الرئيسية › دليل الباحثين › Youssef Abida
Youssef Abida
الانتماء : Tunis University · Hôpital Razi de La Manouba · Faculté de médecine de Tunis · Tunis El Manar University
- 60منشورات (انتماء تونسي)
- 66مجموع المنشورات
- 89الاستشهادات
- 5مؤشر h
الملف البحثي
لدى Youssef Abida 60 منشور(ات) مفهرسة (2020–2026). تُنشر أعماله أساسًا في «Revue Neurologique»، «Multiple Sclerosis and Related Disorders» و«Journal of the Neurological Sciences». أكثر مقالاته استشهادًا هو «Environmental factors related to multiple sclerosis progression» (2024)، وقد استُشهد به 28 مرة. 42 من هذه المنشورات تعود إلى آخر ثلاث سنوات من النشاط. شارك في تأليف أعماله 12 باحثًا على الأقل، منهم باحثون من مؤسسات في إيران، فرنسا.
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إنشاء ملفي المجاني إضافة منشوراتيمجالات البحث
- Multiple Sclerosis Research Studies
- Dementia and Cognitive Impairment Research
- Parkinson's Disease Mechanisms and Treatments
- Neurological disorders and treatments
- Amyotrophic Lateral Sclerosis Research
المنشورات (60)
- Spontaneous Blink Features Extracted from Video for Multi-Class Classification of Parkinson’s Disease
- Le gène MAPT dans la démence à corps de Lewy : est-t-il un facteur pronostique ?
- Facteurs associés à la résilience dans la sclérose en plaques : étude d’une cohorte tunisienne
- Anomalies des mouvements oculaires dans la maladie de Parkinson : analyse vidéo-oculographique et implications cliniques
- Risque de chute dans les troubles neurocognitifs majeurs : facteurs prédictifs et outils d’évaluation
- Évaluation du wearing-off sous ocrélizumab dans la sclérose en plaques
- Determinants of self-management in Multiple Sclerosis: Insights from a Tunisian cross-sectional study
- Clinical and neuropsychological profile of Alzheimer’s disease in Tunisia and the impact of APOE gene
- Risk factors for hypogammaglobulinemia among people with Multiple Sclerosis treated with Ocrelizumab: A Tunisian experience
- Factors associated with stigma among Tunisian people with Multiple Sclerosis
- Seroprevalence of Epstein–Barr virus in Tunisian patients with multiple sclerosis: Associations with clinical characteristics
- Comparative study of Parkinson’s disease phenotypes in homozygous and heterozygous LRRK2-G2019S mutation carriers
- Impact of APOE and MAPT genetic profile on the cognitive functions among Amyotrophic Lateral Sclerosis Tunisian patients
- Parkinson's Disease Database in the Middle East, North Africa, and South Asia Countries
- Impact of autonomic dysfunction on Multiple Sclerosis characteristics: Insights from a Tunisian cohort study
- Motor and non-motor features in progressive supranuclear palsy: the impact of microtubule associated protein tau haplotypes among a Tunisian cohort
- Lien entre la dysautonomie et la fatigue au cours de la Sclérose en plaques
- Corrélations génotype-phénotype dans le syndrome corticobasal chez les patients tunisiens
- Signes précoces d’évolution vers une maladie de Parkinson chez les patients atteints de tremblement essentiel : étude clinique et neurophysiologique
- Impact du gène GBA sur la survie dans la démence à corps de Lewy
- Usefulness of Neurofilaments in Serum and Cerebrospinal Fluid as Biomarker for Tunisian Patients with Amyotrophic Lateral Sclerosis (P3-11.031)
- Health-related Quality of Life in Tunisian Patients with Paramyotonia Congenita (P3-11.028)
- Neurobrucellosis
- Pursuit Regularity Index for Parkinson's Disease Detection via Videonystagmography
- Effects of music therapy on cognitive and behavioral disorders in major neurocognitive disorders of neurodegenerative origin
- Early-onset and late-onset Alzheimer's disease: Epidemiological and clinical features
- Efficacy and tolerability of a high-intensity functional exercise program in Parkinson's
- Recessive patterns of ALS Tunisian patients and their impact on clinical features
- Sex effect on time to diagnosis in narcolepsy in a Tunisian cohort
- Environmental factors related to multiple sclerosis progression
- Phenotypic Spectrum of Progressive Supranuclear Palsy: Clinical Study and Apolipoprotein E Effect
- The Impact of LRRK2 G2019S on Parkinson’s Disease: Clinical Phenotype and Treatment in Tunisian Patients
- Study of Eye Movements Abnormalities in Epilepsy
- Clinical and molecular predictors of survival among atypical parkinsonian syndromes in a North African tertiary referral center
- Manifestations neurologiques liées aux anti-Zic 4 : entre phénotypes classiques et atypiques
- Facteurs associés aux troubles du sommeil dans la maladie d’Alzheimer
- Étude des troubles motivationnels chez les patients tunisiens atteints de maladie de Parkinson
- Neurofilaments light chains as a diagnostic and predictive biomarker for Tunisian Multiple Sclerosis patients
- 35. Cerebrospinal Fluid and Serum Neurofilament Light Chain Levels at Baseline Predict Disease Activity and Severity in Neuromyelitis Optica Spectrum Disorder Patients
- 74. Impact of Vascular Disease Risk Factors on Multiple Sclerosis
- 28. Relationship between Neurofilament Light Chain levels and Disability Progression in Patients with Multiple Sclerosis
- 77. Sleep Disturbances and Associated Factors in Multiple Sclerosis
- Eye movement study in essential tremor patients and its clinical correlates
- LGMDR1 with Prominent Limb–Joint Contractures and Inflammatory Changes Misdiagnosed as Scleromyositis with a Novel CAPN3 Mutation: A Case Report
- Optineurin in patients with Amyotrophic Lateral Sclerosis associated to atypical Parkinsonism in Tunisian population
- Effect of Fasting on Multiple Sclerosis Symptoms
- Work Difficulties Evaluation in People with Multiple Sclerosis: A Tunisian Study
- Profil cognitif de la sclérose en plaques à début pédiatrique
- Variabilité phénotypique intrafamiliale dans la paramyotonie congénitale
- Facteurs pronostiques précoces dans la myasthénie auto-immune
- Sleep Disorders in Tunisian Patients with Multiple Sclerosis
- Predictors of Survival in Atypical Parkinsonian Syndromes in a Tunisian Cohort (P8-11.006)
- Phenotypic spectrum of progressive supranuclear palsy: clinical study and APOE effect
- Clinical and genetic features in young-adult amyotrophic lateral sclerosis – a Tunisian cohort study
- Arabic adaptation of the Edinburgh cognitive and behavioural Amyotrophic lateral sclerosis screen (ECAS-AR)
- Stroke in Djibouti
- The oligogenic model of amyotrophic lateral sclerosis; phenotypes of three Tunisian families
- Facteurs prédictifs du déclin moteur dans la dystrophie musculaire de Duchenne chez les patients traités par corticoïdes
- Validation de la version arabe de l’Edinburgh Cognitive and Behavioral Amyotrophic Lateral Sclerosis Screen
- Angiopathie amyloïde : étude d’une série tunisienne
مجلات النشر
- Revue Neurologique × 19
- Multiple Sclerosis and Related Disorders × 13
- Journal of the Neurological Sciences × 8
- Journal of Neural Transmission × 3
- Neurology × 3
- Journal of Movement Disorders × 2
المنشورات حسب السنة
- 202612
- 202517
- 202413
- 202312
- 20224
- 20211
- 20201
التعاون العلمي
المؤسسات الشريكة : Manouba University · National Institute of Neurology Mongi-Ben Hamida · Razi University · Razi Hospital · National Engineering School of Tunis
بلدان المؤلفين المشاركين : إيران · فرنسا
المؤلفون المشاركون
- Riadh Gouider
- Alya Gharbi
- Imen Kacem
- Amira Souissi
- Amina Gargouri
- Saloua Mrabet
- Ikram Sghaier
- Amal Atrous
- Amina Nasri
- Amina Gargouri-Berrechid
- Imen Kacem
- Mouna Ben Djebara
البيانات البيبليوغرافية مصدرها OpenAlex (قاعدة مفتوحة).
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