Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Nedia Ben Achour"'
Autor:
Ichraf Kraoua, Aida Rouissi, Nedia Ben Achour, Hedia Klaa, Hanene Benrhouma, Amina Nasri, Ilhem Turki
Publikováno v:
Pediatric Emergency Care. 37:e719-e725
Objectives Acute movement disorders (AMD) are frequent in neurological and pediatric emergencies. Few studies analyzed AMD in children, none in Tunisia or other African country. The purpose of this study was to describe the peculiarities of AMD in a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::74294e63fc7bae4de2b71e7935956d10
https://doi.org/10.1097/pec.0000000000002017
https://doi.org/10.1097/pec.0000000000002017
Publikováno v:
European Journal of Paediatric Neurology
European Journal of Paediatric Neurology, Elsevier, 2018, 22 (3), pp.548--551. ⟨10.1016/j.ejpn.2018.01.004⟩
European Journal of Paediatric Neurology, Elsevier, 2018, 22 (3), pp.548--551. ⟨10.1016/j.ejpn.2018.01.004⟩
International audience; Introduction Anti-glutamic acid decarboxylase (anti-GAD65) antibodies are a rare cause of autoimmune encephalitis. This entity is mainly recognized in adults and very few cases were reported in children. We report on a paediat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f1be7e2b29e7df0298f3906af94d071
https://hal.archives-ouvertes.fr/hal-01876256
https://hal.archives-ouvertes.fr/hal-01876256
Publikováno v:
Braindevelopment. 39(9)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dd7737c05f4e6e3cffc063631157cdd1
https://pubmed.ncbi.nlm.nih.gov/28668234
https://pubmed.ncbi.nlm.nih.gov/28668234
Autor:
Aida Rouissi, H. Klaa, H. Benrhouma, I. Kraoua, Ibtihel Rebai, Saloua Mrabet, Nedia Ben Achour, Ines Abid, Ilhem Turki
Publikováno v:
Braindevelopment. 39(9)
Introduction Opsoclonus myoclonus syndrome (OMS) is a rare immune-mediated disorder characterized by opsoclonus, myoclonus, ataxia and behavioral changes. The aim of our study was to investigate the epidemiology, clinical features, etiological aspect
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4e5c2fce0b957023eb60f3837e02a615
https://pubmed.ncbi.nlm.nih.gov/28549713
https://pubmed.ncbi.nlm.nih.gov/28549713
Autor:
H. Klaa, Sarra Raddadi, Nedia Ben Achour, H. Benrhouma, Ilhem Turki, Aida Rouissi, I. Kraoua, Ibtihel Rebai
Publikováno v:
BioMed Research International, Vol 2017 (2017)
BioMed Research International
BioMed Research International
Introduction. Pediatric multiple sclerosis (pMS) is a rare demyelinating disorder with an onset before the age of 18 years. In this study, we aimed to investigate the characteristics of pMS in Tunisian children. Patients and Methods. We conducted a r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::18364a1cb8f0af0ca24a18600429d94c
Autor:
Hanene Benrhouma, Rebai Ibtihel, Hedia Klaa, Ichraf Kraoua, Thouraya Ben Younes, Nedia Ben Achour, Ilhem Turki
Publikováno v:
Revue Neurologique. 173:S178-S179
Introduction La cerebellite aigue (CA) est une affection inflammatoire rare chez l’enfant dont les presentations cliniques et radiologiques sont variees. Elle peut etre d’origine infectieuse, post infectieuse ou post vaccinale. Objectifs Determin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4ee386e361c3373f9b60a0e7eff18706
https://doi.org/10.1016/j.neurol.2017.01.347
https://doi.org/10.1016/j.neurol.2017.01.347
Autor:
Sinda Makhlouf, Nedia Ben Achour, Hedia Klaa, Ilhem Turki, Ichraf Kraoua, Hanene Benrhouma, Aida Rouissi
Publikováno v:
Revue Neurologique. 173:S84-S85
Introduction Les manifestations neurologiques d’origine iatrogene (MNOI) representent un motif frequent de consultation chez l’enfant. Leur expression clinique est polymorphe touchant aussi bien le systeme nerveux central que peripherique. Object
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ebfac0e521465975564e4325212ceca9
https://doi.org/10.1016/j.neurol.2017.01.121
https://doi.org/10.1016/j.neurol.2017.01.121
Autor:
Hedia Klaa, Hanene Benrhouma, Ilhem Turki, Ichraf Kraoua, Ibtihel Rebai, Nedia Ben Achour, Sinda Makhlouf
Publikováno v:
Revue Neurologique. 173:S159-S160
Introduction L’encephalite herpetique (EH) est la cause la plus frequente d’encephalite chez l’enfant. L’encephalite limbique auto-immune (ELAI) succedant a une EH est une entite meconnue et deroutante. Objectifs Decrire les caracteristiques
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8f593c2178866c8d707afcf9d77e4a95
https://doi.org/10.1016/j.neurol.2017.01.299
https://doi.org/10.1016/j.neurol.2017.01.299
Autor:
Ichraf Kraoua, Ibtihel Rebai, Mejri Imene, Nedia Ben Achour, Hanene Benrhouma, Hedia Klaa, Ilhem Turki
Publikováno v:
Revue Neurologique. 173:S128-S129
Introduction Les aspects neurocognitifs au cours de la sclerose en plaques (SEP) ont fait l’objet de plusieurs etudes chez l’adulte. Cependant, ils sont peu connus dans les formes pediatriques de SEP. Objectifs Decrire le profil neurocognitif dan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bf04104830f7d19fdcc631963920ca68
https://doi.org/10.1016/j.neurol.2017.01.227
https://doi.org/10.1016/j.neurol.2017.01.227
Autor:
Hanene Benrhouma, Ilhem Turki, Aida Rouissi, Hedia Klaa, Ichraf Kraoua, Nedia Ben Achour, Saloua Mrabet, Malika Ben Ahmed
Publikováno v:
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society. 19(6)
Background Anti-Ma2-associated encephalitis is a rare paraneoplastic neurological syndrome characterized by isolated or combined limbic, diencephalic, or brainstem dysfunction. It is rarely reported in children. Case study We describe the clinical da
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cd70ed34e13b4e273b9d338cd1b49f4a
https://pubmed.ncbi.nlm.nih.gov/26190012
https://pubmed.ncbi.nlm.nih.gov/26190012