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E

Emna Ellouz

universite de sfax

5H指数
76论文数
63被引数
收录论文 10
发表时间
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Transverse Myelitis: A Case Report of an Overlap Syndrome横贯性脊髓炎：一例重叠综合征病例报告
errNeurological Sciences and Neurophysiology
IF0.2
err2026-01-01
err0
PREAI
errKetata, Imen; Ellouz, Emna; Ketata, Ahmed; Ben Kraeim, Imen
err分享
err收藏
Artificial intelligence-driven eye tracker models for Alzheimer's disease diagnosis: A systematic review and meta-analysis人工智能驱动的眼动追踪模型在阿尔茨海默病诊断中的应用：一项系统评价和荟萃分析
errJournal of Alzheimer’s Disease
IF0
err2025-10-24
err0
PREAI
errImen Ketata; Emna Ellouz
err分享
err收藏
Psychoses onset in multiple sclerosis: A systematic review and meta-analysis多发性硬化中的精神疾病发作：一项系统综述和荟萃分析
errRevue Neurologique
IF2.3
err2025-04-15
err0
PREAI
errI. Ketata; E. Ellouz; A. Ketata
err分享
err收藏
Cerebellar ataxia and epilepsy revealing aceruloplasminemia in a Tunisian family
errJOURNAL OF THE NEUROLOGICAL SCIENCES
IF3.2
err2023-12-01
err0
PREAI
errEllouz, Emna; Ketata, Imen; Sellami, Rahma; Chaabouni, Mariem
err分享
err收藏
Rasmussen encephalitis: A challenging diagnosis in children
errJOURNAL OF THE NEUROLOGICAL SCIENCES
IF3.2
err2023-12-01
err0
PREAI
errDridi, Fawez; Ellouz, Emna
err分享
err收藏
Clinical and etiological features of acute transverse myelitis
errJOURNAL OF THE NEUROLOGICAL SCIENCES
IF3.2
err2023-12-01
err0
PREAI
errKetata, Imen; Sellami, Rahma; Ellouz, Emna
err分享
err收藏
Late-onset multiple sclerosis
errJOURNAL OF THE NEUROLOGICAL SCIENCES
IF3.2
err2023-12-01
err0
PREAI
errKetata, Imen; Dorgham, Dorra; Bouaziz, Fatma; Sellami, Rahma; Ellouz, Emna
err分享
err收藏
Socio-demographic and clinical features of patients with dementia attended in the psychiatry department
errEUROPEAN PSYCHIATRY
IF6.7
err2021-08-13
err0
errOAAI
errBader, S.; Ellouz, E.; Abderrahim, R.; Abbas, M.; Mdhaffer, K.
err分享
err收藏
Ischemic stroke in a case of Koyanagi Harada syndrome
errJOURNAL OF THE NEUROLOGICAL SCIENCES
IF3.2
err2019-10-01
err0
PREAI
errEllouz, E.; Daoud, S.
err分享
err收藏
Phenotypic variability in a Tunisian family with X-linked adrenoleukodystrophy caused by the p.Gln316Pro novel mutation由p.Gln316Pro新突变引起的突尼斯X连锁肾上腺脑白质营养不良家庭的表型变异
errCLINICA CHIMICA ACTA
IF2.9
err2016-01-01
err3
PREAI
errKallabi, Fakhri; Ellouz, Emna; Tabebi, Mouna; Ben Salah, Ghada; Kaabechi, Naziha; Keskes, Leila; Triki, Chahnez; Kamoun, Hassen
err分享
err收藏

研究方向

暂时未获取到该数据
合作学者
合作期刊
M
Mohamed Abbas
H 指数: 33 · 论文数: 185
L
Leila Keskes
H 指数: 27 · 论文数: 167
C
Chahnez Triki
H 指数: 24 · 论文数: 170
H
Hassen Kamoun
H 指数: 17 · 论文数: 113
G
Ghada Ben Salah
H 指数: 12 · 论文数: 49
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