Zobrazeno 1 - 10
of 98
pro vyhledávání: '"Hanene, Benrhouma"'
Autor:
Ichraf Kraoua, Maha Jamoussi, Cyrine Drissi, Lilia Kraoua, Séverine Drunat, Hanene Benrhouma, Thouraya Ben Younes, Sonia Nagi, Sonia Abdelhak, Odile Boespflug Tanguy, Ilhem Ben Youssef‐Turki, Mediha Trabelsi, Imen Dorboz
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 12, Iss 10, Pp n/a-n/a (2024)
ABSTRACT Background POLIII‐related leukodystrophies are a group of recently recognized hereditary white matter diseases with a similar clinical and radiological phenotype. No Tunisian studies have been published about POLIII‐related leukodystroph
Externí odkaz:
https://doaj.org/article/42e56d894f30444d9f78ebe123d5a36b
Autor:
Bissene Douma, Thouraya Ben Younes, Hanene Benrhouma, Zouhour Miladi, Imen Zamali, Aida Rouissi, Hedia Klaa, Ichraf Kraoua, Melika Ben Ahmed, Ilhem Ben Youssef Turki
Publikováno v:
Journal of Immunology Research, Vol 2021 (2021)
Background. Autoimmune encephalitis (AE) is a rapidly progressive encephalopathy caused by antibodies targeting neurons in the central nervous system generating specific immune responses. It is increasingly recognized in children. Objective. To descr
Externí odkaz:
https://doaj.org/article/e41b602af7574fbea3fbf76cd741638d
Autor:
Maha Jamoussi, Hanene Benrhouma, Zouhour Miladi, Thouraya Ben Younes, Hedia Klaa, Aïda Rouissi, Ichraf Kraoua, Ilhem Ben Youssef
Publikováno v:
European Journal of Paediatric Neurology. 43:6-11
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a75993ae4bb1b931346c0e5c746b87e6
https://doi.org/10.1016/j.ejpn.2023.01.012
https://doi.org/10.1016/j.ejpn.2023.01.012
Autor:
Hedia Klaa, Thouraya Ben Younes, Hanene Benrhouma, Sonia Nagi, Aida Rouissi, Ichraf Kraoua, Ilhem Ben Youssef-Turki
Publikováno v:
Case Reports in Neurological Medicine, Vol 2020 (2020)
Rasmussen’s encephalitis (RE) is a rare progressive inflammatory disease of the central nervous system. It is characterized by unilateral hemispheric atrophy, pharmacoresistant focal seizures, and progressive neurological deficit. The exact etiopat
Externí odkaz:
https://doaj.org/article/27181193de8146b59e490f00664dab27
Autor:
Thouraya Ben Younes, Ichraf Kraoua, Sarah Snanoudj, Hedia Klaa, Hanene Benrhouma, Aida Rouissi, Catherine Caillaud, Myriam Chaabouni, Najoua Miladi, Soumeya Bekri, Ilhem Ben Youssef‐Turki
Publikováno v:
Clinical Genetics. 102:157-160
Our study included 13 patients diagnosed with neuronal ceroidlipofuscinosis. It is a group of rare genetically-determined neurodegenerativediseases characterized by clinical and genetic heterogeneity. brain MRI andelectroencephalogram facilitate diag
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f0e594bee9d19faa2666095d5da8eeff
https://doi.org/10.1111/cge.14145
https://doi.org/10.1111/cge.14145
Autor:
Ichraf Kraoua, Adnane Karkar, Cyrine Drissi, Hanene Benrhouma, Hedia Klaa, Simon Samaan, Florence Renaldo, Monique Elmaleh, Mohamed Ben Hamouda, Sonia Abdelhak, Odile Boespflug‐Tanguy, Ilfghem Ben Youssef‐Turki, Imen Dorboz
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 7, Iss 9, Pp n/a-n/a (2019)
Abstract Introduction RNA polymerase III (Pol III)‐related leukodystrophies are a group of autosomal recessive neurodegenerative disorders caused by mutations in POLR3A and POLR3B. Recently a recessive mutation in POLR1C causative of Pol III‐rela
Externí odkaz:
https://doaj.org/article/871d5ae0d1a844b1a34b8a79f7458804
Autor:
Aicha Kalfat, Abir Zioudi, Kraoua Ichraf, Thouraya Ben Younes, Hedia Klaa, Zouhour Miladi, Hanene Benrhouma, Ilhem Ben Youssef-Turki
Publikováno v:
Revue Neurologique. 179:S38-S39
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::20e57824419863f8dddf44674b48b205
https://doi.org/10.1016/j.neurol.2023.01.077
https://doi.org/10.1016/j.neurol.2023.01.077
Autor:
Nadia Sallem, Thouraya Ben Younes, Hanene Benrhouma, Abir Zioudi, Hedia Klaa, Zouhour Miladi, Kraoua Ichraf, Ilhem Ben Youssef Turki
Publikováno v:
Revue Neurologique. 179:S127-S128
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b214ac6ec256afb4ffc604cdb6264007
https://doi.org/10.1016/j.neurol.2023.01.619
https://doi.org/10.1016/j.neurol.2023.01.619
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
Autor:
Thouraya Ben Younes, Hanene Benrhouma, Imen Zamali, Zouhour Miladi, I. Turki, Bissene Douma, Aida Rouissi, Melika Ben Ahmed, Ichraf Kraoua, Hedia Klaa
Publikováno v:
Journal of Immunology Research
Journal of Immunology Research, Vol 2021 (2021)
Journal of Immunology Research, Vol 2021 (2021)
Background. Autoimmune encephalitis (AE) is a rapidly progressive encephalopathy caused by antibodies targeting neurons in the central nervous system generating specific immune responses. It is increasingly recognized in children. Objective. To descr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::94b1c7ebb8cf02a3ec4f9157f15d23ea
https://doi.org/10.1155/2021/6666117
https://doi.org/10.1155/2021/6666117