Home › Researcher directory › Samir Blel

Samir Blel

Affiliation : National Institute of Neurology Mongi-Ben Hamida

• 12Publications (affiliation in Tunisia)
• 14Total publications
• 407Citations
• 4h-index

OpenAlex

Research profile

Samir Blel has 12 indexed publications (1993–2022). Their work appears mainly in “Revue Neurologique”, “Journal of the Neurological Sciences” and “Neurology”. Their most cited article, “Linkage of a locus (CMT4A) for autosomal recessive Charcot-Marie-Tooth disease to chromosome 8q” (1993), has been cited 180 times. 7 of these publications date from the last three years of activity. Their work is co-authored with at least 12 researchers.

Is this you? Get your research seen

Create your free DzCademia profile and add your articles: they will show up more easily on Google and in AI assistants like ChatGPT, so more people can read and cite your work.

Create my free profile Add my publications

Research areas

• Dementia and Cognitive Impairment Research
• Hereditary Neurological Disorders
• Alzheimer's disease research and treatments
• Multiple Sclerosis Research Studies
• Acute Ischemic Stroke Management

Publications (12)

• Myoclonus status revealing COVID 19 infection
  2022 · Seizure · cited 11 times
• Étude d’association entre les polymorphismes des gènes ApoE et TREM2 et la maladie d’Alzheimer dans une population tunisienne
  2022 · Revue Neurologique
• Encéphalopathies de Gayet–Wernicke : étude d’une cohorte tunisienne de 20 patients
  2022 · Revue Neurologique
• Étude du polymorphisme de l’ApoE dans les démences chez une population tunisienne
  2021 · Revue Neurologique
• Une ataxie aiguë révélant une thrombose veineuse cérébrale : à propos de 2 cas
  2021 · Revue Neurologique
• Efficacy of fingolimod in the 2nd line treatment of active relapsing-remitting multiple sclerosis: About a Tunisian cohort of 50 patients
  2021 · Journal of the Neurological Sciences
• Neurological manifestations of coeliac disease: A case report
  2021 · Journal of the Neurological Sciences
• Accident vasculaire cérébral ischémique du sujet jeune : principales étiologies
  2019 · Revue Neurologique · cited 1 times
• A comparative study of the clinical and electrophysiological features between Friedreich ataxia and Ataxia with isolated vitamin E deficiency in Tunisia (P1.064)
  2018 · Neurology · cited 1 times
• Ataxia with Oculomotor Apraxia 2 : Clinical and Genetic study of 17 patients (P5.081)
  2018 · Neurology
• Troubles cognitifs dans la sclérose en plaques : rôle de la dépression
  2015 · Revue Neurologique
• Linkage of a locus (CMT4A) for autosomal recessive Charcot-Marie-Tooth disease to chromosome 8q
  1993 · Human Molecular Genetics · cited 180 times

Publication venues

• Revue Neurologique × 6
• Journal of the Neurological Sciences × 2
• Neurology × 2
• Seizure × 1
• Human Molecular Genetics × 1

Publications per year

• 20223
• 20214
• 20191
• 20182
• 20151
• 19931

Collaborations

Partner institutions : Faculté de médecine de Tunis · Hôpital Charles-Nicolle · Tunis University

Co-authors

• Samia Ben Sassi
• Fatma Nabli
• Zakaria Saied
• Cyrine Jeridi
• Cyrine Jridi
• Saloua Fray
• Rania Zouari
• Fayçal Hentati
• Haifa Kharrat
• Afef Achouri-Rassas
• Ichrak Ghachem
• Emine Rachdi

Bibliographic data from OpenAlex (open database).