الرئيسية › دليل الباحثين › Fatma Nabli
Fatma Nabli
الانتماء : National Institute of Neurology Mongi-Ben Hamida
- 85منشورات (انتماء تونسي)
- 101مجموع المنشورات
- 450الاستشهادات
- 9مؤشر h
الملف البحثي
لدى Fatma Nabli 85 منشور(ات) مفهرسة (2010–2026). تُنشر أعماله أساسًا في «Revue Neurologique»، «Journal of the Neurological Sciences» و«Multiple Sclerosis and Related Disorders». أكثر مقالاته استشهادًا هو «A comparative study of Parkinson's disease and leucine-rich repeat kinase 2 p.G2019S parkinsonism» (2013)، وقد استُشهد به 95 مرة. 27 من هذه المنشورات تعود إلى آخر ثلاث سنوات من النشاط. شارك في تأليف أعماله 12 باحثًا على الأقل.
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إنشاء ملفي المجاني إضافة منشوراتيمجالات البحث
- Peripheral Neuropathies and Disorders
- Multiple Sclerosis Research Studies
- Parkinson's Disease Mechanisms and Treatments
- Hereditary Neurological Disorders
- Neurological disorders and treatments
المنشورات (85)
- LRRK2 G2019S as a shared mutation in two distinct double-mutant Parkinson's disease cases: First cases from Tunisia
- Favorable seizure control with a gluten-free diet in a patient with drug-resistant epilepsy and celiac disease: a case report
- EVALUATION DE L’APPORT DES SCORES PROBABILISTES À L’ IRM DANS LE DIAGNOSTIC D’HYPOTENSION INTRA CRÂNIENNE
- AB-392. Myasthenia Gravis: Factors associated with altered quality of life in a Tunisian cohort
- PO 92 Acute-Onset Chronic inflammatory demyelinating polyneuropathy Mimicking Guillain-Barré Syndrome: Clinical and Electrophysiological Insights
- PO 93 Chronic inflammatory demyelinating polyneuropathy: clinical spectrum, electrophysiological features, and treatment outcomes in a Tunisian cohort
- Un lymphome à grandes cellules B révélé par une méningomyélite : à propos d’un cas clinique
- Phénotype moteur et non moteur de la maladie de Parkinson liée à la mutation G2019S sur le gène LRRK2
- Chorea associated with vitamin B12 deficiency in adults: a case report and review of literature
- Dépression et anxiété dans la maladie de parkinson familiale : fréquence et facteurs pronostiques
- Profil cognitif associé à la maladie de Parkinson familiale : à propos d’une cohorte tunisienne
- Guillain-Barré Syndrome After COVID19 Vaccination: A Single-Center Study in Tunisia and 1 Year Follow-Up
- Sexual dysfunction in G2019S LRRK2 Parkinson's disease
- Fatigue in multiple sclerosis: Exploring its prevalence and impact on mental health and quality of life
- Occurrence of myasthenia gravis with myotonic dystrophy
- PINK1-associated Parkinson's disease: Motor and non-motor signs
- Depression in multiple sclerosis: Prevalence and impact on quality of life in Tunisian patients
- Spinal cord ischemia: A descriptive study of clinical features, risk factors and outcomes
- Anxiety in multiple sclerosis: An invisible symptom with powerful impact
- Characterizing tremor in chronic inflammatory demyelinating polyneuropathy: Clinical and electrophysiological insights
- Cerebral large vessels vasculitis following Guillain-Barré syndrome as first clinical manifestations of primary Sjogren's syndrome: A case based – Review
- 114. Prognosis Predictors in Neuromyelitis Optica Spectrum Disorder: A Tunisian Cohort Study
- Myopathies inflammatoires idiopathiques : apport de la biopsie neuromusculaire
- Troubles du sommeil dans la maladie de Parkinson : lien avec la sévérité de la maladie et les autres signes non-moteurs
- Une neuro-sarcoïdose révélée par un tableau psychotique : une présentation inhabituelle
- 116. Late-onset Neuromyelitis Optica Spectrum Disorders: Clinical, Radiological Features and Prognostic Factors
- 158. The Impact of Natalizumab on Neuropsychological Function in Multiple Sclerosis Patients
- Sexual dysfunction and motor disability in Parkinson’s disease: any link?
- Genetic heterogeneity within a consanguineous family involving TTPA and SETX genes
- Toxic encephalopathy after an overdose of cocaine : a case serie
- Cerebral large vessels vasculitis following Guillain-Barré syndrome as first clinical manifestations of primary Sjogren’s syndrome : a case report and review of the literature
- Neuromyelitis Optica Spectrum Disorder: Clinical, Radiological Features of Seropositive Patients
- Factors Associated with Fatigue in Neuromyelitis Optica Spectrum Disorder in a Tunisian Cohort
- Factors Associated with Altered Quality of Life in Neuromyelitis Optica Spectrum Disorder in a Tunisian Cohort
- Factors Associated with Neuropathic Pain in Neuromyelitis Optica Spectrum Disorder in a Tunisian Cohort
- Spinal cord ischemia in beta thalassemia major
- Neurosarcoidosis: Clinical aspects and diagnostic challenges
- Neurological manifestations of creatine transporter deficiency: Two case reports
- Myoclonus status revealing COVID 19 infection
- B Cells Specific CpG Induces High IL-10 and IL-6 Expression In Vitro in Neuro-Behçet’s Disease
- Atypical anti-NMDA receptor encephalitis associated with varicella zoster virus infection
- A Tunisian patient with CLCN2 ‐related leukoencephalopathy
- Imaging of Central Nervous System Tuberculosis
- Les manifestations neurologiques associées à la maladie cœliaque
- Extending brainstem and capsule-thalamic lesions in a patient with parenchymal neuro-Behçet disease
- Letter to editor response: Why myoclonus is linked to COVID19 infection, not to anti-COVID 19 vaccine
- Myasthenia gravis and COVID‐19: A case series and comparison with literature
- Acquired pial arteriovenous fistula secondary to cerebral cortical vein thrombosis: A case report and review of the literature
- Neuromyelitis optica and concomitant pulmonary tuberculosis: a case report
- Une ataxie aiguë révélant une thrombose veineuse cérébrale : à propos de 2 cas
- Association rare de myasthénie et lymphome lymphoblastique à cellules T(LLCT) : à propos d’un cas
- Post-abortum Anti-N-Methyl-D-aspartate encephalitis mimicking herpetic encephalitis: a case report and literature review
- Efficacy of fingolimod in the 2nd line treatment of active relapsing-remitting multiple sclerosis: About a Tunisian cohort of 50 patients
- Corpus callosum lesion as the main clinical and radiological expression of Neurobehçet: A case report
- Primary Spinal Hydatidosis Revealed by Spinal Cord Compression
- Radiculopathie et malformation de la veine cave inférieure : un lien improbable
- Le spectre de la neuromyélite optique : caractéristiques épidémiologiques et cliniques d’une série Tunisienne
- Stroke in the Middle-East and North Africa: A 2-year prospective observational study of stroke characteristics in the region—Results from the Safe Implementation of Treatments in Stroke (SITS)–Middle-East and North African (MENA)
- Stroke revealing Neuro-Behçet's disease with parenchymal and extensive vascular involvement
- Les troubles neurologiques par carence en vitamine B12 : à propos de 17 cas
- Disability progression in multiple sclerosis: a Tunisian prospective cohort study
- Neuromyélitie optique (NMO) et spectre NMO (SNMO) : caractéristiques cliniques, radiologiques et évolutives d’une série Tunisienne
- A comparative study of the clinical and electrophysiological features between Friedreich ataxia and Ataxia with isolated vitamin E deficiency in Tunisia (P1.064)
- Caractéristiques cliniques ; électrophysiologiques et évolutives des formes atypiques de l’ataxie héréditaire de Friedreich : à propos sept cas
- Syndrome de Parinaud aigu : à propos d’un cas
- Ataxia with Oculomotor Apraxia 2 : Clinical and Genetic study of 17 patients (P5.081)
- DNM3 and genetic modifiers of age of onset in LRRK2 Gly2019Ser parkinsonism: a genome-wide linkage and association study
- AVC ischémique révélant la maladie de Takayasu : à propos d’un cas et revue de la littérature
- Un syndrome parkinsonien typique comme première manifestation d’une atteinte neurologique au cours de la maladie de Behçet
- Hypotension intracrânienne spontanée associée à une syringomyélie
- Motor phenotype of LRRK2‐associated Parkinson's disease: A tunisian longitudinal study
- Pseudotumoral brain lesion as the presenting feature of primary Sjögren's syndrome
- A comparative study of Parkinson's disease and leucine-rich repeat kinase 2 p.G2019S parkinsonism
- Autonomic dysfunction in Tunisian patients with Parkinson's disease
- Une dysphagie révélant une myosite à anticorps antisynthétases
- Clinical features of myelopathies: A cohort study in Tunisia
- Cryoglobulinaemia and peripheral neuropathy
- Clinical manifestations of chronic inflammatory demyelinating polyradiculoneuropathies: A retrospective study of fourty cases
- Clinical and epidemiological profile of Guillain–/INS;Barre syndrome in Tunisia
- Neurosarcoidosis: A Tunisian case series
- Clinical and Molecular Findings of Ataxia With Oculomotor Apraxia Type 2 (AOA2) in 5 Tunisian Families
- Myélopathie chronique révélant une infection à VIH : à propos d’une observation
- Cognitive dysfunction in Tunisian LRRK2 associated Parkinson’s disease
- Cerebral Venous Thrombosis Presenting With Cerebellar Ataxia and Cortical Blindness
- Cerebral venous thrombosis in inflammatory bowel disease: a case series
مجلات النشر
- Revue Neurologique × 20
- Journal of the Neurological Sciences × 20
- Multiple Sclerosis and Related Disorders × 7
- Clinical Neurophysiology × 3
- Parkinsonism & Related Disorders × 2
- La Revue de Médecine Interne × 2
المنشورات حسب السنة
- 20268
- 202512
- 20247
- 202311
- 20228
- 20218
- 20203
- 20193
- 20186
- 20163
التعاون العلمي
المؤسسات الشريكة : Faculté de médecine de Tunis · Tunis El Manar University · Tunis University · Hôpital La Rabta · Centre of Biotechnology of Sfax
المؤلفون المشاركون
- Samia Ben Sassi
- Rania Zouari
- Amine Rachdi
- Zakaria Saied
- Dina Ben Mohamed
- Fayçal Hentati
- Samir Belal
- Cyrine Jeridi
- Anissa Azza Mousli
- Mourad Zouari
- Fayçel Hentati
- Ben Sassi Samia
البيانات البيبليوغرافية مصدرها OpenAlex (قاعدة مفتوحة).
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