 1, Iss 1 (2024)
Résumé Objectifs - Cette étude vise à caractériser des familles comptant plusieurs individus épileptiques, à étudier les modes de transmission de l’épilepsie au sein de ces familles, à rechercher des variants génétiques de vulnérabilit
Externí odkaz:
https://doaj.org/article/15f3a7eaf25f41d8beff4aad0dd4dc99
Autor:
Amina CHENTOUF, Souad DAOUD
Publikováno v:
Journal de la Faculté de Médecine d'Oran, Vol 3, Iss 2 (2022)
Celiac disease is a common autoimmune disease that affects the small intestineof genetically predisposed individuals. This disease can be expressed by a widerange of extra-digestive signs including cutaneous, endocrine, hepatic, skeletal,hematologica
Externí odkaz:
https://doaj.org/article/ba93440ca6b24b49aef0a61a9aa67314
Dysembryoplastic neuroepithelial tumors and refractory epilepsy: a case report and literature review
Autor:
Souad DAOUD, Amina CHENTOUF, Salim BENAMARA, Ryad Moumen AYOUN, Kaouter YZIDI, Mammar BOUCHAKOUR
Publikováno v:
Journal de la Faculté de Médecine d'Oran, Vol 3, Iss 2 (2022)
IntroductionNeuroepithelial dysembryoplastic tumors are grade I benign tumors, typicallylocalized in the suprententorial cortex and usually revealed by drug-resistantepilepsy. Very rare, they represent less than 1% of all brain tumors.ObservationWe r
Externí odkaz:
https://doaj.org/article/d62306a18357417895da98e6ae0a5b25
Autor:
Amina Chentouf, Mohand Laid Oubaiche, Aicha Dahdouh, Annick Salzmann, Michel Guipponi, Stylianos Antonarakis, Malika Chaouch
Publikováno v:
Journal de la Faculté de Médecine d'Oran, Vol 1, Iss 4 (2022)
Introduction - Several studies have shown a strong relationship between schizophrenia and epilepsy. This association implies a common genetic susceptibility for both conditions. This study aims to identify genetic variants of susceptibility to epilep
Externí odkaz:
https://doaj.org/article/d136881ba74b44f685fc82ba38ab9e6c
Autor:
Amina Chentouf, Randa Talhi, Aicha Dahdouh, Soumia Benilha, Mohand Laid Oubaiche, Malika Chaouch
Publikováno v:
Journal de la Faculté de Médecine d'Oran, Vol 1, Iss 3 (2022)
Introduction - Epilepsy is a chronic neurological disease whose risk factors are very heterogeneous from one population to another. The role attributed to inbreeding in the development of genetically determined diseases has been well documented. Howe
Externí odkaz:
https://doaj.org/article/a0278b88611240c28c4355f91fbe8f04
Publikováno v:
Journal de la Faculté de Médecine d'Oran, Vol 1, Iss 1 (2022)
Objectives - This study aims to investigate the surrounding family when several cases of epileptics are found, the goal is to establish inheritance patterns and to identify genetic variants and to document the genotype/phenotype correlation. Material
Externí odkaz:
https://doaj.org/article/8eb21e67d2674e05a3cdf9ccc776b55c
Autor:
Amina Chentouf
Publikováno v:
Türk Nöroloji Dergisi, Vol 27, Iss s1, Pp 56-57 (2021)
Externí odkaz:
https://doaj.org/article/092948405ace4b7e9d7aa29dffa03a7b
Autor:
Amina CHENTOUF
Publikováno v:
Journal de la Faculté de Médecine d'Oran, Vol 4, Iss 2 (2020)
Introduction Fibrodysplasia Ossificans Progressiva (FOP) is an extremely rare genetic disease characterized by heterotopic ossification of muscles and connective tissue occurring in relapses, which can lead to the creation of a real second skeleton.
Externí odkaz:
https://doaj.org/article/9a9551e8bcf74256bca583a2485b5f07